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内皮功能障碍:COPD 炎症衰老现象与心血管合并症之间的可能联系。

Endothelial dysfunction: The possible link between cardiovascular comorbidities and phenomenon of inflammaging from COPD.

机构信息

Center for Research and Innovation in Personalized Medicine of Respiratory Diseases, XIII Department - Pulmonology Discipline, "Victor Babes" University of Medicine and Pharmacy Timisoara, Timișoara, Romania.

I and II Clinic of Pulmonary Diseases, Clinical Hospital of Infectious Diseases and Pneumophthisiology "Dr. Victor Babes" Timisoara, Timisoara, Romania.

出版信息

Medicine (Baltimore). 2022 Aug 19;101(33):e30078. doi: 10.1097/MD.0000000000030078.

DOI:10.1097/MD.0000000000030078
PMID:35984178
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9388037/
Abstract

Aging is a risk factor for many chronic noncommunicable diseases, including chronic obstructive pulmonary disease (COPD), which is often associated with cardiovascular disease (CVD). Moreover, aging is associated with a mild form of systemic inflammation. The aim of our study was to analyze the relationship between age, systemic and vascular inflammation, and the presence of CVD comorbidities in a stable COPD population. Forty COPD patients were divided into 2 age groups (<65 and ≥65 years of age), from which we collected the following inflammatory biomarkers: C-reactive protein, tumor necrosis factor alpha (TNF-α), interleukin-6 (IL-6), and endothelin-1 (ET-1). Elderly COPD patients had more frequent exacerbation events per year (2 vs 1, P = .06), a higher prevalence of CVD (3 vs 2, P = .04), more limited exercise tolerance (6-minute walking test distance, 343 [283-403] vs 434 [384-484]; P = .02), and mild systemic inflammation (TNF-α, 9.02 [7.08-10.96] vs 6.48 [5.21-7.76]; P = .03; ET-1, 2.24 [1.76-2.71] vs 1.67 [1.36-1.98] pg/mL; P = .04). A weak correlation between age and ET-1 (r = 0.32, P = .04) was observed. Mild systemic inflammation, characterized by a slightly increased level of TNF-α, and endothelial dysfunction, marked by elevated ET-1, could be liaisons between aging, COPD, and CVD comorbidities.

摘要

衰老是许多慢性非传染性疾病(包括慢性阻塞性肺疾病,简称 COPD)的一个风险因素,而 COPD 常伴有心血管疾病(CVD)。此外,衰老是轻度全身炎症的一个相关因素。我们的研究目的是分析在稳定期 COPD 患者中,年龄、全身和血管炎症与 CVD 合并症之间的关系。40 名 COPD 患者被分为 2 个年龄组(<65 岁和≥65 岁),我们从这些患者中收集了以下炎症生物标志物:C 反应蛋白、肿瘤坏死因子-α(TNF-α)、白细胞介素-6(IL-6)和内皮素-1(ET-1)。老年 COPD 患者每年发生急性加重的次数更多(2 次与 1 次,P=.06),CVD 患病率更高(3 次与 2 次,P=.04),运动耐量更差(6 分钟步行试验距离,343[283-403]与 434[384-484];P=.02),且存在轻度全身炎症(TNF-α,9.02[7.08-10.96]与 6.48[5.21-7.76];P=.03;ET-1,2.24[1.76-2.71]与 1.67[1.36-1.98]pg/mL;P=.04)。观察到年龄与 ET-1 之间存在弱相关性(r=0.32,P=.04)。轻度全身炎症,表现为 TNF-α 水平略有升高,以及内皮功能障碍,表现为 ET-1 升高,可能是衰老、COPD 和 CVD 合并症之间的联系。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4884/9388037/6d9861e9ac0f/medi-101-e30078-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4884/9388037/17c2181ed66d/medi-101-e30078-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4884/9388037/8fbe85cf34c6/medi-101-e30078-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4884/9388037/6d9861e9ac0f/medi-101-e30078-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4884/9388037/17c2181ed66d/medi-101-e30078-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4884/9388037/8fbe85cf34c6/medi-101-e30078-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4884/9388037/6d9861e9ac0f/medi-101-e30078-g003.jpg

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