Abstract
Schizophrenia, one of the most common psychiatric disorders, with a worldwide annual incidence rate of approximately 0.3-0.7%, known to affect the population below 25 years of age, is persistent throughout lifetime and includes people from all layers of society. With recent technological progress that allows better imaging techniques, such as the ones provided by computed tomography and particularly magnetic resonance imaging (MRI), research on schizophrenia imaging has grown considerably. The purpose of this review is to establish the importance of using imaging techniques in the early detection of brain abnormalities in patients diagnosed with schizophrenia. We reviewed all articles which reported on MRI imaging in schizophrenia. In order to do this, we used the PubMed database, using as search words ‘MRI’ and ‘schizophrenia’. MRI studies of first episode patients and chronic patients, suggest reduction of the whole brain volume. Enlargement of lateral ventricles was described as positive in 15 studies out of 19 and was similar to findings in chronic patients. Moreover, for the first episode patients, all data collected point to important changes in medial temporal lobe structures, diminished hippocampal volume, the whole frontal lobe, asymmetry in prefrontal cortex, diminished volume in cingulate, corpus callosum, and cavum septum pellucidum reported abnormalities. MRI is recommended as an important tool in the follow-up process of patients with schizophrenia. Yet, it is still under debate whether the abnormalities described in this condition are able to be used as diagnostic biomarkers.
Keywords: schizophrenia, neuroleptic, magnetic resonance imaging, biomarkers, structural abnormalities, gray matter, white matter, diagnosis
1. Introduction
Schizophrenia, one of the most common psychiatric disorders, with a worldwide annual incidence rate of approximately 0.3-0.7%, known to affect the population below 25 years of age, is persistent throughout lifetime and includes people from all layers of society (1). The main signs and symptoms may differ among patients as well as the debut period and can include perceptual abnormalities, delusions, deterioration of cognitive function and emotional impairment. It affects both patients and their families, manifesting in poor care and social exclusion because of the widespread ignorance about the disorder (2). Although schizophrenia has been studied for more than a century, the neuropathology of schizophrenia is still unknown, with no single set of causes that can be pinned down as an underlying mechanism for this condition (2-5). Najjar and Pearlman described, in a review of 15 studies that involved 792 patients, that schizophrenia is strongly related with white matter abnormalities and it could lead to structural and functional dysconnectivity, even in an early development of psychosis (6).
With recent technological progress that allows better imaging techniques, such as the ones provided by computed tomography (CT) and particularly magnetic resonance imaging (MRI), research on schizophrenia imaging has grown considerably. Multiple neuroimaging studies have identified substantial evidence of structural and functional brain alterations in schizophrenia. There is no specific region in which these alterations occur, but they are frequently found in the association cortex and subcortical (limbic, striatal) brain regions. These findings still do not have diagnostic value (7-9).
In the 19th and 20th century, there were numerous attempts to identify brain abnormalities that led to discouraging results because of the lack of technology. Although the benefits of using CT to discover brain abnormalities in vivo were important, using the newer technique of MRI, allowed researchers to better analyze different regions of the brain due to an improved picture of the gray matter (10).
2. Scope of the review
The main method of diagnosing schizophrenia is based on clinical diagnostic criteria, psychiatric history and mental examination of the patient, with imaging techniques being used for differential diagnosis with other disorders that could cause psychosis. The purpose of this review was to establish the importance of using imaging techniques in the early detection of brain abnormalities in patients diagnosed with schizophrenia.
3. Literature search methods
We reviewed all articles which reported on MRI imaging in schizophrenia. In order to do this, we used PubMed database, using as search words ‘MRI’ and ‘schizophrenia’. Only articles indexed in PubMed, written in English and published between 1988 to 2020 were reviewed for this study.
A total of 197 article were reviewed. From these we selected 84 articles which offered information about significant brain structures mainly linked with schizophrenia: Lateral ventricles, third ventricle, fourth ventricle, temporal lobe, frontal lobe, parietal lobe, occipital lobe, cerebellum, basal ganglia structures, thalamus, corpus callosum and septum pellucidum.
4. Results
Although large individual variations in brain size in the general population such as gender, age, economic and social status, perinatal factors and potential nutritional deficits are reported, there are no statistically eloquent differences in MRI studies between patients diagnosed with schizophrenia and normal controls (10).
In the review conducted by Shenton et al concerning 55 MRI studies in patients with schizophrenia, 44 reported structural modifications such as enlarged lateral ventricles (10). While lateral ventricle enlargement was not always identified in some studies, enlargement of the temporal horn portion, which is commonly found on the left sided ventricle, has been mentioned (11-20).
