Association of Androgen Hormones, Sex Hormone-Binding Globulin, and the Menopausal Transition With Incident Diabetes Mellitus in Women With and Without HIV.


Journal

Journal of acquired immune deficiency syndromes (1999)
ISSN: 1944-7884
Titre abrégé: J Acquir Immune Defic Syndr
Pays: United States
ID NLM: 100892005

Informations de publication

Date de publication:
15 Apr 2024
Historique:
received: 24 08 2023
accepted: 01 12 2023
medline: 18 3 2024
pubmed: 5 1 2024
entrez: 5 1 2024
Statut: ppublish

Résumé

HIV is associated with alterations in androgen hormone levels and sex hormone-binding globulin (SHBG) in women. Higher SHBG has been associated with a lower risk of diabetes in the general population, but the contribution of HIV, androgen hormones, SHBG, and menopausal phase to diabetes is unclear. From April 2003 through February 2020, 896 women with HIV (WWH) and 343 women without HIV (WWOH) from the Women's Interagency HIV Study with morning total testosterone, dehydroepiandrosterone sulfate (DHEAS), and SHBG levels were followed to assess for incident diabetes. Parametric regression models were used with age as the time scale and relative times (RT) as the measure of association of hormone level and menopausal phase with incident diabetes. Analyses incorporated time-dependent androgen hormone, SHBG levels, and menopausal phase and were adjusted for race/ethnicity, enrollment year, smoking status, BMI, hepatitis C virus status, and HIV-related factors. In total, 128 (14%) WWH and 47 (14%) WWOH developed diabetes. In WWH, a doubling of SHBG and DHEAS were associated with a 7% (RT = 1.07 [95% CI: 0.82 to 1.40] and 15% (RT = 1.15 [95% CI: 0.95 to 1.39]) longer time to diabetes, respectively; in WWOH, a doubling of SHBG and DHEAS were associated with 84% (RT = 1.84 [95% CI: 0.89 to 3.82]) and 41% (RT= 1.41 [95% CI: 0.82 to 2.44]) longer times to diabetes. Total testosterone was not associated. In WWH, later menopausal phase was associated with shorter times to diabetes. Despite alterations in androgen hormone and SHBG levels in HIV, regardless of HIV status, higher SHBG and DHEAS were associated with nonstatistically significant slower progression to diabetes. The menopausal transition may be a better hormonal indicator of diabetes risk in WWH.

Sections du résumé

BACKGROUND BACKGROUND
HIV is associated with alterations in androgen hormone levels and sex hormone-binding globulin (SHBG) in women. Higher SHBG has been associated with a lower risk of diabetes in the general population, but the contribution of HIV, androgen hormones, SHBG, and menopausal phase to diabetes is unclear.
METHODS METHODS
From April 2003 through February 2020, 896 women with HIV (WWH) and 343 women without HIV (WWOH) from the Women's Interagency HIV Study with morning total testosterone, dehydroepiandrosterone sulfate (DHEAS), and SHBG levels were followed to assess for incident diabetes. Parametric regression models were used with age as the time scale and relative times (RT) as the measure of association of hormone level and menopausal phase with incident diabetes. Analyses incorporated time-dependent androgen hormone, SHBG levels, and menopausal phase and were adjusted for race/ethnicity, enrollment year, smoking status, BMI, hepatitis C virus status, and HIV-related factors.
RESULTS RESULTS
In total, 128 (14%) WWH and 47 (14%) WWOH developed diabetes. In WWH, a doubling of SHBG and DHEAS were associated with a 7% (RT = 1.07 [95% CI: 0.82 to 1.40] and 15% (RT = 1.15 [95% CI: 0.95 to 1.39]) longer time to diabetes, respectively; in WWOH, a doubling of SHBG and DHEAS were associated with 84% (RT = 1.84 [95% CI: 0.89 to 3.82]) and 41% (RT= 1.41 [95% CI: 0.82 to 2.44]) longer times to diabetes. Total testosterone was not associated. In WWH, later menopausal phase was associated with shorter times to diabetes.
CONCLUSIONS CONCLUSIONS
Despite alterations in androgen hormone and SHBG levels in HIV, regardless of HIV status, higher SHBG and DHEAS were associated with nonstatistically significant slower progression to diabetes. The menopausal transition may be a better hormonal indicator of diabetes risk in WWH.

Identifiants

pubmed: 38180885
doi: 10.1097/QAI.0000000000003380
pii: 00126334-990000000-00360
doi:

Substances chimiques

Androgens 0
Sex Hormone-Binding Globulin 0
Testosterone 3XMK78S47O

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

486-493

Subventions

Organisme : NHLBI NIH HHS
ID : U01 HL146204
Pays : United States
Organisme : NHLBI NIH HHS
ID : U01 HL146242
Pays : United States
Organisme : NHLBI NIH HHS
ID : U01-HL146242
Pays : United States
Organisme : NHLBI NIH HHS
ID : U01-HL146204
Pays : United States
Organisme : NHLBI NIH HHS
ID : U01-HL146245
Pays : United States
Organisme : NHLBI NIH HHS
ID : U01-HL146202
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK 109823
Pays : United States
Organisme : NHLBI NIH HHS
ID : 5K12HL143961-02
Pays : United States

Informations de copyright

Copyright © 2024 Wolters Kluwer Health, Inc. All rights reserved.

Déclaration de conflit d'intérêts

P.C.T.: Grant support from Merck. The remaining authors have no conflicts of interest to disclose.

Références

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Auteurs

Rebecca A Abelman (RA)

Department of Medicine, University of California San Francisco, San Francisco, CA.

Michael F Schneider (MF)

Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD.

Christopher Cox (C)

Department of Epidemiology, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD.

Geralyn Messerlian (G)

Department of Pathology and Laboratory Medicine, Brown University, Providence, RI.

Mardge Cohen (M)

Department of Medicine, Stroger Hospital, Cook County Health, Chicago, IL.

Deborah Gustafson (D)

Department of Neurology, State University of New York Downstate Health Sciences University, Brooklyn, NY.

Michael Plankey (M)

Department of Medicine, Georgetown University Medical Center, Washington, DC.

Anjali Sharma (A)

Department of Medicine, Albert Einstein College of Medicine, Bronx, NY; and.

Jennifer Price (J)

Department of Medicine, University of California San Francisco, San Francisco, CA.

Carl Grunfeld (C)

Department of Medicine, University of California San Francisco, San Francisco, CA.
Medical Service, Department of Veteran Affairs Medical Center, San Francisco, CA.

Phyllis C Tien (PC)

Department of Medicine, University of California San Francisco, San Francisco, CA.
Medical Service, Department of Veteran Affairs Medical Center, San Francisco, CA.

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