Cortical gyrification in women and men and the (missing) link to prenatal androgens

Author:

Luders Eileen1234ORCID,Gaser Christian567,Spencer Debra8,Thankamony Ajay910,Hughes Ieuan9,Simpson Helen11,Srirangalingam Umasuthan11,Gleeson Helena12,Hines Melissa8,Kurth Florian313ORCID

Affiliation:

1. Department of Women's and Children's Health Uppsala University Uppsala Sweden

2. Swedish Collegium for Advanced Study (SCAS) Uppsala Sweden

3. School of Psychology University of Auckland Auckland New Zealand

4. Laboratory of Neuro Imaging, School of Medicine University of Southern California Los Angeles California USA

5. Department of Neurology Jena University Hospital Jena Germany

6. Department of Psychiatry and Psychotherapy Jena University Hospital Jena Germany

7. German Center for Mental Health (DZPG) Jena Germany

8. Department of Psychology University of Cambridge Cambridge UK

9. Department of Paediatrics, Addenbrooke's Hospital University of Cambridge Cambridge UK

10. Weston Centre for Paediatric Endocrinology and Diabetes, Addenbrooke's Hospital University of Cambridge Cambridge UK

11. Department of Endocrinology and Diabetes University College Hospital London London UK

12. Queen Elizabeth Hospital Birmingham UK

13. Department of Neuroradiology and Radiology Jena University Hospital Jena Germany

Abstract

AbstractPrevious studies have reported sex differences in cortical gyrification. Since most cortical folding is principally defined in utero, sex chromosomes as well as gonadal hormones are likely to influence sex‐specific aspects of local gyrification. Classic congenital adrenal hyperplasia (CAH) causes high levels of androgens during gestation in females, whereas levels in males are largely within the typical male range. Therefore, CAH provides an opportunity to study the possible effects of prenatal androgens on cortical gyrification. Here, we examined the vertex‐wise absolute mean curvature—a common estimate for cortical gyrification—in individuals with CAH (33 women and 20 men) and pair‐wise matched controls (33 women and 20 men). There was no significant main effect of CAH and no significant CAH‐by‐sex interaction. However, there was a significant main effect of sex in five cortical regions, where gyrification was increased in women compared to men. These regions were located on the lateral surface of the brain, specifically left middle frontal (rostral and caudal), right inferior frontal, left inferior parietal, and right occipital. There was no cortical region where gyrification was increased in men compared to women. Our findings do not only confirm prior reports of increased cortical gyrification in female brains but also suggest that cortical gyrification is not significantly affected by prenatal androgen exposure. Instead, cortical gyrification might be determined by sex chromosomes either directly or indirectly—the latter potentially by affecting the underlying architecture of the cortex or the size of the intracranial cavity, which is smaller in women.

Funder

National Institutes of Health

Publisher

Wiley

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