The DOI matches its Crossref record; 66 of the 66 references it cites were found in a registry or an index.
Heritability of Changes in Brain Volume Over Time in Twin Pairs Discordant for Schizophrenia
Abstract
CONTEXT: Structural brain abnormalities have consistently been found in schizophrenia, with increased familial risk for the disease associated with these abnormalities. Some brain volume changes are progressive over the course of the illness. Whether these progressive brain volume changes are mediated by genetic or disease-related factors is unknown. OBJECTIVE: To investigate whether genetic and/or environmental factors are associated with progressive brain volume changes in schizophrenia. DESIGN: Longitudinal 5-year follow-up in monozygotic (MZ) and dizygotic (DZ) twin pairs discordant for schizophrenia and healthy comparison twin pairs using brain magnetic resonance imaging. SETTING: Participants were recruited from the twin pair cohort at the University Medical Center Utrecht. PARTICIPANTS: A total of 92 participants completed the study: 9 MZ and 10 DZ twin pairs discordant for schizophrenia and 14 MZ and 13 DZ healthy twin pairs. MAIN OUTCOME MEASURES: Percentage volume changes of the whole brain; cerebral gray and white matter of the frontal, temporal, parietal, and occipital lobes; cerebellum; and lateral and third ventricles over time between and within twin pairs were compared using repeated measures analysis of covariance. Structural equation modeling was applied to estimate contributions of additive genetic and common and unique environmental factors. RESULTS: Significant decreases over time in whole brain and frontal and temporal lobe volumes were found in patients with schizophrenia and their unaffected co-twins compared with control twins. Bivariate structural equation modeling using cross-trait/cross-twin correlations revealed significant additive genetic influences on the correlations between schizophrenia liability and progressive whole brain (66%; 95% confidence interval [CI], 51%-100%), frontal lobe (76%; 95% CI, 54%-100%), and temporal lobe (79%; CI, 56%-100%) volume change. CONCLUSION: The progressive brain volume loss found in patients with schizophrenia and their unaffected co-twins is at least partly attributable to genetic factors related to the illness.
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“The (progressive) brain tissue loss has been associated with genetic factors and with disease-related factors 11,12 as well as effects of antipsychotic medication intake. 13”
From Physical exercise keeps the brain connected: biking increases white matter integrity in patients with schizophrenia and healthy controls. (2015) · cites this paper as [11]
In the citing paper
“Interestingly, progressive brain changes are also present in discordant cotwins of patients with schizophrenia, suggesting that these changes are familial, and possibly genetic, and can therefore not solely be explained by antipsychotic medication intake.9”
From Glutamate in Schizophrenia: A Focused Review and Meta-Analysis of 1H-MRS Studies (2013) · cites this paper as [9]
In the citing paper
“Interestingly, progressive brain changes are also present in discordant cotwins of patients with schizophrenia, suggesting that these changes are familial, and possibly genetic, and can therefore not solely be explained by antipsychotic medication intake.9”
From Glutamate in Schizophrenia: A Focused Review and Meta-Analysis of 1H-MRS Studies (2013) · cites this paper as [9]
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Course of Schizophrenia: What Has Been Learned from Longitudinal Studies?
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¿Neurodesarrollo o neurodegeneración? Estado actual
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Исследования структурных характеристик мозга в психогенетике
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Structural Methods in Gray Matter
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Gross Pathology in Schizophrenia
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Gray Matter Abnormalities Associated with the Risk for the Schizophrenia-Bipolar Disorder Spectrum
Cattarinussi, G., Fazio, G., & Sambataro, F. (2024) · Springer eBooks · doi:10.1007/978-3-031-32035-4_81-1
Gray Matter Abnormalities Associated with the Risk for the Schizophrenia-Bipolar Disorder Spectrum
Cattarinussi, G., Fazio, G., & Sambataro, F. (2025) · Springer eBooks · doi:10.1007/978-3-031-73368-0_81
An exploratory study of endophenotype markers for schizophrenia
Picchioni, M. M. (2012) · UPT. Syiah Kuala University Library (Syiah Kuala University)
Metadata
- Authors
- Brans, R. G. H., van Haren, N. E. M., van Baal, G. C. M., Schnack, H. G., Kahn, R. S., & Pol, H. E. H.
- Affiliations
- University Medical Center Utrecht (NL)
- Venue
- Archives of General Psychiatry
- Publisher
- American Medical Association (AMA)
- Published
- 2008-11-03
- Volume
- 65
- Issue
- 11
- Pages
- 1259
- ISSN
- 0003-990X (ISSN-L)
- OpenAlex
- W2124863104
- Cited by
- 129
- References
- 66
- Citations by year
- 2025: 1 · 2024: 2 · 2023: 4 · 2022: 4 · 2021: 3 · 2020: 8 · 2019: 4 · 2018: 4 · 2017: 2 · 2016: 11 · 2015: 14 · 2014: 7 · 2013: 11 · 2012: 18
- FWCI
- 8.41
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Archives of General Psychiatry (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Psychiatry and Mental health › Schizophrenia research and treatment
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Keywords
- schizophrenia, brain volume changes, heritability, monozygotic twins, dizygotic twins, discordant twins, gray matter, white matter, frontal lobe, temporal lobe, cerebellum, ventricles, genetic susceptibility, environmental factors, structural brain abnormalities
- MeSH terms
- Adjustment Disorders, Adult, Brain, Marijuana Abuse, Cerebellum, Cerebral Cortex, Major Depressive Disorder, Diseases in Twins, Female, Humans, Image Processing, Computer-Assisted, Longitudinal Studies, Magnetic Resonance Imaging, Male, Middle Aged, Organ Size, Phenotype, Psychotic Disorders, Reference Values, Schizophrenia, Schizotypal Personality Disorder, Twins, Dizygotic, Twins, Monozygotic, Cohort Studies, Comorbidity, Conduct Disorder, Genetic Predisposition to Disease, Third Ventricle, Lateral Ventricles
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