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皮肤弹性丧失与肺气肿、吸烟者的炎症生物标志物和基质金属蛋白酶活性有关。

Loss of skin elasticity is associated with pulmonary emphysema, biomarkers of inflammation, and matrix metalloproteinase activity in smokers.

机构信息

Division of Pulmonary Allergy and Critical Care Medicine Department of Medicine, University of Pittsburgh School of Medicine and University of Pittsburgh Medical Center, Kaufmann Building, Suite 1211, 3471 Fifth Ave, Pittsburgh, PA, 15213, USA.

Department of Radiology, University of Pittsburgh, Pittsburgh, PA, USA.

出版信息

Respir Res. 2019 Jun 24;20(1):128. doi: 10.1186/s12931-019-1098-7.

Abstract

BACKGROUND

Elastin breakdown and the resultant loss of lung elastic recoil is a hallmark of pulmonary emphysema in susceptible individuals as a consequence of tobacco smoke exposure. Systemic alterations to the synthesis and degradation of elastin may be important to our understanding of disease phenotypes in chronic obstructive pulmonary disease. We investigated the association of skin elasticity with pulmonary emphysema, obstructive lung disease, and blood biomarkers of inflammation and tissue protease activity in tobacco-exposed individuals.

METHODS

Two hundred and thirty-six Caucasian individuals were recruited into a sub-study of the University of Pittsburgh Specialized Center for Clinically Orientated Research in chronic obstructive pulmonary disease, a prospective cohort study of current and former smokers. The skin viscoelastic modulus (VE), a determinant of skin elasticity, was recorded from the volar forearm and facial wrinkling severity was determined using the Daniell scoring system.

RESULTS

In a multiple regression analysis, reduced VE was significantly associated with cross-sectional measurement of airflow obstruction (FEV1/FVC) and emphysema quantified from computed tomography (CT) images, β = 0.26, p = 0.001 and β = 0.24, p = 0.001 respectively. In emphysema-susceptible individuals, elasticity-determined skin age was increased (median 4.6 years) compared to the chronological age of subjects without emphysema. Plasma biomarkers of inflammation (TNFR1, TNFR2, CRP, PTX3, and SAA) and matrix metalloproteinase activity (MMP1, TIMP1, TIMP2, and TIMP4) were inversely associated with skin elasticity.

CONCLUSIONS

We report that an objective non-invasive determinant of skin elasticity is independently associated with measures of lung function, pulmonary emphysema, and biomarkers of inflammation and tissue proteolysis in tobacco-exposed individuals. Loss of skin elasticity is a novel observation that may link the common pathological processes that drive tissue elastolysis in the extracellular matrix of the skin and lung in emphysema-susceptible individuals.

摘要

背景

在易患个体中,弹性蛋白的崩解和由此导致的肺弹性回缩丧失是吸烟引起的肺气肿的标志。弹性蛋白的合成和降解的系统改变对于我们理解慢性阻塞性肺疾病的疾病表型可能很重要。我们研究了皮肤弹性与吸烟人群中的肺气肿、阻塞性肺疾病以及炎症和组织蛋白酶活性的血液生物标志物之间的关系。

方法

我们从匹兹堡大学慢性阻塞性肺疾病专门临床导向研究中心的一个前瞻性队列研究中的当前和以前的吸烟者中招募了 236 名白种人个体作为子研究的一部分。记录了掌侧前臂的皮肤粘弹性模量(VE),这是皮肤弹性的一个决定因素,并使用 Daniell 评分系统确定面部皱纹的严重程度。

结果

在多元回归分析中,VE 的降低与 CT 图像量化的气流阻塞(FEV1/FVC)和肺气肿的横断面测量显著相关,β=0.26,p=0.001 和 β=0.24,p=0.001。在肺气肿易感个体中,由弹性决定的皮肤年龄比没有肺气肿的受试者的实际年龄大(中位数为 4.6 岁)。炎症的血浆生物标志物(TNFR1、TNFR2、CRP、PTX3 和 SAA)和基质金属蛋白酶活性(MMP1、TIMP1、TIMP2 和 TIMP4)与皮肤弹性呈负相关。

结论

我们报告说,皮肤弹性的一个客观的非侵入性决定因素与吸烟人群中的肺功能、肺气肿以及炎症和组织蛋白酶活性的生物标志物独立相关。皮肤弹性的丧失是一个新的观察结果,可能将导致易患个体皮肤和肺细胞外基质中组织弹性蛋白降解的常见病理过程联系起来。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f913/6591816/840f5cb7c6c3/12931_2019_1098_Fig1_HTML.jpg

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