Oh GYeon, Moga Daniela C, Fardo David W, Abner Erin L
Sanders-Brown Center on Aging, University of Kentucky, Lexington, KY, United States.
Department of Epidemiology and Environmental Health, University of Kentucky, Lexington, KY, United States.
Front Pharmacol. 2022 Nov 25;13:910719. doi: 10.3389/fphar.2022.910719. eCollection 2022.
Gabapentin is increasingly prescribed to older adults, which raises concerns about its potential to cause neurocognitive changes. Therefore, we aimed to examine the association of gabapentin use with neurocognitive changes (i.e., cognitive decline, functional status decline, and motor function change) in older adults. We conducted a retrospective cohort study using the National Alzheimer's Coordinating Center Uniform Data Set (UDS; September 2005-March 2021 data freeze). From the eligible sample (≥age 65 years), we identified cognitively normal new-users of gabapentin and the visit they initiated gabapentin (i.e., index visit). Initiators were matched to randomly selected nonusers on year of UDS enrollment and visit number from enrollment to index. Cognitive decline was defined as any increase in the Clinical Dementia Rating global score (CDRGLOB) and as a 1-point increase in CDR sum of boxes (CDR-SB). Functional status decline was defined as a 3-point increase in the sum of the Functional Activities Questionnaire (FAQ) and as 0.3-point increase in mean FAQ. Decline in motor function was defined as new clinician reports of gait disorder, falls, and slowness. To mitigate confounding and selection bias, we used joint stabilized inverse probability of treatment weights and stabilized inverse probability of censoring weights. All analyses were conducted comparing index to index+1 and index+2 visits. From the eligible UDS participants (N = 23,059), we included 480 initiators (mean age [SD]: 78.7 [6.9]; male 34.4%); 4,320 nonusers (78.3 [7.0]; 34.4%). Gabapentin initiation was significantly associated with cognitive/functional status decline: worsening CDRGLOB at index+1 visit (odds ratio [95% confidence interval]: 1.55 [1.07, 2.25]); CDR-SB at index+1 visit (1.94 [1.22, 3.09]); and mean of FAQ at index+2 visit (1.78 [1.12, 2.83]). After excluding initiators with extant motor dysfunction (n = 21), we identified 459 initiators (78.7 [6.9]; 34.0%) and 4,131 nonusers (78.2 [6.9]; 34.7%); in this sample, gabapentin initiation was associated with increased falls at the index+2 visit (2.51 [1.19, 5.31]). Gabapentin initiation was significantly associated with deleterious neurocognitive changes among older adults with initially normal cognition. Further studies are needed to examine the risk/benefit of prescribing gabapentin in older adults.
加巴喷丁越来越多地被开给老年人,这引发了人们对其可能导致神经认知改变的担忧。因此,我们旨在研究加巴喷丁的使用与老年人神经认知改变(即认知能力下降、功能状态下降和运动功能改变)之间的关联。我们使用国家阿尔茨海默病协调中心统一数据集(UDS;2005年9月 - 2021年3月数据冻结)进行了一项回顾性队列研究。从符合条件的样本(年龄≥65岁)中,我们确定了认知正常的加巴喷丁新使用者以及他们开始使用加巴喷丁的就诊时间(即索引就诊)。发起者与在UDS登记年份和从登记到索引就诊的就诊次数方面随机选择的非使用者进行匹配。认知能力下降定义为临床痴呆评定量表总体评分(CDRGLOB)的任何增加以及CDR方框总和(CDR - SB)增加1分。功能状态下降定义为功能活动问卷(FAQ)总和增加3分以及平均FAQ增加0.3分。运动功能下降定义为新的临床医生报告的步态障碍、跌倒和行动迟缓。为了减轻混杂和选择偏倚,我们使用了联合稳定的治疗权重逆概率和稳定的删失权重逆概率。所有分析都是将索引就诊与索引 + 1和索引 + 2就诊进行比较。从符合条件的UDS参与者(N = 23,059)中,我们纳入了480名发起者(平均年龄[标准差]:78.7[6.9];男性34.4%);4320名非使用者(78.3[7.0];34.4%)。开始使用加巴喷丁与认知/功能状态下降显著相关:索引 + 1就诊时CDRGLOB恶化(优势比[95%置信区间]:1.55[1.07, 2.25]);索引 + 1就诊时CDR - SB(1.94[1.22, 3.09]);以及索引 + 2就诊时FAQ平均值(1.78[1.12, 2.83])。在排除已有运动功能障碍的发起者(n = 21)后,我们确定了459名发起者(78.7[6.9];34.0%)和4131名非使用者(78.2[6.9];34.7%);在这个样本中,开始使用加巴喷丁与索引 + 2就诊时跌倒增加相关(2.51[1.19, 5.31])。开始使用加巴喷丁与认知最初正常的老年人中有害的神经认知改变显著相关。需要进一步研究来检查在老年人中开具加巴喷丁的风险/益处。