Sarcopenia in interstitial lung disease.

IF 9 1区 医学 Q1 RESPIRATORY SYSTEM
European Respiratory Review Pub Date : 2024-12-04 Print Date: 2024-10-01 DOI:10.1183/16000617.0126-2024
Robert Sheehy, Samuel McCormack, Caitlin Fermoyle, Tamera Corte
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引用次数: 0

Abstract

Background: Interstitial lung disease (ILD) encompasses a heterogeneous group of chronic lung conditions with considerable variability in prognosis and response to treatment. People with reduced muscle mass and function, known as sarcopenia, have a higher risk of mortality and adverse clinical outcomes both in the general population and in other chronic disease states. The importance of sarcopenia across the spectrum of patients with ILD is not well established.

Objectives: In this narrative review, we explore the prevalence and clinical implications of sarcopenia in patients with ILD, evaluate the optimal methods to diagnose sarcopenia in this patient population and review treatment interventions.

Findings: Almost one third of patients with chronic forms of ILD have evidence of sarcopenia. Sarcopenia is associated with adverse clinical outcomes and increased risk of mortality in select populations with ILD. Screening tests such as the SARC-F (strength, assistance walking, rise from a chair, climb stairs, falls) questionnaire and clinical assessment tools (including grip strength dynamometry) are well validated. Medical imaging modalities, including computed tomography, are hampered by lack of a gold standard and normative values, but have been used in patients with ILD in acute care and research settings. If sarcopenia is identified, multidimensional interventions such as pulmonary rehabilitation are beneficial.

Conclusion: Sarcopenia is common in patients with ILD and is associated with poorer outcomes. Accordingly, if identified, targeted interventions should be considered. Validated diagnostic criteria exist, but the optimal use of medical imaging techniques in this patient cohort remains an area of uncertainty.

肺间质性疾病中的肌肉减少症。
背景:间质性肺病(ILD)包括一组异质性的慢性肺部疾病,在预后和治疗反应方面具有相当大的差异。肌肉质量和功能减少的人,即肌肉减少症,无论是在普通人群还是在其他慢性疾病状态下,都有更高的死亡率和不良临床结果风险。肌少症在ILD患者谱系中的重要性尚未得到很好的证实。目的:在这篇叙述性综述中,我们探讨了ILD患者肌肉减少症的患病率和临床意义,评估了诊断该患者群体肌肉减少症的最佳方法,并回顾了治疗干预措施。结果:几乎三分之一的慢性ILD患者有肌少症的证据。骨骼肌减少症与不良临床结果和特定ILD患者死亡风险增加有关。筛选试验,如SARC-F(力量、辅助行走、从椅子上站起来、爬楼梯、跌倒)问卷和临床评估工具(包括握力测功)得到了很好的验证。医学成像模式,包括计算机断层扫描,由于缺乏黄金标准和规范值而受到阻碍,但已在急性护理和研究环境中用于ILD患者。如果发现肌肉减少症,多维干预如肺部康复是有益的。结论:骨骼肌减少症在ILD患者中很常见,并与较差的预后相关。因此,如果确定,应考虑有针对性的干预措施。存在有效的诊断标准,但在该患者队列中最佳使用医学成像技术仍然是一个不确定的领域。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
European Respiratory Review
European Respiratory Review Medicine-Pulmonary and Respiratory Medicine
CiteScore
14.40
自引率
1.30%
发文量
91
审稿时长
24 weeks
期刊介绍: The European Respiratory Review (ERR) is an open-access journal published by the European Respiratory Society (ERS), serving as a vital resource for respiratory professionals by delivering updates on medicine, science, and surgery in the field. ERR features state-of-the-art review articles, editorials, correspondence, and summaries of recent research findings and studies covering a wide range of topics including COPD, asthma, pulmonary hypertension, interstitial lung disease, lung cancer, tuberculosis, and pulmonary infections. Articles are published continuously and compiled into quarterly issues within a single annual volume.
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