Brain Changes Occur in Mentally Ill Who Have Never Been Medicated
People with schizophrenia may have different brain structure for two reasons
1. The illness itself. These changes are not associated with taking medications.
2. The antipsychotic medications used to treat the illnesses. These changes can explain why the medicines work or could be a side-effect of the medication.
These two articles explain changes that are due to the disease and changes that are due to medications.
Schizophrenia changes brain structure: A Review of Studies of Individuals with Schizophrenia Never Treated with Antipsychotic Medications
By E. Fuller Torrey, M.D.
Stanley Medical Research Institute
5430 Grosvenor Lane, Suite 200, Bethesda, MD 20814-2142
A review of 56 studies of individuals with schizophrenia who had never been treated with antipsychotic medications indicates significant abnormalities in brain structure and function. Neurological and neuropsychological measures show the most consistent and largest group differences between those affected and normal controls. Measures of structural differences and cerebral metabolic function are significant but less impressive. Electrophysiological differences also are found, but most such studies are older and have methodological problems. The brain abnormalities implicate a variety of interrelated brain regions, primarily the medial temporal, prefrontal, thalamic, and basal ganglia areas. It is concluded that schizophrenia is a brain disease in the same sense that Parkinson’s disease and multiple sclerosis are, and that the brain abnormalities in schizophrenia are inherent in the disease process and not medication-related. The challenge for the future is to use the new molecular techniques to study these brain areas and elevate our understanding of schizophrenia’s etiology to the next level.
One of the defining characteristics of 20th-century psychiatry was an ongoing controversy regarding the nature of schizophrenia. Sociologists, psychologists, psychoanalysts, family interaction theorists, geneticists, and a variety of neuroscientists all weighed in, often generating more heat than light. Szasz (1976) even claimed that schizophrenia does not exist but is merely “the sacred symbol of psychiatry.”
In recent years, as evidence has accumulated that there are abnormalities in brain structure and function in individuals with schizophrenia, the controversy has shifted. Critics of psychiatry have argued that, insofar as brain abnormalities do exist, they are caused by the use of antipsychotic medications. Breggin (1991), for example, claimed: “Dozens of studies have since come out indicating that neuroleptic-treated patients have such severe brain damage that it can be detected as shrinkage of the brain on the newer radiology techniques, such as the CT scan….”
Such views have been widely cited by Scientologists and other antipsychiatry advocates and continue to be repeated in the media. For example, science journalist Robert Whitaker, in his 2002 book Mad in America, described schizophrenia as “a term being loosely applied to people with widely disparate emotional problems” and asserted that most of the symptoms of schizophrenia are induced by antipsychotic medications:
The image we have today of schizophrenia is not that of madness—whatever that might be—in its natural state. All of the traits that we have come to associate with schizophrenia—the awkward gait, the jerking arm movements, the vacant facial expression, the sleepiness, the lack of initiative—are symptoms due, at least in large part, to a drug-induced deficiency in dopamine transmission. (Whitaker, 2002)
The best way to ascertain the validity of such claims is to examine studies of schizophrenia carried out on individuals who have never been treated with antipsychotic medications. At least 56 such studies now exist; they can be grouped into those examining structural, neurological, neuropsychological, electrophysiological, and cerebral metabolic abnormalities of the brain.
Structural Abnormalities In People with Mental Illness Never Treated with Antipsychotics.
- Structural abnormalities of the brains of individuals with schizophrenia have been observed for two centuries. Haslam, who examined the brains of individuals with insanity after their deaths, reported in 1809 that in many cases “the lateral ventricles were very much enlarged” (Haslam, 1809). Hecker (1871) in Germany and Southard (1915) in the United States made similar observations; the latter reported moderate or marked hydrocephalus in 8 of 25 consecutive cases of schizophrenia autopsied.
- Following the development of pneumoencephalography in the 1920s, Jacobi and Winkler (1927) used this technique on 19 patients with schizophrenia and reported that 18 of them had enlarged cerebral ventricles. Table 1 summarizes other pneumoencephalographic studies carried out on individuals with schizophrenia prior to the introduction of antipsychotic medications. Some of the patients had been previously treated with electro-convulsive therapy (ECT), but Huber (1957) specifically compared those who had had ECT and those who had not and reported no difference in the ventricular size.
- Since the introduction of CT and MRI technology, over 200 studies have examined brain structure in individuals with schizophrenia. It is now known that such studies require an adequate control group, since some psychiatrically normal individuals also have structural changes in their brains (Buckley et al., 1992). It is also known that antipsychotic medications may increase the size of the basal ganglia and thalamus (Chakos et al., 1994; Gur et al, 1998), so structural studies should be carried out, whenever possible, on individuals who have never been treated with antipsychotic medications. Such studies have examined various brain structures in seven different groups of patients (Schulz et al., 1983; Lieberman et al., 1992, Degreef et al., 1992, Chakos et al., 1994; Shihabuddin et al., 1998; Keshaven et al., 1998, 2002; Corson et al., 1999; Gur et al., 1998, 1999, 2000a, 2000b; McCreadie et al., 2002).
- Ventricular size was assessed for four of these groups. Schulz et al. (1983), using CT, compared 8 never-treated adolescents with schizophrenia and 18 normal controls; 7 of the 8 had enlarged ventricles, defined as “larger than the value of the mean plus two standard deviations of the control group.” Lieberman et al. (1992), using MRI to compare 62 never-treated patients with 42 normal controls, reported enlarged ventricles in 18 percent of the former and 2 percent of the latter (p<0.05). Gur et al. (1999 and personal communication 2002), using MRI to compare 33 never-treated patients with 65 normal controls, reported a 16 percent increase in ventricular volume in the patients (p=0.052, t test, 2-tailed). McCreadie et al. (2002), using MRI to compare 42 never-treated patients with 31 normal controls, reported a 20 percent increase in total ventricular (right and left) volume (p=0.098, t test, 2-tailed). Thus, modern studies, using CT and MRI, have confirmed older studies, using pneumoencephalography, showing increased ventricular size in individuals with schizophrenia who have never been treated.
- Studies of other cerebral structures have been less conclusive. Within the basal ganglia, six studies have been done on the size of the caudate; three of these reported it to be significantly smaller in never-treated patients (Keshaven et al., 1998; Shihabbudin et al., 1998; Corson et al., 1999), one reported a trend in this direction for total caudate and a significant decrease for left caudate alone (McCreadie et al., 2002), and two other studies reported no differences between patients and controls (Chakos et al., 1994; Gur et al., 1998 and personal communication 2002). A significant increase in the size of the globus pallidus was reported by Gur et al. (1998 and personal communication 2002) (p=0.024, t test, 2-tailed). Gur et al. (1998 and personal communication 2002) also found a trend toward an increase in the size of the putamen (p=0.064), whereas Keshaven et al. (1998) reported a trend in the opposite direction.
- A single study measured the size of the thalamus in never-treated patients. Gur et al. (1998 and personal communication 2002), comparing 42 patients and 94 normal controls, reported a 10 percent reduction in the thalamus in the patients (p=0.042, t test, 2-tailed).
- Examining cortical structures, Lieberman et al. (1992), comparing 62 never-treated patients with 42 normal controls, found that 24 percent of the patients and 7 percent of the controls had “questionable” or “abnormal” frontal/parietal cortex (p<0.05), and that 44 percent of the patients and 21 percent of the controls had “questionable” or “abnormal” medial temporal structures (p<0.01). Gur et al. (1999, 2000a, 2000b, personal communication 2002), comparing up to 36 never-treated patients with up to 62 normal controls, assessed gray and white matter volume on a variety of frontal and temporal lobe regions. Although the gray matter was reduced in most regions in the patient group compared to the controls, the differences achieved statistical significance only for the lateral dorsal prefrontal area (p=0.02, t test, 2-tailed).
