Ahn Nayeon, Nolde Michael, Krause Evamaria, Güntner Florian, Günter Alexander, Tauscher Martin, Gerlach Roman, Meisinger Christa, Linseisen Jakob, Baumeister Sebastian-Edgar, Rückert-Eheberg Ina-Maria
Institute for Medical Information Processing, Biometry, and Epidemiology (IBE), Ludwig Maximilian University of Munich, Munich, Germany.
Chair of Epidemiology, University of Augsburg, University Hospital Augsburg, Augsburg, Germany.
Br J Clin Pharmacol. 2023 Feb;89(2):602-616. doi: 10.1111/bcp.15583. Epub 2022 Nov 23.
Previous studies on the association between proton pump inhibitor (PPI) intake and the increased risk of dementia has shown discrepancies in their conclusions. We aimed to provide updated evidence based on extensive bias assessments and quantitative sensitivity analyses.
We searched the databases PubMed, EMBASE, SCOPUS, CENTRAL and clinicaltrials.gov for prospective studies that examined an association between PPI use and dementia, up to February 2022. Each study was assessed using the Cochrane risk of bias assessment tools for non-randomized studies of interventions (ROBINS-I) or randomized trials (RoB2). Pooled risk ratios (RRs) and 95% prediction intervals were computed using random-effects models. Sensitivity analyses were adjusted for small-study bias.
We included nine observational studies with 204 108 dementia cases in the primary analysis on the association between PPI use vs. non-use and dementia, and the RR was 1.16 (95% CI = 1.00; 1.35). After adjusting for small-study bias by Copas selection model and Rücker's shrinkage procedure, the RR was 1.16 (1.02; 1.32) and 1.15 (1.13; 1.17), respectively. A subgroup analysis of PPI use vs. non-use regarding Alzheimer's disease risk yielded an RR of 1.15 (0.89; 1.50). The secondary analysis on the risk of dementia by use of PPI vs. histamine-2 receptor antagonist showed an RR of 1.03 (0.66; 1.62).
This meta-analysis provided no clear evidence for an association between PPI intake and the risk of dementia. Due to discrepancies in sensitivity analyses, however, some risk of dementia by PPI use cannot be ruled out. Since an unequivocal conclusion is still pending, further research is warranted.
先前关于质子泵抑制剂(PPI)摄入与痴呆风险增加之间关联的研究结论存在差异。我们旨在通过广泛的偏倚评估和定量敏感性分析提供最新证据。
我们检索了PubMed、EMBASE、SCOPUS、CENTRAL和clinicaltrials.gov数据库,以查找截至2022年2月研究PPI使用与痴呆之间关联的前瞻性研究。每项研究使用Cochrane干预性非随机研究偏倚风险评估工具(ROBINS-I)或随机试验(RoB2)进行评估。使用随机效应模型计算合并风险比(RRs)和95%预测区间。敏感性分析针对小型研究偏倚进行了调整。
在关于PPI使用与未使用和痴呆之间关联的主要分析中,我们纳入了9项观察性研究,共204108例痴呆病例,RR为1.16(95%CI = 1.00;1.35)。通过Copas选择模型和Rücker收缩程序对小型研究偏倚进行调整后,RR分别为1.16(1.02;1.32)和1.15(1.13;1.17)。关于PPI使用与未使用对阿尔茨海默病风险的亚组分析得出RR为1.15(0.89;1.50)。使用PPI与组胺-2受体拮抗剂对痴呆风险的二次分析显示RR为1.03(0.66;1.62)。
这项荟萃分析没有提供PPI摄入与痴呆风险之间关联的明确证据。然而,由于敏感性分析存在差异,不能排除PPI使用导致痴呆的一些风险。由于仍未得出明确结论,因此有必要进行进一步研究。