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特发性肺纤维化患者中肌少症的频率及其对临床结局的影响。

Frequency and impact on clinical outcomes of sarcopenia in patients with idiopathic pulmonary fibrosis.

机构信息

Department of Respiratory Medicine, Allergy and Clinical Immunology, 38386Nagoya City University Graduate School of Medical Sciences, Nagoya, Japan.

Department of Respiratory Medicine, 36975Nagoya City University East Medical Center, Nagoya, Japan.

出版信息

Chron Respir Dis. 2022 Jan-Dec;19:14799731221117298. doi: 10.1177/14799731221117298.

Abstract

OBJECTIVES

Sarcopenia is a syndrome characterized by reduced muscle mass and function. It is well-recognized as a complication in chronic diseases such as chronic obstructive pulmonary disease. However, little is known about sarcopenia in patients with idiopathic pulmonary fibrosis (IPF). This study aimed to investigate the clinical characteristics of sarcopenia and the association between quality of life and sarcopenia in patients with IPF.

METHODS

In this pilot cross-sectional study, 56 Japanese outpatients with IPF (49 men) were enrolled prospectively. Sarcopenia was diagnosed according to the criteria of the Asian Working Group for Sarcopenia 2019. Its associations with clinical parameters including age, pulmonary functions, physical performance, and patient-reported outcomes (PROs) were examined.

RESULTS

The frequency of sarcopenia was 39.3% ( = 22) in this cohort. There were significant differences in St George's Respiratory Questionnaire ( = .005), modified Medical Research Council score ( = .004), and Hospital and Anxiety Depression Scale depression score ( = .030) between the sarcopenic and non-sarcopenic groups. On multivariate regression analysis, 6-min walk distance (6MWD) was an independent factor associated with sarcopenia (odds ratio 1.241, 95% confidence interval 1.016-1.515, = .034).

CONCLUSION

Sarcopenia was associated with PROs and physical performance in patients with IPF.

摘要

目的

肌少症是一种以肌肉质量和功能下降为特征的综合征。它是慢性阻塞性肺疾病等慢性疾病的公认并发症。然而,对于特发性肺纤维化(IPF)患者的肌少症知之甚少。本研究旨在探讨肌少症的临床特征以及 IPF 患者生活质量与肌少症之间的关系。

方法

在这项前瞻性的初步横断面研究中,共纳入了 56 名日本特发性肺纤维化门诊患者(49 名男性)。根据亚洲肌少症工作组 2019 年的标准诊断肌少症。检查了其与临床参数(包括年龄、肺功能、身体机能和患者报告的结局)的相关性。

结果

在该队列中,肌少症的发生率为 39.3%(=22)。在圣乔治呼吸问卷(=0.005)、改良医学研究委员会评分(=0.004)和医院焦虑抑郁量表抑郁评分(=0.030)方面,肌少症组和非肌少症组存在显著差异。在多变量回归分析中,6 分钟步行距离(6MWD)是与肌少症相关的独立因素(比值比 1.241,95%置信区间 1.016-1.515,=0.034)。

结论

肌少症与 IPF 患者的生活质量和身体机能相关。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/2fa0/9358593/c29a9a23c7f7/10.1177_14799731221117298-fig1.jpg

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