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Grand Multiparity Is Associated With Type 2 Diabetes in Filipino American Women, Independent of Visceral Fat and Adiponectin

OBJECTIVE: To determine whether multiparity is associated with type 2 diabetes, independent of visceral adipose tissue (VAT) and adipokines. RESEARCH DESIGN AND METHODS: Participants were from the University of California San Diego Filipino Women's Health Study with at least one live birth. A 2...

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Detalles Bibliográficos
Autores principales: Araneta, Maria Rosario G., Barrett-Connor, Elizabeth
Formato: Texto
Lenguaje:English
Publicado: American Diabetes Association 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2809288/
https://www.ncbi.nlm.nih.gov/pubmed/19918009
http://dx.doi.org/10.2337/dc09-1477
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author Araneta, Maria Rosario G.
Barrett-Connor, Elizabeth
author_facet Araneta, Maria Rosario G.
Barrett-Connor, Elizabeth
author_sort Araneta, Maria Rosario G.
collection PubMed
description OBJECTIVE: To determine whether multiparity is associated with type 2 diabetes, independent of visceral adipose tissue (VAT) and adipokines. RESEARCH DESIGN AND METHODS: Participants were from the University of California San Diego Filipino Women's Health Study with at least one live birth. A 2-h 75-g oral glucose tolerance test was administered; adiponectin, leptin, ghrelin, reproductive history, family history of diabetes, VAT, and lifestyle behaviors were measured between 1995 and 2002. RESULTS: Among 152 women, mean age was 59.5 years (range 48–73 years) and mean parity was 4.3 (range 1–12 births). Type 2 diabetes prevalence increased by parity group (low parity, 1–2 births, 25%; medium parity, 3–5 births, 30.3%; and grand multiparity: 6–12 births, 50%; P = 0.048). Family history of diabetes, exercise, insulin resistance, and leptin and ghrelin levels did not differ by parity group. Compared with women in the low parity group, women with ≥6 births were significantly older (62 vs. 57 years), had lower college completion (22 vs. 58%, P = 0.006), more hypertension (72 vs. 55%), higher VAT (74.9 vs. 58.4 cm(3)), and lower adiponectin concentration (5.79 vs. 7.61 μg/ml). In multivariate analysis adjusting for adiponectin, VAT, family history of diabetes, age, education, hypertension, and estrogen use, grand multiparous women had a threefold higher odds of type 2 diabetes (adjusted odds ratio 3.40 [95% CI 1.13–10.2]) compared with low parity women. No differences were observed in the odds of diabetes between women in the medium (1.10 [0.41–2.91]) and low parity groups. CONCLUSIONS: Having ≥6 children was associated with type 2 diabetes, independent of adiponectin, VAT, family history, and other measured diabetes risk factors.
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spelling pubmed-28092882011-02-01 Grand Multiparity Is Associated With Type 2 Diabetes in Filipino American Women, Independent of Visceral Fat and Adiponectin Araneta, Maria Rosario G. Barrett-Connor, Elizabeth Diabetes Care Original Research OBJECTIVE: To determine whether multiparity is associated with type 2 diabetes, independent of visceral adipose tissue (VAT) and adipokines. RESEARCH DESIGN AND METHODS: Participants were from the University of California San Diego Filipino Women's Health Study with at least one live birth. A 2-h 75-g oral glucose tolerance test was administered; adiponectin, leptin, ghrelin, reproductive history, family history of diabetes, VAT, and lifestyle behaviors were measured between 1995 and 2002. RESULTS: Among 152 women, mean age was 59.5 years (range 48–73 years) and mean parity was 4.3 (range 1–12 births). Type 2 diabetes prevalence increased by parity group (low parity, 1–2 births, 25%; medium parity, 3–5 births, 30.3%; and grand multiparity: 6–12 births, 50%; P = 0.048). Family history of diabetes, exercise, insulin resistance, and leptin and ghrelin levels did not differ by parity group. Compared with women in the low parity group, women with ≥6 births were significantly older (62 vs. 57 years), had lower college completion (22 vs. 58%, P = 0.006), more hypertension (72 vs. 55%), higher VAT (74.9 vs. 58.4 cm(3)), and lower adiponectin concentration (5.79 vs. 7.61 μg/ml). In multivariate analysis adjusting for adiponectin, VAT, family history of diabetes, age, education, hypertension, and estrogen use, grand multiparous women had a threefold higher odds of type 2 diabetes (adjusted odds ratio 3.40 [95% CI 1.13–10.2]) compared with low parity women. No differences were observed in the odds of diabetes between women in the medium (1.10 [0.41–2.91]) and low parity groups. CONCLUSIONS: Having ≥6 children was associated with type 2 diabetes, independent of adiponectin, VAT, family history, and other measured diabetes risk factors. American Diabetes Association 2010-02 2009-11-16 /pmc/articles/PMC2809288/ /pubmed/19918009 http://dx.doi.org/10.2337/dc09-1477 Text en © 2010 by the American Diabetes Association. Readers may use this article as long as the work is properly cited, the use is educational and not for profit, and the work is not altered. See http://creativecommons.org/licenses/by-nc-nd/3.0/ for details.
spellingShingle Original Research
Araneta, Maria Rosario G.
Barrett-Connor, Elizabeth
Grand Multiparity Is Associated With Type 2 Diabetes in Filipino American Women, Independent of Visceral Fat and Adiponectin
title Grand Multiparity Is Associated With Type 2 Diabetes in Filipino American Women, Independent of Visceral Fat and Adiponectin
title_full Grand Multiparity Is Associated With Type 2 Diabetes in Filipino American Women, Independent of Visceral Fat and Adiponectin
title_fullStr Grand Multiparity Is Associated With Type 2 Diabetes in Filipino American Women, Independent of Visceral Fat and Adiponectin
title_full_unstemmed Grand Multiparity Is Associated With Type 2 Diabetes in Filipino American Women, Independent of Visceral Fat and Adiponectin
title_short Grand Multiparity Is Associated With Type 2 Diabetes in Filipino American Women, Independent of Visceral Fat and Adiponectin
title_sort grand multiparity is associated with type 2 diabetes in filipino american women, independent of visceral fat and adiponectin
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2809288/
https://www.ncbi.nlm.nih.gov/pubmed/19918009
http://dx.doi.org/10.2337/dc09-1477
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