Veronese Nicola, Stubbs Brendon, Noale Marianna, Solmi Marco, Pilotto Alberto, Vaona Alberto, Demurtas Jacopo, Mueller Christoph, Huntley Jonathan, Crepaldi Gaetano, Maggi Stefania
National Research Council, Neuroscience Institute, Aging Branch, Padua, Italy; Institute for clinical Research and Education in Medicine, IREM, Padua, Italy; Department of Geriatric Care, OrthoGeriatrics and Rehabilitation, E.O. Galliera Hospital, Genova, Italy.
South London and Maudsley NHS Foundation Trust, Denmark Hill, London, United Kingdom; Faculty of Health, Social care and Education, Anglia Ruskin University, Chelmsford, United Kingdom; Institute of Psychiatry, Psychology and Neuroscience (IoPPN) King's College London, London, United Kingdom.
J Am Med Dir Assoc. 2017 Jul 1;18(7):624-628. doi: 10.1016/j.jamda.2017.02.009. Epub 2017 Apr 7.
To investigate whether polypharmacy is associated with a higher incidence of frailty in a large cohort of North Americans during 8 years of follow-up.
Longitudinal study, follow-up of 8 years.
A total of 4402 individuals at high risk or having knee osteoarthritis free from frailty at baseline.
Details regarding medication prescription were captured and categorized as 0-3, 4-6, and ≥7. Frailty was defined using the Study of Osteoporotic Fracture index as the presence of ≥2 out of (1) weight loss ≥5% between baseline and the subsequent follow-up visit; (2) inability to do 5 chair stands; and (3) low energy level according to the Study of Osteoporotic Fracture definition. Cox's regression models calculating a hazard ratio (HR) with 95% confidence intervals (CIs), adjusted for potential confounders, were undertaken.
During the 8-year follow-up, from 4402 participants at baseline, 361 became frail. Compared with participants taking 0-3 medications, the incidence of frailty was approximately double in those taking 4-6 medications and 6 times higher in people taking ≥7 medications. After adjusting for 11 potential baseline confounders, participants using 4-6 medications had a higher risk of frailty of 55% (HR = 1.55; 95% CI 1.22-1.96; P < .0001), whereas those using more than 7 drugs were at approximately 147% (HR = 2.47; 95% CI 1.78-3.43; P < .0001). Each additional drug used at the baseline increased the risk of frailty at the follow-up of 11% (HR = 1.11; 95% CI 1.07-1.15; P < .0001).
Polypharmacy is associated with a higher incidence of frailty over 8-year follow-up period. Our data suggest evidence of a dose response relationship. Future research is required to confirm our findings and explore underlying mechanisms.
调查在8年随访期间,多种药物联合使用是否与北美一大群人更高的衰弱发生率相关。
纵向研究,8年随访。
共有4402名基线时无衰弱的高危或患有膝关节骨关节炎的个体。
记录药物处方的详细信息,并分为0 - 3种、4 - 6种和≥7种。衰弱采用骨质疏松性骨折研究指数定义,即基线与后续随访之间体重减轻≥5%、无法完成5次从椅子上站起以及根据骨质疏松性骨折研究定义能量水平低这三项中出现≥2项。采用Cox回归模型计算风险比(HR)及95%置信区间(CI),并对潜在混杂因素进行校正。
在8年随访期间,4402名基线参与者中有361人变得衰弱。与服用0 - 3种药物的参与者相比,服用4 - 6种药物的参与者衰弱发生率约为两倍,服用≥7种药物的人则高6倍。在对11个潜在基线混杂因素进行校正后,使用4 - 6种药物的参与者衰弱风险高55%(HR = 1.55;95% CI 1.22 - 1.96;P <.0001),而使用超过7种药物的参与者约高147%(HR = 2.47;95% CI 1.78 - 3.43;P <.0001)。基线时每多使用一种药物,随访时衰弱风险增加11%(HR = 1.11;95% CI 1.07 - 1.15;P <.0001)。
在8年随访期内,多种药物联合使用与更高的衰弱发生率相关。我们的数据表明存在剂量反应关系的证据。需要进一步研究来证实我们的发现并探索潜在机制。