- Finally, two studies have looked at the incidence of cavum septum pellucidum, a structural abnormality of the brain membranes. Degreef et al. (1992) found such abnormalities in 14 of 62 (23%) never-treated individuals with schizophrenia compared to 1 of 46 (2%) controls (p<0.02). However, Keshaven et al. (2002), comparing 40 never-treated patients and 59 normal controls, found no difference in the incidence of this structural abnormality between the groups.
Neurological Abnormalities Abnormalities In People with Mental Illness Never Treated with Antipsychotics.
A wide variety of neurological abnormalities have been reported in individuals with schizophrenia who have never been treated with antipsychotic medications. These include dyskinesias, parkinsonian or extrapyrimidal signs, neurological soft signs, and decreased pain perception.
Dyskinesias occur spontaneously in individuals with schizophrenia and may also be caused by antipsychotic medications; the latter is called tardive dyskinesia. Dyskinesias in schizophrenia most commonly include involuntary movements of the tongue or mouth (oro-facial dyskinesias) or the upper limbs.
Prior to the introduction of antipsychotic medications, dyskinesias were frequently described as occurring in individuals with schizophrenia. Turner (1989), in a review of the records of over 600 individuals in an English asylum between 1850 and 1890, reported that “movement disorder, often equivalent to tardive dyskinesia, was noted in nearly one-third of schizophrenics.” Kraepelin, in his 1919 textbook on schizophrenia, provided an extended description of dyskinesia, and in the ensuing decades other psychiatrists elaborated on it. For example, in 1926, Reiter described 10 cases of schizophrenia with “marked and well-observed motor disturbances” such as “peculiar twitchings of the facial muscles” and “myoclonic jerkings of forearms and hands” (Reiter, 1926). Similarly, Farran-Ridge (1926) noted that “choreiform manifestations” were frequently observed in individuals with schizophrenia: “Of these, by far the commonest are all those spasmodic movements of expression which are grouped together under the heading of ‘making faces’ or ‘grimacing’.” In a review of pre–antipsychotic medications–era studies, Casey and Hansen (1984) concluded: “The question is not whether these types of abnormal movements occurred prior to the drug treatment era. They surely did. Rather, it is a question of how much of what is now called ‘neuroleptic-induced TD’ should actually be attributed to the natural history of psychosis, aging, or other nondrug causes.”
Between 1959 and 1984, at least 29 studies assessed the prevalence of dyskinesia in individuals with schizophrenia who had not been treated with antipsychotic drugs. One review of these studies concluded that the prevalence of spontaneous dyskinesias was 4.2 percent (Casey and Hansen, 1984); another review of a subset of these studies came to a similar conclusion of 5 percent (Kane and Smith, 1982). Much of the variation among studies can be attributed to the use of different scales and thresholds in the measurements.
More recently published studies of dyskinesias in individuals with schizophrenia who had never been treated with antipsychotic medications are summarized in Table 2. The average dyskinesia prevalence rate of 12 percent is modestly above the conclusions of earlier studies, possibly because more older patients were included in the recent studies and it is known that spontaneous dyskinesias increase with age (Fenton, 2000). Another confounding factor is that some of the study patients had been previously treated with ECT and/or insulin shock, including more than half the patients in the Fenton et al. (1997) study. The authors examined this issue and noted that “exposure to such treatments was not significantly related to the presence or absence of movement disorders in these samples.” If this study is deleted from the list of recent studies, the average prevalence of spontaneous dyskinesias in the other recent studies is 23/278, or 8 percent.
The rate of tardive dyskinesia in individuals with schizophrenia who have been treated with antipsychotic medications has been estimated to be 15–20 percent in most studies (Casey and Hansen, 1984; Gerlach and Casey, 1988), although it increases over the age of 60. Thus, it appears that one-quarter to one-third of that prevalence is attributable to spontaneous dyskinesias and is not medication-related. The true prevalence of tardive dyskinesia, i.e., related to antipsychotic medications, is therefore no higher than 15 percent. As summarized by Khot and Wyatt (1991): “Not all that moves is tardive dyskinesia.”
Parkinsonian Signs In People with Mental Illness Never Treated with Antipsychotics.
Parkinsonian or extrapyrimidal motor signs were noted in individuals with schizophrenia for many years before antipsychotic medications were introduced. Kraepelin, in 1919, described patients with rigidity and bradykinesia as well as those with a tremor (Kraepelin, 1919). Similarly, in 1926, Reiter described patients with schizophrenia with a “well-defined parkinsonian syndrome, which overshadows all other symptoms” (Reiter, 1926).
Since 1993, six studies have been published that assessed parkinsonian motor signs in individuals with schizophrenia who had never been treated with antipsychotic medications (Table 3). Rigidity, bradykinesia, and tremor were assessed in three studies using the Simpson-Angus Scale and in three using the Extrapyrimidal Symptom Rating Scale. A total of 82 out of 353 patients (23 percent) showed some combination of parkinsonian signs.
Neurological Soft Signs In People with Mental Illness Never Treated with Antipsychotics.
It has become customary in neurology to divide neurological abnormalities into “hard” signs, such as the patellar tendon reflex, and “soft” signs, such as being unable to identify a coin in one’s hand without looking at it (astereognosis). In the former, it is often possible to specify which part of the brain is affected, while the latter represent more complex brain functions. Heinrichs and Buchanan (1988), in a lucid discussion of neurological soft signs, claimed that they involve impairments in “three higher-order functional areas: the integration of more complex sensory units, the coordination of motor activity, and the sequencing of motor patterns.” Neurological soft signs are found in a variety of central nervous system (CNS) disorders, including dyslexia and attention-deficit/hyperactivity disorder (ADHD), and are less commonly found in individuals with no known CNS disorder.
Seven studies have assessed neurological soft signs in individuals with schizophrenia who had never received antipsychotic medications (Table 4). In all five studies that included normal controls, the never-treated patients had significantly more soft signs. Five of the studies also compared never-treated and treated patients; in three studies the two groups had approximately the same degree of neurological dysfunction, and in the other two studies the treated patients had higher scores, suggesting that antipsychotic medications also contribute to neurological dysfunction.
These findings are consistent with more than 50 studies that have reported that individuals with schizophrenia who are being treated with medications have significantly more neurological soft signs than normal controls. The present studies suggest that antipsychotic medications are not the main cause of the neurological abnormalities but rather a contributing cause. This confirms previous reports that whether patients were on or off medications at the time of testing had little effect on the presence of neurological soft signs (Manschreck et al., 1982; Kolakowska et al, 1985). It also confirms the schizophrenia twin study by Mosher et al. (1971) that concluded that “total previous drug intake … did not correlate significantly with the two neurologic scores.”
Decreased pain perception In People with Mental Illness Never Treated with Antipsychotics.
Anecdotal accounts of decreased pain perception, occasionally accompanied by self-mutilation, are abundant in historical accounts of schizophrenia from the years before antipsychotic medications were introduced. In the 1798 edition of his textbook, Haslam noted that “in many cases of insanity there prevails a great degree of insensibility, so that patients have appeared hardly to feel … the application of blisters or the operation of cupping” (Haslam, 1798). In the 1809 edition, Haslam added a description of an insane patient who amputated his own penis (Haslam, 1809). Similarly, Esquirol in 1838 described cases of insanity in which “pain may cease altogether, or be changed into a state of well-being. We see mad men frequently commit horrid mutilations with very blunt instruments, sometimes with red hot iron, without exhibiting the least symptom of pain, but, on the contrary, the strongest appearances of pleasure” (anonymous, 1838).
In the 20th century, Kraepelin (1919) observed that “patients often become less sensitive to bodily discomfort … pricks of a needle, injuries, without thinking much about it; burn themselves with their cigar…” Kraepelin’s observation was followed by numerous similar reports, and by 1930 it was observed that “nearly every textbook of psychiatry mentions that the reaction to pain in catatonics is incomplete or absent” (Bender and Schilder, 1930). Two studies of psychotic patients who had sustained myocardial infarctions noted that 87 percent (Lieberman, 1955) and 83 percent (Marchand, 1955) of them did not complain of pain. In a study in a large Veterans Administration Hospital, in which 79 percent of the residents were diagnosed with schizophrenia, pain appeared to be absent in 21 percent of patients with an acute perforated ulcer, 37 percent of patients with acute appendicitis, and 41 percent of patients with a fractured femur. As the authors noted: “The lack of complaint of pain by psychotic patients when afflicted by painful disorders has been an observation of every physician practicing in a mental institution” (Marchand et al., 1959).
