Open AccessGenetic variation in the vitamin D pathway CYP2R1 gene predicts sustained HBeAg seroconversion in chronic hepatitis B patients treated with pegylated interferon: A multicenter study
Author(s) -
Kessarin Thanapirom,
Sirinporn Suksawatamnuay,
Wattana Sukeepaisarnjareon,
Tawesak Tanwandee,
Phunchai Charatcharoenwitthaya,
Satawat Thongsawat,
Apinya Leerapun,
Teerha Piratvisuth,
Rattana Boonsirichan,
Chalermrat Bunchorntavakul,
Chaowalit Pattanasirigool,
Bubpha Pornthisarn,
Supot Tantipanichtheerakul,
Ekawee Sripariwuth,
Woramon Jeamsripong,
Teeranan Sanpajit,
Yong Poovorawan,
Piyawat Komolmit
Publication year - 2017
Publication title -
plos one
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.99
H-Index - 332
ISSN - 1932-6203
DOI - 10.1371/journal.pone.0173263
Subject(s) - foki , vitamin d and neurology , calcitriol receptor , pegylated interferon , single nucleotide polymorphism , medicine , taqi , seroconversion , hbsag , genotype , hbeag , vitamin d deficiency , immunology , biology , gastroenterology , hepatitis b virus , hepatitis c virus , restriction fragment length polymorphism , ribavirin , polymorphism (computer science) , genetics , virus , gene
Evidence of a role of vitamin D in the immune system is increasing. Low serum vitamin D is associated with increased hepatitis B virus replication. Genome-wide association study (GWAS) data has revealed a number of the single nucleotide polymorphisms (SNPs) within the vitamin D synthetic pathway that affect vitamin D functions. We aimed to determine the association between SNPs in the vitamin D gene cascade and response to pegylated interferon (PegIFN) therapy in hepatitis B e-antigen (HBeAg)-positive patients. One hundred and eleven patients treated for 48 weeks with PegIFN-alfa 2a at 13 hospitals were retrospectively evaluated. Thirteen SNPs derived from vitamin D cascade-related genes, including DHCR7 (rs12785878), CYP27B1 (rs10877012), CYP2R1 (rs2060793, rs12794714), GC (rs4588, rs7041, rs222020, rs2282679), and VDR ( Fok I, Bsm I, Tru 9I, Apa I, Taq I), were genotyped. Thirty-one patients (27.9%) seroconverted to HBeAg after 24 weeks of treatment. Multivariate analysis found pretreatment qHBsAg <10,000 IU/mL (OR = 7.73, 95% CI: 2.36–25.31, P = 0.001), CYP2R1 rs12794714 TT genotype (OR = 4.16, 95% CI: 1.07–16.25, P = 0.04), and baseline ALT >2 times the upper limit of normal (OR = 3.83, 95% CI: 1.31–11.22, P = 0.014) predicted sustained HBeAg seroconversion after completion of PegIFN treatment. HBV DNA during study period tended to be lower with the rs12794714 CYP2R1 TT than the non-TT genotype. The rs12794714 CYP2R1 polymorphism may be a useful pretreatment factor predictive of sustained HBeAg seroconversion after PegIFN therapy. This study provides evidence that not only vitamin D level but also genetic variation of CYP2R1 in the vitamin D cascade influences host immune response in chronic HBV infection.