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Plasminogen activator inhibitor-1 and type 2 diabetes: a systematic review and meta-analysis of observational studies

An emerging body of evidence has implicated plasminogen activator inhibitor-1 (PAI-1) in the development of type 2 diabetes (T2D), though findings have not always been consistent. We systematically reviewed epidemiological studies examining the association of PAI-1 with T2D. EMBASE, PubMed, Web of S...

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Autores principales: Yarmolinsky, James, Bordin Barbieri, Natália, Weinmann, Tobias, Ziegelmann, Patricia K., Duncan, Bruce B., Inês Schmidt, Maria
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4728395/
https://www.ncbi.nlm.nih.gov/pubmed/26813008
http://dx.doi.org/10.1038/srep17714
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author Yarmolinsky, James
Bordin Barbieri, Natália
Weinmann, Tobias
Ziegelmann, Patricia K.
Duncan, Bruce B.
Inês Schmidt, Maria
author_facet Yarmolinsky, James
Bordin Barbieri, Natália
Weinmann, Tobias
Ziegelmann, Patricia K.
Duncan, Bruce B.
Inês Schmidt, Maria
author_sort Yarmolinsky, James
collection PubMed
description An emerging body of evidence has implicated plasminogen activator inhibitor-1 (PAI-1) in the development of type 2 diabetes (T2D), though findings have not always been consistent. We systematically reviewed epidemiological studies examining the association of PAI-1 with T2D. EMBASE, PubMed, Web of Science, and the Cochrane Library were searched to identify studies for inclusion. Fifty-two studies (44 cross-sectional with 47 unique analytical comparisons and 8 prospective) were included. In pooled random-effects analyses of prospective studies, a comparison of the top third vs. bottom third of baseline PAI-1 values generated a RR of T2D of 1.67 (95% CI 1.28–2.18) with moderate heterogeneity (I(2) = 38%). Additionally, of 47 cross-sectional comparisons, 34(72%) reported significantly elevated PAI-1 among diabetes cases versus controls, 2(4%) reported significantly elevated PAI-1 among controls, and 11(24%) reported null effects. Results from pooled analyses of prospective studies did not differ substantially by study design, length of follow-up, adjustment for various putative confounding factors, or study quality, and were robust to sensitivity analyses. Findings from this systematic review of the available epidemiological literature support a link between PAI-1 and T2D, independent of established diabetes risk factors. Given the moderate size of the association and heterogeneity across studies, future prospective studies are warranted.
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spelling pubmed-47283952016-02-01 Plasminogen activator inhibitor-1 and type 2 diabetes: a systematic review and meta-analysis of observational studies Yarmolinsky, James Bordin Barbieri, Natália Weinmann, Tobias Ziegelmann, Patricia K. Duncan, Bruce B. Inês Schmidt, Maria Sci Rep Article An emerging body of evidence has implicated plasminogen activator inhibitor-1 (PAI-1) in the development of type 2 diabetes (T2D), though findings have not always been consistent. We systematically reviewed epidemiological studies examining the association of PAI-1 with T2D. EMBASE, PubMed, Web of Science, and the Cochrane Library were searched to identify studies for inclusion. Fifty-two studies (44 cross-sectional with 47 unique analytical comparisons and 8 prospective) were included. In pooled random-effects analyses of prospective studies, a comparison of the top third vs. bottom third of baseline PAI-1 values generated a RR of T2D of 1.67 (95% CI 1.28–2.18) with moderate heterogeneity (I(2) = 38%). Additionally, of 47 cross-sectional comparisons, 34(72%) reported significantly elevated PAI-1 among diabetes cases versus controls, 2(4%) reported significantly elevated PAI-1 among controls, and 11(24%) reported null effects. Results from pooled analyses of prospective studies did not differ substantially by study design, length of follow-up, adjustment for various putative confounding factors, or study quality, and were robust to sensitivity analyses. Findings from this systematic review of the available epidemiological literature support a link between PAI-1 and T2D, independent of established diabetes risk factors. Given the moderate size of the association and heterogeneity across studies, future prospective studies are warranted. Nature Publishing Group 2016-01-27 /pmc/articles/PMC4728395/ /pubmed/26813008 http://dx.doi.org/10.1038/srep17714 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Yarmolinsky, James
Bordin Barbieri, Natália
Weinmann, Tobias
Ziegelmann, Patricia K.
Duncan, Bruce B.
Inês Schmidt, Maria
Plasminogen activator inhibitor-1 and type 2 diabetes: a systematic review and meta-analysis of observational studies
title Plasminogen activator inhibitor-1 and type 2 diabetes: a systematic review and meta-analysis of observational studies
title_full Plasminogen activator inhibitor-1 and type 2 diabetes: a systematic review and meta-analysis of observational studies
title_fullStr Plasminogen activator inhibitor-1 and type 2 diabetes: a systematic review and meta-analysis of observational studies
title_full_unstemmed Plasminogen activator inhibitor-1 and type 2 diabetes: a systematic review and meta-analysis of observational studies
title_short Plasminogen activator inhibitor-1 and type 2 diabetes: a systematic review and meta-analysis of observational studies
title_sort plasminogen activator inhibitor-1 and type 2 diabetes: a systematic review and meta-analysis of observational studies
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4728395/
https://www.ncbi.nlm.nih.gov/pubmed/26813008
http://dx.doi.org/10.1038/srep17714
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