White matter microstructure and functional connectivity in the brains of infants with Turner syndrome
Turner syndrome, caused by complete or partial loss of an X-chromosome, is often accompanied by specific cognitive challenges. Magnetic resonance imaging studies of adults and children with Turner syndrome suggest these deficits reflect differences in anatomical and functional connectivity. However, no imaging studies have explored connectivity in infants with Turner syndrome. Consequently, it is unclear when in development connectivity differences emerge. To address this gap, we compared functional connectivity and white matter microstructure of 1-year-old infants with Turner syndrome to typically developing 1-year-old boys and girls. We examined functional connectivity between the right precentral gyrus and five regions that show reduced volume in 1-year old infants with Turner syndrome compared to controls and found no differences. However, exploratory analyses suggested infants with Turner syndrome have altered connectivity between right supramarginal gyrus and left insula and right putamen. To assess anatomical connectivity, we examined diffusivity indices along the superior longitudinal fasciculus and found no differences. However, an exploratory analysis of 46 additional white matter tracts revealed significant group differences in nine tracts. Results suggest that the first year of life is a window in which interventions might prevent connectivity differences observed at later ages, and by extension, some of the cognitive challenges associated with Turner syndrome.
Authors
- Debra B. Reinhartsen (ORCID: https://orcid.org/0000-0003-4641-7015)
- Maria T. Maza (ORCID: https://orcid.org/0000-0002-1603-960X)
- Reid Blanchett (ORCID: https://orcid.org/0000-0003-4082-7603)
- Stephen R. Hooper (ORCID: https://orcid.org/0000-0002-6761-4504)
- Rebecca Knickmeyer (ORCID: https://orcid.org/0000-0001-7708-1388)
- Emil Cornea (ORCID: https://orcid.org/0000-0001-8582-1729)
- John H. Gilmore (ORCID: https://orcid.org/0000-0002-0939-6764)
- Wei Gao (ORCID: https://orcid.org/0000-0002-9260-2601)
- Margaret DeRamus
- Martin Styner (ORCID: https://orcid.org/0000-0002-8747-5118)
- Roza Vlasova (ORCID: https://orcid.org/0000-0002-6455-8949)
- Rebecca Edmondson Pretzel (ORCID: https://orcid.org/0000-0001-7817-8624)
- Haitao Chen (ORCID: https://orcid.org/0000-0002-6108-6640)
- Marsha L. Davenport
Institutions
- University of North Carolina at Chapel Hill (US)
- Cedars-Sinai Medical Center (US)
- Van Andel Institute (US)
- Quantitative BioSciences (US)
- Michigan State University (US)
Publication Details
- Journal
- Cerebral Cortex
- Published
- 2024-09-01
- DOI
- https://doi.org/10.1093/cercor/bhae351
- Citations
- 1
- Primary Topic
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Type
- article
- Field-Weighted Citation Impact
- 0.55
Funders
- Pfizer
- National Institutes of Health
- National Institute of Mental Health
- National Institute of Child Health and Human Development
- National Center for Advancing Translational Sciences
- Eunice Kennedy Shriver National Institute of Child Health and Human Development