Hanai Tatsunori, Nishimura Kayoko, Miwa Takao, Maeda Toshihide, Imai Kenji, Suetsugu Atsushi, Takai Koji, Shimizu Masahito
Department of Gastroenterology/Internal Medicine Gifu University Graduate School of Medicine Gifu Japan.
Center for Nutrition Support and Infection Control Gifu University Hospital Gifu Japan.
JGH Open. 2023 Feb 12;7(3):208-214. doi: 10.1002/jgh3.12877. eCollection 2023 Mar.
Polypharmacy and sarcopenia are increasing public health problems worldwide. However, data on the prevalence, association, and prognostic significance of polypharmacy and sarcopenia in patients with liver cirrhosis are limited.
Polypharmacy and sarcopenia were assessed in 239 patients with liver cirrhosis. Polypharmacy was defined as the daily use of six or more medications, and sarcopenia was diagnosed based on muscle strength and mass evaluated on computed tomography. The association between polypharmacy and sarcopenia and their effects on mortality were analyzed using logistic regression and Cox proportional hazards models.
Among the 239 patients, 52% were men, the median age was 68 years, and the number of medications used per patient was 6. Further, 53% and 29% patients had polypharmacy and sarcopenia, respectively. The number of medications used and the prevalence of sarcopenia increased with age. Patients with polypharmacy and sarcopenia had similar characteristics, such as older age, increased medication use, advanced liver disease, and decreased muscle strength and mass. After adjusting for confounders, polypharmacy was significantly associated with sarcopenia (odds ratio, 2.11; 95% confidence interval [CI], 1.07-4.17). During the median follow-up of 2.2 years, 62 (26%) patients died. Polypharmacy (hazard ratio [HR], 1.83; 95% CI, 1.01-3.37) and sarcopenia (HR, 2.00; 95% CI, 1.12-3.50) independently predicted mortality. The prognostic significance of polypharmacy was more prominent in older adults than in younger adults (HR, 2.31; 95% CI, 1.01-5.67).
Polypharmacy and sarcopenia are interrelated and associated with poor prognosis in patients with cirrhosis. Further large, prospective, population-based studies are required to validate these findings.
多重用药和肌肉减少症是全球日益严重的公共卫生问题。然而,肝硬化患者中多重用药和肌肉减少症的患病率、关联性及预后意义的数据有限。
对239例肝硬化患者进行了多重用药和肌肉减少症评估。多重用药定义为每日使用六种或更多药物,肌肉减少症根据计算机断层扫描评估的肌肉力量和质量进行诊断。使用逻辑回归和Cox比例风险模型分析多重用药与肌肉减少症之间的关联及其对死亡率的影响。
在239例患者中,52%为男性,中位年龄为68岁,每位患者使用的药物数量为6种。此外,分别有53%和29%的患者存在多重用药和肌肉减少症。使用的药物数量和肌肉减少症的患病率随年龄增加而升高。多重用药和肌肉减少症患者具有相似的特征,如年龄较大、用药增加、肝病进展以及肌肉力量和质量下降。在调整混杂因素后,多重用药与肌肉减少症显著相关(优势比,2.11;95%置信区间[CI],1.07 - 4.17)。在中位随访2.2年期间,62例(26%)患者死亡。多重用药(风险比[HR],1.83;95%CI,1.01 - 3.37)和肌肉减少症(HR,2.00;95%CI,1.12 - 3.50)独立预测死亡率。多重用药的预后意义在老年人中比在年轻人中更显著(HR,2.31;95%CI,1.01 - 5.67)。
多重用药和肌肉减少症相互关联,且与肝硬化患者的不良预后相关。需要进一步开展大规模、前瞻性、基于人群的研究来验证这些发现。