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Prospective evaluation of vascular changes in acute respiratory infections in children with cystic fibrosis

BACKGROUND/AIM: Acute exacerbations and chronic inflammation are risk factors for cardiovascular disease (CVD) in cystic fibrosis (CF) patients. The aim of this study was to investigate the effects of acute exacerbation therapy on arterial stiffness in children with CF. MATERIALS AND METHODS: Augmen...

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Autores principales: KARTAL ÖZTÜRK, Gökçen, EŞKİ, Aykut, ÇELEBİ ÇELİK, Figen, CONKAR, Seçil, GÜLEN, Figen, DEMİR, Esen, KESKİNOĞLU, Ahmet
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The Scientific and Technological Research Council of Turkey 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7379472/
https://www.ncbi.nlm.nih.gov/pubmed/32421279
http://dx.doi.org/10.3906/sag-2002-61
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author KARTAL ÖZTÜRK, Gökçen
EŞKİ, Aykut
ÇELEBİ ÇELİK, Figen
CONKAR, Seçil
GÜLEN, Figen
DEMİR, Esen
KESKİNOĞLU, Ahmet
author_facet KARTAL ÖZTÜRK, Gökçen
EŞKİ, Aykut
ÇELEBİ ÇELİK, Figen
CONKAR, Seçil
GÜLEN, Figen
DEMİR, Esen
KESKİNOĞLU, Ahmet
author_sort KARTAL ÖZTÜRK, Gökçen
collection PubMed
description BACKGROUND/AIM: Acute exacerbations and chronic inflammation are risk factors for cardiovascular disease (CVD) in cystic fibrosis (CF) patients. The aim of this study was to investigate the effects of acute exacerbation therapy on arterial stiffness in children with CF. MATERIALS AND METHODS: Augmentation index (Aix) and pulse wave velocity (PWV) were measured before and after treatment and 1 month after the end of treatment in patients with acute exacerbation. The relationship between hemodynamic measurements and c-reactive protein (CRP) and pulmonary function tests (PFTs) was investigated. RESULTS: Measurements before and after treatment were evaluated in 27 patients and were repeated in 21 patients who were clinically stable 1 month following acute exacerbation. There was a significant decrease in CRP and an increase in spirometry parameters after treatment. While no significant difference was found between PWV (P = 0.33), a significant difference for Aix before (41.95 ± 12.96%) and after (30.95 ± 11.47%) treatment and before treatment and stable clinical condition (34.19 ± 14.36%) was obtained (P =0.00, and P =0.01, respectively). No significant difference in heart rate and other hemodynamic measurements was found. Pretreatment Aix is associated with poor clinical condition (PFTs, BMI, and clinical score) and systemic inflammation (CRP) (P <0.05). CONCLUSION: The decrease of arterial stiffness (Aix) with acute exacerbation treatment in children with CF has been demonstrated. This result shows that systemic inflammation in CF may cause an increase in arterial stiffness and recurrent exacerbations may increase the risk of CVD.
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spelling pubmed-73794722020-07-27 Prospective evaluation of vascular changes in acute respiratory infections in children with cystic fibrosis KARTAL ÖZTÜRK, Gökçen EŞKİ, Aykut ÇELEBİ ÇELİK, Figen CONKAR, Seçil GÜLEN, Figen DEMİR, Esen KESKİNOĞLU, Ahmet Turk J Med Sci Article BACKGROUND/AIM: Acute exacerbations and chronic inflammation are risk factors for cardiovascular disease (CVD) in cystic fibrosis (CF) patients. The aim of this study was to investigate the effects of acute exacerbation therapy on arterial stiffness in children with CF. MATERIALS AND METHODS: Augmentation index (Aix) and pulse wave velocity (PWV) were measured before and after treatment and 1 month after the end of treatment in patients with acute exacerbation. The relationship between hemodynamic measurements and c-reactive protein (CRP) and pulmonary function tests (PFTs) was investigated. RESULTS: Measurements before and after treatment were evaluated in 27 patients and were repeated in 21 patients who were clinically stable 1 month following acute exacerbation. There was a significant decrease in CRP and an increase in spirometry parameters after treatment. While no significant difference was found between PWV (P = 0.33), a significant difference for Aix before (41.95 ± 12.96%) and after (30.95 ± 11.47%) treatment and before treatment and stable clinical condition (34.19 ± 14.36%) was obtained (P =0.00, and P =0.01, respectively). No significant difference in heart rate and other hemodynamic measurements was found. Pretreatment Aix is associated with poor clinical condition (PFTs, BMI, and clinical score) and systemic inflammation (CRP) (P <0.05). CONCLUSION: The decrease of arterial stiffness (Aix) with acute exacerbation treatment in children with CF has been demonstrated. This result shows that systemic inflammation in CF may cause an increase in arterial stiffness and recurrent exacerbations may increase the risk of CVD. The Scientific and Technological Research Council of Turkey 2020-06-23 /pmc/articles/PMC7379472/ /pubmed/32421279 http://dx.doi.org/10.3906/sag-2002-61 Text en Copyright © 2020 The Author(s) This article is distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use and redistribution provided that the original author and source are credited.
spellingShingle Article
KARTAL ÖZTÜRK, Gökçen
EŞKİ, Aykut
ÇELEBİ ÇELİK, Figen
CONKAR, Seçil
GÜLEN, Figen
DEMİR, Esen
KESKİNOĞLU, Ahmet
Prospective evaluation of vascular changes in acute respiratory infections in children with cystic fibrosis
title Prospective evaluation of vascular changes in acute respiratory infections in children with cystic fibrosis
title_full Prospective evaluation of vascular changes in acute respiratory infections in children with cystic fibrosis
title_fullStr Prospective evaluation of vascular changes in acute respiratory infections in children with cystic fibrosis
title_full_unstemmed Prospective evaluation of vascular changes in acute respiratory infections in children with cystic fibrosis
title_short Prospective evaluation of vascular changes in acute respiratory infections in children with cystic fibrosis
title_sort prospective evaluation of vascular changes in acute respiratory infections in children with cystic fibrosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7379472/
https://www.ncbi.nlm.nih.gov/pubmed/32421279
http://dx.doi.org/10.3906/sag-2002-61
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