In 33 MRI studies of the third ventricle, 24 (73%) describe an enlargement of this area, and 9 (27%) report negative findings (10,21-23).
The fourth ventricle was investigated in 5 MRI studies, and only one of them reported positive findings, representing 20%; the remaining 4 studies were negative (10,24,25).
Of 51 MRI studies evaluating the volume of temporal lobe, 31 (61%) reported smaller temporal lobe volume, while 20 (39%) reported negative findings (10,26-29).
MRI findings of frontal lobe abnormalities in schizophrenia are vague. From 50 MRI studies, 30 (60%) reported volumetric reduction, while 20 (40%) reported negative findings (10,30-33).
An important brain region involved in processes that are altered in schizophrenia, such as attention (34), spatial working memory (35) and language (36) is the parietal lobe. In 15 studies regarding the MRI of the parietal lobe, only 9 (60%) describe abnormalities in this region (7,10,37,38).
Four of the studies that describe the occipital lobe, representing 44%, showed a reduction in the volume of patients diagnosed with schizophrenia (8,9,39,40).
Four (31%) out of 13 MRI studies of the cerebellum in schizophrenia, reported positive findings, while 9 (69%) reported negative findings (41,42). Nopoulos and coworkers (43) reported negative findings, but they did report a reduction in volume in the anterior lobe of the vermis and Rossi and coworkers (44) showed a decrease in vermal-to-brain ratio in male patients with schizophrenia compared to female patients with schizophrenia.
From 25 studies involving the basal ganglia structures, 17 of them, representing 68%, described increased volume (45-47) and 8 reporting negative results (48,49). Recent studies describe that the enlargement of the basal ganglia is rather caused by neuroleptic medication (10,47).
The thalamus, although an important relay station in the brain, which is involved in modulating the input from various levels such as the cortical areas, limbic system and reticular activating system, has been little scanned, mainly because this area fades from gray matter to white matter. From 12 MRI studies, 5 (42%) describe a reduction in the volume and 7 (58%) reported no discrepancy between the control group and the patients with schizophrenia (50-53).
Corpus callosum, a brain structure composed of white matter, has been reviewed in 27 MRI studies, 17 (63%) of them reporting reduction in thickness all along its structures (10,54-57).
One of the most important findings in literature is related to MRI studies of septum pellucidum, 11 (92%) describing an enlargement of this region in schizophrenia (10).
Akhtar et al conducted an MRI study of 66 subjects (33 with schizophrenia and 33 control test) and found that brain atrophy was present only in 13 patients with schizophrenia (39.4%) and none of the control group. The presence of prominent cavum septum pellucidum was described in 10 cases of schizophrenia representing 30% and none in the control. Prominent Virchow Robin spaces were significantly associated with schizophrenia (30.3%) as compared to the control group. Enlargement of ventricles was reported only in 4 cases (12%) and 2 (6%) of the control group (58).
5. First episode patient data
MRI studies of first episode patients are quite comparable with those of chronic patients, especially in data regarding the reduction of the whole brain volume. Enlargement of lateral ventricles was described as positive in 15 studies out of 19 and is similar to the findings of chronic patients (59-61). Also, several researchers note the increase in volume of the left temporal horn of the lateral ventricles which is comparable with data gathered from chronic patients (10,62,63).
Five out of 6 studies regarding medial temporal lobe structures report positive data for schizophrenic patients (10), in comparison with 5 out of 11 MRI studies that examined the whole temporal lobe volume (45,64). When investigating the hippocampus and amygdala independently, 8 out of 10 studies report a diminished hippocampal volume and only 1 out of 5 studies report a decreased amygdala volume (29,64,65).
Regarding the whole frontal lobe, 7 out of 10 MRI studies showed abnormalities, one of them noted asymmetry in the prefrontal cortex (9) and another one a diminished volume in the cingulate, while the other study reported negative findings (65).
For other brain regions, MRIs also gathered important data. From 4 studies of corpus callosum, 3 reported abnormalities; 7 out of 10 basal ganglia studies, and 3 out of 3 studies of cavum septum pellucidum reported abnormalities (10,47,65-68).
6. Chronic patient data
The inceptive reports (45,66,69) noted that there were no differences between the patients with first episode and the control group regarding the volume of ventricles. Previous studies revealed increased volume of lateral ventricles as the subject sample grew larger (66,70).
In a 4-year study, DeLisi and coworkers (66) noted that there were no modifications in temporal lobe volume or in the amygdala-hippocampal complex.
