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CYP24A1 genetic variants in the vitamin D metabolic pathway are involved in the outcomes of hepatitis C virus infection among high-risk Chinese population
Author(s) -
Haozhi Fan,
Ru Zhang,
Ting Tian,
Yuling Zhong,
Mengping Wu,
Chao-nan Xie,
Jingjing Yang,
Peng Huang,
Rongbin Yu,
Yun Zhang,
Jie Wang
Publication year - 2019
Publication title -
international journal of infectious diseases
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.278
H-Index - 89
eISSN - 1878-3511
pISSN - 1201-9712
DOI - 10.1016/j.ijid.2019.04.032
Subject(s) - cyp24a1 , hepatitis c virus , vitamin d and neurology , medicine , population , genetic variants , hepatitis c , virology , biology , virus , gene , genetics , environmental health , calcitriol receptor , genotype
It has been demonstrated that 1,25-hydroxyvitamin-D3-24-hydroxylase, encoded by CYP24A1 gene, is a key enzyme that neutralizes the active vitamin D3 metabolite 1,25-dihydroxyvitamin D3 [1,25(OH) 2 D 3 ] in response to hepatitis C virus (HCV) infection. This study aimed to investigate whether CYP24A1 genetic variation is associated with HCV infection outcomes.

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