• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

肌无力和肌少症作为间质性肺疾病患者死亡的危险因素

Dynapenia and Sarcopenia as Risk Factors for Mortality in Interstitial Lung Disease.

作者信息

Ibarra-Fernández Alan Aldair, Robles-Hernández Robinson, Orea-Tejeda Arturo, González-Islas Dulce, Jiménez-Valentín Angelia, Sánchez-Santillán Rocío, Arcos-Pacheco Laura Patricia, Gutiérrez-Luna Emilio, Zurita-Sandoval Andrea, Peña-Espinosa Tomas, Gutiérrez-Vargas Rosaura, Flores-Cisneros Laura

机构信息

Tuberculosis Clinic, Instituto Nacional de Enfermedades Respiratorias "Ismael Cosío Villegas", Mexico City, Mexico.

Department of Research in Tobacco Smoking and COPD, Instituto Nacional de Enfermedades Respiratorias "Ismael Cosío Villegas", Mexico City, Mexico.

出版信息

Respirology. 2025 May;30(5):424-434. doi: 10.1111/resp.14892. Epub 2025 Feb 4.

DOI:10.1111/resp.14892
PMID:39905591
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12060744/
Abstract

BACKGROUND AND OBJECTIVE

Fibrotic interstitial lung disease (ILD) is associated with high morbidity and mortality. Patients often exhibit impaired nutritional status and alterations in body composition, such as dynapenia and sarcopenia, which correlate with poor pulmonary function, reduced exercise tolerance and diminished quality of life. However, the impact of dynapenia and sarcopenia on prognosis has not been examined extensively in ILD patients. We assessed the impact of dynapenia and sarcopenia as risk factors for mortality and their prevalence in ILD.

METHODS

Prospective cohort study. ILD was classified into idiopathic pulmonary fibrosis (IPF), connective tissue disease-related ILD (CTD-ILD) and chronic hypersensitivity pneumonitis (CHP). Patients over 18 years old with a confirmed diagnosis of ILD were included, while those with diagnoses of cancer, human immunodeficiency virus and neurological disease were excluded. Dynapenia and sarcopenia were determined according to EWGSOP2 criteria.

RESULTS

Ninety-eight ILD patients were included; 33.66% had IPF, 47.96% had CTD-ILD, and 18.37% had CHP. The mean age was 63.89 ± 12.02 years; 37.76% were male. The risk factors associated with mortality included dynapenia (HR: 2.04, 95% CI: 1.10-3.77, p = 0.022), sarcopenia (HR: 1.88, 95% CI; 1.00-3.33, p = 0.049) and exercise tolerance (HR: 0.99, 95% CI; 0.99-0.99, p = 0.023), adjusted for confounding variables. The prevalence of dynapenia was 45% in ILD; 51% in IPF, 35% in CTD-ILD and 61% in CHP. The prevalence of sarcopenia was 29%; both IPF (39%) and CHP (50%) had a higher prevalence of sarcopenia than CTD-ILD (14%).

CONCLUSION

Sarcopenia and dynapenia are independent risk factors for mortality in ILD.

摘要

背景与目的

纤维化间质性肺疾病(ILD)与高发病率和死亡率相关。患者常表现出营养状况受损和身体成分改变,如肌无力和肌肉减少症,这与肺功能差、运动耐力降低及生活质量下降相关。然而,肌无力和肌肉减少症对ILD患者预后的影响尚未得到广泛研究。我们评估了肌无力和肌肉减少症作为ILD患者死亡风险因素的影响及其患病率。

方法

前瞻性队列研究。ILD分为特发性肺纤维化(IPF)、结缔组织病相关ILD(CTD-ILD)和慢性过敏性肺炎(CHP)。纳入确诊为ILD的18岁以上患者,排除患有癌症、人类免疫缺陷病毒和神经系统疾病的患者。根据EWGSOP2标准确定肌无力和肌肉减少症。

结果

纳入98例ILD患者;33.66%患有IPF,47.96%患有CTD-ILD,18.37%患有CHP。平均年龄为63.89±12.02岁;37.76%为男性。调整混杂变量后,与死亡相关的风险因素包括肌无力(HR:2.04,95%CI:1.10-3.77,p = 0.022)、肌肉减少症(HR:1.88,95%CI;1.00-3.33,p = 0.用调整后的混杂变量分析。ILD患者中肌无力的患病率为45%;IPF中为51%,CTD-ILD中为35%,CHP中为61%。肌肉减少症的患病率为29%;IPF(39%)和CHP(50%)的肌肉减少症患病率均高于CTD-ILD(14%)。

