Pediatric Features of Genetic Predisposition to Polycystic Ovary Syndrome

Author:

Zhu Jia123ORCID,Eliasen Anders U45,Aris Izzuddin M6,Stinson Sara E7ORCID,Holm Jens-Christian78,Hansen Torben7ORCID,Hivert Marie-France69ORCID,Bønnelykke Klaus4,Salem Rany M10,Hirschhorn Joel N12311ORCID,Chan Yee-Ming123ORCID

Affiliation:

1. Division of Endocrinology, Boston Children's Hospital , Boston, MA 02115 , USA

2. Programs in Metabolism and Medical and Population Genetics, The Broad Institute of MIT and Harvard , Cambridge, MA 02142 , USA

3. Department of Pediatrics, Harvard Medical School , Boston, MA 02115 , USA

4. Copenhagen Prospective Studies on Asthma in Childhood Research Center (COPSAC), Copenhagen University Hospital, Herlev-Gentofte , Copenhagen 2820 , Denmark

5. Department of Health Technology, Section for Bioinformatics, Technical University of Denmark , Kongens Lyngby 2800 , Denmark

6. Division of Chronic Disease Research Across the Lifecourse, Department of Population Medicine, Harvard Medical School, Harvard University and Harvard Pilgrim Health Care Institute , Boston, MA 02215 , USA

7. Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen , Copenhagen 2200 , Denmark

8. The Children's Obesity Clinic, Accredited European Centre for Obesity Management, Department of Pediatrics, Copenhagen University Hospital Holbæk , Holbæk 4300 , Denmark

9. Diabetes Unit, Massachusetts General Hospital , Boston, MA 02114 , USA

10. Herbert Wertheim School of Public Health and Human Longevity Science, University of California San Diego , La Jolla, CA 92093 , USA

11. Department of Genetics, Harvard Medical School , Boston, MA 02115 , USA

Abstract

Abstract Context Polycystic ovary syndrome (PCOS) has historically been conceptualized as a disorder of the reproductive system in women. However, offspring of women with PCOS begin to show metabolic features of PCOS in childhood, suggestive of childhood manifestations. Objective To identify childhood manifestations of genetic risk for PCOS. Methods We calculated a PCOS polygenic risk score (PRS) for 12 350 girls and boys in 4 pediatric cohorts—ALSPAC (UK), COPSAC (Denmark), Project Viva (USA), and The HOLBÆK Study (Denmark). We tested for association of the PRS with PCOS-related phenotypes throughout childhood and with age at pubarche and age at peak height velocity and meta-analyzed effects across cohorts using fixed-effect models. Results Higher PRS for PCOS was associated with higher body mass index in midchildhood (0.05 kg/m2 increase per 1 SD of PRS, 95% CI 0.03, 0.07, P = 3 × 10−5) and higher risk of obesity in early childhood (OR 1.34, 95% CI 1.13, 1.59, P = .0009); both persisted through late adolescence (P all ≤.03). Higher PCOS PRS was associated with earlier age at pubarche (0.85-month decrease per 1 SD of PRS, 95% CI −1.44, −0.26, P = .005) and younger age at peak height velocity (0.64-month decrease per 1 SD of PRS, 95% CI −0.94, −0.33, P = 4 × 10−5). Conclusion Genetic risk factors for PCOS are associated with alterations in metabolic, growth, and developmental traits in childhood. Thus, PCOS may not simply be a condition that affects women of reproductive age but, rather, a possible manifestation of an underlying condition that affects both sexes starting in early life.

Funder

National Institute of Child Health and Human Development

American Heart Association

Pediatric Endocrine Society

Boston Children’s Hospital Office of Faculty Development

National Institute of Diabetes and Digestive and Kidney Diseases

UK Medical Research Council and Wellcome Trust

UK Medical Research Council and the Wellcome Trust

National Institutes of Health

Novo Nordisk Foundation

Innovation Fund Denmark

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

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