Sickle cell trait as a limiting factor for high-level performance in a semi-marathon

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Deutscher übersetzter Titel:Sichelzellanlage als limitierender Faktor fuer Hoechstleistungen im Semimarathon
Autor:Préfaut, C.; Mercier, J.; Bile, A.; Bogui, P.; Lonsdorfer, J.; LeGallais, D.
Erschienen in:International journal of sports medicine
Veröffentlicht:15 (1994), 7, S. 399-402, Lit.
Format: Literatur (SPOLIT)
Publikationstyp: Zeitschriftenartikel
Medienart: Gedruckte Ressource Elektronische Ressource (online)
Sprache:Englisch
ISSN:0172-4622, 1439-3964
DOI:10.1055/s-2007-1021077
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Erfassungsnummer:PU199511103509
Quelle:BISp

Abstract des Autors

Of 1506 black males participating in the first Abidjan semi-marathon, 123 subjects with sickle cell trait (SCT) were detected, i.e., 8.7%. Twenty-nine of these subjects with hemoglobin S (HbS) were ranked among the first 332 participants to finish the race, a percentage of 8.2. These percentages did not significantly differ from the prevalence of SCT observed in the general Ivory Coast population (12.0%). Only one subject with SCT was found among the 22 internationally-ranked athletes. The concentration of HbS found in this athlete (37.7%), his mean globular volume (87 fl), and his hemoglobin concentration (13.8 g/100 ml) suggest the coexistence of alpha-thalassemia with SCT. These results indicate that the percentage of SCT individuals participating in a semi-marathon is equal to the prevalence of SCT found in the local population. Furthermore, the general ranking of SCT indviduals is comparable to that of non-SCT individuals. Nevertheless, at the level of internationally-ranked performance, no subject with SCT only, was ranked; the one ranked subject with SCT presented an associated alpha-thalassemia. We thus hypothesize that SCT may be a limiting factor for high level performance in a semi-marathon and alpha-thalassemia an enhancing factor for subjects with SCT to succeed in long distance races. Verf.-Referat