Goldstein Felicia C, Steenland Kyle, Zhao Liping, Wharton Whitney, Levey Allan I, Hajjar Ihab
Department of Neurology, School of Medicine, Emory University, Atlanta, Georgia.
Department of Environmental and Occupational Health, School of Public Health, Emory University, Atlanta, Georgia.
J Am Geriatr Soc. 2017 Sep;65(9):1969-1974. doi: 10.1111/jgs.14956. Epub 2017 Jun 7.
To examine the risk associated with the use of proton pump inhibitors (PPIs) of conversion to mild cognitive impairment (MCI), dementia, and specifically Alzheimer's disease (AD).
Observational, longitudinal study.
Tertiary academic Alzheimer's Disease Centers funded by the National Institute on Aging.
Research volunteers aged 50 and older with two to six annual visits; 884 were taking PPIs at every visit, 1,925 took PPIs intermittently, and 7,677 never reported taking PPIs. All had baseline normal cognition or MCI.
Multivariable Cox regression analyses evaluated the association between PPI use and annual conversion of baseline normal cognition to MCI or dementia or annual conversion of baseline MCI to dementia, controlling for demographic characteristics, vascular comorbidities, mood, and use of anticholinergics and histamine-2 receptor antagonists.
Continuous (always vs never) PPI use was associated with lower risk of decline in cognitive function (hazard ratio (HR) = 0.78, 95% confidence interval (CI) =0.66-0.93, P = .005) and lower risk of conversion to MCI or AD (HR = 0.82, 95% CI = 0.69-0.98, P = .03). Intermittent use was also associated with lower risk of decline in cognitive function (HR = 0.84, 95% CI = 0.76-0.93, P = .001) and risk of conversion to MCI or AD (HR = 0.82, 95% CI = 0.74-0.91, P = .001). This lower risk was found for persons with normal cognition or MCI.
Proton pump inhibitors were not associated with greater risk of dementia or of AD, in contrast to recent reports. Study limitations include reliance on self-reported PPI use and lack of dispensing data. Prospective studies are needed to confirm these results to guide empirically based clinical treatment recommendations.
研究使用质子泵抑制剂(PPI)与转化为轻度认知障碍(MCI)、痴呆症,尤其是阿尔茨海默病(AD)之间的风险。
观察性纵向研究。
由美国国立衰老研究所资助的三级学术性阿尔茨海默病中心。
年龄在50岁及以上的研究志愿者,每年进行两到六次随访;884人每次随访时都在服用PPI,1925人间歇性服用PPI,7677人从未报告服用过PPI。所有参与者基线认知正常或为MCI。
多变量Cox回归分析评估了PPI使用与基线正常认知向MCI或痴呆症的年度转化率,或基线MCI向痴呆症的年度转化率之间的关联,并对人口统计学特征、血管合并症、情绪以及抗胆碱能药物和组胺-2受体拮抗剂的使用情况进行了控制。
持续(始终服用与从未服用)使用PPI与认知功能下降风险较低相关(风险比(HR)=0.78,95%置信区间(CI)=0.66 - 0.93,P = 0.005),以及转化为MCI或AD的风险较低相关(HR = 0.82,95% CI = 0.69 - 0.98,P = 0.03)。间歇性使用也与认知功能下降风险较低相关(HR = 0.84,95% CI = 0.76 - 0.93,P = 0.001)以及转化为MCI或AD的风险较低相关(HR = 0.82,95% CI = 0.74 - 0.91,P = 0.001)。在认知正常或为MCI的人群中发现了这种较低风险。
与近期报告相反,质子泵抑制剂与痴呆症或AD的较高风险无关。研究局限性包括依赖自我报告的PPI使用情况以及缺乏配药数据。需要进行前瞻性研究以证实这些结果,从而指导基于经验的临床治疗建议。