Risk of dementia associated with anticholinergic drugs for overactive bladder in adults aged ≥55 years: nested case-control study.

BMJ medicine Pub Date : 2024-11-12 eCollection Date: 2024-01-01 DOI:10.1136/bmjmed-2023-000799
Barbara Iyen, Carol Coupland, Brian Gregory Bell, Darren M Ashcroft, Martin William Orrell, Delia Bishara, Tom Dening, Anthony J Avery
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Abstract

Abstract:

Objective: To investigate whether different anticholinergic drug treatments for overactive bladder have differential risks for incident dementia, in a large representative population of older adults in England.

Design: Nested case-control study.

Setting: General practices in England providing data to the Clinical Practice Research Datalink (CPRD) GOLD database, with linked patient admission records from secondary care (Hospital Episode Statistics), 1 January 2006 and 16 February 2022.

Participants: 170 742 patients aged ≥55 years, with a first reported diagnosis of dementia during the study period, matched by age, sex, and general practice with 804 385 individuals without dementia (controls).

Interventions: Cumulative drug use (defined using total standardised daily dose) of different anticholinergic drugs used for the treatment of an overactive bladder, and a non-anticholinergic drug, mirabegron, in the period 3-16 years before a diagnosis of dementia (or equivalent date in matched controls).

Main outcome measures: Odds ratios for onset of dementia associated with the different anticholinergic drugs used for the treatment of an overactive bladder, adjusted for sociodemographic characteristics, clinical comorbidities, and use of other anticholinergic drug treatments.

Results: The study population comprised 62.6% women, and median age was 83 (interquartile range 77-87) years. 15 418 (9.0%) patients with dementia and 63 369 (7.9%) controls without dementia had used anticholinergic drugs for the treatment of an overactive bladder in the 3-16 years before diagnosis (or equivalent date for controls). The adjusted odds ratio for dementia associated with the use of any anticholinergic drug used to treat an overactive bladder was 1.18 (95% confidence interval (CI) 1.16 to 1.20), and was higher in men (1.22, 1.18 to 1.26) than women (1.16, 1.13 to 1.19). The risk of dementia was substantially increased with the use of oxybutynin hydrochloride (adjusted odds ratio 1.31, 95% CI 1.21 to 1.42 and 1.28, 1.15 to 1.43 for use of 366-1095 and >1095 total standardised daily doses, respectively), solifenacin succinate (1.18, 1.09 to 1.27 and 1.29, 1.19 to 1.39), and tolterodine tartrate (1.27, 1.19 to 1.37 and 1.25, 1.17 to 1.34). No significant increases in the risk of dementia associated with darifenacin, fesoterodine fumarate, flavoxate hydrochloride, propiverine hydrochloride, and trospium chloride were found. The association between mirabegron, a non-anticholinergic drug, and dementia was variable across the dose categories and might be caused by previous use of anticholinergic drugs for the treatment of an overactive bladder in these individuals.

Conclusions: Of the different anticholinergic drugs used to treat an overactive bladder, oxybutynin hydrochloride, solifenacin succinate, and tolterodine tartrate were found to be most strongly associated with the risk of dementia in older adults. This finding emphasises the need for clinicians to take into account the possible long term risks and consequences of the available treatment options for an overactive bladder in older adults, and to consider prescribing alternative treatments that might be associated with a lower risk of dementia.

与抗胆碱能药物治疗膀胱过度活动症相关的痴呆症风险:巢式病例对照研究。
摘要:目的:在英格兰具有代表性的老年人群中,研究治疗膀胱过度活动症的不同抗胆碱能药物是否会导致不同的痴呆症发病风险:在英格兰一个具有代表性的大型老年人群中,调查不同的抗胆碱能药物治疗膀胱过度活动症是否会导致不同的痴呆症发病风险:设计:嵌套病例对照研究:英国全科医生向临床实践研究数据链接(CPRD)GOLD数据库提供数据,并与二级医疗机构(医院病历统计)2006年1月1日至2022年2月16日的患者入院记录相链接:170 742 名年龄≥55 岁、在研究期间首次报告诊断为痴呆症的患者,与 804 385 名无痴呆症的患者(对照组)进行年龄、性别和全科匹配:干预措施:在痴呆症确诊前 3-16 年内(或匹配对照组的同等日期),累计使用用于治疗膀胱过度活动症的不同抗胆碱能药物和非抗胆碱能药物米拉贝琼(mirabegron)(以标准化每日总剂量定义):与治疗膀胱过度活动症的不同抗胆碱能药物相关的痴呆症发病率,并根据社会人口学特征、临床合并症和使用其他抗胆碱能药物治疗进行调整:研究对象中 62.6% 为女性,中位年龄为 83 岁(四分位数间距为 77-87 岁)。15 418 名(9.0%)痴呆症患者和 63 369 名(7.9%)非痴呆症对照组患者在确诊前 3-16 年内(或对照组的同等日期)曾使用抗胆碱能药物治疗膀胱过度活动症。与使用任何抗胆碱能药物治疗膀胱过度活动症相关的痴呆调整后几率为 1.18(95% 置信区间 (CI) 1.16 至 1.20),男性(1.22,1.18 至 1.26)高于女性(1.16,1.13 至 1.19)。使用盐酸奥昔布宁会大大增加痴呆症的风险(调整后的几率比为 1.31,95% CI 为 1.21 至 1.42 和 1.28,1.15 至 1.43)。43)、琥珀酸索利那新(1.18,1.09 至 1.27 和 1.29,1.19 至 1.39)和酒石酸托特罗定(1.27,1.19 至 1.37 和 1.25,1.17 至 1.34)。没有发现达非那新、富马酸非索特罗定、盐酸黄连素、盐酸丙哌维林和氯化曲司铵会明显增加痴呆症风险。米拉贝琼(一种非抗胆碱能药物)与痴呆症之间的关联在不同剂量类别之间存在差异,这可能是由于这些患者以前曾使用抗胆碱能药物治疗膀胱过度活动症所致:结论:在用于治疗膀胱过度活动症的各种抗胆碱能药物中,盐酸奥昔布宁、琥珀酸索利那新和酒石酸托特罗定与老年人痴呆症风险的关系最为密切。这一发现强调临床医生有必要考虑到现有治疗老年人膀胱过度活动症的方案可能带来的长期风险和后果,并考虑开具可能与较低痴呆症风险相关的替代治疗处方。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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