Literature DB >> 28340403

Micro- and macrovascular function in children with sickle cell anaemia and sickle cell haemoglobin C disease.

Berenike Möckesch1, Keyne Charlot1, Stéphane Jumet2, Marc Romana3, Lydia Divialle-Doumdo4, Marie-Dominique Hardy-Dessources3, Marie Petras4, Benoît Tressieres5, Vanessa Tarer4, Olivier Hue2, Maryse Etienne-Julan4, Philippe Connes6, Sophie Antoine-Jonville7.   

Abstract

It is unclear whether vascular function is affected similarly in children with sickle cell anaemia (SS) and children with sickle haemoglobin C (SC) disease. Therefore, we compared micro and macrovascular functions in healthy (AA) children, children with SS and SC disease, and assessed their association with physical activity. Participants (24 SS, 22 SC and 16 AA), were compared in terms of 1) thermal hyperaemic response (finger pad warming to 42°C) measured by Laser Doppler techniques, 2) arterial stiffness determined by pulse wave velocity, 3) daily energy expenditure related to moderate and intense physical activities estimated by questionnaire and 4) fitness level, evaluated by the six-minute walk test. Response to heating differed between SS, SC and controls. Peripheral microvascular reactivity was lower and pulse wave velocity higher in SS compared to AA. SC had blunted microvascular reactivity in response to heating compared to AA but pulse wave velocity was not different within the two groups. Physical activity and fitness levels were markedly lower in sickle cell patients compared to healthy controls but no association was observed with vascular function. Microvasodilatory reserve is decreased in both SS and SC patients but only SS patients were also characterised by impaired macrovascular function.
Copyright © 2017. Published by Elsevier Inc.

Entities:  

Keywords:  Physical activity; Sickle cell anaemia; Sickle cell haemoglobin C disease; Vascular function

Mesh:

Year:  2017        PMID: 28340403     DOI: 10.1016/j.bcmd.2017.02.001

Source DB:  PubMed          Journal:  Blood Cells Mol Dis        ISSN: 1079-9796            Impact factor:   3.039


  3 in total

1.  Unusually High Prevalence of Stroke and Cerebral Vasculopathy in Hemoglobin SC Disease: A Retrospective Single Institution Study.

Authors:  Bindu Kanathezhath Sathi; Yilin Yoshida; Michael Raymond Weaver; Lila S Nolan; Barbara Gruner; Vinod Balasa; Talissa Altes; Carlos Leiva-Salinas
Journal:  Acta Haematol       Date:  2021-11-08       Impact factor: 3.068

2.  Association Between Nitric Oxide, Oxidative Stress, Eryptosis, Red Blood Cell Microparticles, and Vascular Function in Sickle Cell Anemia.

Authors:  Elie Nader; Marc Romana; Nicolas Guillot; Romain Fort; Emeric Stauffer; Nathalie Lemonne; Yohann Garnier; Sarah Chambers Skinner; Maryse Etienne-Julan; Mélanie Robert; Alexandra Gauthier; Giovanna Cannas; Sophie Antoine-Jonville; Benoît Tressières; Marie-Dominique Hardy-Dessources; Yves Bertrand; Cyril Martin; Céline Renoux; Philippe Joly; Marijke Grau; Philippe Connes
Journal:  Front Immunol       Date:  2020-11-04       Impact factor: 7.561

Review 3.  The Red Blood Cell-Inflammation Vicious Circle in Sickle Cell Disease.

Authors:  Elie Nader; Marc Romana; Philippe Connes
Journal:  Front Immunol       Date:  2020-03-13       Impact factor: 7.561

  3 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.