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TNF-Block Genotypes Influence Susceptibility to HIV-Associated Sensory Neuropathy in Indonesians and South Africans

HIV-associated sensory neuropathy (HIV-SN) is a disabling complication of HIV disease and antiretroviral therapies (ART). Since stavudine was removed from recommended treatment schedules, the prevalence of HIV-SN has declined and associated risk factors have changed. With stavudine, rs1799964*C (TNF...

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Autores principales: Gaff, Jessica, Octaviana, Fitri, Pillay, Prinisha, Ngassa Mbenda, Huguette Gaelle, Ariyanto, Ibnu A., Gan, June Anne, Cherry, Catherine L., Kamerman, Peter, Laws, Simon M., Price, Patricia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7014294/
https://www.ncbi.nlm.nih.gov/pubmed/31936167
http://dx.doi.org/10.3390/ijms21020380
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author Gaff, Jessica
Octaviana, Fitri
Pillay, Prinisha
Ngassa Mbenda, Huguette Gaelle
Ariyanto, Ibnu A.
Gan, June Anne
Cherry, Catherine L.
Kamerman, Peter
Laws, Simon M.
Price, Patricia
author_facet Gaff, Jessica
Octaviana, Fitri
Pillay, Prinisha
Ngassa Mbenda, Huguette Gaelle
Ariyanto, Ibnu A.
Gan, June Anne
Cherry, Catherine L.
Kamerman, Peter
Laws, Simon M.
Price, Patricia
author_sort Gaff, Jessica
collection PubMed
description HIV-associated sensory neuropathy (HIV-SN) is a disabling complication of HIV disease and antiretroviral therapies (ART). Since stavudine was removed from recommended treatment schedules, the prevalence of HIV-SN has declined and associated risk factors have changed. With stavudine, rs1799964*C (TNF-1031) associated with HIV-SN in Caucasians and Indonesians but not in South Africans. Here, we investigate associations between HIV-SN and rs1799964*C and 12 other polymorphisms spanning TNF and seven neighboring genes (the TNF-block) in Indonesians (n = 202; 34/168 cases) and South Africans (n = 75; 29/75 cases) treated without stavudine. Haplotypes were derived using fastPHASE and haplotype networks built with PopART. There were no associations with rs1799964*C in either population. However, rs9281523*C in intron 10 of BAT1 (alternatively DDX39B) independently associated with HIV-SN in Indonesians after correcting for lower CD4 T-cell counts and >500 copies of HIV RNA/mL (model p = 0.0011, Pseudo R(2) = 0.09). rs4947324*T (between NFKBIL1 and LTA) independently associated with reduced risk of HIV-SN and shared haplotype 1 (containing no minor alleles) associated with increased risk of HIV-SN after correcting for greater body weight, a history of tuberculosis and nadir CD4 T-cell counts (model: p = 0.0003, Pseudo R(2) = 0.22). These results confirm TNF-block genotypes influence susceptibility of HIV-SN. However, critical genotypes differ between ethnicities and with stavudine use.
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spelling pubmed-70142942020-03-09 TNF-Block Genotypes Influence Susceptibility to HIV-Associated Sensory Neuropathy in Indonesians and South Africans Gaff, Jessica Octaviana, Fitri Pillay, Prinisha Ngassa Mbenda, Huguette Gaelle Ariyanto, Ibnu A. Gan, June Anne Cherry, Catherine L. Kamerman, Peter Laws, Simon M. Price, Patricia Int J Mol Sci Article HIV-associated sensory neuropathy (HIV-SN) is a disabling complication of HIV disease and antiretroviral therapies (ART). Since stavudine was removed from recommended treatment schedules, the prevalence of HIV-SN has declined and associated risk factors have changed. With stavudine, rs1799964*C (TNF-1031) associated with HIV-SN in Caucasians and Indonesians but not in South Africans. Here, we investigate associations between HIV-SN and rs1799964*C and 12 other polymorphisms spanning TNF and seven neighboring genes (the TNF-block) in Indonesians (n = 202; 34/168 cases) and South Africans (n = 75; 29/75 cases) treated without stavudine. Haplotypes were derived using fastPHASE and haplotype networks built with PopART. There were no associations with rs1799964*C in either population. However, rs9281523*C in intron 10 of BAT1 (alternatively DDX39B) independently associated with HIV-SN in Indonesians after correcting for lower CD4 T-cell counts and >500 copies of HIV RNA/mL (model p = 0.0011, Pseudo R(2) = 0.09). rs4947324*T (between NFKBIL1 and LTA) independently associated with reduced risk of HIV-SN and shared haplotype 1 (containing no minor alleles) associated with increased risk of HIV-SN after correcting for greater body weight, a history of tuberculosis and nadir CD4 T-cell counts (model: p = 0.0003, Pseudo R(2) = 0.22). These results confirm TNF-block genotypes influence susceptibility of HIV-SN. However, critical genotypes differ between ethnicities and with stavudine use. MDPI 2020-01-07 /pmc/articles/PMC7014294/ /pubmed/31936167 http://dx.doi.org/10.3390/ijms21020380 Text en © 2020 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Gaff, Jessica
Octaviana, Fitri
Pillay, Prinisha
Ngassa Mbenda, Huguette Gaelle
Ariyanto, Ibnu A.
Gan, June Anne
Cherry, Catherine L.
Kamerman, Peter
Laws, Simon M.
Price, Patricia
TNF-Block Genotypes Influence Susceptibility to HIV-Associated Sensory Neuropathy in Indonesians and South Africans
title TNF-Block Genotypes Influence Susceptibility to HIV-Associated Sensory Neuropathy in Indonesians and South Africans
title_full TNF-Block Genotypes Influence Susceptibility to HIV-Associated Sensory Neuropathy in Indonesians and South Africans
title_fullStr TNF-Block Genotypes Influence Susceptibility to HIV-Associated Sensory Neuropathy in Indonesians and South Africans
title_full_unstemmed TNF-Block Genotypes Influence Susceptibility to HIV-Associated Sensory Neuropathy in Indonesians and South Africans
title_short TNF-Block Genotypes Influence Susceptibility to HIV-Associated Sensory Neuropathy in Indonesians and South Africans
title_sort tnf-block genotypes influence susceptibility to hiv-associated sensory neuropathy in indonesians and south africans
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7014294/
https://www.ncbi.nlm.nih.gov/pubmed/31936167
http://dx.doi.org/10.3390/ijms21020380
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