Hyperandrogenemia in Early Adulthood Is an Independent Risk Factor for Abnormal Glucose Metabolism in Middle Age

Author:

Tuorila Katri1ORCID,Ollila Meri-Maija1ORCID,Järvelin Marjo-Riitta2345,Tapanainen Juha S16,Franks Stephen7,Puukka Katri8,Piltonen Terhi T1ORCID,Morin-Papunen Laure1ORCID

Affiliation:

1. Department of Obstetrics and Gynecology, University of Oulu and Oulu University Hospital, Medical Research Center, PEDEGO Research Unit, Oulu, Finland

2. MRC-PHE Centre for Environment and Health, Department of Epidemiology and Biostatistics, School of Public Health, Imperial College London, London, UK

3. Center for Life Course Health Research, Faculty of Medicine, University of Oulu, Oulu, Finland

4. Unit of Primary Health Care, Oulu University Hospital, OYS, Oulu, Finland

5. Department of Life Sciences, College of Health and Life Sciences, Brunel University London, London, UK

6. Department of Obstetrics and Gynecology, University of Helsinki and Helsinki University Hospital, Helsinki, Finland

7. Institute of Reproductive and Developmental Biology, Imperial College London, London, UK

8. NordLab Oulu, Department of Clinical Chemistry, University of Oulu and Oulu University Hospital, Medical Research Center Oulu, Oulu, Finland

Abstract

Abstract Context The role of androgen excess as a contributing factor to abnormal glucose metabolism (AGM) and insulin resistance in women remains controversial. Objective To investigate whether hyperandrogenemia (HA) estimated by serum testosterone (T) level and free androgen index (FAI) at ages 31 and 46 years is associated with insulin resistance, insulin secretion and AGM by age 46. Design Prospective study including 5889 females followed at ages 31 and 46 years. Setting General community. Participants Women with HA were compared with normoandrogenic women at ages 31 and 46 years. Intervention None. Main outcome measurements AGM, including prediabetes and type 2 diabetes mellitus, homeostatic model assessments of insulin resistance (HOMA-IR) and of pancreatic β-cell function (HOMA-B). Results At age 31 years, HA women displayed increased HOMA-IR (P = 0.002), HOMA-B (P = 0.007), and higher fasting insulin (P = 0.03) than normoandrogenic women after adjusting for body mass index (BMI). At age 46 years, there was a nonsignificant trend toward higher fasting glucose (P = 0.07) and glycated hemoglobin A1 (P = 0.07) levels in HA women. Women in the highest T quartile (odds ratio [OR] = 1.80; 95%CI, 1.15-2.82) at age 31 years and in the 2 highest FAI quartiles at ages 31 (Q4: OR = 3.76; 95% CI, 2.24-6.32) and 46 (Q4: OR = 2.79; 95% CI, 1.74-4.46) years had increased risk for AGM, independently of BMI, when compared with women in Q1. SHBG was inversely associated with AGM (at age 31 years: Q4: OR = 0.37; 95% CI, 0.23-0.60, at age 46 years: Q4: OR = 0.28; 95% CI, 0.17-0.44). Conclusion Hyperandrogenemia and low SHBG in early and middle age associates with AGM independently of BMI.

Funder

University of Oulu

Socialdepartementet

Ministry of Health and Social Affairs

National Institute for Health and Welfare

Regional Institute of Occupational Health, Oulu, Finland

ERDF European Regional Development Fund

National Institute for Health Research

Medical Research Council

Genesis Research Trust

Finnish Medical Foundation

North Ostrobothnia Regional Fund

Academy of Finland

Sigrid Juselius Foundation and Medical Research Center Oulu

Publisher

The Endocrine Society

Subject

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

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