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首页> 外文期刊>Public health genomics >Interleukin 10 gene polymorphisms and development of post kala-azar dermal leishmaniasis in a selected sudanese population
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Interleukin 10 gene polymorphisms and development of post kala-azar dermal leishmaniasis in a selected sudanese population

机译:苏丹人群中白介素10基因多态性与黑热病后皮肤利什曼病的发展

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Background: Post kala-azar dermal leishmaniasis (PKDL) is a cutaneous form of disease that develops at variable times after individuals have received treatment for clinical visceral leishmaniasis (VL). The study aimed to investigate the possible role of interleukin 10 (IL-10) and development of PKDL. Methods: 77 families composed of 41 complete case-parent trios and 36 case-parent pairs from the Masalit ethnic group were genotyped for 3 IL10 promoter polymorphisms: -1082A/G, -819C/T and -592C/A. Results: Single point analysis using the transmission disequilibrium test showed no evidence of association between any of these IL10 promoter single nucleotide polymorphisms (SNPs) and development of PKDL. Haplotype analysis performed using TRANSMIT showed borderline significance between PKDL and the haplotype AA across -592C/A and -1082A/G (p = 0.053). Haplotypes GCC (0.33) and ATA (0.30) were the common haplotypes in this Sudanese population. Allele frequencies for the 3 SNPs differed significantly in Sudan compared to other African (Gambian, Malawian, YRI) populations. Conclusion: There is no evidence for an association between 3 SNPs in the IL10 gene promoter and susceptibility to PKDL in the Masalit ethnic group in Sudan, although some evidence for haplotype association was observed.
机译:背景:黑热病后皮肤利什曼病(PKDL)是一种皮肤病,在个人接受临床内脏利什曼病(VL)治疗后,会在不同时间发展。该研究旨在调查白介素10(IL-10)和PKDL的发展的可能作用。方法:对来自Masalit族的41个完整的个案父母三重奏和36个个案父母对组成的77个家庭进行基因分型,确定其3个IL10启动子多态性:-1082A / G,-819C / T和-592C / A。结果:使用传输不平衡测试的单点分析显示,这些IL10启动子单核苷酸多态性(SNP)与PKDL的发生之间没有关联的证据。使用TRANSMIT进行的单倍型分析显示,在-592C / A和-1082A / G之间,PKDL与单倍型AA之间具有临界界限(p = 0.053)。 GCC(0.33)和ATA(0.30)的单倍型是该苏丹人口中常见的单倍型。与其他非洲(冈比亚,马拉维,YRI)人群相比,苏丹3个SNP的等位基因频率存在显着差异。结论:苏丹苏丹Masalit族群中没有证据显示IL10基因启动子中的3个SNP与PKDL的易感性相关,尽管有一些单倍型关联的证据。

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