Pectoralis muscle area and its association with indices of disease severity in interstitial lung disease

医学 DLCO公司 肺活量 内科学 间质性肺病 瘦体质量 肺功能测试 心脏病学 肺容积 危险系数 扩散能力 肺功能 置信区间 体重
作者
Yannick Molgat‐Seon,Sabina A. Guler,Carli M. Peters,Dragoş M. Vasilescu,Joseph H. Puyat,Harvey O. Coxson,Christopher J. Ryerson,Jordan A. Guenette
出处
期刊:Respiratory Medicine [Elsevier]
卷期号:186: 106539-106539 被引量:18
标识
DOI:10.1016/j.rmed.2021.106539
摘要

Rationale The pathophysiology of interstitial lung disease (ILD) impacts body composition, whereby ILD severity is linked to lower lean mass. Objectives To determine i) if pectoralis muscle area (PMA) is a surrogate for whole-body lean mass in ILD, ii) whether PMA is associated with ILD severity, and iii) if the longitudinal change in PMA is associated with pulmonary function and mortality in ILD. Methods Patients with ILD (n = 164) were analyzed retrospectively. PMA was quantified from a chest computed tomography scan. Peripheral oxygen saturation (SpO2), 6-min walk distance (6MWD), and pulmonary function were obtained as part of routine clinical care. Dyspnea and quality of life were assessed using the UCSD Shortness of Breath Questionnaire and European Quality of Life 5 Dimensions questionnaire, respectively. Results PMA was associated with whole-body lean mass (p < 0.001). After adjusting for age, sex, height, body mass, and prednisone status, PMA was associated with %-predicted forced vital capacity (FVC), %-predicted diffusion capacity (DLCO), resting and exertional SpO2, and dyspnea (all p < 0.05), but not forced expiratory volume in 1 s (FEV1), FEV1/FVC, 6MWD, or quality of life (all p > 0.05). The annual negative PMA slope was associated with annual negative slopes in FVC, FEV1, and DLCO (all p < 0.05), but not FEV1/FVC (p = 0.46). Annual slope in PMA was associated with all-cause mortality (hazard ratio = −0.80, 95% CI:0.889–0.959; p < 0.001). Conclusion In patients with ILD, PMA is a suitable surrogate for whole-body lean mass. A lower PMA is associated with indices of ILD severity, which supports the notion that ILD progression may involve sarcopenia.
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