7. Conclusions
Summarizing all of these studies regarding MRI imaging in patients with schizophrenia, the most frequent findings are enlargement of lateral ventricles, cortical atrophy, affecting mostly temporal and frontal lobes, and white matter abnormalities.
MRI findings thus demonstrate that brain abnormalities are present at first episode of the illness, and that the brain regions involved are the same brain regions observed in more chronic patients. There are some anomalies which progress over time, such as reduction in the volume of frontal and parietal lobes, superior temporal gyrus and lateral ventricles (10).
The changes in the volume of the basal ganglia seem to be related rather to the type and duration of neuroleptic treatment, whereas the volume of amygdala-hippocamp appears not to change over time.
It is still under debate whether the abnormalities described in this condition could be used as a biomarker for diagnosis. Hopefully, the new MRI technique with a higher resolution will offer new data regarding the brain anomalies in schizophrenia with a better understanding of the innermost pathogenic mechanism of this devastating disease, subsequently impacting the therapeutic interventions in these patients.
These data recommend MRI investigation as an important tool in the follow-up process of patients with schizophrenia.
In conclusion, regarding the continuous evolution of technology, MRI investigation may be considered a necessity and no longer a luxury in early schizophrenia diagnosis.
Acknowledgements
Not applicable.
Funding Statement
Funding: The present work was supported partially by a grant from the Romanian National Authority for Scientific Research and Innovation CCCDI-UEFISCDI project number COFUND-ERANET NEURON SYNSCHIZ 6/2018.
Availability of data and materials
All information included in this Review is documented by relevant references.
Authors' contributions
FPI analyzed and collected data regarding the MRI findings. MCM analyzed and collected data regarding the MRI findings. MB was involved in revising the review critically for important intellectual content. AMC was involved in revising the review critically for important intellectual content. MM critically revised the manuscript. All authors read and approved the final manuscript for publication.
Ethics approval and consent to participate
Not applicable.
Patient consent for publication
Not applicable.
Competing interests
The authors declare that they have no competing interests.
References
- 1.van OS J, Kapur S. Schizophrenia. Lancet. 2009;374:635–645. doi: 10.1016/S0140-6736(09)60995-8. [DOI] [PubMed] [Google Scholar]
- 2.Rofman ES. Kaplan and Sadock's synopsis of psychiatry. J Clin Psychiatry. 2015;11(303) [Google Scholar]
- 3.McClellan J, Stock S. Practice parameter for the assessment and treatment of children and adolescents with schizophrenia. J Am Acad Child Adolesc Psychiatry. 2013;52:976–990. doi: 10.1016/j.jaac.2013.02.008. American Academy of Child and Adolescent Psychiatry (AACAP) Committee on Quality Issues (CQI) [DOI] [PubMed] [Google Scholar]
- 4.Davis J, Eyre H, Jacka FN, Dodd S, Dean O, McEwen S, Debnath M, McGrath J, Maes M, Amminger P, et al. A review of vulnerability and risks for schizophrenia: Beyond the two hit hypothesis. Neurosci Biobehav Rev. 2016;65:185–194. doi: 10.1016/j.neubiorev.2016.03.017. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Murray RM, Bhavsar V, Tripoli G, Howes O. 30 years on: How the neurodevelopmental hypothesis of schizophrenia morphed into the developmental risk factor model of psychosis. Schizophr Bull. 2017;43:1190–1196. doi: 10.1093/schbul/sbx121. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Najjar S, Pearlman DM. Neuroinflammation and white matter pathology in schizophrenia: Systematic review. Schizophr Res. 2015;161:102–112. doi: 10.1016/j.schres.2014.04.041. [DOI] [PubMed] [Google Scholar]
