Assessment of endothelial dysfunction in idiopathic pulmonary fibrosis
Background: Idiopathic pulmonary fibrosis (IPF) is defined as a specific form of chronic fibrosing interstitial pneumonia limited to the lung, with the histopathology of UIP on surgical lung biopsy. Recent epidemiological evidence indicates that patients with IPF have an increased risk of cardiovasc...
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Wolters Kluwer Medknow Publications
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doaj-1513c0408f854509a8ffb7f62c7984952020-11-25T00:36:33ZengWolters Kluwer Medknow PublicationsEgyptian Journal of Chest Disease and Tuberculosis0422-76382013-10-0162458959210.1016/j.ejcdt.2013.08.016Assessment of endothelial dysfunction in idiopathic pulmonary fibrosisM. Elshazly0H. Hosny1H. Abdel-Hafiz2A. Zakaria3K. Elkaffas4N. Okasha5Department of Chest Diseases, Faculty of Medicine, Cairo University, EgyptDepartment of Chest Diseases, Faculty of Medicine, Cairo University, EgyptDepartment of Chest Diseases, Faculty of Medicine, Cairo University, EgyptDepartment of Internal Medicine, Faculty of Medicine, Cairo University, EgyptDepartment of Radiology, Faculty of Medicine, Cairo University, EgyptDepartment of Chest Diseases, Helwan University, EgyptBackground: Idiopathic pulmonary fibrosis (IPF) is defined as a specific form of chronic fibrosing interstitial pneumonia limited to the lung, with the histopathology of UIP on surgical lung biopsy. Recent epidemiological evidence indicates that patients with IPF have an increased risk of cardiovascular disease. The vascular endothelium acts to maintain vascular homeostasis through multiple mechanisms, and alteration in its function precedes the development, progression and clinical expression of atherosclerosis. Aim of the work: To assess the prevalence of endothelial dysfunction in patients with idiopathic pulmonary fibrosis and its correlation with pulmonary hypertension. Subjects and methods: The study included two groups. The patient group included 30 IPF patients subdivided into 2 subgroups: Subgroup I (15 IPF cases) with pulmonary hypertension; Subgroup II (15 IPF cases) without pulmonary hypertension. The control group included 10 normal healthy individuals. Patients were subjected to written informed consent, detailed history taking, thorough clinical examination, collagen profile, arterial blood gases (PaO2, SaO2), Pulmonary function tests (spirometry), 6 min walk test, HRCT chest scan, echocardiography, and brachial artery duplex to assess endothelial dysfunction. Results: Subgroup (I) and Subgroup (II) showed a statistically highly significant difference in brachial artery flow mediated dilatation (BADFMD) and endothelium – reactive dilatation (ERD) which indicate endothelial dysfunction compared to the control group. Conclusion: This work concluded that BADFMD and ERD more affected in IPF patients regardless of presence or absence of PH than normal population. So, endothelial dysfunction is a possible link between IPF and cardiovascular disease.http://www.sciencedirect.com/science/article/pii/S0422763813001921Idiopathic pulmonary fibrosis (IPF)Brachial artery flow mediated dilatationEndothelial dysfunction |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
M. Elshazly H. Hosny H. Abdel-Hafiz A. Zakaria K. Elkaffas N. Okasha |
spellingShingle |
M. Elshazly H. Hosny H. Abdel-Hafiz A. Zakaria K. Elkaffas N. Okasha Assessment of endothelial dysfunction in idiopathic pulmonary fibrosis Egyptian Journal of Chest Disease and Tuberculosis Idiopathic pulmonary fibrosis (IPF) Brachial artery flow mediated dilatation Endothelial dysfunction |
author_facet |
M. Elshazly H. Hosny H. Abdel-Hafiz A. Zakaria K. Elkaffas N. Okasha |
author_sort |
M. Elshazly |
title |
Assessment of endothelial dysfunction in idiopathic pulmonary fibrosis |
title_short |
Assessment of endothelial dysfunction in idiopathic pulmonary fibrosis |
title_full |
Assessment of endothelial dysfunction in idiopathic pulmonary fibrosis |
title_fullStr |
Assessment of endothelial dysfunction in idiopathic pulmonary fibrosis |
title_full_unstemmed |
Assessment of endothelial dysfunction in idiopathic pulmonary fibrosis |
title_sort |
assessment of endothelial dysfunction in idiopathic pulmonary fibrosis |
publisher |
Wolters Kluwer Medknow Publications |
series |
Egyptian Journal of Chest Disease and Tuberculosis |
issn |
0422-7638 |
publishDate |
2013-10-01 |
description |
Background: Idiopathic pulmonary fibrosis (IPF) is defined as a specific form of chronic fibrosing interstitial pneumonia limited to the lung, with the histopathology of UIP on surgical lung biopsy. Recent epidemiological evidence indicates that patients with IPF have an increased risk of cardiovascular disease. The vascular endothelium acts to maintain vascular homeostasis through multiple mechanisms, and alteration in its function precedes the development, progression and clinical expression of atherosclerosis.
Aim of the work: To assess the prevalence of endothelial dysfunction in patients with idiopathic pulmonary fibrosis and its correlation with pulmonary hypertension.
Subjects and methods: The study included two groups. The patient group included 30 IPF patients subdivided into 2 subgroups: Subgroup I (15 IPF cases) with pulmonary hypertension; Subgroup II (15 IPF cases) without pulmonary hypertension. The control group included 10 normal healthy individuals. Patients were subjected to written informed consent, detailed history taking, thorough clinical examination, collagen profile, arterial blood gases (PaO2, SaO2), Pulmonary function tests (spirometry), 6 min walk test, HRCT chest scan, echocardiography, and brachial artery duplex to assess endothelial dysfunction.
Results: Subgroup (I) and Subgroup (II) showed a statistically highly significant difference in brachial artery flow mediated dilatation (BADFMD) and endothelium – reactive dilatation (ERD) which indicate endothelial dysfunction compared to the control group.
Conclusion: This work concluded that BADFMD and ERD more affected in IPF patients regardless of presence or absence of PH than normal population. So, endothelial dysfunction is a possible link between IPF and cardiovascular disease. |
topic |
Idiopathic pulmonary fibrosis (IPF) Brachial artery flow mediated dilatation Endothelial dysfunction |
url |
http://www.sciencedirect.com/science/article/pii/S0422763813001921 |
work_keys_str_mv |
AT melshazly assessmentofendothelialdysfunctioninidiopathicpulmonaryfibrosis AT hhosny assessmentofendothelialdysfunctioninidiopathicpulmonaryfibrosis AT habdelhafiz assessmentofendothelialdysfunctioninidiopathicpulmonaryfibrosis AT azakaria assessmentofendothelialdysfunctioninidiopathicpulmonaryfibrosis AT kelkaffas assessmentofendothelialdysfunctioninidiopathicpulmonaryfibrosis AT nokasha assessmentofendothelialdysfunctioninidiopathicpulmonaryfibrosis |
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