Literature DB >> 16986131

Physical fitness indices and anthropometrics profiles in schoolchildren with sickle cell trait/disease.

Hisham Moheeb1, Yasser A Wali, Mahmoud S El-Sayed.   

Abstract

The current studies aimed at determining physical fitness indices and anthropometrics profiles of school children with sickle cell trait (SCT) and sickle cell disease (SCD). Male school children (150) comprising 3 Groups participated in the studies. Group 1 has 50 normal healthy controls, while Groups 2 and 3 each has 50 children who were suffering from SCT and SCD, respectively. Anthropometrics measurement and parameters of physical fitness were assessed in all subjects. All children were also subjected to a 5-min running exercise test on a flat motorized treadmill at speed corresponding to 5 km/hr. Throughout the test, heart rate was monitored and recorded during exercise and for 10-min during recovery. Blood lactate was measured before and 5 min following the completion of test. The mean values of lean body mass and height were lower in the SCD children (P < 0.05) compared with the healthy subjects and SCT individuals. Children with SCD exhibited a higher mean value (P < 0.05) for percent body fat and fat mass than the normal healthy subjects and SCT individuals. Although all groups tolerated well the treadmill exercise protocol, the SCD group exhibited higher (P < 0.05) mean values of heart rate during exercise than those observed in the SCT and normal control children. In addition, SCD children showed higher serum lactate values before and after treadmill exercise compared to the other groups. Children with SCD exhibit high level of adiposity; low level of fitness and their exercise performance appears to be physiologically more stressful as indicated by heart rate and blood lactate concentration responses. (c) 2006 Wiley-Liss, Inc.

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Year:  2007        PMID: 16986131     DOI: 10.1002/ajh.20755

Source DB:  PubMed          Journal:  Am J Hematol        ISSN: 0361-8609            Impact factor:   10.047


  11 in total

1.  Muscle Strength, Power, and Torque Deficits in Children With Type SS Sickle Cell Disease.

Authors:  Kelly A Dougherty; Chiara Bertolaso; Joan I Schall; Kim Smith-Whitley; Virginia A Stallings
Journal:  J Pediatr Hematol Oncol       Date:  2018-07       Impact factor: 1.289

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.  Attenuated maximal muscle strength and peak power in children with sickle cell disease.

Authors:  Kelly A Dougherty; Joan I Schall; Alisha J Rovner; Virginia A Stallings; Babette S Zemel
Journal:  J Pediatr Hematol Oncol       Date:  2011-03       Impact factor: 1.289

4.  Fracture prevalence and relationship to endocrinopathy in iron overloaded patients with sickle cell disease and thalassemia.

Authors:  Ellen B Fung; Paul R Harmatz; Meredith Milet; Thomas D Coates; Alexis A Thompson; Mark Ranalli; Robert Mignaca; Charles Scher; Patricia Giardina; Shanda Robertson; Lynne Neumayr; Elliott P Vichinsky
Journal:  Bone       Date:  2008-03-15       Impact factor: 4.398

Review 5.  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

6.  Impact of a submaximal mono-articular exercise on the skeletal muscle function of patients with sickle cell disease.

Authors:  Etienne Gouraud; Philippe Connes; Alexandra Gauthier-Vasserot; Camille Faes; Salima Merazga; Solène Poutrel; Céline Renoux; Camille Boisson; Philippe Joly; Yves Bertrand; Arnaud Hot; Giovanna Cannas; Christophe Hautier
Journal:  Eur J Appl Physiol       Date:  2021-05-22       Impact factor: 3.078

7.  Exercise Testing In Patients with Sickle Cell Disease: Safety, Feasibility and Potential Prognostic Implication.

Authors:  Christiano Gonçalves de Araújo; Maria Betânia Solis Resende; Julia Teixeira Tupinambás; Rebeca Coeli Teodoro Maciel Dias; Flávio Coelho Barros; Maria Carmen Melo Vasconcelos; José Nelio Januário; Antonio Luiz Pinho Ribeiro; Maria Carmo P Nunes
Journal:  Arq Bras Cardiol       Date:  2022-03       Impact factor: 2.000

8.  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

9.  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

10.  Dietary intakes and nutritional status of children with sickle cell disease at the Princess Marie Louise Hospital, Accra - a survey.

Authors:  Isaac Boadu; Agartha Ohemeng; Lorna Awo Renner
Journal:  BMC Nutr       Date:  2018-08-23
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