- 7.Bilder RM, Wu H, Bogerts B, Ashtari M, Robinson D, Woerner M, Lieberman JA, Degreef G. Cerebral volume asymmetries in schizophrenia and mood disorders: A quantitative magnetic resonance imaging study. Int J Psychophysiol. 1999;34:197–205. doi: 10.1016/s0167-8760(99)00077-x. [DOI] [PubMed] [Google Scholar]
- 8.Andreasen NC, Flashman L, Flaum M, Arndt S, Swayze V II, O'Leary DS, Ehrhardt JC, Yuh WT. Regional brain abnormalities in schizophrenia measured with magnetic resonance imaging. JAMA. 1994;272:1763–1769. [PubMed] [Google Scholar]
- 9.Bilder RM, Wu H, Bogerts B, Degreef G, Ashtari M, Alvir JM, Snyder PJ, Lieberman JA. Absence of regional hemispheric volume asymmetries in first-episode schizophrenia. Am J Psychiatry. 1994;151:1437–1447. doi: 10.1176/ajp.151.10.1437. [DOI] [PubMed] [Google Scholar]
- 10.Shenton ME, Dickey CC, Frumin M, McCarley RW. A review of MRI findings in schizophrenia. Schizophr Res. 2001;49:1–52. doi: 10.1016/s0920-9964(01)00163-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Blackwood DH, Young AH, McQueen JK, Martin MJ, Roxborough HM, Muir WJ, St Clair DM, Kean DM. Magnetic resonance imaging in schizophrenia: Altered brain morphology associated with P300 abnormalities and eye tracking dysfunction. Biol Psychiatry. 1991;30:753–769. doi: 10.1016/0006-3223(91)90232-b. [DOI] [PubMed] [Google Scholar]
- 12.Colombo C, Abbruzzese M, Livian S, Scotti G, Locatelli M, Bonfanti A, Scarone S. Memory functions and temporal-limbic morphology in schizophrenia. Psychiatry Res. 1993;50:45–56. doi: 10.1016/0925-4927(93)90023-b. [DOI] [PubMed] [Google Scholar]
- 13.Hoff AL, Riordan H, O'Donnell D, Stritzke P, Neale C, Boccio A, Anand AK, DeLisi LE. Anomalous lateral sulcus asymmetry and cognitive function in first-episode schizophrenia. Schizophr Bull. 1992;18:257–272. doi: 10.1093/schbul/18.2.257. [DOI] [PubMed] [Google Scholar]
- 14.Jernigan TL, Zisook S, Heaton RK, Moranville JT, Hesselink JR, Braff DL. Magnetic resonance imaging abnormalities in lenticular nuclei and cerebral cortex in schizophrenia. Arch Gen Psychiatry. 1991;48:881–890. doi: 10.1001/archpsyc.1991.01810340013002. [DOI] [PubMed] [Google Scholar]
- 15.Lawrie SM, Whalley H, Kestelman JN, Abukmeil SS, Byrne M, Hodges A, Rimmington JE, Best JJ, Owens DG, Johnstone EC. Magnetic resonance imaging of brain in people at high risk of developing schizophrenia. Lancet. 1999;353:30–33. doi: 10.1016/S0140-6736(98)06244-8. [DOI] [PubMed] [Google Scholar]
- 16.Rossi A, Stratta P, D'Albenzio L, Tartaro A, Schiazza G, di Michele V, Bolino F, Casacchia M. Reduced temporal lobe areas in schizophrenia: Preliminary evidences from a controlled multiplanar magnetic resonance imaging study. Biol Psychiatry. 1990;27:61–68. doi: 10.1016/0006-3223(90)90020-3. [DOI] [PubMed] [Google Scholar]
- 17.Rossi A, Stratta P, Mancini F, Gallucci M, Mattei P, Core L, di Michele V, Casacchia M. Magnetic resonance imaging findings of amygdala-anterior hippocampus shrinkage in male patients with schizophrenia. Psychiatry Res. 1994;52:43–53. doi: 10.1016/0165-1781(94)90119-8. [DOI] [PubMed] [Google Scholar]
- 18.Schwartz JM, Aylward E, Barta PE, Tune LE, Pearlson GD. Sylvian fissure size in schizophrenia measured with the magnetic resonance imaging rating protocol of the Consortium to Establish a Registry for Alzheimer's disease. Am J Psychiatry. 1992;149:1195–1198. doi: 10.1176/ajp.149.9.1195. [DOI] [PubMed] [Google Scholar]
