Abstract

Host genetics in dengue hemorrhagic fever (DHF) pathophysiology has not been extensively investigated. Most studies have focused on HLA in different populations; however these reported associations have not been replicated. We performed a case–control study to analyze possible associations of HLA-A, HLA-B, HLA-Cw, HLA-DRB1 and HLA-DQB1 alleles with clinical disease severity caused by dengue virus infection. Our population consisted of 39 individuals (DF: 23, DHF: 16) and 34 healthy controls from the State of Morelos, Mexico. HLA loci were genotyped by nucleotide sequencing method. Statistical analyses revealed associations in three alleles: HLA-B*35 was negatively associated with symptomatic disease ( p < 1 × 10 −4, p c = 0.01, OR = 0.12, 95%CI = 0.037–0.39), and DF ( p = 0.0007, p c = 0.03, OR = 0.13, 95%CI = 0.031–0.51). HLA-DQB1*0302 was positively associated with DHF ( p = 0.018, p c = NS, OR = 5.02, 95%CI = 1.05–25.34), and negatively with DF ( p = 0.011, p c = NS, OR = 0.23, 95%CI = 0.06–0.84). HLA-DQB1*0202 was positively associated with DF only ( p = 0.012, p c = NS, OR = 7.0, 95%CI = 1.11–73.8). We identified possible associations of HLA-B and HLA-DQB1 alleles with the risk of developing symptomatic disease, DF and DHF in a Mexican Mestizo population.

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