For ethical reasons, it would not be possible today to do research on the pain threshold of individuals with schizophrenia. Such studies were, however, carried out prior to the introduction of antipsychotic medications. For example, Stengel et al. (1955) studied 13 individuals with schizophrenia and reported that they had decreased pain perception for pin-prick or pressure. Malmo et al. (1951) subjected 17 individuals with schizophrenia to “thermal stimulations” to the forehead, asking each to press a button “when he felt that the stimulus was about to become painful.” The individuals with schizophrenia had a much “lower responsiveness to the pain stimulus” than individuals with psychoneuroses or normal controls. Hall and Stride (1954) carried out a similar study of 14 individuals with schizophrenia and also reported that “the overall results for the group show a very high [threshold for] V.R.P. [verbal report of pain] and P.R.P. [pain reaction point].”
The incidence of having a decreased pain threshold in individuals with schizophrenia is unknown. A questionnaire to members of the National Schizophrenia Fellowship in England reported that 16 percent said they had “insensitivity to pain” (Tyler, 1995). Anecdotal evidence also suggests that some individuals with schizophrenia may have the opposite and be unusually sensitive to pain and/or suffer from paresthesias, e.g., a feeling that insects are crawling on one’s skin.
The mechanism responsible for decreased pain perception in individuals with schizophrenia is not known but most likely includes the thalamus, for which neuropathological abnormalities have been reported. In recent years, some observers (Fishbain, 1982; Guieu et al., 1994) have suggested that the decreased pain perception is a consequence of antipsychotic medications but, given the previous studies carried out prior to the use of such medications, this is unlikely. Brain endorphins and opiates have also been suggested as being involved. Finally, there is a lively debate whether individuals with schizophrenia do not feel the pain, or feel the pain but underreact; this debate is well summarized by Dworkin (1994).
Neuropsychological Abnormalities In People with Mental Illness Never Treated with Antipsychotics.
Haslam, in his 1809 Observations on Madness and Melancholy, observed that recent memory was often impaired in individuals with insanity:
In persons of sound mind, as well as in maniacs, the memory is the first power which decays; and there is something remarkable in the manner of its decline. The transactions of the latter part of life are feebly recollected, whilst the scenes of youth and of manhood, remain more strongly impressed. (Haslam, 1809)
Over the ensuing century and a half, anecdotal accounts continued to describe memory and other neuropsychological deficits in individuals diagnosed with insanity, dementia praecox, and schizophrenia.
In the 1940s, Rapaport and his colleagues carried out extensive neuropsychological testing on hospitalized patients with schizophrenia. Their two-volume report concluded that patients with schizophrenia differed markedly both from normal controls and from patients with depression on many neuropsychological tests, including “association thought processes” and “loose sortings, syncretistic, fabulated, or symbolic definitions” (Rapaport, 1946).
In recent years, four studies have reported neuropsychological test results in individuals with schizophrenia never treated with antipsychotic medications (Table 5). Saykin et al. (1994), studying 37 antipsychotic-naïve individuals with schizophrenia, reported “generalized impairment of approximately 2 SD units magnitude relative to healthy controls,” with the greatest difference seen on tests of verbal memory and learning. They concluded that “this pattern is evident already in patients experiencing FE [first episode] of psychosis, who have never been exposed to neuroleptics.”
Censits et al. (1997), comparing 30 first-episode patients (of which 28 were antipsychotic-naïve) to 30 previously treated patients and 38 normal controls, reported that “patients’ neuropsychological performance was equally impaired for first-episode [antipsychotic-naïve] and previously treated patients.” The data in this study were reanalyzed by Ragland to include only the 28 antipsychotic-naïve patients in the 30 first-episode group (Ragland, personal communication 2002); maximum deficits in the patients were seen for tests of abstraction, attention, verbal memory, spatial memory, and language abilities (p<0.0000 for each).
McCreadie et al. (1997), comparing 19 antipsychotic-naïve patients to 55 normal controls, reported that memory was most impaired and that the degree of memory impairment correlated with the severity of the patients negative symptoms. Lussier and Stip (2001), comparing 16 antipsychotic-naïve patients to 20 normal controls, found that the patients were “mildly impaired” and that tests of attention were most affected.
In addition to these four neuropsychological studies utilizing exclusively antipsychotic-naïve patients, two other studies included a subset of antipsychotic-naïve patients and reported that this subset did not differ on neuropsychological testing from patients who had been treated with medications. Mohamed et al. (1999) included 77 antipsychotic-naïve patients with 21 others who had received medications and compared them to 305 normal controls on a broad neuropsychological test battery. The patients displayed “substantial impairments in most aspects of cognition,” especially on tests of memory, speeded cognitive tasks, attention, social cognition, and executive skills (e.g., sequencing, organization, and flexibility). Similarly, Riley et al. (2000) included 15 antipsychotic-naïve patients with 25 other first-episode patients and compared them to 22 matched controls. The patients showed “significant impairment on tasks of executive function, verbal learning, delayed recall from non-verbal memory, and psychomotor speed.”
It should be noted that these neuropsychological studies of individuals with schizophrenia who have never been treated with antipsychotic medications yield results remarkably similar to neuropsychological studies of patients who have been treated with antipsychotic medications for varying lengths of time. Between 1980 and 1997, 204 such studies were published, covering 7,420 individuals with schizophrenia and 5,865 normal controls. In their analysis of these studies, Heinrichs and Zakzanis (1998) reported that deficits of memory, attention, and executive function were most prominent. Studies of medicated, previously medicated, and never medicated patients thus yield similar results, suggesting that antipsychotic medications have relatively little effect on most neuropsychological functions. This conclusion is also consistent with Mortimer (1997), who noted that “the effects of conventional neuroleptics on cognition in schizophrenia are minor according to numerous studies.”
Electrophysiological Abnormalities In People with Mental Illness Never Treated with Antipsychotics.
The most common way to assess electrophysiological function in individuals with schizophrenia is with an electroencephalogram (EEG). EEGs have been used for psychiatric research since the early 1930s. Between 1941 and 1954, five EEG studies of individuals with schizophrenia were carried out in which normal control groups were also included. An additional study by Colony and Willis (1956) is not included in this analysis because it is unclear whether or not the patients with schizophrenia were being medicated and also because the “control” group consisted of other psychiatrically hospitalized patients, including those diagnosed with schizoid personalities and paranoid states.
Evaluation of EEG tracings is somewhat subjective. Thus, estimates of abnormal EEGs among groups of normal controls done at that time ranged from 5 to 20 percent (Ellingson, 1954). As summarized by Chamberlain and Russell (1952): “In general, while the proportion of subjects with abnormal EEGs varies with the group selected for study, it probably does not exceed 15 percent in the general population, and 10 percent probably is a fair approximation.”
All five controlled studies of EEGs on individuals with schizophrenia carried out prior to the introduction of antipsychotic medications reported significantly more abnormal EEGs in the patients. As shown in Table 6, the rate of abnormal EEGs in these studies ranged from 28 to 44 percent. It is noteworthy that no single pattern of abnormality was found. A 1952 study of 100 patients with schizophrenia of varying degrees of severity reported that “abnormal electroencephalograms were quite definitely more frequent in the group of cases in which the psychopathologic process was most severe” (Kennard and Levy, 1952).
