Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.14279/29620
DC FieldValueLanguage
dc.contributor.authorWander, Pandora L-
dc.contributor.authorChristophi, Costas A.-
dc.contributor.authorAraneta, Maria Rosario G-
dc.contributor.authorBoyko, Edward J-
dc.contributor.authorEnquobahrie, Daniel A-
dc.contributor.authorDabelea, Dana-
dc.contributor.authorGoldberg, Ronald B-
dc.contributor.authorKahn, Steven E-
dc.contributor.authorKim, Catherine-
dc.contributor.authorPi-Sunyer, Xavier-
dc.contributor.authorKnowler, William C-
dc.date.accessioned2023-07-04T11:22:36Z-
dc.date.available2023-07-04T11:22:36Z-
dc.date.issued2022-01-01-
dc.identifier.citationObesity, 2022, vol.30, iss.1, pp. 221 - 228en_US
dc.identifier.issn19307381-
dc.identifier.urihttps://hdl.handle.net/20.500.14279/29620-
dc.description.abstractObjective: This study investigated associations of adiposity and adiposity-related biomarkers with incident type 2 diabetes (T2D) among parous women. Methods: 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. Results: 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). Conclusions: 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. © 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.en_US
dc.language.isoenen_US
dc.rights© The Obesity Societyen_US
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 International*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/*
dc.subjectAdiposityen_US
dc.subjectBiomarkersen_US
dc.subjectDiabetes Mellitusen_US
dc.subjectDiabetesen_US
dc.subjectGestationalen_US
dc.subjectHumansen_US
dc.subjectObesityen_US
dc.subjectPregnancyen_US
dc.titleAdiposity, related biomarkers, and type 2 diabetes after gestational diabetes: The Diabetes Prevention Programen_US
dc.typeArticleen_US
dc.collaborationVeterans Affairs Puget Sound Health Care Systemen_US
dc.collaborationUniversity of Washingtonen_US
dc.collaborationGeorge Washington Universityen_US
dc.collaborationUniversity of California, San Diegoen_US
dc.collaborationColorado School of Public Healthen_US
dc.collaborationUniversity of Miamien_US
dc.collaborationUniversity of Michiganen_US
dc.collaborationColumbia University Medical Centeren_US
dc.collaborationNational Institute of Diabetes and Digestive and Kidney Diseasesen_US
dc.subject.categoryHealth Sciencesen_US
dc.journalsSubscriptionen_US
dc.countryUnited Statesen_US
dc.subject.fieldMedical and Health Sciencesen_US
dc.publicationPeer Revieweden_US
dc.identifier.doi10.1002/oby.23291en_US
dc.identifier.pmid34796678-
dc.identifier.scopus2-s2.0-85119257240-
dc.identifier.urlhttps://api.elsevier.com/content/abstract/scopus_id/85119257240-
dc.relation.issue1en_US
dc.relation.volume30en_US
cut.common.academicyear2022-2023en_US
dc.identifier.spage221en_US
dc.identifier.epage228en_US
item.openairecristypehttp://purl.org/coar/resource_type/c_6501-
item.openairetypearticle-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.languageiso639-1en-
item.fulltextNo Fulltext-
crisitem.author.deptDepartment of Rehabilitation Sciences-
crisitem.author.facultyFaculty of Health Sciences-
crisitem.author.orcid0000-0003-0503-1538-
crisitem.author.parentorgFaculty of Health Sciences-
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