Associations between urate-lowering therapy and the risk of type 2 diabetes mellitus.

<h4>Background</h4>Gout is independently associated with increased risk of type 2 diabetes mellitus (T2DM). Urate-lowering therapy (ULT) might be beneficial in lowering the risks of T2DM. Therefore, we conducted a nested case-control study to evaluate the associations between ULT and T2D...

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Main Authors: Hsin-Wen Chang, Ya-Wen Lin, Ming-Hung Lin, Yu-Ching Lan, Ruey-Yun Wang
Format: Article
Language:English
Published: Public Library of Science (PLoS) 2019-01-01
Series:PLoS ONE
Online Access:https://doi.org/10.1371/journal.pone.0210085
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spelling doaj-2812f0d1d1274aebb3b44696c6f7adae2021-03-04T10:38:28ZengPublic Library of Science (PLoS)PLoS ONE1932-62032019-01-01141e021008510.1371/journal.pone.0210085Associations between urate-lowering therapy and the risk of type 2 diabetes mellitus.Hsin-Wen ChangYa-Wen LinMing-Hung LinYu-Ching LanRuey-Yun Wang<h4>Background</h4>Gout is independently associated with increased risk of type 2 diabetes mellitus (T2DM). Urate-lowering therapy (ULT) might be beneficial in lowering the risks of T2DM. Therefore, we conducted a nested case-control study to evaluate the associations between ULT and T2DM.<h4>Methods</h4>This study retrieved the data of 29,765 gout patients from the period of 1998-2010 by using data from Taiwan's National Health Insurance Research Database. Controls (n = 59,530) were matched at a 1:2 ratio by age, sex, and region. Multivariate Cox proportional hazards regression were performed to examine the dose-dependent relationship between ULT and T2DM.<h4>Results</h4>The adjusted Hazard ratio (HR) for the association of T2DM with allopurinol or benzbromarone exposure was 1.17 (95% confidence interval (CI) 1.07-1.28) and1.09 (95% CI 1.03-1.15), respectively. The HR for the cumulative allopurinol dose was 0.87 (95% CI 0.71-1.07) for patients with dose ≤1.3 mg/day and was 1.31 (95% CI 1.13-1.52) for those with a dose >15.2 mg/day. Similarly, the HR for the cumulative benzbromarone dose was 0.85(95% CI 0.75-0.96) for patients with a dose ≤1.3 mg/day and 1.42 (95% CI 1.30-1.55) for patients with a dose>9.4 mg/day, respectively. Moreover, the average exposure dose of >100 mg/day for allopurinol and >100 mg/day for benzbromarone was associated with a 1.28-fold (95% CI 1.11-1.48) and 1.47-fold (95% CI 1.23-1.76) T2DM risk respectively. The HR for patients in aged >50 years group with cumulative dose ≤1.3 mg/day of allopurinol or benzbromarone had lower risk of T2DM (HR = 0.74, 95% CI 0.58-0.94 for allopurinol; HR = 0.79, 95% CI 0.69-0.90 for benzbromarone).<h4>Conclusion</h4>Gout patients with prolonged ULT and a high dose of ULT were associated with a significant increase in T2DM risk. Although gout patients with age greater than 50 years and a lower dose of ULT may be beneficial in lowering T2DM risk, further clinical studies need to be confirmed these associations.https://doi.org/10.1371/journal.pone.0210085
collection DOAJ
language English
format Article
sources DOAJ
author Hsin-Wen Chang
Ya-Wen Lin
Ming-Hung Lin
Yu-Ching Lan
Ruey-Yun Wang
spellingShingle Hsin-Wen Chang
Ya-Wen Lin
Ming-Hung Lin
Yu-Ching Lan
Ruey-Yun Wang
Associations between urate-lowering therapy and the risk of type 2 diabetes mellitus.
PLoS ONE
author_facet Hsin-Wen Chang
Ya-Wen Lin
Ming-Hung Lin
Yu-Ching Lan
Ruey-Yun Wang
author_sort Hsin-Wen Chang
title Associations between urate-lowering therapy and the risk of type 2 diabetes mellitus.
title_short Associations between urate-lowering therapy and the risk of type 2 diabetes mellitus.
title_full Associations between urate-lowering therapy and the risk of type 2 diabetes mellitus.
title_fullStr Associations between urate-lowering therapy and the risk of type 2 diabetes mellitus.
title_full_unstemmed Associations between urate-lowering therapy and the risk of type 2 diabetes mellitus.
title_sort associations between urate-lowering therapy and the risk of type 2 diabetes mellitus.
publisher Public Library of Science (PLoS)
series PLoS ONE
issn 1932-6203
publishDate 2019-01-01
description <h4>Background</h4>Gout is independently associated with increased risk of type 2 diabetes mellitus (T2DM). Urate-lowering therapy (ULT) might be beneficial in lowering the risks of T2DM. Therefore, we conducted a nested case-control study to evaluate the associations between ULT and T2DM.<h4>Methods</h4>This study retrieved the data of 29,765 gout patients from the period of 1998-2010 by using data from Taiwan's National Health Insurance Research Database. Controls (n = 59,530) were matched at a 1:2 ratio by age, sex, and region. Multivariate Cox proportional hazards regression were performed to examine the dose-dependent relationship between ULT and T2DM.<h4>Results</h4>The adjusted Hazard ratio (HR) for the association of T2DM with allopurinol or benzbromarone exposure was 1.17 (95% confidence interval (CI) 1.07-1.28) and1.09 (95% CI 1.03-1.15), respectively. The HR for the cumulative allopurinol dose was 0.87 (95% CI 0.71-1.07) for patients with dose ≤1.3 mg/day and was 1.31 (95% CI 1.13-1.52) for those with a dose >15.2 mg/day. Similarly, the HR for the cumulative benzbromarone dose was 0.85(95% CI 0.75-0.96) for patients with a dose ≤1.3 mg/day and 1.42 (95% CI 1.30-1.55) for patients with a dose>9.4 mg/day, respectively. Moreover, the average exposure dose of >100 mg/day for allopurinol and >100 mg/day for benzbromarone was associated with a 1.28-fold (95% CI 1.11-1.48) and 1.47-fold (95% CI 1.23-1.76) T2DM risk respectively. The HR for patients in aged >50 years group with cumulative dose ≤1.3 mg/day of allopurinol or benzbromarone had lower risk of T2DM (HR = 0.74, 95% CI 0.58-0.94 for allopurinol; HR = 0.79, 95% CI 0.69-0.90 for benzbromarone).<h4>Conclusion</h4>Gout patients with prolonged ULT and a high dose of ULT were associated with a significant increase in T2DM risk. Although gout patients with age greater than 50 years and a lower dose of ULT may be beneficial in lowering T2DM risk, further clinical studies need to be confirmed these associations.
url https://doi.org/10.1371/journal.pone.0210085
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