In addition to the above EEG studies using scalp electrodes, at least two groups carried out studies using deeply implanted electrodes in the years before the introduction of antipsychotic medications. Heath and his colleagues studied 26 patients with schizophrenia and reported spike abnormalities in the septal region and secondarily in the hippocampus and amydgala; such spikes were not found in nonpsychotic patients being treated for conditions such as chronic pain or Parkinson’s disease (Heath and Walker, 1985). Similarly, Peterson et al. (1953) used depth electrodes on four individuals with schizophrenia and reported abnormal electrical activity in the “deep frontal” and “subthalamic” regions.
In more recent years, many researchers have reported abnormal EEG activity in individuals with schizophrenia, but in almost all cases, they had been treated previously with antipsychotic medications. One exception to this was a sleep EEG study carried out on 8 individuals with schizophrenia and 16 normal controls. Compared to the controls, the patients showed diminished slow-wave sleep that was inversely “correlated with the severity of negative symptoms” (Ganguli et al., 1987).
Cerebral Metabolic Abnormalities In People with Mental Illness Never Treated with Antipsychotics.
The measurement of cerebral activity is comparatively new and technically complex. Three ways of doing this are by positron emission tomography (PET), single photon emission computed tomography (SPECT), and functional magnetic resonance imaging (fMRI). Since it is known that antipsychotic medications can affect these tests (Loeber et al., 2002), it is important to use individuals who have not been treated, whenever possible.
To date, seven small studies have demonstrated metabolic abnormalities in individuals with schizophrenia never treated with antipsychotic medications (Table 7). Three of the studies used fMRI, three used PET, and one used SPECT. Representative of these studies is that by Barch et al. (2001), in which 14 antipsychotic-naïve individuals with schizophrenia, compared to 12 normal controls, failed to activate the dorsolateral prefrontal cortex (DLPFC) in response to neuropsychological tasks. The authors conclude “that DLPFC deficits are present at the onset of the first acute exacerbation in this illness and are not due to current or previous medication effects.”
This review of 56 studies, carried out on individuals with schizophrenia who had never received antipsychotic medications, indicates that the brains of these individuals have abnormalities in both brain structure and function that are inherent in the schizophrenia disease process, not medication-related. As such, schizophrenia is a disease of the brain in the same sense that Parkinson’s disease and multiple sclerosis are diseases of the brain. Amariah Brigham (1844), a founding member of the American Psychiatric Association, expressed this clearly in 1844:
Insanity is a chronic disease of the brain, producing either derangement of the intellectual faculties, or, prolonged change of the feelings, affections, and habits of an individual.
The best indicators of schizophrenia as a brain disease appear to be neurological and neuropsychological measures, since these studies are the most numerous and generally show the greatest differences between individuals with this disease and normal controls. Structural differences, as measured by CT or MRI, and cerebral metabolic differences, as measured by fMRI, PET, or SPECT, have been more highly publicized, but the differences between patients and normal controls are less impressive. Electrophysiological measures also show significant differences, but most of the antipsychotic-naïve studies were done in the early 20th century, when research methodology was less rigorous.
The importance of neurological and neuropsychological measures as indicators of adult schizophrenia is also consistent with findings from prospective studies of children who later develop schizophrenia. Compared to controls, the children who later develop schizophrenia have delayed developmental milestones such as walking and talking (Isohanni et al., 2001); “poorer fine and gross motor coordination” from ages 0 to 5 (Walker and Lewine, 1990); lower educational test scores at age 8 (Jones et al., 1994); and deficits in gross motor skills, in verbal memory and attention, and “cognitive and neurointegrative deficits” at ages 7 to 12 (Fish et al., 1992; Cannon et al., 1999; Erlenmeyer-Kimling et al., 2000). Thus, the neurological and neuropsychological deficits seen in adults with schizophrenia are adult manifestations of deficits that were apparent premorbidly, many years before the symptoms became manifest or the individuals received any antipsychotic medications.
It should be emphasized, however, that there is no single abnormality in brain structure or function that is pathognomonic for schizophrenia. All deficits cited above can be found in some other brain diseases and, occasionally, in normal individuals, although statistically they occur more frequently in individuals with schizophrenia. Thus, we do not yet have a specific diagnostic test that points conclusively and exclusively to schizophrenia as the diagnosis.
It is also apparent from reviewing studies of individuals with schizophrenia who were antipsychotic-naïve that the schizophrenia disease process is not confined to a single part of the brain. Structural studies suggest involvement of the periventriculararea, caudate, thalamus, and gray matter in general; neurological studies point to the basal ganglia (dyskinesias and extrapyramidal symptoms) and thalamus (decreased pain perception); neuropsychological studies suggest dysfunction of the prefrontal and medial temporal areas; depth electrophysiological studies implicate the medial temporal and septal areas; and cerebral metabolic studies point toward the prefrontal cortex. It should be emphasized that these various structures are extensively interconnected and function as part of complex circuits, not as discrete brain areas.
It may also be asked whether the same individuals have abnormal findings in each of the five measures of brain structure and function. There are correlations between some findings in the same patients, such as neurological soft signs and Parkinsonian signs (Gupta et al., 1995), but not between others, such as neurological soft signs and ventricular enlargement (Kolakowska et al., 1985) or cerebral metabolism (Rubin et al., 1994). Overall, the correlations between abnormal findings in the same patients are not impressive, suggesting that abnormalities in brain structure and function are probably present in a large percentage of individuals with schizophrenia and not merely in a small subset. What this percentage is remains to be ascertained.
What are the limitations of this review of antipsychotic-naïve patients? The main limitation is that some of the patients, especially those in studies carried out prior to the introduction of antipsychotic medications, had been treated with somatic therapies (e.g., ECT or insulin coma therapy) or were being treated with sedatives or other medications. Studies that took this into account reported no differences between patients who had and had not been so treated. In most of the studies done in more recent years, however, the individuals with schizophrenia were experiencing their first episode of illness and had received no treatment whatsoever.
Now that schizophrenia is firmly established as a disease of brain structure and function, the next challenge is to identify the predisposing genes and biological insults that interact to cause the damage. This is the challenge for emerging molecular psychiatry, which, by focusing on the brain areas apparently affected in schizophrenia, will increase knowledge regarding the nature of the disease process and elevate our understanding of schizophrenia’s etiology to another level. With such understanding should come new and better medications.
I am grateful to Daniel Ragland, Ph.D., Raquel Gur, M.D., and Ruben Gur, Ph.D., for kindly recomputing their data to include only those subjects who were antipsychotic naïve; to Dave Luckenbaugh for his statistical help; and to Judy Miller for preparing the manuscript.
Anonymous, 1838. Statistics of insanity in Europe (review article on M. Esquirol’s Statistique de la Maison Royale de Charenton, dans les Annales d’Hygiène Publique). Foreign Quarterly 20, 39–54.
Barch, D.M., Carter, C.S., Braver, T.S. et al., 2001. Selective deficits in prefrontal cortex function in medication-naïve patients with schizophrenia. Arch. Gen. Psychiatry 58, 280–288.
Bender, L. and Schilder, P., 1930. Unconditioned and conditioned reactions to pain in schizophrenia. Am. J. Psychiatry 10, 365–384.
Braus, D.F., Weber-Fahr, W., Tost, H. et al., 2002. Visuo-acoustic information processing in neuroleptic-naïve first-episode schizophrenic patients [abstract]. Schizophr. Res. 53 (suppl), 221.
Breggin, P.R., 1991. Toxic Psychiatry. St. Martin’s Press, New York, p. 84.
Brewer, W.J., McGorry, P.D., O’Keefe, G. et al., 2002. Functional neuroimaging follow-up of stroop performance n neuroleptic-naïve first-episode psychosis [abstract]. Schizophr. Res. 53 (suppl), 109.
Brigham, Amariah, 1844, Annual report. Am. J. Insanity 1, 97, quoted in Dain, N., 1964. Concepts of Insanity in the United States, 1789–1865. Rutgers University Press, New Brunswick, N.J., p. 72.
Browne, S., Clarke, M., Gervin, M. et al., 2000. Determinants of neurological dysfunction in first episode schizophrenia. Psychol. Med. 30, 1433–1441.
