Laboratory of Ageing and Pharmacology, Kolling Institute of Medical Research, Royal North Shore Hospital and University of Sydney, St Leonards, New South Wales, Australia.
Departments of Clinical Pharmacology and Aged Care, Royal North Shore Hospital, St Leonards, New South Wales, Australia.
J Gerontol A Biol Sci Med Sci. 2021 May 22;76(6):1010-1018. doi: 10.1093/gerona/glaa060.
Polypharmacy (use of ≥5 medications) and increasing Drug Burden Index (DBI) score (measure of person's total exposure to anticholinergic/sedative medications) are associated with impaired physical function in observational studies of older adults. Deprescribing, the supervised withdrawal of medications for which harms outweigh benefits for an individual, may be a useful intervention. Current knowledge is limited to clinical observational studies that are unable to determine causality. Here, we establish a preclinical model that investigates the effects of chronic polypharmacy, increasing DBI, and deprescribing on global health outcomes in aging. In a longitudinal study, middle-aged (12 months) male C57BL/6J (B6) mice were administered control feed or feed and/or water containing polypharmacy or monotherapy with different DBI scores. At 21 months, each treatment group was subdivided (stratified by frailty at 21 months) to either continue on treatment for life or to have treatment withdrawn (deprescribed). Frailty and physical function were evaluated at 12, 15, 18, and 24 months, and were analyzed using a mixed modeling approach. Polypharmacy with increasing DBI and monotherapy with citalopram caused mice to become frailer, less mobile, and impaired their strength and functional activities. Critically, deprescribing in old age reversed a number of these outcomes. This is the first preclinical study to demonstrate that chronic polypharmacy with increasing DBI augments frailty and impairs function in old age, and that drug withdrawal in old age reversed these outcomes. It was not the number of drugs (polypharmacy) but the type and dose of drugs (DBI) that caused adverse geriatric outcomes.
多药治疗(使用≥5 种药物)和不断增加的药物负担指数(衡量个体接触抗胆碱能/镇静药物总量的指标)与观察性研究中老年患者身体功能受损有关。药物撤停(即停止使用对个人利小于弊的药物)可能是一种有用的干预措施。目前的知识仅限于无法确定因果关系的临床观察性研究。在这里,我们建立了一个临床前模型,用于研究慢性多药治疗、不断增加的 DBI 和药物撤停对衰老个体整体健康结果的影响。在一项纵向研究中,中年(12 个月)雄性 C57BL/6J(B6)小鼠给予对照饲料或含有多药治疗或不同 DBI 评分的单药治疗的饲料和/或水。在 21 个月时,每个治疗组被进一步细分(根据 21 个月时的脆弱性分层),要么继续终生治疗,要么停止治疗(撤停)。在 12、15、18 和 24 个月时评估虚弱和身体功能,并使用混合建模方法进行分析。随着 DBI 的增加,慢性多药治疗和西酞普兰单药治疗使小鼠变得更加脆弱、活动能力降低,并损害了它们的力量和功能活动。关键的是,老年时的撤停逆转了其中的一些结果。这是第一项临床前研究,证明随着 DBI 的增加,慢性多药治疗会加剧老年时的脆弱性并损害功能,而老年时的药物撤停可以逆转这些结果。导致老年不良结局的不是药物数量(多药治疗),而是药物类型和剂量(DBI)。