Adiposity, related biomarkers, and type 2 diabetes after gestational diabetes: The Diabetes Prevention Program.


Journal

Obesity (Silver Spring, Md.)
ISSN: 1930-739X
Titre abrégé: Obesity (Silver Spring)
Pays: United States
ID NLM: 101264860

Informations de publication

Date de publication:
01 2022
Historique:
revised: 23 07 2021
received: 21 04 2021
accepted: 15 08 2021
pubmed: 20 11 2021
medline: 15 3 2022
entrez: 19 11 2021
Statut: ppublish

Résumé

This study investigated associations of adiposity and adiposity-related biomarkers with incident type 2 diabetes (T2D) among parous women. Among women in the Diabetes Prevention Program (DPP) who reported a previous live birth, circulating biomarkers (leptin, adiponectin, sex hormone-binding globulin, and alanine aminotransferase; n = 1,711) were measured at enrollment (average: 12 years post partum). Visceral (VAT) and subcutaneous adipose tissue areas at the L2-L3 region and the L3-L4 region were quantified by computed tomography (n = 477). Overall and stratified (by history of gestational diabetes mellitus [GDM]) adjusted Cox proportional hazards models were fit. Alanine aminotransferase, L2-L3 VAT, and L3-L4 VAT were positively associated (hazard ratio [HR] for 1-SD increases: 1.073, p = 0.024; 1.251, p = 0.009; 1.272, p = 0.004, respectively), and adiponectin concentration was inversely associated with T2D (HR 0.762, p < 0.001). Whereas leptin concentration was not associated with T2D overall, in GDM-stratified models, a 1-SD higher leptin was positively associated with risk of T2D in women without GDM (HR: 1.126, p = 0.016) and inversely in women with a history of GDM (HR: 0.776, p = 0.013, interaction p = 0.002). Among parous women, alanine aminotransferase and VAT are positively associated with incident T2D, whereas adiponectin is inversely associated. Leptin is associated with higher risk of T2D in women with a history of GDM but a lower risk in women without a history of GDM.

Identifiants

pubmed: 34796678
doi: 10.1002/oby.23291
pmc: PMC8692336
mid: NIHMS1736212
doi:

Substances chimiques

Biomarkers 0

Banques de données

ClinicalTrials.gov
['NCT00004992']

Types de publication

Journal Article Research Support, N.I.H., Extramural

Langues

eng

Sous-ensembles de citation

IM

Pagination

221-228

Subventions

Organisme : NIDDK NIH HHS
ID : U01 DK048412
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK048375
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK048434
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK048413
Pays : United States
Organisme : NIDDK NIH HHS
ID : K08 DK103945
Pays : United States
Organisme : NCRR NIH HHS
ID : M01 RR016587
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK048339
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK048443
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK048387
Pays : United States
Organisme : NIDDK NIH HHS
ID : P30 DK017047
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK048406
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK048407
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK048397
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK048381
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK048514
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK048485
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK048380
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK048400
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK048489
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK048349
Pays : United States

Commentaires et corrections

Type : ErratumIn

Informations de copyright

© 2021 The Obesity Society (TOS). This article has been contributed to by US Government employees and their work is in the public domain in the USA.

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Auteurs

Pandora L Wander (PL)

Veterans Affairs Puget Sound Health Care System, Seattle, Washington, USA.
Department of Medicine, University of Washington, Seattle, Washington, USA.

Costas A Christophi (CA)

Biostatistics Center, George Washington University, Rockville, Maryland, USA.

Maria Rosario G Araneta (MRG)

Department of Family Medicine and Public Health, University of California San Diego, La Jolla, California, USA.

Edward J Boyko (EJ)

Veterans Affairs Puget Sound Health Care System, Seattle, Washington, USA.
Department of Medicine, University of Washington, Seattle, Washington, USA.

Daniel A Enquobahrie (DA)

Department of Epidemiology, University of Washington, Seattle, Washington, USA.

Dana Dabelea (D)

Department of Preventive Medicine and Biometrics, Colorado School of Public Health, Aurora, Colorado, USA.

Ronald B Goldberg (RB)

Department of Medicine, University of Miami, Miami, Florida, USA.

Steven E Kahn (SE)

Veterans Affairs Puget Sound Health Care System, Seattle, Washington, USA.
Department of Medicine, University of Washington, Seattle, Washington, USA.

Catherine Kim (C)

Departments of Medicine and Obstetrics and Gynecology, University of Michigan, Ann Arbor, Michigan, USA.

Xavier Pi-Sunyer (X)

Division of Endocrinology, Columbia University Medical Center, New York, New York, USA.

William C Knowler (WC)

National Institute of Diabetes and Digestive and Kidney Diseases, Phoenix, Arizona, USA.

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