Buchsbaum, M.S., Haier, R.J., Potkin, S.G. et al., 1992. Frontostriatal disorder of cerebral metabolism in never-medicated schizophrenics. Arch. Gen. Psychiatry 49, 935–942.
Buckley, P., O’Callaghan, E., Larkin, C. et al., 1992. Schizophrenia research: the problem of controls [editorial]. Biol. Psychiatry 32, 215–217.
Caligiuri, M.P., Lohr, J.B. and Jeste, D.V., 1993. Parkinsonism in neuroleptic-naive schizophrenic patients. Am. J. Psychiatry 150, 1343–1348.
Cannon, M., Jones, P., Huttunen, M.O. et al., 1999. School performance in Finnish children and later development of schizophrenia: a population-based longitudinal study. Arch. Gen. Psychiatry 56, 457–463.
Casey, D.E. and Hansen, T.E., 1984. Spontaneous dyskinesias. In: Jeste, D.V. and Wyatt, R.J. (eds), Neuropsychiatric Movement Disorders. American Psychiatric Press, Washington, D.C., pp. 68–95.
Censits, D.M., Ragland, J.D., Gur, R.C. et al., 1997. Neuropsychological evidence supporting a neurodevelopmental model of schizophrenia: a longitudinal study. Schizophr. Res. 24, 289–298.
Chakos, M.H., Lieberman, J.A., Bilder, R.M. et al., 1994. Increase in caudate nuclei volumes of first-episode schizophrenic patients taking antipsychotic drugs. Am. J. Psychiatry 151, 1430–1436
Chamberlain, G.H.A. and Russell, J.G., 1952. The E.E.G.s of the relatives of schizophrenics. J. Ment. Sci. 98, 654–659.
Chatterjee, A., Chakos, M., Koreen, A. et al., 1995. Prevalence and clinical correlates of extrapyramidal signs and spontaneous dyskinesia in never-medicated schizophrenic patients. Am. J. Psychiatry 152, 1724–1729.
Chorfi, M. and Moussaoui, D., 1989. Lack of dyskinesias in unmedicated schizophrenics [letter]. Psychopharmacology 97, 423.
Cleghorn, J.M., Szechtman, H., Garnett, E.S. et al., 1991. Apomorphine effects on brain metabolism in neuroleptic-naïve schizophrenic patients. Psychiatry Res.: Neuroimaging 40, 135–153.
Colony, H.S. and Willis, S.E., 1956. Electroencephalographic studies of 1,000 schizophrenic patients. Am. J. Psychiatry 113, 163–169.
Corson, P.W., Nopoulos, P., Andreasen, N.C. et al., 1999. Caudate size in first-episode neuroleptic-naïve schizophrenic patients measured using an artificial neural network. Biol. Psychiatry 46, 712–720.
Cortese, L., Norman, R., Townsend, L. et al., 2002. Motor abnormalities and clinical correlates in drug-naïve, first episode patients with schizophrenia [abstract]. Schizophr. Res. 53, 55.
Degreef, G., Bogerts, B., Falkai, P. et al., 1992. Increased prevalence of the cavum septum pellucidum in magnetic resonance scans and post-mortem brains of schizophrenic patients. Psychiatry Res.: Neuroimaging 45, 1–13.
Donovan, J.F., Galbraith, A.J. and Jackson, H., 1949. Some observations on leucotomy and investigations by pneumoencephalography. J. Ment. Sci. 95, 655–666.
Dworkin, R.H., 1994. Pain insensitivity in schizophrenia: a neglected phenomenon and some implications. Schizophr. Bull. 20, 235–248.
Ellingson, R.J., 1954. The incidence of EEG abnormality among patients with mental disorders of apparently nonorganic origin: a critical review. Am. J. Psychiatry 111, 263–275.
Erlenmeyer-Kimling, L., Rock, D., Roberts, S.A. et al., 2000. Attention, memory, and motor skills as childhood predictors of schizophrenia-related psychoses: the New York High-Risk Project. Am. J. Psychiatry 157, 1416–1422.
Farran-Ridge, C., 1926. Some symptoms referable to the basal ganglia occurring in dementia praecox and epidemic encephalitis. J. Ment. Sci. 72, 513–523.
Fenn, D.S., Moussaoui, D., Hoffman, W.F. et al., 1996. Movements in never-medicated schizophrenics: a preliminary study. Psychopharmacology 123, 206–210.
Fenton, W.S., 2000. Prevalence of spontaneous dyskinesia in schizophrenia. J. Clin. Psychiatry 61 (suppl 4), 10–14.
Fenton, W.S., Blyler, C.R., Wyatt, R.J. et al., 1997. Prevalence of spontaneous dyskinesia in schizophrenic and non-schizophrenic psychiatric patients. Br. J. Psychiatry 171, 265–268.
Finley, K.H. and Campbell, C.M., 1941. Electroencephalography in schizophrenia. Am. J. Psychiatry 98, 374–381.
Fish, B., Marcus, J., Hans, S.L. et al., 1992. Infants at risk for schizophrenia: sequelae of a genetic neurointegrative defect: a review and replication analysis of pandysmaturation in the Jerusalem Infant Development Study. Arch. Gen. Psychiatry 49, 221–235.
Fishbain, D.A., 1982. Pain insensitivity in psychosis. Ann. Emerg. Med. 11, 630–632.
Ganguli, R., Reynolds, C.F. and Kupfer, D.J., 1987. Electroencephalographic sleep in young, never-medicated schizophrenics. Arch. Gen. Psychiatry 44, 36–44.
Gerlach, J. and Casey D.E., 1988. Tardive dyskinesia. Acta Psychiatr. Scand. 77, 369–378.
Gervin, M., Browne, S., Lane, A. et al., 1998. Spontaneous abnormal involuntary movements in first-episode schizophrenia and schizophreniform disorder: baseline rate in a group of patients from an Irish catchment area. Am. J. Psychiatry 155, 1202–1206.
Greenblatt, M., 1944. Age and electroencephalographic abnormality in neuropsychiatric patients: a study of 1593 cases. Am. J. Psychiatry 101, 82–90.
Guieu, R., Samuélian, J.C. and Coulouvrat, H., 1994. Objective evaluation of pain perception in patients with schizophrenia. Br. J. Psychiatry 164, 253–255.
Gupta, S., Andreasen, N.C., Arndt, S. et al., 1995. Neurological soft signs in neuroleptic-naïve and neuroleptic-treated schizophrenic patients and in normal comparison subjects. Am. J. Psychiatry 152, 191–196.
Gur, R.E., Maany, V., Mozley, P.D. et al., 1998. Subcortical MRI volumes in neuroleptic-naïve and treated patients with schizophrenia. Am. J. Psychiatry 155, 1711–1717.
Gur, R.E., Turetsky, B.I., Bilker, W.B. et al., 1999. Reduced gray matter volume in schizophrenia. Arch. Gen. Psychiatry 56, 905–911.
Gur, R.E., Cowell, P.E., Latshaw, A. et al., 2000a. Reduced dorsal and orbital prefrontal gray matter volumes in schizophrenia. Arch. Gen. Psychiatry 57, 761–768.
Gur, R.E., Turetsky, B.I., Cowell, P.E. et al., 2000b. Temporolimbic volume reductions in schizophrenia. Arch. Gen. Psychiatry 57, 769–775.
Hall, K.R.L. and Stride, E., 1954. The varying response to pain in psychiatric disorders: a study in abnormal psychology. Br. J. Med. Path. 27, 48–60.
Haslam, 1798. Observations on Insanity: With Practical Remarks on the Disease…. F. and C. Rivington, London.
Haslam, J., 1809. Observations on Madness and Melancholy. The Classics of Psychiatry and Behavioral Science Library, New York, 1992, pp. 49, 140.
Heath, R.G. and Walker, C.F., 1985. Correlation of deep and surface electroencephalograms with psychosis and hallucinations in schizophrenics: a report of two cases. Biol. Psychiatry 20, 669–674.
