Literature DB >> 22414551

Delayed beneficial effect of acute exercise on red blood cell aggregate strength in patients with sickle cell anemia.

Xavier Waltz1, Mona Hedreville, Stéphane Sinnapah, Yann Lamarre, Valérie Soter, Nathalie Lemonne, Maryse Etienne-Julan, Eric Beltan, Tawfik Chalabi, Roger Chout, Olivier Hue, Danièle Mougenel, Marie-Dominique Hardy-Dessources, Philippe Connes.   

Abstract

Because of the metabolic changes induced by a physical activity, the hemorheological properties of patients with sickle cell anemia could be further impaired and increase the risks for vaso-occlusive complications. However, few studies suggest that moderate physical activity could be beneficial rather than harmful in patients with sickle cell anemia (SCA). However, the definition of what can be considered as a moderate physical activity in SCA patients is imprecise. The present study tested the effects of a short incremental cycling exercise test conducted until the first ventilatory threshold on different biomarkers. Hematological and hemorheological parameters were compared between 8 patients with SCA and 13 healthy subjects (CONT) before, immediately after the end of the exercise and at 12, 36 and 60 hours after the exercise. We observed no significant hematological or hemorheological alteration induced by the exercise in the two groups. However, the exercise resulted in a delayed improvement of the red blood cell disaggregation threshold at 36 and 60 hrs after exercise in the SCA group which was paralleled to the decrease in the platelet count in this group. The present study suggests that such an exercise might be beneficial for microcirculatory blood flow.

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Year:  2012        PMID: 22414551     DOI: 10.3233/CH-2012-1540

Source DB:  PubMed          Journal:  Clin Hemorheol Microcirc        ISSN: 1386-0291            Impact factor:   2.375


  14 in total

1.  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

2.  Exercise Testing of Adolescents and Young Adults With Sickle Cell Disease: Perceptual Responses and the Gas Exchange Threshold.

Authors:  Suzanne Ameringer; R K Elswick; India Sisler; Wally Smith; Thokozeni Lipato; Edmund O Acevedo
Journal:  J Pediatr Oncol Nurs       Date:  2019-04-26       Impact factor: 1.636

3.  Severe proliferative retinopathy is associated with blood hyperviscosity in sickle cell hemoglobin-C disease but not in sickle cell anemia.

Authors:  Clément Lemaire; Yann Lamarre; Nathalie Lemonne; Xavier Waltz; Sadri Chahed; Florence Cabot; Ioana Botez; Benoit Tressieres; Marie-Laure Lalanne-Mistrih; Maryse Etienne-Julan; Philippe Connes
Journal:  Clin Hemorheol Microcirc       Date:  2013-01-01       Impact factor: 2.375

Review 4.  Role of Exercise-Induced Oxidative Stress in Sickle Cell Trait and Disease.

Authors:  Erica N Chirico; Camille Faës; Philippe Connes; Emmanuelle Canet-Soulas; Cyril Martin; Vincent Pialoux
Journal:  Sports Med       Date:  2016-05       Impact factor: 11.136

5.  The Role of Inspiratory Muscle Training in Sickle Cell Anemia Related Pulmonary Damage due to Recurrent Acute Chest Syndrome Attacks.

Authors:  Burcu Camcıoğlu; Meral Boşnak-Güçlü; Müşerrefe Nur Karadallı; Şahika Zeynep Akı; Gülsan Türköz-Sucak
Journal:  Case Rep Hematol       Date:  2015-04-28

6.  Comment on: Relationship between lipid and hematological profiles and adiposity in obese adolescents.

Authors:  Ricardo Luís Fernandes Guerra
Journal:  Rev Bras Hematol Hemoter       Date:  2013

7.  Blood thixotropy in patients with sickle cell anaemia: role of haematocrit and red blood cell rheological properties.

Authors:  Jens Vent-Schmidt; Xavier Waltz; Marc Romana; Marie-Dominique Hardy-Dessources; Nathalie Lemonne; Marie Billaud; Maryse Etienne-Julan; Philippe Connes
Journal:  PLoS One       Date:  2014-12-11       Impact factor: 3.240

8.  Normal muscle oxygen consumption and fatigability in sickle cell patients despite reduced microvascular oxygenation and hemorheological abnormalities.

Authors:  Xavier Waltz; Aurélien Pichon; Nathalie Lemonne; Danièle Mougenel; Marie-Laure Lalanne-Mistrih; Yann Lamarre; Vanessa Tarer; Benoit Tressières; Maryse Etienne-Julan; Marie-Dominique Hardy-Dessources; Olivier Hue; Philippe Connes
Journal:  PLoS One       Date:  2012-12-20       Impact factor: 3.240

9.  Hematological and hemorheological determinants of the six-minute walk test performance in children with sickle cell anemia.

Authors:  Xavier Waltz; Marc Romana; Marie-Dominique Hardy-Dessources; Yann Lamarre; Lydia Divialle-Doumdo; Marie Petras; Vanessa Tarer; Régine Hierso; Kizzy-Clara Baltyde; Benoît Tressières; Marie-Laure Lalanne-Mistrih; Fréderic Maillard; Olivier Hue; Maryse Etienne-Julan; Philippe Connes
Journal:  PLoS One       Date:  2013-10-17       Impact factor: 3.240

10.  Acute moderate exercise does not further alter the autonomic nervous system activity in patients with sickle cell anemia.

Authors:  Mona Hedreville; Keyne Charlot; Xavier Waltz; Stéphane Sinnapah; Nathalie Lemonne; Maryse Etienne-Julan; Valérie Soter; Olivier Hue; Marie-Dominique Hardy-Dessources; Jean-Claude Barthélémy; Philippe Connes
Journal:  PLoS One       Date:  2014-04-16       Impact factor: 3.240

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