噻嗪类利尿剂或他汀类药物使用者的基因表达与 2 型糖尿病发病率的关系。

International journal of molecular epidemiology and genetics Pub Date : 2014-02-17 eCollection Date: 2014-01-01
Astrid Suchy-Dicey, Susan R Heckbert, Nicholas L Smith, Barbara McKnight, Jerome I Rotter, Yd Ida Chen, Bruce M Psaty, Daniel A Enquobahrie
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引用次数: 0

摘要

噻嗪类利尿剂和他汀类药物用于改善心血管疾病的预后,但也可能导致 2 型糖尿病(T2DM),尽管其机制尚不清楚。基因表达研究有助于了解这些关联。这些外周血微阵列基因表达纵向研究从正在进行的人群研究中抽取受试者样本,并随访至糖尿病发病。所有抽样对象均为他汀类药物或噻嗪类药物使用者。在随访期间患上糖尿病的受试者包括病例(44 名噻嗪类药物使用者;19 名他汀类药物使用者),他们与未患糖尿病的用药对照组在多个因素上匹配。监督归一化和替代变量分析消除了技术偏差和混杂因素。差异表达基因是那些假发现率Q值为
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Gene expression in thiazide diuretic or statin users in relation to incident type 2 diabetes.

Gene expression in thiazide diuretic or statin users in relation to incident type 2 diabetes.

Gene expression in thiazide diuretic or statin users in relation to incident type 2 diabetes.

Thiazide diuretics and statins are used to improve cardiovascular outcomes, but may also cause type 2 diabetes (T2DM), although mechanisms are unknown. Gene expression studies may facilitate understanding of these associations. Participants from ongoing population-based studies were sampled for these longitudinal studies of peripheral blood microarray gene expression, and followed to incident diabetes. All sampled subjects were statin or thiazide users. Those who developed diabetes during follow-up comprised cases (44 thiazide users; 19 statin users), and were matched to drug-using controls who did not develop diabetes on several factors. Supervised normalization, surrogate variable analyses removed technical bias and confounding. Differentially-expressed genes were those with a false discovery rate Q-value<0.05. Among thiazide users, diabetes cases had significantly different expression of CCL14 (down-regulated 6%, Q-value=0.0257), compared with controls. Among statin users, diabetes cases had marginal but insignificantly different expression of ZNF532 (up-regulated 15%, Q-value=0.0584), CXORF21 (up-regulated 11%, Q-value=0.0584), and ZNHIT3 (up-regulated 19%, Q-value=0.0959), compared with controls. These genes comprise potential targets for future expression or mechanistic research on medication-related diabetes development.

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