Hecker, E., 1871. Die Hebephrenie. Arch. Pathol. Anat. Physiol. Klin. Med. 52, 394–409.
Heinrichs, D.W. and Buchanan, R.W., 1988. Significance and meaning of neurological signs in schizophrenia. Am. J. Psychiatry 145, 11–18.
Heinrichs, R.W. and Zakzanis, K.K., 1998. Neurocognitive deficit in schizophrenia: a quantitative review of the evidence. Neuropsychology 12, 426–445.
Hill, D., 1952. EEG in episodic psychotic and psychopathic behaviour: a classification of data. EEG Clin. Neurophysiol. 4, 419–442.
Honer, W.G., Kopala, L.C. and Rabinowitz, J., 2002. Are movement disorders a part of the syndrome or consequences of treatment? [abstract] Schizophr. Res. 53, 11.
Huber, G., 1957. Pneumoencephalographische und Psychopathologische Bilder bei Endogenen Psychosen. Springer, Berlin.
Isohanni, M., Jones, P.B., Moilanen, K. et al., 2001. Early developmental milestones in adult schizophrenia and other psychoses. A 31-year follow-up of the Northern Finland 1966 birth cohort. Schizophr. Res. 52, 1–19.
Jacobi, W. and Winkler, H., 1927. Encephalographische studien auf chronischen schizophrenen. Archiv für Psychiatrie und Nervenkrankheiten 81, 299–332.
Jones, P., Rodgers, B., Murray, R. et al., 1994 . Child developmental risk factors for adult schizophrenia in the British 1946 birth cohort. Lancet 344, 1398–1402.
Kane, J.M. and Smith, J.M., 1982. Tardive dyskinesia: prevalence and risk factors, 1959 to 1979. Arch. Gen. Psychiatry 39, 473–481.
Kennard, M.A. and Levy, S., 1952. The meaning of the abnormal electroencephalogram in schizophrenia. J. Nerv. Ment. Dis. 116, 413–423.
Keshaven, M.S., Rosenberg, D., Sweeney, J.A. et al., 1998. Decreased caudate volume in neuroleptic-naïve psychotic patients. Am. J. Psychiatry 155, 774–778.
Keshaven, M.S., Jayakumar, P.N., Diwadkar, V.A. et al., 2002. Cavum septi pellucidi in first-episode patients and young relatives at risk for schizophrenia. CNS Spectrums 7, 155–158.
Khot, V. and Wyatt, R.J., 1991. Not all that moves is tardive dyskinesia. Am. J. Psychiatry 148, 661–666.
Kolakowska, T., Williams, A.O., Jambor, K. et al., 1985. Schizophrenia with good and poor outcome. III: Neurological ‘soft’ signs, cognitive impairment and their clinical significance. Br. J. Psychiatry 146, 348–357.
Kraepelin, 1919. Dementia Praecox and Paraphrenia, Robertson, G.M. (ed), Barclay, M. (Transl.), Livingstone, Edinburgh, p. 34.
Krebs, M.-O., Gut-Fayand, A., Bourdel, M.-C. et al., 2000. Validation and factorial structure of a standardized neurological examination assessing neurological soft signs in schizophrenia. Schizophr. Res. 45, 245–260.
Krebs, M.-O., Gut-Fayand, A., Bourdel, M.-C. et al., 2002. Disorganisation syndrome is correlated to sensory neurological soft signs in medicated and neuroleptic naïve schizophrenic patients [abstract]. Schizophr. Res. 53, 232.
Laruelle, M., Abi-Dargham, A., Gil, R. et al., 1999. Increased dopamine transmission in schizophrenia: relationship to illness phases. Biol. Psychiatry 46, 56–72.
Lemke, R., 1935. Untersuchungen über die soziale Prognose der Schizophrenia unter besonderer Berücksichtigung des encephalographischen Befundes. Arch. Psychiat. Nervenkr. 104, 89–136.
Lieberman, A.L., 1955. Painless myocardial infarction in psychotic patients. Geriatrics 10, 579–580.
Lieberman, J., Bogerts, B., Degreef, G. et al., 1992. Qualitative assessment of brain morphology in acute and chronic schizophrenia. Am. J. Psychiatry 149, 784–794.
Loeber, R.T., Gruber S.A., Cohen, B.M. et al., 2002. Cerebellar blood volume in bipolar patients correlates with medication. Biol. Psychiatry 51, 370–376.
Lussier, I. and Stip, E., 2001. Memory and attention deficits in drug naïve patients with schizophrenia. Schizophr. Res. 48, 45–55.
McCreadie, R.G. and Ohaeri, J.U., 1994. Movement disorder in never and minimally treated Nigerian schizophrenic patients. Br. J. Psychiatry 164, 184–189.
McCreadie, R.G., Thara, R., Kamath, S. et al., 1996. Abnormal movements in never-medicated Indian patients with schizophrenia. Br. J. Psychiatry 168, 221–226.
McCreadie, R.G., Latha, S., Thara, R. et al., 1997. Poor memory, negative symptoms and abnormal movements in never-treated Indian patients with schizophrenia. Br. J. Psychiatry 171, 360–363.
McCreadie, R.G., Thara, R., Padmavati, R. et al., 2002. Structural brain differences between never-treated patients with schizophrenia, with and without dyskinesia, and normal control subjects: a magnetic imaging study. Arch. Gen. Psychiatry 59, 332–336.
Malmo, R.B., Shagass, C. and Smith, A.A., 1951. Responsiveness in chronic schizophrenia. J. Pers. 19, 359–375.
Manschreck, T.C., Maher, B.A., Rucklos, M.E. et al., 1982. Disturbed voluntary motor activity in schizophrenic disorder. Psychol. Med. 12, 73–84.
Marchand, W.E., 1955. Occurrence of painless myocardial infarction in psychotic patients. N. Engl. J. Med. 253, 51–55.
Marchand, W.E., Sarota, B., Marble, H.C. et al., 1959. Occurrence of painless acute surgical disorders in psychotic patients. N. Engl. J. Med. 260, 580–585.
Mohamed, S., Paulsen, J.S., O’Leary, D. et al., 1999. Generalized cognitive deficits in schizophrenia: a study of first-episode patients. Arch. Gen. Psychiatry 56, 749–754.
Moore, M., Nathan, D., Elliot, A.R. et al., 1933. Encephalographic studies in schizophrenia (dementia praecox). Am. J. Psychiatry 89, 801–810.
Mortimer, A.M., 1997. Cognitive function in schizophrenia—do neuroleptics make a difference? Pharmacol. Biochem. Behav. 56, 789–795.
Mosher, L.R., Pollin, W. and Stabenau, J.R., 1971. Identical twins discordant for schizophrenia: neurologic findings. Arch. Gen. Psychiatry 24, 422–430.
Peterson, M.C., Bickford, R.G., Sem-Jacobsen, C.W. et al., 1953. The depth electrogram in schizophrenic patients. Mayo Clin. Proc. 28, 170–175.
Puri, B.K., Barnes, T.R.E., Chapman, M.J. et al., 1999. Spontaneous dyskinesia in first episode schizophrenia. J. Neurol. Neurosurg. Psychiatry 66, 76–78.
Rapaport, D., 1946. Diagnostic Psychological Testing. Year Book Publishers, Chicago, vol. 1, p. 452, and vol. 2, p. 76.
Reiter, P.J., 1926. Extrapyramidal motor-disturbances in dementia praecox. Acta Psychiatr. Neurol. Scand. 1, 287–309.
Riley, E.M., McGovern, D., Mockler, D. et al., 2000. Neuropsychological functioning in first-episode psychosis—evidence of specific deficits. Schizophr. Res. 43, 47–55.
Rogers, D., 1985. The motor disorders of severe psychiatric illness: a conflict of paradigms. Br. J. Psychiatry 147, 221–232.
