A Comprehensive Analysis of Cerebellar Volumes in the 22q11.2 Deletion Syndrome
| Autor: | T. Blaine Crowley, Beverly S. Emanuel, Khaled Khairy, Walter J. Akers, Stanislav S. Zakharenko, R. Sean Gallagher, Jeffrey Steinberg, J. Eric Schmitt, Shahinur Alam, David R. Roalf, Ruben C. Gur, Donna M. McDonald-McGinn, Raquel E. Gur, Kosha Ruparel, Tae-Yeon Eom, Aaron Alexander-Bloch, John J. DeBevits |
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| Rok vydání: | 2023 |
| Předmět: |
Cerebellum
Psychosis Cognitive Neuroscience Biology medicine.disease Hierarchical clustering medicine.anatomical_structure nervous system Schizophrenia Principal component analysis Linear regression medicine Radiology Nuclear Medicine and imaging Deletion syndrome Neurology (clinical) Neuroscience Biological Psychiatry Neuroanatomy |
| Zdroj: | Biological Psychiatry: Cognitive Neuroscience and Neuroimaging. 8:79-90 |
| ISSN: | 2451-9022 |
| DOI: | 10.1016/j.bpsc.2021.11.008 |
| Popis: | The presence of a 22q11.2 microdeletion (22q11.2 deletion syndrome [22q11DS]) ranks among the greatest known genetic risk factors for the development of psychotic disorders. There is emerging evidence that the cerebellum is important in the pathophysiology of psychosis. However, there is currently limited information on cerebellar neuroanatomy in 22q11DS specifically.High-resolution 3T magnetic resonance imaging was acquired in 79 individuals with 22q11DS and 70 typically developing control subjects (N = 149). Lobar and lobule-level cerebellar volumes were estimated using validated automated segmentation algorithms, and subsequently group differences were compared. Hierarchical clustering, principal component analysis, and graph theoretical models were used to explore intercerebellar relationships. Cerebrocerebellar structural connectivity with cortical thickness was examined via linear regression models.Individuals with 22q11DS had, on average, 17.3% smaller total cerebellar volumes relative to typically developing subjects (p.0001). The lobules of the superior posterior cerebellum (e.g., VII and VIII) were particularly affected in 22q11DS. However, all cerebellar lobules were significantly smaller, even after adjusting for total brain volumes (all cerebellar lobules p.0002). The superior posterior lobule was disproportionately associated with cortical thickness in the frontal lobes and cingulate cortex, brain regions known be affected in 22q11DS. Exploratory analyses suggested that the superior posterior lobule, particularly Crus I, may be associated with psychotic symptoms in 22q11DS.The cerebellum is a critical but understudied component of the 22q11DS neuroendophenotype. |
| Databáze: | OpenAIRE |
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