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肿瘤坏死因子阻断基因变异在南非黑人HIV相关感觉神经病变中的作用。

Role of TNF block genetic variants in HIV-associated sensory neuropathy in black Southern Africans.

作者信息

Wadley Antonia L, Hendry Liesl M, Kamerman Peter R, Chew Constance S N, Price Patricia, Cherry Catherine L, Lombard Zané

机构信息

Brain Function Research Group, School of Physiology, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.

1] Brain Function Research Group, School of Physiology, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa [2] Division of Human Genetics, School of Pathology, Faculty of Health Sciences, National Health Laboratory Service and University of the Witwatersrand, Johannesburg, South Africa.

出版信息

Eur J Hum Genet. 2015 Mar;23(3):363-8. doi: 10.1038/ejhg.2014.104. Epub 2014 Jun 4.

Abstract

HIV-associated sensory neuropathy (HIV-SN) is a common neurological complication of HIV infection. The TNF block is a region within the central MHC that contains many immunoregulatory genes. Polymorphisms and haplotypes of the TNF block have been associated with increased risk of HIV-SN in Asians and whites. Here we investigated genetic associations with HIV-SN in 342 black Southern Africans (190 cases and 152 neuropathy-free controls) using single nucleotide polymorphisms (SNPs) spanning the TNF block and a set of haplotypes defined by 31 SNPs in Asian and white populations (denoted FVa). We included population-appropriate tagSNPs derived from an African population (Yoruban, YRI, HapMap) and derived extended haplotypes comprising 61 SNPs (denoted FVa_ext b). We found no association between HIV-SN and carriage of two SNPs (TNF-1031/rs1799964C and BAT1 (intron10)/rs9281523C) associated with HIV-SN in whites and Asians. Additionally, a haplotype containing TNF-1031/rs1799964C associated with increased risk of HIV-SN in Asians, but was not present in this African population. However, alleles of seven SNPs associated with reduced risk of HIV-SN (corrected for age, height and multiple comparisons). These were rs11796A, rs3130059G, rs2071594C, NFKBIL1-62/rs2071592A, rs2071591A, LTA+252/rs909253G, rs1041981C. One haplotype (FV18_ext1), not containing these alleles, was associated with increased risk of HIV-SN after correction for age, height and multiple comparisons. Our results confirm the involvement of genes in the TNF block in altering risk for HIV-SN, but genotypes critical in this African population differed from those affecting HIV-SN in whites and Asians. These differences support the need for genetic association studies in diverse populations.

摘要

人类免疫缺陷病毒相关感觉神经病变(HIV-SN)是HIV感染常见的神经并发症。肿瘤坏死因子(TNF)区域是主要组织相容性复合体(MHC)内的一个区域,包含许多免疫调节基因。TNF区域的多态性和单倍型与亚洲人和白人患HIV-SN的风险增加有关。在此,我们使用跨越TNF区域的单核苷酸多态性(SNP)以及在亚洲人和白人人群中由31个SNP定义的一组单倍型(表示为FVa),对342名南非黑人(190例患者和152名无神经病变对照)进行了HIV-SN的基因关联研究。我们纳入了源自非洲人群(约鲁巴人,YRI,HapMap)的适合该人群的标签SNP以及由61个SNP组成的扩展单倍型(表示为FVa_ext b)。我们发现,在白人和亚洲人中与HIV-SN相关的两个SNP(TNF-1031/rs1799964C和BAT1(内含子10)/rs9281523C)的携带情况与HIV-SN之间无关联。此外,一个包含与亚洲人患HIV-SN风险增加相关的TNF-1031/rs1799964C的单倍型在该非洲人群中不存在。然而,7个SNP的等位基因与HIV-SN风险降低相关(校正了年龄、身高和多重比较)。这些SNP分别是rs11796A、rs3130059G、rs2071594C、NFKBIL1-62/rs2071592A、rs2071591A、LTA+252/rs909253G、rs1041981C。在对年龄、身高和多重比较进行校正后,一个不包含这些等位基因的单倍型(FV18_ext1)与HIV-SN风险增加相关。我们的结果证实了TNF区域的基因参与改变HIV-SN的风险,但在该非洲人群中起关键作用的基因型与影响白人和亚洲人HIV-SN的基因型不同。这些差异支持了在不同人群中进行基因关联研究的必要性。

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