- 19.Schwarzkopf SB, Olson SC, Coffman JA, Nasrallah HA. Third and lateral ventricular volumes in schizophrenia: Support for progressive enlargement of both structures. Psychopharmacol Bull. 1990;26:385–391. [PubMed] [Google Scholar]
- 20.Shenton ME, Kikinis R, McCarley RW, Metcalf D, Tieman J, Jolesz FA. Application of automated MRI volumetric measurement techniques to the ventricular system in schizophrenics and normal controls. Schizophr Res. 1991;5:103–113. doi: 10.1016/0920-9964(91)90037-r. [DOI] [PubMed] [Google Scholar]
- 21.Woodruff PW, Wright IC, Shuriquie N, Russouw H, Rushe T, Howard RJ, Graves M, Bullmore ET, Murray RM. Structural brain abnormalities in male schizophrenics reflect fronto-temporal dissociation. Psychol Med. 1997;27:1257–1266. doi: 10.1017/s0033291797005229. [DOI] [PubMed] [Google Scholar]
- 22.Andreasen NC, Ehrhardt JC, Swayze VW II, Alliger RJ, Yuh WT, Cohen G, Ziebell S. Magnetic resonance imaging of the brain in schizophrenia. The pathophysiologic significance of structural abnormalities. Arch Gen Psychiatry. 1990;47:35–44. doi: 10.1001/archpsyc.1990.01810130037006. [DOI] [PubMed] [Google Scholar]
- 23.Roy PD, Zipursky RB, Saint-Cyr JA, Bury A, Langevin R, Seeman MV. Temporal horn enlargement is present in schizophrenia and bipolar disorder. Biol Psychiatry. 1998;44:418–422. doi: 10.1016/s0006-3223(98)00105-x. [DOI] [PubMed] [Google Scholar]
- 24.Keshavan MS, Haas GL, Kahn CE, Aguilar E, Dick EL, Schooler NR, Sweeny JA, Pettegrew JW. Superior temporal gyrus and the course of early schizophrenia: Progressive, static, or reversible? J Psychiatr Res. 1998;32:161–167. doi: 10.1016/s0022-3956(97)00038-1. [DOI] [PubMed] [Google Scholar]
- 25.Stratta P, Rossi A, Gallucci M, Amicarelli I, Passariello R, Casacchia M. Hemispheric asymmetries and schizophrenia: A preliminary magnetic resonance imaging study. Biol Psychiatry. 1989;25:275–284. doi: 10.1016/0006-3223(89)90175-3. [DOI] [PubMed] [Google Scholar]
- 26.Cannon TD, van Erp TG, Huttunen M, Lönnqvist J, Salonen O, Valanne L, Poutanen VP, Standertskjöld-Nordenstam CG, Gur RE, Yan M. Regional gray matter, white matter, and cerebrospinal fluid distributions in schizophrenic patients, their siblings, and controls. Arch Gen Psychiatry. 1998;55:1084–1091. doi: 10.1001/archpsyc.55.12.1084. [DOI] [PubMed] [Google Scholar]
- 27.Gur RE, Cowell P, Turetsky BI, Gallacher F, Cannon T, Bilker W, Gur RC. A follow-up magnetic resonance imaging study of schizophrenia. Relationship of neuroanatomical changes to clinical and neurobehavioral measures. Arch Gen Psychiatry. 1998;55:145–152. doi: 10.1001/archpsyc.55.2.145. [DOI] [PubMed] [Google Scholar]
- 28.Altshuler LL, Bartzokis G, Grieder T, Curran J, Mintz J. Amygdala enlargement in bipolar disorder and hippocampal reduction in schizophrenia: An MRI study demonstrating neuroanatomic specificity. Arch Gen Psychiatry. 1998;55:663–664. doi: 10.1001/archpsyc.55.7.663. [DOI] [PubMed] [Google Scholar]
- 29.Niemann K, Hammers A, Coenen VA, Thron A, Klosterkötter J. Evidence of a smaller left hippocampus and left temporal horn in both patients with first episode schizophrenia and normal control subjects. Psychiatry Res. 2000;99:93–110. doi: 10.1016/s0925-4927(00)00059-7. [DOI] [PubMed] [Google Scholar]
- 30.Szeszko PR, Bilder RM, Lencz T, Pollack S, Alvir JM, Ashtari M, Wu H, Lieberman JA. Investigation of frontal lobe subregions in first-episode schizophrenia. Psychiatry Res. 1999;90:1–15. doi: 10.1016/s0925-4927(99)00002-5. [DOI] [PubMed] [Google Scholar]
