Northuis Carin A, Bell Elizabeth J, Lutsey Pamela L, George Kristen M, Gottesman Rebecca F, Mosley Tom H, Whitsel Eric A, Lakshminarayan Kamakshi
From the University of Minnesota (C.A.N., P.L.L., K.L.), Minneapolis; Optum (E.J.B.), Minneapolis, MN; University of California, Davis (K.M.G.); National Institute of Neurological Disorders and Stroke (R.F.G.), Washington, DC; University of Mississippi Medical Center (T.H.M.), Jackson; and University of North Carolina (E.A.W.), Chapel Hill.
Neurology. 2023 Oct 31;101(18):e1771-e1778. doi: 10.1212/WNL.0000000000207747. Epub 2023 Aug 9.
Studies on the association between proton pump inhibitor (PPI) use and dementia report mixed results and do not examine the impact of cumulative PPI use. We evaluated the associations between current and cumulative PPI use and risk of incident dementia in the Atherosclerosis Risk in Communities (ARIC) Study.
These analyses used participants from a community-based cohort (ARIC) from the time of enrollment (1987-1989) through 2017. PPI use was assessed through visual medication inventory at clinic visits 1 (1987-1989) to 5 (2011-2013) and reported annually in study phone calls (2006-2011). This study uses ARIC visit 5 as baseline because this was the first visit in which PPI use was common. PPI use was examined 2 ways: current use at visit 5 and duration of use before visit 5 (from visit 1 to 2011, exposure categories: 0 day, 1 day-2.8 years, 2.8-4.4 years, >4.4 years). The outcome was incident dementia after visit 5. Cox proportional hazard models were used, adjusted for demographics, comorbid conditions, and other medication use.
A total of 5,712 dementia-free participants at visit 5 (mean age 75.4 ± 5.1 years; 22% Black race; 58% female) were included in our analysis. The median follow-up was 5.5 years. The minimum cumulative PPI use was 112 days, and the maximum use was 20.3 years. There were 585 cases of incident dementia identified during follow-up. Participants using PPIs at visit 5 were not at a significantly higher risk of developing dementia during subsequent follow-up than those not using PPIs (hazard ratio (HR): 1.1 [95% confidence interval (CI) 0.9-1.3]). Those who used PPIs for >4.4 cumulative years before visit 5 were at 33% higher risk of developing dementia during follow-up (HR: 1.3 [95% CI 1.0-1.8]) than those reporting no use. Associations were not significant for lesser durations of PPI use.
Future studies are needed to understand possible pathways between cumulative PPI use and the development of dementia.
This study provides Class III evidence that the use of prescribed PPIs for >4.4 years by individuals aged 45 years and older is associated with a higher incidence of newly diagnosed dementia.
关于质子泵抑制剂(PPI)使用与痴呆症之间关联的研究结果不一,且未考察累积使用PPI的影响。我们在社区动脉粥样硬化风险研究(ARIC研究)中评估了当前及累积使用PPI与新发痴呆症风险之间的关联。
这些分析使用了来自社区队列(ARIC)的参与者,时间跨度从入组时(1987 - 1989年)至2017年。通过在第1次门诊就诊(1987 - 1989年)至第5次门诊就诊(2011 - 2013年)时的可视药物清单评估PPI使用情况,并在研究电话随访(2006 - 2011年)中每年报告一次。本研究以ARIC第5次就诊作为基线,因为这是首次PPI使用较为普遍的就诊。PPI使用情况通过两种方式进行考察:第5次就诊时的当前使用情况以及第5次就诊前的使用时长(从第1次就诊至2011年,暴露类别:0天、1天 - 2.8年、2.8 - 4.4年、>4.4年)。结局为第5次就诊后的新发痴呆症。使用Cox比例风险模型,并对人口统计学特征、合并症及其他药物使用情况进行了调整。
我们的分析纳入了第5次就诊时无痴呆症的5712名参与者(平均年龄75.4 ± 5.1岁;22%为黑人;58%为女性)。中位随访时间为5.5年。PPI的最小累积使用天数为112天,最大使用时长为20.3年。随访期间共确定了585例新发痴呆症病例。在第5次就诊时使用PPI的参与者在后续随访中发生痴呆症的风险并不显著高于未使用PPI的参与者(风险比(HR):1.1 [95%置信区间(CI)0.9 - 1.3])。在第5次就诊前累积使用PPI超过4.4年的参与者在随访期间发生痴呆症的风险比未使用PPI的参与者高33%(HR:1.3 [95% CI 1.0 - 1.8])。对于较短的PPI使用时长,关联并不显著。
需要开展进一步研究以了解累积使用PPI与痴呆症发生之间可能的途径。
本研究提供了III类证据,即45岁及以上个体使用处方PPI超过4.4年与新诊断痴呆症的较高发病率相关。