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Association between liver enzymes and incident type 2 diabetes in Singapore Chinese men and women

AIMS: To assess the association between liver enzymes and the risk of type 2 diabetes (T2D) in a Chinese population. METHODS: A nested case–control study comprising 571 T2D cases and 571 matched controls was conducted within the Singapore Chinese Health Study. Alanine aminotransferase (ALT), asparta...

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Autores principales: Wang, Ye-Li, Koh, Woon-Puay, Yuan, Jian-Min, Pan, An
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5030569/
https://www.ncbi.nlm.nih.gov/pubmed/27738514
http://dx.doi.org/10.1136/bmjdrc-2016-000296
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author Wang, Ye-Li
Koh, Woon-Puay
Yuan, Jian-Min
Pan, An
author_facet Wang, Ye-Li
Koh, Woon-Puay
Yuan, Jian-Min
Pan, An
author_sort Wang, Ye-Li
collection PubMed
description AIMS: To assess the association between liver enzymes and the risk of type 2 diabetes (T2D) in a Chinese population. METHODS: A nested case–control study comprising 571 T2D cases and 571 matched controls was conducted within the Singapore Chinese Health Study. Alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase (ALP), and lactate dehydrogenase (LDH) were quantified in baseline plasma collected from them, while γ-glutamyltransferase (GGT) was assayed among 255 T2D cases with baseline hemoglobin A1c <6.5% and 255 matched controls. Participants were free of diagnosed diabetes, cardiovascular disease, and cancer at blood collections (1999–2004). Incident self-reported T2D cases were identified at follow-up II interview (2006–2010). Controls were matched to cases on age, sex, dialect group, and date of blood collection. RESULTS: Higher levels of ALT and GGT were significantly associated with increased risk of T2D (p for trend <0.001 for ALT, p for trend=0.03 for GGT), and the ORs (95% CIs) comparing highest versus lowest tertiles of ALT and GGT were 2.00 (1.01 to 3.96) and 2.38 (1.21 to 4.66), respectively. A null association was observed for AST, ALP, and LDH with T2D risk. Adding GGT (<23 vs ≥23 IU/L) or ALT (<21 vs ≥21 IU/L) to a prediction model resulted in significant gain in net reclassification improvement and integrated discrimination improvement of T2D prediction (all p<0.001). CONCLUSIONS: Higher levels of GGT and ALT are associated with increased T2D risk. GGT ≥23 IU/L and ALT ≥21 IU/L may identify people at higher risk of developing T2D in this Chinese population.
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spelling pubmed-50305692016-10-13 Association between liver enzymes and incident type 2 diabetes in Singapore Chinese men and women Wang, Ye-Li Koh, Woon-Puay Yuan, Jian-Min Pan, An BMJ Open Diabetes Res Care Epidemiology/Health Services Research AIMS: To assess the association between liver enzymes and the risk of type 2 diabetes (T2D) in a Chinese population. METHODS: A nested case–control study comprising 571 T2D cases and 571 matched controls was conducted within the Singapore Chinese Health Study. Alanine aminotransferase (ALT), aspartate aminotransferase (AST), alkaline phosphatase (ALP), and lactate dehydrogenase (LDH) were quantified in baseline plasma collected from them, while γ-glutamyltransferase (GGT) was assayed among 255 T2D cases with baseline hemoglobin A1c <6.5% and 255 matched controls. Participants were free of diagnosed diabetes, cardiovascular disease, and cancer at blood collections (1999–2004). Incident self-reported T2D cases were identified at follow-up II interview (2006–2010). Controls were matched to cases on age, sex, dialect group, and date of blood collection. RESULTS: Higher levels of ALT and GGT were significantly associated with increased risk of T2D (p for trend <0.001 for ALT, p for trend=0.03 for GGT), and the ORs (95% CIs) comparing highest versus lowest tertiles of ALT and GGT were 2.00 (1.01 to 3.96) and 2.38 (1.21 to 4.66), respectively. A null association was observed for AST, ALP, and LDH with T2D risk. Adding GGT (<23 vs ≥23 IU/L) or ALT (<21 vs ≥21 IU/L) to a prediction model resulted in significant gain in net reclassification improvement and integrated discrimination improvement of T2D prediction (all p<0.001). CONCLUSIONS: Higher levels of GGT and ALT are associated with increased T2D risk. GGT ≥23 IU/L and ALT ≥21 IU/L may identify people at higher risk of developing T2D in this Chinese population. BMJ Publishing Group 2016-09-19 /pmc/articles/PMC5030569/ /pubmed/27738514 http://dx.doi.org/10.1136/bmjdrc-2016-000296 Text en Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://www.bmj.com/company/products-services/rights-and-licensing/ This is an Open Access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/
spellingShingle Epidemiology/Health Services Research
Wang, Ye-Li
Koh, Woon-Puay
Yuan, Jian-Min
Pan, An
Association between liver enzymes and incident type 2 diabetes in Singapore Chinese men and women
title Association between liver enzymes and incident type 2 diabetes in Singapore Chinese men and women
title_full Association between liver enzymes and incident type 2 diabetes in Singapore Chinese men and women
title_fullStr Association between liver enzymes and incident type 2 diabetes in Singapore Chinese men and women
title_full_unstemmed Association between liver enzymes and incident type 2 diabetes in Singapore Chinese men and women
title_short Association between liver enzymes and incident type 2 diabetes in Singapore Chinese men and women
title_sort association between liver enzymes and incident type 2 diabetes in singapore chinese men and women
topic Epidemiology/Health Services Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5030569/
https://www.ncbi.nlm.nih.gov/pubmed/27738514
http://dx.doi.org/10.1136/bmjdrc-2016-000296
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