Polycystic Ovary Syndrome, Combined Oral Contraceptives, and the Risk of Dysglycemia: A Population-Based Cohort Study With a Nested Pharmacoepidemiological Case-Control Study.


Journal

Diabetes care
ISSN: 1935-5548
Titre abrégé: Diabetes Care
Pays: United States
ID NLM: 7805975

Informations de publication

Date de publication:
12 2021
Historique:
received: 22 02 2021
accepted: 08 09 2021
pubmed: 16 10 2021
medline: 8 3 2022
entrez: 15 10 2021
Statut: ppublish

Résumé

Irregular menstrual cycles are associated with increased cardiovascular mortality. Polycystic ovary syndrome (PCOS) is characterized by androgen excess and irregular menses; androgens are drivers of increased metabolic risk in women with PCOS. Combined oral contraceptive pills (COCPs) are used in PCOS both for cycle regulation and to reduce the biologically active androgen fraction. We examined COCP use and risk of dysglycemia (prediabetes and type 2 diabetes) in women with PCOS. Using a large U.K. primary care database (The Health Improvement Network [THIN]; 3.7 million patients from 787 practices), we carried out a retrospective population-based cohort study to determine dysglycemia risk (64,051 women with PCOS and 123,545 matched control subjects), as well as a nested pharmacoepidemiological case-control study to investigate COCP use in relation to dysglycemia risk (2,407 women with PCOS with [case subjects] and without [control subjects] a diagnosis of dysglycemia during follow-up). Cox models were used to estimate the unadjusted and adjusted hazard ratio, and conditional logistic regression was used to obtain adjusted odds ratios (aORs). The adjusted hazard ratio for dysglycemia in women with PCOS was 1.87 (95% CI 1.78-1.97, In this study, limited by its retrospective nature and the use of routinely collected electronic general practice record data, which does not allow for exclusion of the impact of prescription-by-indication bias, women with PCOS exposed to COCPs had a reduced risk of dysglycemia across all BMI subgroups. Future prospective studies should be considered for further understanding of these observations and potential causality.

Identifiants

pubmed: 34649997
pii: dc21-0437
doi: 10.2337/dc21-0437
pmc: PMC8669537
doi:

Substances chimiques

Contraceptives, Oral, Combined 0

Banques de données

figshare
['10.2337/figshare.16608068']

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2758-2766

Subventions

Organisme : Wellcome Trust
Pays : United Kingdom
Organisme : Medical Research Council
ID : MR/S003878/1
Pays : United Kingdom
Organisme : Wellcome Trust
ID : WT209492/Z/17/Z
Pays : United Kingdom
Organisme : Department of Health
ID : BRC-1215-20009
Pays : United Kingdom

Informations de copyright

© 2021 by the American Diabetes Association.

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Auteurs

Balachandran Kumarendran (B)

Institute of Applied Health Research, University of Birmingham, Edgbaston, Birmingham, U.K.
Department of Community and Family Medicine, Faculty of Medicine, University of Jaffna, Kokkuvil, Sri Lanka.

Michael W O'Reilly (MW)

Department of Medicine, Royal College of Surgeons in Ireland, University of Medicine and Health Sciences, Dublin, Republic of Ireland.
Institute of Metabolism and Systems Research, University of Birmingham, Birmingham, U.K.

Anuradhaa Subramanian (A)

Institute of Applied Health Research, University of Birmingham, Edgbaston, Birmingham, U.K.

Dana Šumilo (D)

Institute of Applied Health Research, University of Birmingham, Edgbaston, Birmingham, U.K.

Konstantinos Toulis (K)

Institute of Applied Health Research, University of Birmingham, Edgbaston, Birmingham, U.K.

Krishna M Gokhale (KM)

Institute of Applied Health Research, University of Birmingham, Edgbaston, Birmingham, U.K.

Chandrika N Wijeratne (CN)

Department of Obstetrics and Gynecology, Faculty of Medicine, University of Colombo, Colombo, Sri Lanka.

Arri Coomarasamy (A)

Institute of Metabolism and Systems Research, University of Birmingham, Birmingham, U.K.

Abd A Tahrani (AA)

Institute of Metabolism and Systems Research, University of Birmingham, Birmingham, U.K.

Laurent Azoulay (L)

Department of Epidemiology, Biostatistics and Occupational Health and Gerald Bronfman Department of Oncology, McGill University, Toronto, Canada.

Wiebke Arlt (W)

Institute of Metabolism and Systems Research, University of Birmingham, Birmingham, U.K. w.arlt@bham.ac.uk k.nirantharan@bham.ac.uk.
NIHR Birmingham Biomedical Research Centre, University of Birmingham and University Hospitals Birmingham NHS Foundation Trust, Birmingham, U.K.

Krishnarajah Nirantharakumar (K)

Institute of Applied Health Research, University of Birmingham, Edgbaston, Birmingham, U.K. w.arlt@bham.ac.uk k.nirantharan@bham.ac.uk.
Institute of Metabolism and Systems Research, University of Birmingham, Birmingham, U.K.

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