Publications & Reports

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

Wadley AL, Hendry LM, Kamerman PR, Chew CS, Price P, Cherry CL, Lombard Z
Brain Function Research Group, School of Physiology, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.

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.European Journal of Human Genetics advance online publication, 4 June 2014; doi:10.1038/ejhg.2014.104.

Project

Publication

  • Journal: European Journal of Human Genetics : EJHG
  • Published: 01/03/2015
  • Volume: 23
  • Issue: 3
  • Pagination: 363-368

Author

Health Issue