Rubin, P., Vorstrup, S., Hemmingsen, R. et al., 1994. Neurological abnormalities in patients with schizophrenia or schizophreniform disorder at first admission to hospital: correlations with computerized tomography and regional cerebral blood flow findings. Acta Psychiatr. Scand. 90, 385–390.
Sanders, R.D., Keshavan, M.S. and Schooler, N.R., 1994. Neurological examination abnormalities in neuroleptic-naive patients with first-break schizophrenia: preliminary results. Am. J. Psychiatry 151, 1231–1233.
Saykin, A.J., Shtasel, D.L., Gur, R. E. et al., 1994. Neuropsychological deficits in neuroleptic naïve patients with first-episode schizophrenia. Arch. Gen. Psychiatry 51, 124–131.
Schröder, J., Niethammer, R., Geider, F.-J. et al., 1992. Neurological soft signs in schizophrenia. Schizophr. Res. 6, 25–30.
Schulz, S.C., Sinicrope, P., Kishore P. et al., 1983. Treatment response and ventricular brain enlargement in young schizophrenic patients. Psychopharmacol. Bull. 19, 510–512.
Shibre, T., Kebede, D., Alem, A. et al., in press. Neurological soft signs (NSS) in 200 treatment naïve cases with schizophrenia: a community based study in a rural setting. Nordic J. Psychiatry.
Shihabuddin, L, Buchsbaum, M.S., Hazlett, E.A. et al., 1998. Dorsal striatal size, shape, and metabolic rate in never-medicated and previously medicated schizophrenics performing a verbal learning task. Arch. Gen. Psychiatry 55, 235–243.
Southard, E.E., 1915. On the topographical distribution of cortex lesions and anomalies in dementia praecox, with some account of their functional significance. Am. J. Insanity 71, 603–671.
Stengel, E., Oldham, A.J. and Ehrenberg, A.S.C., 1955. Reactions to pain in various abnormal mental states. J. Ment. Sci. 101, 52–69.
Szasz, T.S., 1976. Schizophrenia: The Sacred Symbol of Psychiatry. Basic Books, New York.
Turner, T., 1989. Rich and mad in Victorian England. Psychol. Med. 19, 29–44.
Tyler, M., 1995. Somatic symptoms in schizophrenia. Schizophr. Res. 18, 87–88.
Walker, E. and Lewine, R.J., 1990. Prediction of adult-onset schizophrenia from childhood home movies of the patients. Am. J. Psychiatry 147, 1052–1056.
Whitaker, R., 2002. Mad in America: Bad Science, Bad Medicine, and the Enduring Mistreatment of the Mentally Ill. Perseus Publishing, New York, pp. 164–165.
Table 1. Pneumoencephalography Studies of Individuals with Schizophrenia Never Treated with Antipsychotic Medications
Enlargement of Cerebral Ventricles
|1927||Jacobi and Winkler||18/19 95%|
|1933||Moore et al.||25/60 42%|
|1949||Donovan et al.||16/19 84%|
Table 2. Recent Studies of the Prevalence of Dyskinesia in Individuals with Schizophrenia Never Treated with Antipsychotic Medications
|1989||Chorfi and Moussaoui||Morocco|| |
|1994||McCreadie and Ohaeri||Nigeria|| |
|1995||Chatterjee et al.||United States|| |
|1996||Fenn et al.||Morocco|| |
|1996||McCreadie et al.||India|| |
|1997||Fenton et al.||United States|| |
|1998||Gervin et al.||Ireland|| |
|1999||Puri et al.||England|| |
Table 3. Recent Studies of the Prevalence of Parkinsonian Signs in Individuals with Schizophrenia Never Treated with Antipsychotic Medications
|1993||Caligiuri et al.||United States|| |
|1995||Chatterjee et al.||United States|| |
|1996||McCreadie et al.||India|| |
|1999||Puri et al.||England|| |
|2002||Honer et al.||Canada|| |
|2002||Cortese et al.||Canada|| |
Table 4. Studies of Neurological Soft Signs in Individuals with Schizophrenia Never Treated with Antipsychotic Medications
|1992||Schröder et al.||Germany||On a 17-item scale, compared 17 never-treated patients to 33 receiving treatment and 34 normal controls. The patient group had significantly more soft signs than controls (p<0.0001), and the scores of the never-treated patients “did not differ from that of the remaining patients.”|
|1994||Rubin et al.||Denmark||Compared 12 never-treated patients to 33 receiving treatment and 24 normal controls. The never-treated group had a significantly higher total neurological abnormality score than the controls (p=0.03) and was virtually identical to the group receiving treatment.|
|1994||Sanders et al.||United States||On a 27-item scale, compared 17 never-treated patients to 15 normal controls. The former had significantly more neurological abnormalities (p=0.0001).|
|1995||Gupta et al.||United States||On a 13-item scale, compared 26 never-treated patients to 126 receiving treatment and 117 normal controls. Compared to the controls, the never-treated patients had more soft signs (23% vs. 0%) and developmental reflexes (19% vs. 0%). The treated patients had even more soft signs (46%).|
|2000||Browne et al.||Ireland||On a 26-item scale, compared 35 never-treated patients to 31 receiving treatment. Sixty-three percent (63%) of the never-treated patients had at least two abnormal soft signs, and they did not differ significantly from those receiving treatment.|
|2000 & 2002||Krebs et al. |
Krebs et al.
|France||Compared 54 never-treated patients to 51 receiving treatment and 48 normal controls on a 23-item scale. The mean scores of the groups were 10.8 for never-treated, 13.7 for treated, and 5.0 for normal controls. Using their data, we compared the never-treated and normal controls by t test (p<0.0001).|
|2002||Shibre et al.||Ethiopia||On a 26-item scale, compared 200 never-treated patients to 78 normal controls. The median scores of neurological abnormalities were 5.0 for patients and 1.5 for controls (p=0.000).|
Table 5. Studies of Neuropsychological Function in Individuals with Schizophrenia Never Treated with Antipsychotic Medications
|1994||Saykin et al.||Thirty-seven (37) patients, compared to 131 normal controls, had marked impairment in tests of verbal memory and learning (p<0.001).|
|1997||Censits et al., reanalyzed by Ragland to include only the antipsychotic-naïve patients||Twenty-eight (28) patients, compared to 38 normal controls, showed generalized impairment that was most marked for tests of abstraction, attention, verbal memory, spatial memory, and language abilities (p<0.0000 for each).|
|1997||McCreadie et al.||Nineteen (19) patients, compared to 55 normal controls, performed more poorly on some memory tests including memory quotient (p=0.008) and digit span (p=0.0009).|
|2001||Lussier and Stip||Sixteen (16) patients, compared to 20 normal controls, showed the greatest deficits on tests of attention (p<0.001).|
Table 6. EEG Studies of Individuals with Schizophrenia Never Treated with Antipsychotic Medications
Number of individuals with schizophrenia
|Percent abnormal EEGS |
Number of controls
|Percent abnormal EEGs |
|1941||Finley and Campbell|| |
|1952||Chamberlain and Russell|| |
Table 7. Studies of Cerebral Metabolic Abnormalities in Individuals with Schizophrenia Never Treated with Antipsychotic Medications
|1991||Cleghorn et al.||PET||Eleven (11) patients, compared to 8 normal controls, showed significantly altered glucose metabolism in the striatum (p=0.02), superior temporal (p=0.02), and posterior frontal (p=0.02) regions.|
|1992||Buchsbaum et al.||PET||Eighteen (18) patients, compared to 20 normal controls, showed significantly reduced glucose metabolism in the frontal regions (p=0.03) and basal ganglia (p<0.05).|
|1998||Shihabuddin et al.||PET||Seven (7) patients, compared to 24 controls, had a lower metabolic rate in the right putamen (p<0.05).|
|1999||Laruelle et al.||SPECT||Seven (7) patients, compared to 36 normal controls, showed significant increase in dopamine displacement in response to amphetamine challenge (p<0.001).|
|2001||Barch et al.||fMRI||Fourteen (14) patients, compared to 12 normal controls, showed deficits in activation of the prefrontal cortex in response to neuropsychological tasks (p=0.007).|
|2002||Braus et al.||fMRI||Twelve (12) patients, compared to 11 normal controls, showed reduced activation in the right thalamus and right prefrontal cortex in response to visual and auditory stimuli (p<0.01).|
|2002||Brewer et al.||fMRI||Eight (8) patients, compared to an unspecified number of normal controls, failed to activate the anterior cingulate in response to neurospsychological tasks.|
Antipsychotic drugs may work by changing brain structure. Other changes may be due to side-effects.
