A whole genome association study of mother-to-child transmission of HIV in Malawi

被引:34
|
作者
Joubert, Bonnie R. [1 ]
Lange, Ethan M. [2 ,3 ,4 ]
Franceschini, Nora [1 ]
Mwapasa, Victor [5 ]
North, Kari E. [1 ,4 ]
Meshnick, Steven R. [1 ]
机构
[1] Univ N Carolina, Dept Epidemiol, Gillings Sch Global Publ Hlth, Chapel Hill, NC 27599 USA
[2] Univ N Carolina, Sch Med, Dept Genet, Chapel Hill, NC 27599 USA
[3] Univ N Carolina, Dept Biostat, Gillings Sch Global Publ Hlth, Chapel Hill, NC 27599 USA
[4] Univ N Carolina, Carolina Ctr Genome Sci, Chapel Hill, NC 27599 USA
[5] Univ Malawi, Coll Med, Blantyre, Malawi
来源
GENOME MEDICINE | 2010年 / 2卷
关键词
IMMUNODEFICIENCY-VIRUS TYPE-1; MANNOSE-BINDING LECTIN; SURFACE HEPARAN-SULFATE; DISEASE PROGRESSION; FACTOR-I; DC-SIGN; VERTICAL TRANSMISSION; GENETIC RESTRICTION; AIDS PATHOGENESIS; DENDRITIC CELL;
D O I
10.1186/gm138
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
Background: More than 300,000 children are newly infected with HIV each year, predominantly through mother-to-child transmission (HIV MTCT). Identification of host genetic traits associated with transmission may more clearly explain the mechanisms of HIV MTCT and further the development of a vaccine to protect infants from infection. Associations between transmission and a selection of genes or single nucleotide polymorphisms (SNP)s may give an incomplete picture of HIV MTCT etiology. Thus, this study employed a genome-wide association approach to identify novel variants associated with HIV MTCT. Methods: We conducted a nested case-control study of HIV MTCT using infants of HIV(+) mothers, drawn from a cohort study of malaria and HIV in pregnancy in Blantyre, Malawi. Whole genome scans (650,000 SNPs genotyped using Illumina genotyping assays) were obtained for each infant. Logistic regression was used to evaluate the association between each SNP and HIV MTCT. Results: Genotype results were available for 100 HIV(+) infants (at birth, 6, or 12 weeks) and 126 HIV(-) infants (at birth, 6, and 12 weeks). We identified 9 SNPs within 6 genes with a P-value <5 x 10(-5) associated with the risk of transmission, in either unadjusted or adjusted by maternal HIV viral load analyses. Carriers of the rs8069770 variant allele were associated with a lower risk of HIV MTCT (odds ratio = 0.27, 95% confidence interval = 0.14, 0.51), where rs8069770 is located within HS3ST3A1, a gene involved in heparan sulfate biosynthesis. Interesting associations for SNPs located within or near genes involved in pregnancy and development, innate immunological response, or HIV protein interactions were also observed. Conclusions: This study used a genome-wide approach to identify novel variants associated with the risk of HIV MTCT in order to gain new insights into HIV MTCT etiology. Replication of this work using a larger sample size will help us to differentiate true positive findings.
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页数:11
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