Diabetes Obes Metab:老年2型糖尿病患者采用吡格列酮与其他治疗发生膀胱癌的风险比较!

2017-06-30 xing.T MedSci原创

由此可见,吡格列酮治疗与膀胱癌风险升高相关,相比于DPP-4s和磺脲类药物。升高的风险发生在治疗前2年内,并在停药后有所减弱。吡格列酮的相对有效性应与较小的膀胱癌风险绝对增加相权衡。

近日,代谢内分泌疾病领域权威杂志Diabetes Obesity & Metabolism上发表了一篇研究文章,研究人员旨在比较服用吡格列酮的患者和服用二肽基肽酶4抑制剂(DPP-4s)或磺脲类药物的患者膀胱癌的发病率。

研究人员确定了年龄>65岁的在2007年至2014年期间服用吡格列酮(n=38700)、DPP-4s(n=82552)或磺脲类药物(n=126104)的医疗保险受益人,并且这些患者在6个月后没有再服用过这些药物。在2014年底审查了治疗变化、死亡。研究人员使用倾向评分加权Cox比例风险模型来获得调整后的风险比率(aHR)以及95%可信区间。

总体平均年龄为75岁,男性占41%。在1.2年的中位治疗期间,727名受益人患了膀胱癌。服用吡格列酮会增加膀胱癌的发病率(308 vs. 204(DPP-4s)或231(磺脲类)每100000人每年;aHR=1.57[1.23-2.00]) vs. DPP-4s和1.32 [1.02-1.70] vs. 磺脲类药物。增加的风险出现在治疗的前2年内(aHR=1.63[1.22-2.17] vs. DPP-4s和1.32[0.98-1.78] vs. 磺脲类药物)。如果在治疗后2年内停止治疗,在服药2年后风险减弱(aHR=0.89[0.61-1.28]),相比于治疗超过2年的患者(aHR=1.45[0.93-2.26],均与DPP-4s相比)。次要和敏感性分析的结果是一致的。

由此可见,吡格列酮治疗与膀胱癌风险升高相关,相比于DPP-4s和磺脲类药物。升高的风险发生在治疗前2年内,并在停药后有所减弱。吡格列酮的相对有效性应与较小的膀胱癌风险绝对增加相权衡。

原始出处:

Elizabeth M. Garry,et al. Comparative Safety of Pioglitazone versus Clinically Meaningful Treatment Alternatives on the Risk of Bladder Cancer in Older US Adults with Type 2 Diabetes. Diabetes Obesity & Metabolism.2017. http://onlinelibrary.wiley.com/doi/10.1111/dom.13049/full

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    2017-08-25 guojianrong
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    2017-09-17 一闲
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status=1, ipAttribution=), GetPortalCommentsPageByObjectIdResponse(id=1474235, encodeId=34f914e423533, content=<a href='/topic/show?id=935fe6718e3' target=_blank style='color:#2F92EE;'>#糖尿病患者#</a>, beContent=null, objectType=article, channel=null, level=null, likeNumber=31, replyNumber=0, topicName=null, topicId=null, topicList=[TopicDto(id=76718, encryptionId=935fe6718e3, topicName=糖尿病患者)], attachment=null, authenticateStatus=null, createdAvatar=, createdBy=a38f7243741, createdName=xue8604, createdTime=Sun Jul 02 03:37:00 CST 2017, time=2017-07-02, status=1, ipAttribution=)]
    2017-07-04 lou.minghong

    学习了,谢谢分享!

    0

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口服降糖药控制不佳的中国2型糖尿病患者(T2DM)真实生活中基础胰岛素的使用情况如何呢?2017年6月,发表在《Diabetes Obes Metab》的一项研究对此进行分析。

Metabolism:2型糖尿病患者apoC-III、内皮依赖性血管舒张功能与周围神经病变有啥关系?

由此可见,DPN患者血浆中apoC-III水平较高。血脂与大血管并发症除了已知的相关性外,该研究还提示它与DPN有关。调节apoC-III代谢是否是2型糖尿病患者管理血脂异常和微血管并发症的一个重要的新的治疗方法还有待在今后的机理和临床研究予以证明。