Changes in brain structure are caused both by the disease process of schizophrenia and bipolar disorder and by the antipsychotic drugs used to treat these diseases. Different antipsychotic drugs may have different effects. It is important to study the brain changes caused by antipsychotic drugs, since this may tell us how these drugs work and/or predict which individuals are more likely to experience side effects. The changes caused by antipsychotic drugs used to treat schizophrenia and bipolar disorder are similar in kind to structural brain changes caused by drugs used to treat Parkinson’s disease, epilepsy, and other brain diseases. It is incorrect to characterize these brain changes as an indication that these drugs are dangerous or should not be used.
The findings that antipsychotic drugs produce structural brain changes should not be a surprise. Schizophrenia and bipolar disorder are known to produce structural brain changes as part of the disease process, so it is reasonable to expect drugs that are effective in treating these diseases to do likewise. Some opponents of the use of antipsychotic medication misunderstand such research, arguing that brain changes prove that antipsychotic drugs are dangerous and should not be used. On the contrary, this research is very important and may eventually led to better and more effective medications.
Furthermore, many drugs known to be effective in other brain disorders also produce structural brain changes. For example, levodopa, a mainstay of treatment for Parkinson’s disease, has been shown to produce some changes in the cellular mitochondria and neuronal degeneration. Phenobarbital, widely used for many years to treat some forms of epilepsy, has been shown to produce “lasting effects on fine structure of cells” in the cerebellum. And diphenylhydantoin, also commonly used to treat epilepsy, has been shown to produce “marked dystrophic changes in the Purkinje cell axons” and to interfere with the formation of neuronal processes. Drugs used to treat diseases of other parts of the body (e.g., heart, joints) also may cause structural changes to those parts.
Ogawa N, Edamatsu R, Mizukawa K et al. Degeneration of dopaminergic neurons and free radicals. Advances in Neurology 1993;60:242–250.
Fishman RHB, Ornoy A, Yanai J. Correlated ultrastructural damage between cerebellum cells after early anticonvulsant treatment in mice. International Journal of Developmental Neuroscience 1989;7:15–26.
Volk B, Kirchgässner N. Damage of Purkinje cell axons following chronic phenytoin administration: an animal model of distal axonopathy. Acta Neuropathologica 1985;67:67–74.
Bahn S, Ganter U,Bauer J et al. Influence of phenytoin on cytoskeletal organization and cell viability of immortalized mouse hippocampal neurons. Brain Research 1993;615:160–169.
Strucutural changes caused by antipsychotic medications.
There is considerable ongoing work in this research area. The majority of the work to date has been carried out in rats and needs to be replicated in humans, since there are substantial species variation in brain structure and function. The following structural brain changes appear to be caused by antipsychotic drugs.
Decreased brain volume with associated increased volume of the ventricles.
These changes appear to be caused both by the disease process and by the effects of antipsychotics, so it is difficult to determine how much is caused by one and how much by the other. In addition, the studies of antipsychotic drug effect have been inconsistent, with the majority of studies showing an effect, but a minority not showing one.
Moncrieff J, Leo J. A systematic review of the effects of antipsychotic drugs on brain volume. Psychological Medicine 2010;40:1409–1422.
Navari S, Dazzan P. Do antipsychotic drugs affect brain structure? A systematic and critical review of MRI findings. Psychological Medicine 2009;39:1763–1777.
Boonstra G, van Haren NEM, Schnack HG et al. Brain volume changes after withdrawal of atypical antipsychotics in patients with first-episode schizophrenia. Journal of Clinical Psychopharmacology 2011;31:146–153.
Increase in size of the striatum.
An increase in the size of the striatum (the striatum is composed of the caudate and putamen and is part of the basal ganglia) has been found in human MRI studies of individuals taking some antipsychotic drugs but not clozapine. The increased size is thought to be due both to increased blood flow and to structural changes of the neurons. It is not known whether this increased blood flow has any relationship to either the efficacy of the drug or its side effects.
Chakos MH, Lieberman JA, Bilder RM et al. Increase in caudate nuclei volumes of first-episode schizophrenic patients taking antipsychotic drugs. American Journal of Psychiatry 1994;151:1430–1436.
Increased density of glial cells in the prefrontal cortex.
Glial proliferation and hypertrophy of the prefrontal cortex is reported to be “a common response to antipsychotic drugs” and may “play a regulatory role in adjusting neurotransmitter levels or metabolic processes.”
Selemon LD, Lidow MS, Goldman-Rakic PS. Increased volume and glial density in primate prefrontal cortex associated with chronic antipsychotic drug exposure. Biological Psychiatry 1999;46:161–172.
Increased number of synapses (connections between neurons) and changes in the proportions and properties of the synapses.
This includes changes in the distribution and subtypes of synapses. The changes have been found primarily in the caudate nucleus of the striatum, and there is some evidence that they may also occur in layer six of the prefrontal cortex but not elsewhere. The changes may be secondary to the effects of the antipsychotic drug on dopamine or glutamate neurotransmitters. It is not yet clear what these changes mean; they may be related to the efficacy of the drug or may possibly be a marker for side effects. If the latter, being able to identify such changes in living individuals could potentially provide an early marker for tardive dyskinesia and thus indicate which individuals should not take these drugs. Most of these studies have been carried out in rats, so it is not yet known how applicable the findings are to humans.
Decrease in the gray matter in the parietal lobe associated with a decrease in glial cells but no decrease in neurons.
This research has been carried out on monkeys by giving them antipsychotic drugs and then assessing the effect on the brain.
Konopaske GT, Dorph-Petersen K-A, Pierri JN et al. Effect of chronic exposure to antipsychotic medication on cell numbers in the parietal cortex of macaque monkeys. Neuropsychopharmacology 2007;32:1216–1223.
Konopaske GT, Dorph-Petersen K-A, Sweet RA et al. Effect of chronic antipsychotic exposure on astrocyte and oligodendrocyte numbers in macaque monkeys. Biological Psychiatry 2008;63:759–765.
Many of these studies assessed the effects of haloperidol (Haldol), a first-generation antipsychotic. Fewer studies have been done with second-generation antipsychotics. Those that have been done suggest that the effects on brain structure may be somewhat different.
Kopelman A, Andreasen NC, Nopoulos P. Morphology of the anterior cingulate gyrus in patients with schizophrenia: relationship to typical neuroleptic exposure. Am J Psychiatry 2005;162:1872–1878.
Massana G, Salgado-Pineda P, Junqué C et al. Volume changes in gray matter in first-episode neuroleptic-naïve schizophrenic patients treated with risperidone. Journal of Clinical Psychopharmacology 2005;25:111–117.
Lieberman JA, Tollefson GD, Charles Cecil et al. Antipsychotic drug effects on brain morphology in first-episode psychosis. Archives of General Psychiatry 2005;62:361–370.
Panenka WJ, Khorram B, Barr AM et al. A longitudinal study on the effects of typical versus atypical antipsychotic drugs on hippocampal volume in schizophrenia. Schizophrenia Research 2007;94:288–292.
Vita A, De Peri L. The effects of antipsychotic treatment on cerebral structure and function in schizophrenia. International Review of Psychiatry 2007;19:431–438.
Koolschijn PCMP, van Haren NEM, Cahn W et al. Hippocampal volume change in schizophrenia. Journal of Clinical Psychiatry 2010;71:737–744.