Negative health implications of sickle cell trait in high income countries: from the football field to the laboratory

被引:37
作者
Key, Nigel S. [1 ]
Connes, Philippe [2 ,3 ]
Derebail, Vimal K. [4 ]
机构
[1] Univ N Carolina, Div Hematol Oncol, Dept Med, Chapel Hill, NC 27599 USA
[2] Univ Claude Bernard Lyon 1, Sect Vasc Biol & Red Blood Cell, Lab CRIS EA647, Lyon, France
[3] Inst Univ France, Paris, France
[4] Univ N Carolina, Div Nephrol, Dept Med, Chapel Hill, NC 27599 USA
基金
美国国家卫生研究院;
关键词
sickle trait; exertional rhabdomyolysis; chronic renal disease; venous thromboembolism; RENAL MEDULLARY CARCINOMA; POLYCYSTIC KIDNEY-DISEASE; VENOUS THROMBOEMBOLISM; ALPHA-THALASSEMIA; SUDDEN-DEATH; OXIDATIVE STRESS; PLASMODIUM-FALCIPARUM; PULMONARY-EMBOLISM; ADHESION MOLECULES; CHRONIC HYPOXIA;
D O I
10.1111/bjh.13363
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Worldwide, sickle cell trait is a highly prevalent gene carrier state. While generally a benign condition with a normal life expectancy, it is becoming increasingly clear that the sickle trait is associated with certain adverse outcomes. This article will focus on three of these outcomes, namely exertional rhabdomyolysis and sudden death, chronic renal dysfunction, and venous thromboembolism. In each case, the epidemiological evidence for the association is reviewed, together with the existing data on potential underlying mechanisms. Because newborn screening programmes for sickle cell anaemia also identify those with sickle cell trait, it is imperative that further studies determine what, if any, preventive measures can be taken to reduce the burden of these uncommon but potentially morbid complications in affected individuals.
引用
收藏
页码:5 / 14
页数:10
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