Literature DB >> 31107040

Macro- and microvascular functions in cystic fibrosis adults without cardiovascular risk factors: A case-control study.

Enrico Vizzardi1, Edoardo Sciatti, Ivano Bonadei, Dario Salvatore Cani, Elisa Menotti, Francesco Prati, Lucia Dallapellegrina, Marco Metra, Marialma Berlendis, Piercarlo Poli, Rita Padoan.   

Abstract

Increasing survival from cystic fibrosis show untypical systems involvement, such as cardiocirculatory. In particular, the presence of CFTR in smooth muscle and endothelial cells, systemic inflammation and oxidative stress could explain vascular alterations in these patients. We aimed at noninvasely evaluating macro- and microvascular dysfunction in cystic fibrosis adults without cardiovascular risk factors. Twenty-twoadults affected by cystic fibrosis and 24 healthy volunteers matched for age and sex were enrolled. None had known cardiovascular risk factors. All people underwent blood pressure measurement, microvascular function assessment by EndoPAT-2000 device (calculating RH-PAT index) and macrovascular evaluation by pulse wave velocity (PWV). RH-PAT index was significantly lower in patients than in controls (1.74±0.59 vs 2.33±0.34; p<0.001). Thirteen patients of 22 had a value inferior to the threshold of 1.67 (59.1%), while no controls had (p<0.001). Carotid-femoral PWV did not differ between the two groups (5.2±1.5 m/s vs 5.4±1.1; p=0.9), while brachial-ankle one did (11.0±2.2 m/s vs 10.1±0.8 m/s; p=0.04).Adults patients affected by cystic fibrosis show peripheral endothelial dysfunction, which is the first alteration in atherosclerotic phenomenon. Moreover, arterial stiffness measured by PWV unclearly seems to differ respect of healthy people, perhaps because PWV alterations are typical of above 50 years old people. It is unclear what prognostic role of future developing of atherosclerotic disease these findings could be, but it seems evident that cystic fibrosis directly affects cardiovascular system itself.

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Year:  2019        PMID: 31107040     DOI: 10.4081/monaldi.2019.1035

Source DB:  PubMed          Journal:  Monaldi Arch Chest Dis        ISSN: 1122-0643


  3 in total

1.  Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) in Human Lung Microvascular Endothelial Cells Controls Oxidative Stress, Reactive Oxygen-Mediated Cell Signaling and Inflammatory Responses.

Authors:  Maha Khalaf; Toby Scott-Ward; Adam Causer; Zoe Saynor; Anthony Shepherd; Dariusz Górecki; Anthony Lewis; David Laight; Janis Shute
Journal:  Front Physiol       Date:  2020-07-29       Impact factor: 4.566

2.  Activated L-Arginine/Nitric Oxide Pathway in Pediatric Cystic Fibrosis and Its Association with Pancreatic Insufficiency, Liver Involvement and Nourishment: An Overview and New Results.

Authors:  Folke Brinkmann; Beatrice Hanusch; Manfred Ballmann; Sebene Mayorandan; Alexander Bollenbach; Kristine Chobanyan-Jürgens; Kathrin Jansen; Anjona Schmidt-Choudhury; Nico Derichs; Dimitrios Tsikas; Thomas Lücke
Journal:  J Clin Med       Date:  2020-06-26       Impact factor: 4.241

3.  Upregulation of CFTR Protects against Palmitate-Induced Endothelial Dysfunction by Enhancing Autophagic Flux.

Authors:  Hongqi Chen; Wenliang Chen; Yinlian Yao; Naobei Ye; Ning Hou; Jiandong Luo
Journal:  Oxid Med Cell Longev       Date:  2020-10-17       Impact factor: 6.543

  3 in total

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