School of Pharmacy, University of Washington, Seattle, Washington.
Kaiser Permanente Washington Health Research Institute, Seattle, Washington.
J Am Geriatr Soc. 2018 Feb;66(2):247-253. doi: 10.1111/jgs.15073. Epub 2017 Nov 14.
To determine whether higher cumulative proton pump inhibitor (PPI) exposure is associated with greater dementia risk.
Prospective population-based cohort study.
Kaiser Permanente Washington, an integrated healthcare delivery system in Seattle, Washington.
Individuals aged 65 and older without dementia at study entry (N = 3,484).
Participants were screened for dementia every 2 years, and those who screened positive underwent extensive evaluation. Dementia outcomes were determined using standard diagnostic criteria. Time-varying PPI exposure was determined from computerized pharmacy data and consisted of total standardized daily doses (TSDDs) dispensed to an individual in the prior 10 years. We also assessed duration of use. Multivariable Cox regression was used to estimate the association between PPI exposure and time to dementia or Alzheimer's disease (AD).
Over a mean follow-up of 7.5 years, 827 participants (23.7%) developed dementia (670 with possible or probable AD). PPI exposure was not associated with risk of dementia (P = .66) or AD (P = .77). For dementia, the risk for specific levels of cumulative exposure compared to no use was: 365 TSDDs (HR 0.87, 95% CI 0.65-1.18), 1,095 TSDDs (HR 0.99, CI 0.75-1.30) and 1,825 TSDDs (HR 1.13, CI 0.82-1.56). These TSDD levels represent approximately 1, 3 and 5 years of daily use respectively. Duration of PPI use was not associated with dementia outcomes either.
Proton pump inhibitor use was not associated with dementia risk, even for people with high cumulative exposure. Although there are other safety concerns with long-term PPI use, results from our study do not support that these medications should be avoided out of concern about dementia risk.
确定累积质子泵抑制剂(PPI)暴露量是否与更高的痴呆风险相关。
前瞻性基于人群的队列研究。
华盛顿凯泽 Permanente,华盛顿州西雅图的一个综合医疗服务系统。
研究入组时无痴呆的年龄在 65 岁及以上的个体(N=3484)。
每两年对参与者进行一次痴呆筛查,对筛查阳性者进行全面评估。痴呆结局采用标准诊断标准确定。通过计算机化的药房数据确定时变 PPI 暴露情况,包括在过去 10 年内给个体开的总标准化日剂量(TSDD)。我们还评估了使用时间。多变量 Cox 回归用于估计 PPI 暴露与痴呆或阿尔茨海默病(AD)发生时间之间的关联。
在平均 7.5 年的随访期间,827 名参与者(23.7%)发生痴呆(670 名患有可能或可能的 AD)。PPI 暴露与痴呆风险无关(P=0.66)或 AD 风险无关(P=0.77)。对于痴呆症,与无使用相比,特定累积暴露水平的风险为:365 TSDD(HR 0.87,95%CI 0.65-1.18),1095 TSDD(HR 0.99,CI 0.75-1.30)和 1825 TSDD(HR 1.13,CI 0.82-1.56)。这些 TSDD 水平分别代表约 1、3 和 5 年的每日使用量。PPI 使用时间也与痴呆结局无关。
即使对于累积暴露量高的人群,PPI 使用与痴呆风险无关。尽管长期使用 PPI 存在其他安全问题,但我们的研究结果不支持出于对痴呆风险的担忧而避免使用这些药物。