- 31.Buchanan RW, Vladar K, Barta PE, Pearlson GD. Structural evaluation of the prefrontal cortex in schizophrenia. Am J Psychiatry. 1998;155:1049–1055. doi: 10.1176/ajp.155.8.1049. [DOI] [PubMed] [Google Scholar]
- 32.Baaré WF, Hulshoff Pol HE, Hijman R, Mali WP, Viergever MA, Kahn RS. Volumetric analysis of frontal lobe regions in schizophrenia: Relation to cognitive function and symptomatology. Biol Psychiatry. 1999;45:1597–1605. doi: 10.1016/s0006-3223(98)00266-2. [DOI] [PubMed] [Google Scholar]
- 33.Wible CG, Shenton ME, Fischer IA, Allard JE, Kikinis R, Jolesz FA, Iosifescu DV, McCarley RW. Parcellation of the human prefrontal cortex using MRI. Psychiatry Res. 1997;76:29–40. doi: 10.1016/s0925-4927(97)00060-7. [DOI] [PubMed] [Google Scholar]
- 34.Nuechterlein KH, Dawson ME. Information processing and attentional functioning in the developmental course of schizophrenic disorders. Schizophr Bull. 1984;10:160–203. doi: 10.1093/schbul/10.2.160. [DOI] [PubMed] [Google Scholar]
- 35.Park S, Holzman PS. Schizophrenics show spatial working memory deficits. Arch Gen Psychiatry. 1992;49:975–982. doi: 10.1001/archpsyc.1992.01820120063009. [DOI] [PubMed] [Google Scholar]
- 36.Mesulam MM. Large-scale neurocognitive networks and distributed processing for attention, language, and memory. Ann Neurol. 1990;28:597–613. doi: 10.1002/ana.410280502. [DOI] [PubMed] [Google Scholar]
- 37.Frederikse M, Lu A, Aylward E, Barta P, Sharma T, Pearlson G. Sex differences in inferior parietal lobule volume in schizophrenia. Am J Psychiatry. 2000;157:422–427. doi: 10.1176/appi.ajp.157.3.422. [DOI] [PubMed] [Google Scholar]
- 38.Nopoulos P, Torres I, Flaum M, Andreasen NC, Ehrhardt JC, Yuh WT. Brain morphology in first-episode schizophrenia. Am J Psychiatry. 1995;152:1721–1723. doi: 10.1176/ajp.152.12.1721. [DOI] [PubMed] [Google Scholar]
- 39.Zipursky RB, Lim KO, Sullivan EV, Brown BW, Pfefferbaum A. Widespread cerebral gray matter volume deficits in schizophrenia. Arch Gen Psychiatry. 1992;49:195–205. doi: 10.1001/archpsyc.1992.01820030027004. [DOI] [PubMed] [Google Scholar]
- 40.Schlaepfer TE, Harris GJ, Tien AY, Peng LW, Lee S, Federman EB, Chase GA, Barta PE, Pearlson GD. Decreased regional cortical gray matter volume in schizophrenia. Am J Psychiatry. 1994;151:842–848. doi: 10.1176/ajp.151.6.842. [DOI] [PubMed] [Google Scholar]
- 41.Levitt JJ, McCarley RW, Nestor PG, Nestor PG, Petrescu C, Donnino R, Hirayasu Y, Kikinis R, Jolesz FA, Shenton ME. Quantitative volumetric MRI study of the cerebellum and vermis in schizophrenia: Clinical and cognitive correlates. Am J Psychiatry. 1999;156:1105–1107. doi: 10.1176/ajp.156.7.1105. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 42.Goldstein JM, Goodman JM, Seidman LJ, Kennedy DN, Makris N, Lee H, Tourville J, Caviness VS Jr, Faraone SV, Tsuang MT. Cortical abnormalities in schizophrenia identified by structural magnetic resonance imaging. Arch Gen Psychiatry. 1999;56:537–547. doi: 10.1001/archpsyc.56.6.537. [DOI] [PubMed] [Google Scholar]
- 43.Nopoulos PC, Ceilley JW, Gailis EA, Andreasen NC. An MRI study of cerebellar vermis morphology in patients with schizophrenia: Evidence in support of the cognitive dysmetria concept. Biol Psychiatry. 1999;46:703–711. doi: 10.1016/s0006-3223(99)00093-1. [DOI] [PubMed] [Google Scholar]
- 44.Rossi A, Stratta P, Fabrizio M, de Cataldo S, Casacchia M. Cerebellar vermal size in schizophrenia: A male effect. Biol Psychiatry. 1993;33:354–357. doi: 10.1016/0006-3223(93)90324-7. [DOI] [PubMed] [Google Scholar]
- 45.DeLisi LE, Hoff AL, Schwartz JE, Shields GW, Halthore SN, Gupta SM, Henn FA, Anand AK. Brain morphology in first-episode schizophrenic-like psychotic patients: A quantitative magnetic resonance imaging study. Biol Psychiatry. 1991;29:159–175. doi: 10.1016/0006-3223(91)90044-m. [DOI] [PubMed] [Google Scholar]
