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Interferon-λ rs12979860 genotype and liver fibrosis in viral and non-viral chronic liver disease

机译:病毒性和非病毒性慢性肝病的干扰素-λrs12979860基因型和肝纤维化

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摘要

Tissue fibrosis is a core pathologic process that contributes to mortality in ~45% of the population and is likely to be influenced by the host genetic architecture. Here we demonstrate, using liver disease as a model, that a single-nucleotide polymorphism (rs12979860) in the intronic region of interferon-λ4 (IFNL4) is a strong predictor of fibrosis in an aetiology-independent manner. In a cohort of 4,172 patients, including 3,129 with chronic hepatitis C (CHC), 555 with chronic hepatitis B (CHB) and 488 with non-alcoholic fatty liver disease (NAFLD), those with rs12979860CC have greater hepatic inflammation and fibrosis. In CHC, those with rs12979860CC also have greater stage-constant and stage-specific fibrosis progression rates (P<0.0001 for all). The impact of rs12979860 genotypes on fibrosis is maximal in young females, especially those with HCV genotype 3. These findings establish rs12979860 genotype as a strong aetiology-independent predictor of tissue inflammation and fibrosis.
机译:组织纤维化是一种核心病理过程,可导致约45%的人口死亡,并可能受到宿主基因结构的影响。在这里,我们以肝脏疾病为模型证明,干扰素-λ4(IFNL4)内含子区域的单核苷酸多态性(rs12979860)是病因学独立的强烈纤维化预测因子。在一个4,172名患者的队列中,包括3,129例慢性丙型肝炎(CHC),555例慢性乙型肝炎(CHB)和488例非酒精性脂肪肝疾病(NAFLD),患有rs12979860CC的患者的肝脏炎症和纤维化程度更高。在CHC中,具有rs12979860CC的患者的阶段恒定和阶段特异性纤维化进展率也更高(所有P均<0.0001)。 rs12979860基因型对纤维化的影响在年轻女性中最大,尤其是那些具有HCV基因型3的女性。这些发现将rs12979860基因型确立为组织炎症和纤维化的强烈病因独立指标。

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