老年慢性阻塞性肺疾病患者肺功能与肌肉减少的相关性及影响肌肉减少的因素分析。

IF 1.6 4区 医学 Q3 MEDICINE, RESEARCH & EXPERIMENTAL American journal of translational research Pub Date : 2025-01-15 eCollection Date: 2025-01-01 DOI:10.62347/OGUT1532
Xiaoran Yang, Yingchun Wei, Jinfeng Zhao, Yuqin Bai
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引用次数: 0

摘要

目的:探讨老年慢性阻塞性肺疾病(COPD)患者肺功能与骨骼肌减少的相关性,并分析影响骨骼肌减少的因素。目的是为COPD患者的综合管理提供证据。方法:选取2022年3月至2024年3月兰州市第一人民医院住院的老年COPD患者294例作为研究对象。将患者按7:3的比例分为训练组(205例)和验证组(89例)。通过肺功能测试评估肺功能,通过生物电阻抗分析评估肌肉质量和肌肉质量来确定肌肉减少症。根据肌少症的诊断标准,将患者分为肌少症组(113例)和非肌少症组(181例)。收集患者基本信息、生活习惯、病史,分析肺功能与肌肉减少症的相关性及影响因素。此外,通过logistic回归分析找出独立的危险因素,并建立nomogram风险预测模型。结果:多因素logistic回归分析显示年龄(p)与老年COPD患者肺功能下降与肌少症的发生密切相关。年龄增加是COPD患者肌肉减少的独立危险因素,而BMI和FEV1/FVC升高是保护因素。基于这些独立危险因素的nomogram模型能够有效预测老年COPD患者的肌肉减少症。
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Correlation of lung function and sarcopenia in elderly patients with chronic obstructive pulmonary disease and analysis of factors influencing sarcopenia.

Objective: This study aims to investigate the correlation between lung function and sarcopenia in elderly patients with chronic obstructive pulmonary disease (COPD) and to analyze the factors influencing sarcopenia. The goal is to provide evidence for comprehensive management of COPD patients.

Methods: A total of 294 elderly COPD patients admitted to Lanzhou City No. 1 People's Hospital from March 2022 to March 2024 were selected as study subjects. The patients were divided into a training group (n=205) and a validation group (n=89) in a 7:3 ratio. Lung function was assessed through pulmonary function tests, and sarcopenia was defined by evaluating muscle mass and muscle quality using bioelectrical impedance analysis. Based on the diagnostic criteria for sarcopenia, patients were categorized into a sarcopenia group (n=113) and a non-sarcopenia group (n=181). Basic information, lifestyle habits, and medical history were collected to analyze the correlation between lung function and sarcopenia, as well as influencing factors. Additionally, logistic regression analysis was conducted to identify independent risk factors, and a nomogram model was developed for risk prediction.

Results: Multivariate logistic regression analysis revealed that age (P<0.001, OR=0.053), weight (P=0.032, OR=3.321), Cys-C (P=0.018, OR=0.283), Hb (P=0.001, OR=7.014), FVC (P=0.04, OR=3.605), FEV1 (P=0.001, OR=9.674), and CAT score (P<0.001, OR=0.085) were independent risk factors for sarcopenia in COPD patients. The nomogram model based on these independent risk factors demonstrated good predictive performance for sarcopenia in elderly COPD patients. ROC curve analysis showed that the area under the curve (AUC) of the nomogram model was 0.886 (95% CI: 0.819-0.932) in the training group and 0.809 (95% CI: 0.726-0.883) in the validation group, indicating a high predictive accuracy. Additionally, ROC curve analysis showed that the AUCs for age, BMI, and FEV1/FVC in diagnosing sarcopenia in elderly COPD patients were 0.710 (95% CI: 0.747-0.863), 0.647 (95% CI: 0.766-0.878), and 0.682 (95% CI: 0.701-0.833), respectively. Gene Set Enrichment Analysis (GSEA) revealed that pathways significantly enriched in the high Cys-C expression group included oxidative phosphorylation, fatty acid biosynthesis, the AMPK signaling pathway, the HIF-1 signaling pathway, and glycolysis/gluconeogenesis pathways, which may play important roles in energy metabolism and muscle function regulation in sarcopenic patients.

Conclusion: Lung function decline in elderly COPD patients is closely associated with the occurrence of sarcopenia. Increasing age is an independent risk factor for sarcopenia in COPD patients, while higher BMI and FEV1/FVC are protective factors. The nomogram model based on these independent risk factors can effectively predict sarcopenia in elderly COPD patients.

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American journal of translational research
American journal of translational research ONCOLOGY-MEDICINE, RESEARCH & EXPERIMENTAL
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