- 46.Shihabuddin L, Buchsbaum MS, Hazlett EA, Haznedar MM, Harvey PD, Newman A, Schnur DB, Spiegel-Cohen J, Wei T, Machac J, et al. Dorsal striatal size, shape, and metabolic rate in never-medicated and previously medicated schizophrenics performing a verbal learning task. Arch Gen Psychiatry. 1998;55:235–243. doi: 10.1001/archpsyc.55.3.235. [DOI] [PubMed] [Google Scholar]
- 47.Corson PW, Nopoulos P, Andreasen NC, Heckel D, Arndt S. Caudate size in first-episode neuroleptic-naive schizophrenic patients measured using an artificial neural network. Biol Psychiatry. 1999;46:712–720. doi: 10.1016/s0006-3223(99)00079-7. [DOI] [PubMed] [Google Scholar]
- 48.Corey-Bloom J, Jernigan T, Archibald S, Harris MJ, Jeste DV. Quantitative magnetic resonance imaging of the brain in late-life schizophrenia. Am J Psychiatry. 1995;152:447–449. doi: 10.1176/ajp.152.3.447. [DOI] [PubMed] [Google Scholar]
- 49.Symonds LL, Archibald SL, Grant I, Zisook S, Jernigan TL. Does an increase in sulcal or ventricular fluid predict where brain tissue is lost? J Neuroimaging. 1999;9:201–209. doi: 10.1111/jon199994201. [DOI] [PubMed] [Google Scholar]
- 50.Staal WG, Hulshoff Pol HE, Schnack H, Van Der Schot AC, Kahn RS. Partial volume decrease of the thalamus in relatives of patients with schizophrenia. Am J Psychiatry. 1998;155:1784–1786. doi: 10.1176/ajp.155.12.1784. [DOI] [PubMed] [Google Scholar]
- 51.Gur RE, Maany V, Mozley PD, Swanson C, Bilker W, Gur RC. Subcortical MRI volumes in neuroleptic-naive and treated patients with schizophrenia. Am J Psychiatry. 1998;155:1711–1717. doi: 10.1176/ajp.155.12.1711. [DOI] [PubMed] [Google Scholar]
- 52.Arciniegas D, Rojas DC, Teale P, Sheeder J, Sandberg E, Reite M. The thalamus and the schizophrenia phenotype: Failure to replicate reduced volume. Biol Psychiatry. 1999;45:1329–1335. doi: 10.1016/s0006-3223(97)00459-9. [DOI] [PubMed] [Google Scholar]
- 53.Hazlett EA, Buchsbaum MS, Byne W, Wei TC, Spiegel-Cohen J, Geneve C, Kinderlehrer R, Haznedar MM, Shihabuddin L, Siever LJ. Three-dimensional analysis with MRI and PET of the size, shape, and function of the thalamus in the schizophrenia spectrum. Am J Psychiatry. 1999;156:1190–1199. doi: 10.1176/ajp.156.8.1190. [DOI] [PubMed] [Google Scholar]
- 54.Narr KL, Thompson PM, Sharma T, Moussai J, Cannestra AF, Toga AW. Mapping morphology of the corpus callosum in schizophrenia. Cereb Cortex. 2000;10:40–49. doi: 10.1093/cercor/10.1.40. [DOI] [PubMed] [Google Scholar]
- 55.Downhill JE Jr, Buchsbaum MS, Wei T, Spiegel-Cohen J, Hazlett EA, Haznedar MM, Silverman J, Siever LJ. Shape and size of the corpus callosum in schizophrenia and schizotypal personality disorder. Schizophr Res. 2000;42:193–208. doi: 10.1016/s0920-9964(99)00123-1. [DOI] [PubMed] [Google Scholar]
- 56.Chua SE, Sharma T, Takei N, Murray RM, Woodruff PWR. A magnetic resonance imaging study of corpus callosum size in familial schizophrenic subjects, their relatives, and normal controls. Schizophr Res. 2000;41:397–403. doi: 10.1016/s0920-9964(99)00081-x. [DOI] [PubMed] [Google Scholar]
- 57.Meisenzahl EM, Frodl T, Greiner J, Leisinger G, Maag KP, Heiss D, Hahn K, Hegerl U, Moller HJ. Corpus callosum size in schizophrenia-a magnetic resonance imaging analysis. Eur Arch Psychiatry Clin Neurosci. 1999;249:305–312. doi: 10.1007/s004060050104. [DOI] [PubMed] [Google Scholar]
- 58.Akhtar W, Naqvi H, Hussain S, Ali A, Ahmad N. Magnetic resonance imaging findings in patients with schizophrenia. J Coll Physicians Surg Pak. 2010;20:167–170. [PubMed] [Google Scholar]
