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IL3 variant on chromosomal region 5q31–33 and protection from recurrent malaria attacks

机译:染色体区域5q31–33上的IL3变异体和对复发性疟疾的防护

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摘要

Using segregation analyses, control of malaria parasites has previously been linked to a major gene within the chromosomal region 5q31–33, but also to complex genetic factors in which effects are under substantial age-dependent influence. However, the responsible gene variants have not yet been identified for this chromosomal region. In order to perform association analyses of 5q31–33 locus candidate single nucleotide polymorphisms (SNPs), 1015 children were recruited at the age of 3 months and followed monthly until the age of 2 years in an area holoendemic for Plasmodium falciparum malaria in Ghana. Quantitative (incidence rates of malaria episodes) and qualitative phenotypes (i.e. ‘more than one malaria episode’ or ‘not more than one malaria episode’) were used in population- and family-based analyses. The strongest signal was observed for the interleukin 3 gene (IL3) SNP rs40401 (P = 3.4 × 10−7, Pc= 1.4 × 10−4). The IL3 genotypes rs40401CT and rs40401TT were found to exert a protective effect of 25% [incidence rate ratio (IRR) 0.75, P = 4.1 × 10−5] and 33% (IRR 0.67, P = 3.2 × 10−8), respectively, against malaria attacks. The association was confirmed in transmission disequilibrium tests (TDT, qTDT). The results could argue for a role of IL3 in the pathophysiology of falciparum malaria.
机译:使用隔离分析,疟疾寄生虫的控制以前与5q31-33染色体区域内的一个主要基因有关,但也与影响年龄受到实质性影响的复杂遗传因素有关。但是,尚未鉴定出该染色体区域的负责基因变体。为了对5q31–33位点候选单核苷酸多态性(SNPs)进行关联分析,在加纳的恶性疟原虫疟疾全流行地区,招募了1015名3个月大的儿童,每个月随访至2岁。在基于人口和家庭的分析中使用了定量(疟疾发作的发生率)和定性表型(即“一个以上疟疾发作”或“一个以下疟疾发作”)。对于白介素3基因(IL3)SNP rs40401观察到最强的信号(P = 3.4×10 -7 ,P c = 1.4×10 -4 < / sup>)。发现IL3基因型rs40401 CT 和rs40401 TT 具有25%的保护作用[发生率比(IRR)0.75,P = 4.1×10 - 5 ]和33%(IRR 0.67,P = 3.2×10 −8 ),以抗击疟疾。该关联在传输不平衡测试(TDT,qTDT)中得到证实。结果可能证明IL3在恶性疟疾的病理生理中的作用。

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  • 来源
    《Human Molecular Genetics》 |2011年第6期|p.1173-1181|共9页
  • 作者单位

    Molecular Medicine and;

    Infectious Disease Epidemiology, Bernhard Nocht Institute for Tropical Medicine, D-20359 Hamburg, Germany,;

    Molecular Medicine and|Infectious Disease Epidemiology, Bernhard Nocht Institute for Tropical Medicine, D-20359 Hamburg, Germany,;

    I. Department of Internal Medicine and;

    Department of Pediatrics, University Medical Center Hamburg-Eppendorf, D-20246 Hamburg, Germany,;

    Infectious Disease Epidemiology, Bernhard Nocht Institute for Tropical Medicine, D-20359 Hamburg, Germany,;

    Kumasi Centre for Collaborative Research in Tropical Medicine, Kumasi, Ghana and;

    Institute of Clinical Molecular Biology, Christian Albrechts University, D-24118 Kiel, Germany;

    Infectious Disease Epidemiology, Bernhard Nocht Institute for Tropical Medicine, D-20359 Hamburg, Germany,;

    Molecular Medicine and;

    Kumasi Centre for Collaborative Research in Tropical Medicine, Kumasi, Ghana and;

    Kumasi Centre for Collaborative Research in Tropical Medicine, Kumasi, Ghana and;

    Molecular Medicine and;

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