Neuroanatomical Profile of Young Females with Fragile X Syndrome: A Voxel-Based Morphometry Analysis

Abstract Fragile X syndrome is a genetic condition associated with alterations in brain and subsequent cognitive development. However, due to a milder phenotype relative to males, females with fragile X syndrome are underrepresented in research studies. In the current study, we investigate neuroanat...

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Published inCerebral cortex (New York, N.Y. 1991) Vol. 32; no. 11; pp. 2310 - 2320
Main Authors Lee, Cindy H, Bartholomay, Kristi L, Marzelli, Matthew J, Miller, Jonas G, Bruno, Jennifer L, Lightbody, Amy A, Reiss, Allan L
Format Journal Article
LanguageEnglish
Published United States Oxford University Press 31.05.2022
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Summary:Abstract Fragile X syndrome is a genetic condition associated with alterations in brain and subsequent cognitive development. However, due to a milder phenotype relative to males, females with fragile X syndrome are underrepresented in research studies. In the current study, we investigate neuroanatomical differences in young females (age range: 6.03–16.32 years) with fragile X syndrome (N = 46) as compared to age-, sex-, and verbal abilities-matched participants (comparison group; N = 35). Between-group analyses of whole-brain and regional brain volumes were assessed using voxel-based morphometry. Results demonstrate significantly larger total gray and white matter volumes in girls with fragile X syndrome compared to a matched comparison group (Ps < 0.001). In addition, the fragile X group showed significantly larger gray matter volume in a bilateral parieto-occipital cluster and a right parieto-occipital cluster (Ps < 0.001). Conversely, the fragile X group showed significantly smaller gray matter volume in the bilateral gyrus rectus (P < 0.03). Associations between these regional brain volumes and key socio-emotional variables provide insight into gene–brain–behavior relationships underlying the fragile X syndrome phenotype in females. These findings represent the first characterization of a neuroanatomical phenotype in a large sample of girls with fragile X syndrome and expand our knowledge about potential neurodevelopmental mechanisms underlying cognitive–behavioral outcomes in this condition.
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Cindy H. Lee and Kristi L. Bartholomay contributed equally to this work.
ISSN:1047-3211
1460-2199
DOI:10.1093/cercor/bhab319