Tseng Chin-Hsiao
Department of Internal Medicine, National Taiwan University College of Medicine, Taipei 10051, Taiwan.
Division of Endocrinology and Metabolism, Department of Internal Medicine, National Taiwan University Hospital, Taipei 10002, Taiwan.
Pharmaceuticals (Basel). 2022 Dec 11;15(12):1538. doi: 10.3390/ph15121538.
Pioglitazone shows potential benefits in inflammatory bowel disease (IBD) in preclinical studies, but its effect in humans has not been researched. We used a nationwide database of Taiwan's National Health Insurance to investigate whether pioglitazone might affect IBD risk. We enrolled 12,763 ever users and 12,763 never users matched on a propensity score from patients who had a new diagnosis of type 2 diabetes mellitus between 1999 and 2008. The patients were alive on 1 January 2009, and they were followed up for a new diagnosis of IBD until 31 December 2011. Propensity score-weighted hazard ratios were estimated, and the interactions between pioglitazone and major risk factors of IBD (i.e., psoriasis, arthropathies, dorsopathies, chronic obstructive pulmonary disease/tobacco abuse, and any of the above) and metformin were investigated. At the end of the follow-up, 113 ever users and 139 never users were diagnosed with IBD. When compared to never users, the hazard ratio for ever users was 0.809 (95% confidence interval: 0.631-1.037); and none of the hazard ratios for ever users categorized by tertiles of cumulative duration and cumulative dose reached statistical significance. No interactions with major risk factors or metformin were observed. Our findings suggested a null effect of pioglitazone on IBD.
吡格列酮在临床前研究中显示出对炎症性肠病(IBD)有潜在益处,但尚未对其在人体中的作用进行研究。我们利用台湾全民健康保险的全国性数据库来调查吡格列酮是否可能影响IBD风险。我们纳入了12763名曾经使用过吡格列酮的使用者和12763名从未使用过吡格列酮的非使用者,这些使用者和非使用者在倾向得分上相匹配,他们均为1999年至2008年间新诊断为2型糖尿病的患者。这些患者在2009年1月1日仍在世,并对他们进行随访,观察是否有新的IBD诊断,直至2011年12月31日。我们估计了倾向得分加权风险比,并研究了吡格列酮与IBD的主要风险因素(即银屑病、关节病、背痛、慢性阻塞性肺疾病/烟草滥用以及上述任何一种情况)和二甲双胍之间的相互作用。在随访结束时,113名曾经使用者和139名从未使用者被诊断为IBD。与从未使用者相比,曾经使用者的风险比为0.809(95%置信区间:0.631 - 1.037);按累积使用时间和累积剂量三分位数分类的曾经使用者的风险比均未达到统计学显著性。未观察到与主要风险因素或二甲双胍的相互作用。我们的研究结果表明吡格列酮对IBD无作用。