Regional Alterations in Cortical Sulcal Depth in Living Fetuses with Down Syndrome

Author:

Yun Hyuk Jin12ORCID,Perez Juan David Ruiz12,Sosa Patricia12,Valdés J Alejandro12,Madan Neel3,Kitano Rie4,Akiyama Shizuko4,Skotko Brian G5,Feldman Henry A26,Bianchi Diana W7,Grant P Ellen128,Tarui Tomo4,Im Kiho12

Affiliation:

1. Fetal Neonatal Neuroimaging and Developmental Science Center, Boston Children’s Hospital, Harvard Medical School, Boston, MA 02115, USA

2. Division of Newborn Medicine, Boston Children’s Hospital, Harvard Medical School, Boston, MA 02115, USA

3. Department of Radiology, Tufts Medical Center, Boston, MA 02111, USA

4. Mother Infant Research Institute, Tufts Medical Center, Boston, MA 02111, USA

5. Down Syndrome Program, Genetics, Pediatrics, Massachusetts General Hospital, Boston, MA 02114, USA

6. Institutional Centers for Clinical and Translational Research, Boston Children’s Hospital, Harvard Medical School, Boston, MA 02115, USA

7. Prenatal Genomics and Fetal Therapy Section, Medical Genetics Branch, National Human Genome Research Institute, Bethesda, MD 20892, USA

8. Department of Radiology, Boston Children’s Hospital, Harvard Medical School, Boston, MA 02115, USA

Abstract

Abstract Down syndrome (DS) is the most common genetic cause of developmental disabilities. Advanced analysis of brain magnetic resonance imaging (MRI) has been used to find brain abnormalities and their relationship to neurocognitive impairments in children and adolescents with DS. Because genetic factors affect brain development in early fetal life, there is a growing interest in analyzing brains from living fetuses with DS. In this study, we investigated regional sulcal folding depth as well as global cortical gyrification from fetal brain MRIs. Nine fetuses with DS (29.1 ± 4.24 gestational weeks [mean ± standard deviation]) were compared with 17 typically developing [TD] fetuses (28.4 ± 3.44). Fetuses with DS showed lower whole-brain average sulcal depths and gyrification index than TD fetuses. Significant decreases in sulcal depth were found in bilateral Sylvian fissures and right central and parieto-occipital sulci. On the other hand, significantly increased sulcal depth was shown in the left superior temporal sulcus, which is related to atypical hemispheric asymmetry of cortical folding. Moreover, these group differences increased as gestation progressed. This study demonstrates that regional sulcal depth is a sensitive marker for detecting alterations of cortical development in DS during fetal life, which may be associated with later neurocognitive impairment.

Funder

National Institutes of Health

Jerome Lejeune Foundation

Susan Saltonstall Foundation

Publisher

Oxford University Press (OUP)

Subject

Cellular and Molecular Neuroscience,Cognitive Neuroscience

Reference93 articles.

1. Abnormal brain synchrony in Down syndrome;Anderson;NeuroImage: Clinical,2013

2. New approaches to studying early brain development in Down syndrome;Baburamani;Dev Med Child Neurol,2019

3. A critical period in cortical interneuron neurogenesis in Down syndrome revealed by human neural progenitor cells;Bhattacharyya;DNE,2009

4. Cerebral asymmetry and language development: cause, correlate or consequence?;Bishop;Science,2013

Cited by 18 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3