Interferon-induced transmembrane protein-3 genetic variant rs12252 is associated with COVID-19 mortality

干扰素诱导的跨膜蛋白 3 基因变异 rs12252 与 COVID-19 死亡率相关

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作者:Jahad Alghamdi, Manal Alaamery, Tlili Barhoumi, Mamoon Rashid, Hala Alajmi, Nasser Aljasser, Yaseen Alhendi, Hind Alkhalaf, Hanadi Alqahtani, Omer Algablan, Abdulraham I Alshaya, Nabiha Tashkandi, Salam Massadeh, Bader Almuzzaini, Salleh N Ehaideb, Mohammad Bosaeed, Kamal Ayoub, Saber Yezli, Anas Kh

Abstract

Interferon-induced membrane proteins (IFITM) 3 gene variants are known risk factor for severe viral diseases. We examined whether IFITM3 variant may underlie the heterogeneous clinical outcomes of SARS-CoV-2 infection-induced COVID-19 in large Arab population. We genotyped 880 Saudi patients; 93.8% were PCR-confirmed SARS-CoV-2 infection, encompassing most COVID-19 phenotypes. Mortality at 90 days was 9.1%. IFITM3-SNP, rs12252-G allele was associated with hospital admission (OR = 1.65 [95% CI; 1.01-2.70], P = 0.04]) and mortality (OR = 2.2 [95% CI; 1.16-4.20], P = 0.01). Patients less than 60 years old had a lower survival probability if they harbor this allele (log-rank test P = 0.002). Plasma levels of IFNγ were significantly lower in a subset of patients with AG/GG genotypes than patients with AA genotype (P = 0.00016). Early identification of these individuals at higher risk of death may inform precision public health response.

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