结论

肌肉减少症和肌无力是ILD患者死亡的独立风险因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6861/12060744/04b5560d980c/RESP-30-424-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6861/12060744/8bd9fa3c1027/RESP-30-424-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6861/12060744/e1a581fba1cc/RESP-30-424-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6861/12060744/04b5560d980c/RESP-30-424-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6861/12060744/8bd9fa3c1027/RESP-30-424-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6861/12060744/e1a581fba1cc/RESP-30-424-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6861/12060744/04b5560d980c/RESP-30-424-g003.jpg

相似文献

1
Dynapenia and Sarcopenia as Risk Factors for Mortality in Interstitial Lung Disease.肌无力和肌少症作为间质性肺疾病患者死亡的危险因素
Respirology. 2025 May;30(5):424-434. doi: 10.1111/resp.14892. Epub 2025 Feb 4.
2
Hospitalization Rates in Interstitial Lung Disease: An Analysis of the Pulmonary Fibrosis Foundation Registry.间质性肺疾病的住院率:对肺纤维化基金会登记处的分析。
Am J Respir Crit Care Med. 2024 Sep 15;210(6):801-813. doi: 10.1164/rccm.202309-1708OC.
3
Comparison of clinical courses and mortality of connective tissue disease-associated interstitial pneumonias and chronic fibrosing idiopathic interstitial pneumonias.结缔组织病相关性间质性肺炎与慢性纤维化特发性间质性肺炎的临床过程和死亡率比较。
Kaohsiung J Med Sci. 2019 Jun;35(6):365-372. doi: 10.1002/kjm2.12066. Epub 2019 Mar 26.
4
High resolution computed tomography patterns in interstitial lung disease (ILD): prevalence and prognosis.高分辨率计算机断层扫描(HRCT)在间质性肺疾病(ILD)中的表现:患病率和预后。
J Bras Pneumol. 2020 Mar 9;46(5):e20190153. doi: 10.36416/1806-3756/e20190153. eCollection 2020.
5
Computed Tomography Honeycombing Identifies a Progressive Fibrotic Phenotype with Increased Mortality across Diverse Interstitial Lung Diseases.计算机断层扫描蜂巢征鉴别不同间质性肺疾病中具有进展性纤维化表型的患者,此类患者的死亡率更高。
Ann Am Thorac Soc. 2019 May;16(5):580-588. doi: 10.1513/AnnalsATS.201807-443OC.
6
Pathological features of connective tissue disease-associated interstitial lung disease in transbronchial cryobiopsies.经支气管冷冻活检中结缔组织病相关间质性肺疾病的病理特征
Histopathology. 2025 Jan;86(2):260-267. doi: 10.1111/his.15311. Epub 2024 Sep 2.
7
Prevalence and characteristics of progressive fibrosing interstitial lung disease in a prospective registry.前瞻性登记研究中进行性纤维化间质性肺疾病的患病率及特征
Eur Respir J. 2022 Oct 6;60(4). doi: 10.1183/13993003.02571-2021. Print 2022 Oct.
8
Comparison of characteristics of connective tissue disease-associated interstitial lung diseases, undifferentiated connective tissue disease-associated interstitial lung diseases, and idiopathic pulmonary fibrosis in Chinese Han population: a retrospective study.中国汉族人群中结缔组织病相关间质性肺疾病、未分化结缔组织病相关间质性肺疾病和特发性肺纤维化的特征比较:一项回顾性研究
Clin Dev Immunol. 2013;2013:121578. doi: 10.1155/2013/121578. Epub 2013 Sep 19.
9
Clinical features and outcome of acute exacerbation in connective tissue disease-associated interstitial lung disease: A single-center study from India.结缔组织病相关间质性肺疾病急性加重的临床特征和结局:来自印度的单中心研究。
Int J Rheum Dis. 2019 Sep;22(9):1741-1745. doi: 10.1111/1756-185X.13666. Epub 2019 Jul 22.
10
Acute exacerbations of fibrosing interstitial lung disease associated with connective tissue diseases: a population-based study.与结缔组织疾病相关的纤维性间质性肺疾病的急性加重:一项基于人群的研究。
BMC Pulm Med. 2019 Nov 14;19(1):215. doi: 10.1186/s12890-019-0960-1.