BACKGROUND: Genetic variations contribute to septic shock mortality. To discover a novel locus, we performed in vitro genome-wide association studies (GWAS) and further tested the result in a cohort of septic shock patients. METHODS: Two in vitro GWAS using a quantitative trait locus analysis of stimulated IL-6 production in lymphoblastoid cells from 60 individuals of European ancestry were performed. VPS13D rs6685273 was genotyped in European ancestry patients (n = 498). The VPS13D gene was silenced in vitro. RESULTS: Two GWAS using lymphoblastoid cells identified the locus of VPS13D rs6685273 that was significant in the same direction in both GWAS. The VPS13D rs6685273 C allele was associated with increased IL-6 production. Patients with septic shock who had the VPS13D rs6685273 CC genotype had an increased 28-day mortality (p = 0.023) and more organ failure (p < 0.05) compared to the CT/TT genotypes. VPS13D in vitro gene silencing in the HeLa cell line increased IL-6 production. Furthermore, the rs6685273 genotype was associated with differential VPS13D splice variant expression. CONCLUSIONS: The VPS13D rs6685273 C allele was associated with increased IL-6 production in vitro. The patients with the VPS13D rs6685273 CC genotype had increased 28-day mortality and increased organ failure. VPS13D appears to regulate IL-6 production.
VPS13D Gene Variant Is Associated with Altered IL-6 Production and Mortality in Septic Shock.
VPS13D 基因变异与脓毒症休克中 IL-6 产生改变和死亡率相关
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作者:Nakada Taka-aki, Boyd John H, Russell James A, Aguirre-Hernández RosalÃa, Wilkinson Mark D, Thair Simone A, Nakada Emiri, McConechy Melissa K, Fjell Christopher D, Walley Keith R
| 期刊: | Journal of Innate Immunity | 影响因子: | 3.000 |
| 时间: | 2015 | 起止号: | 2015;7(5):545-53 |
| doi: | 10.1159/000381265 | 研究方向: | 其它 |
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