Literature DB >> 33815924

Exercise-induced haemoglobin oxygen desaturation in patients with SCD.

Charles Antwi-Boasiako1, Chamila P Asare2, Jane S Afriyie-Mensah3, Charles Hayfron-Benjamin1,4, Isaac Nuako5, Robert Aryee1, Gifty Boatemaa Dankwah1, Michael M Asare6, Kevin Adutwum-Ofosu7.   

Abstract

BACKGROUND: Patients with sickle cell disease (SCD) may experience severe clinical complications when there is low tissue oxygenation due to the increased risk of the polymerization of haemoglobin S in deoxygenated environment. The predictors of oxygen desaturation after exercise is not clear in patients with SCD. The current study compared lung function and six-minute walk test (6MWT) between SCD patients with oxygen desaturation after exercise and those without oxygen desaturation.
METHODOLOGY: A cross-sectional study was conducted among adults with SCD (with HbSS and HbSC genotypes) at a large tertiary hospital in Accra, Ghana. Lung function and exercise tolerance (using the 6MWT) were performed for all the study subjects (n=119). Venous blood was collected from all the study subjects for determination of some haemolytic markers. Oxygen saturation was assessed before and after the 6MWT for all the study subjects, and individuals who had oxygen desaturation of ≥3% after the 6MWT were considered as having exercise-induced haemoglobin oxygen desaturation (EIHOD). The lung function and 6MWT were compared between these two groups. Predictors of EIHOD were determined in both HbSC and HbSS patients.
RESULTS: The prevalence of EIHOD in the HbSS and HbSC adults were 41% and 36.1% respectively. Haemoglobin, aspartate amino transaminase, indirect bilirubin, lactate dehydrogenase and six-minute walk distance did not differ in both HbSS and HbSC patients. Decreasing haemoglobin is a predictor of EIHOD in HbSC adults but not HbSS patients. Lung function abnormalities did not predict EIHOD in both HbSS and HbSC patients.
CONCLUSION: The study demonstrates that SCD patients with EIHOD have similar degree of haemolysis and lung function when compared to those without EIHOD. AJCD
Copyright © 2021.

Entities:  

Keywords:  Sickle cell disease; lung function; oxygen desaturation; six-minute walk test

Year:  2021        PMID: 33815924      PMCID: PMC8012294     

Source DB:  PubMed          Journal:  Am J Cardiovasc Dis        ISSN: 2160-200X


  23 in total

1.  Interpretative strategies for lung function tests.

Authors:  R Pellegrino; G Viegi; V Brusasco; R O Crapo; F Burgos; R Casaburi; A Coates; C P M van der Grinten; P Gustafsson; J Hankinson; R Jensen; D C Johnson; N MacIntyre; R McKay; M R Miller; D Navajas; O F Pedersen; J Wanger
Journal:  Eur Respir J       Date:  2005-11       Impact factor: 16.671

2.  Hydroxyurea treatment does not increase blood viscosity and improves red blood cell rheology in sickle cell anemia.

Authors:  Nathalie Lemonne; Keyne Charlot; Xavier Waltz; Samir K Ballas; Yann Lamarre; Ketty Lee; Régine Hierso; Catherine Connes; Maryse Etienne-Julan; Marc Romana; Philippe Connes
Journal:  Haematologica       Date:  2015-07-02       Impact factor: 9.941

3.  Hematologic and hemorheological determinants of resting and exercise-induced hemoglobin oxygen desaturation in children with sickle cell disease.

Authors:  Xavier Waltz; Marc Romana; Marie-Laure Lalanne-Mistrih; Roberto F Machado; Yann Lamarre; Vanessa Tarer; Marie-Dominique Hardy-Dessources; Benoît Tressières; Lydia Divialle-Doumdo; Marie Petras; Frederic Maillard; Maryse Etienne-Julan; Philippe Connes
Journal:  Haematologica       Date:  2013-03-28       Impact factor: 9.941

Review 4.  Sickle cell disease.

Authors:  Gregory J Kato; Frédéric B Piel; Clarice D Reid; Marilyn H Gaston; Kwaku Ohene-Frempong; Lakshmanan Krishnamurti; Wally R Smith; Julie A Panepinto; David J Weatherall; Fernando F Costa; Elliott P Vichinsky
Journal:  Nat Rev Dis Primers       Date:  2018-03-15       Impact factor: 52.329

5.  Clinical correlates of steady-state oxyhaemoglobin desaturation in children who have sickle cell disease.

Authors:  Charles T Quinn; Naveed Ahmad
Journal:  Br J Haematol       Date:  2005-10       Impact factor: 6.998

6.  Elevated tricuspid regurgitant jet velocity in children and adolescents with sickle cell disease: association with hemolysis and hemoglobin oxygen desaturation.

Authors:  Caterina P Minniti; Craig Sable; Andrew Campbell; Sohail Rana; Gregory Ensing; Niti Dham; Onyinye Onyekwere; Mehdi Nouraie; Gregory J Kato; Mark T Gladwin; Oswaldo L Castro; Victor R Gordeuk
Journal:  Haematologica       Date:  2009-02-11       Impact factor: 9.941

7.  Hypoxaemia in sickle cell disease: biomarker modulation and relevance to pathophysiology.

Authors:  B N Yamaja Setty; Marie J Stuart; Carlton Dampier; Darcy Brodecki; Julian L Allen
Journal:  Lancet       Date:  2003-11-01       Impact factor: 79.321

8.  Hydroxyurea therapy modulates sickle cell anemia red blood cell physiology: Impact on RBC deformability, oxidative stress, nitrite levels and nitric oxide synthase signalling pathway.

Authors:  Elie Nader; Marijke Grau; Romain Fort; Bianca Collins; Giovanna Cannas; Alexandra Gauthier; Katja Walpurgis; Cyril Martin; Wilhelm Bloch; Solène Poutrel; Arnaud Hot; Céline Renoux; Mario Thevis; Philippe Joly; Marc Romana; Nicolas Guillot; Philippe Connes
Journal:  Nitric Oxide       Date:  2018-10-19       Impact factor: 4.427

9.  Sickle cell disease: Classification of clinical complications and approaches to preventive and therapeutic management.

Authors:  Samir K Ballas
Journal:  Clin Hemorheol Microcirc       Date:  2018       Impact factor: 2.375

Review 10.  Sickle cell anemia, the first molecular disease: overview of molecular etiology, pathophysiology, and therapeutic approaches.

Authors:  Martin H Steinberg
Journal:  ScientificWorldJournal       Date:  2008-12-25
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