- 59.Barr WB, Ashtari M, Bilder RM, Degreef G, Lieberman JA. Brain morphometric comparison of first-episode schizophrenia and temporal lobe epilepsy. Br J Psychiatry. 1997;170:515–519. doi: 10.1192/bjp.170.6.515. [DOI] [PubMed] [Google Scholar]
- 60.James AC, Crow TJ, Renowden S, Wardell AM, Smith DM, Anslow P. Is the course of brain development in schizophrenia delayed? Evidence from onsets in adolescence. Schizophr Res. 1999;40:1–10. doi: 10.1016/s0920-9964(99)00042-0. [DOI] [PubMed] [Google Scholar]
- 61.Whitworth AB, Honeder M, Kremser C, Kemmler G, Felber S, Hausmann A, Wanko C, Wechdorn H, Aichner F, Stuppaeck CH, et al. Hippocampal volume reduction in male schizophrenic patients. Schizophr Res. 1998;31:73–81. doi: 10.1016/s0920-9964(98)00013-9. [DOI] [PubMed] [Google Scholar]
- 62.Bogerts B, Ashtari M, Degreef G, Alvir JMJ, Bilder RM, Lieberman JA. Reduced temporal limbic structure volumes on magnetic resonance images in first episode schizophrenia. Psychiatry Res Neuroimaging. 1990;35:1–13. doi: 10.1016/0925-4927(90)90004-p. [DOI] [PubMed] [Google Scholar]
- 63.Degreef G, Ashtari M, Bogerts B, Bilder RM, Jody DN, Alvir JMJ, Lieberman JA. Volumes of ventricular system subdivisions measured from magnetic resonance images in first-episode schizophrenic patients. Arch Gen Psychiatry. 1992;49:531–537. doi: 10.1001/archpsyc.1992.01820070025004. [DOI] [PubMed] [Google Scholar]
- 64.Gur RE, Turetsky BI, Cowell PE, Finkelman C, Maany V, Grossman RI, Arnold SE, Bilker WB, Gur RC. Temporolimbic volume reductions in schizophrenia. Arch Gen Psychiatry. 2000;57:769–775. doi: 10.1001/archpsyc.57.8.769. [DOI] [PubMed] [Google Scholar]
- 65.Ohnuma T, Kimura M, Takahashi T, Iwamoto N, Arai H. A magnetic resonance imaging study in first-episode disorganized-type patients with schizophrenia. Psychiatry Clin Neurosci. 1997;51:9–15. doi: 10.1111/j.1440-1819.1997.tb02359.x. [DOI] [PubMed] [Google Scholar]
- 66.DeLisi LE, Sakuma M, Tew W, Kushner M, Hoff AL, Grimson R. Schizophrenia as a chronic active brain process: A study of progressive brain structural change subsequent to the onset of schizophrenia. Psychiatry Res. 1997;74:129–140. doi: 10.1016/s0925-4927(97)00012-7. [DOI] [PubMed] [Google Scholar]
- 67.Kwon JS, Shenton ME, Hirayasu Y, Salisbury DF, Fischer IA, Dickey CC, Yurgelun-Todd D, Tohen M, Kikinis R, Jolesz FA, et al. MRI study of cavum septi pellucidi in schizophrenia, affective disorder, and schizotypal personality disorder. Am J Psychiatry. 1998;155:509–515. doi: 10.1176/ajp.155.4.509. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 68.DeQuardo JR, Keshavan MS, Bookstein FL, Bagwell WW, Green WD, Sweeney JA, Haas GL, Tandon R, Schooler NR, Pettegrew JW. Landmark-based morphometric analysis of first-episode schizophrenia. Biol Psychiatry. 1999;45:1321–1328. doi: 10.1016/s0006-3223(98)00181-4. [DOI] [PubMed] [Google Scholar]
- 69.DeLisi LE, Stritzke P, Riordan H, Holan V, Boccio A, Kushner M, McClelland J, Van Eyl O, Anand A. The timing of brain morphological changes in schizophrenia and their relationship to clinical outcome. Biol Psychiatry. 1992;31:241–254. doi: 10.1016/0006-3223(92)90047-4. [DOI] [PubMed] [Google Scholar]
- 70.DeLisi LE, Tew W, Xie S, Hoff AL, Sakuma M, Kushner M, Lee G, Shedlack K, Smith AM, Grimson R. A prospective follow-up study of brain morphology and cognition in first-episode schizophrenic patients: Preliminary findings. Biol Psychiatry. 1995;38:349–360. doi: 10.1016/0006-3223(94)00376-e. [DOI] [PubMed] [Google Scholar]
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Data Availability Statement
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