Byun Min Kwang, Cho Eun Na, Chang Joon, Ahn Chul Min, Kim Hyung Jung
Division of Pulmonology, Department of Internal Medicine, Gangnam Severance Hospital.
Division of Pulmonology, Department of Internal Medicine, Severance Hospital, Yonsei University College of Medicine, Seoul, South Korea.
Int J Chron Obstruct Pulmon Dis. 2017 Feb 20;12:669-675. doi: 10.2147/COPD.S130790. eCollection 2017.
Muscle wasting and chronic inflammation are predominant features of patients with COPD. Systemic inflammation is associated with an accelerated decline in lung function. In this study, the prevalence of sarcopenia and the relationships between sarcopenia and systemic inflammations in patients with stable COPD were investigated.
In a cross-sectional design, muscle strength and muscle mass were measured by handgrip strength (HGS) and bioelectrical impedance analysis in 80 patients with stable COPD. Patients (≥40 years old) diagnosed with COPD were recruited from outpatient clinics, and then COPD stages were classified. Sarcopenia was defined as the presence of both low muscle strength (by HGS) and low muscle mass (skeletal muscle mass index [SMMI]). Levels of circulating inflammatory biomarkers (IL-6 and high-sensitivity TNFα [hsTNFα]) were measured.
Sarcopenia was prevalent in 20 (25%) patients. Patients with sarcopenia were older, had lower body mass index, and a higher percentage of cardiovascular diseases. In addition, they had significantly higher modified Medical Research Council scores and lower 6-minute walk distance than those without sarcopenia. HGS was significantly correlated with age, modified Medical Research Council score, and COPD Assessment Test scores. Both HGS and SMMI had associations with IL-6 and hsTNFα (HGS, =-0.35, =0.002; SMMI, =-0.246, =0.044) level. In multivariate analysis, old age, lower body mass index, presence of cardiovascular comorbidities, and higher hsTNFα levels were significant determinants for sarcopenia in patients with stable COPD.
Sarcopenia is very common in patients with stable COPD, and is associated with more severe dyspnea-scale scores and lower exercise tolerance. Systemic inflammation could be an important contributor to sarcopenia in the stable COPD population.
肌肉萎缩和慢性炎症是慢性阻塞性肺疾病(COPD)患者的主要特征。全身炎症与肺功能加速下降有关。在本研究中,调查了稳定期COPD患者中肌肉减少症的患病率以及肌肉减少症与全身炎症之间的关系。
采用横断面设计,通过握力(HGS)和生物电阻抗分析测量80例稳定期COPD患者的肌肉力量和肌肉质量。从门诊招募诊断为COPD(≥40岁)的患者,然后对COPD分期进行分类。肌肉减少症定义为同时存在低肌肉力量(通过HGS测量)和低肌肉质量(骨骼肌质量指数[SMMI])。测量循环炎症生物标志物(IL-6和高敏TNFα[hsTNFα])水平。
20例(25%)患者存在肌肉减少症。肌肉减少症患者年龄更大,体重指数更低,心血管疾病百分比更高。此外,与无肌肉减少症的患者相比,他们的改良医学研究委员会评分显著更高,6分钟步行距离更低。HGS与年龄、改良医学研究委员会评分和COPD评估测试评分显著相关。HGS和SMMI均与IL-6和hsTNFα水平相关(HGS,=-0.35,=0.002;SMMI,=-0.246,=0.044)。在多变量分析中,老年、较低的体重指数、心血管合并症的存在以及较高的hsTNFα水平是稳定期COPD患者肌肉减少症的重要决定因素。
肌肉减少症在稳定期COPD患者中非常常见,并且与更严重的呼吸困难量表评分和更低的运动耐力相关。全身炎症可能是稳定期COPD人群中肌肉减少症的重要促成因素。