APOB codon 4311 polymorphism is associated with hepatitis C virus infection through altered lipid metabolism

Abstract Background It has been reported that some single-nucleotide polymorphisms (SNPs) in lipid regulators such as apolipoproteins and cell surface molecules for hepatitis C virus (HCV) entry into hepatocytes are associated with HCV infection. However, it is unknown how HCV infection is affected...

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Main Authors: Rie Harada, Masako Kimura, Yasushi Sato, Tatsuya Taniguchi, Tetsu Tomonari, Takahiro Tanaka, Hironori Tanaka, Naoki Muguruma, Hirohiko Shinomiya, Hirohito Honda, Issei Imoto, Masahiro Sogabe, Toshiya Okahisa, Tetsuji Takayama
Format: Article
Language:English
Published: BMC 2018-01-01
Series:BMC Gastroenterology
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Online Access:http://link.springer.com/article/10.1186/s12876-018-0747-5
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author Rie Harada
Masako Kimura
Yasushi Sato
Tatsuya Taniguchi
Tetsu Tomonari
Takahiro Tanaka
Hironori Tanaka
Naoki Muguruma
Hirohiko Shinomiya
Hirohito Honda
Issei Imoto
Masahiro Sogabe
Toshiya Okahisa
Tetsuji Takayama
author_facet Rie Harada
Masako Kimura
Yasushi Sato
Tatsuya Taniguchi
Tetsu Tomonari
Takahiro Tanaka
Hironori Tanaka
Naoki Muguruma
Hirohiko Shinomiya
Hirohito Honda
Issei Imoto
Masahiro Sogabe
Toshiya Okahisa
Tetsuji Takayama
author_sort Rie Harada
collection DOAJ
description Abstract Background It has been reported that some single-nucleotide polymorphisms (SNPs) in lipid regulators such as apolipoproteins and cell surface molecules for hepatitis C virus (HCV) entry into hepatocytes are associated with HCV infection. However, it is unknown how HCV infection is affected by altered lipid metabolism resulting from the SNPs. We investigated the relationship between these SNPs and HCV infection status, and also analyzed the mechanism by which these SNPs mediate HCV infection via lipid metabolism alterations. Methods Serum lipid and apolipoprotein profiles were tested in 158 HCV-positive and 220 HCV-negative subjects. We selected 22 SNPs in five lipid regulator genes which were related to HCV entry into hepatocytes and to lipid metabolism (APOA1, APOB, SR-B1, LDLR, and APOE), and their polymorphisms were analyzed using the PCR-sequence-specific oligonucleotide probe-Luminex method. Results An APOB N4311S (g.41553a > g) SNP, rs1042034, was significantly associated with HCV positivity; the HCV positivity rate for the minor allele AA genotype was significantly higher than for genotype AG + GG (P = 0.016). Other SNPs except for APOB P2712L SNP rs676210, which is in linkage disequilibrium with rs1042034, showed no significant difference in genotype distribution. The serum level of low density lipoprotein-cholesterol (LDL-C) in the genotype AA group was significantly lower than in the genotype non-AA group (P = 0.032), whereas the triglyceride (TG) level was significantly higher (P = 0.007). Conclusion An APOB SNP, rs1042034, is closely associated with HCV infection through lipid metabolism alteration. The minor allele AA genotype might contribute to facilitating serum LDL uptake into hepatocytes via LDLR by modifying their affinity and interaction and may have an influence on HCV infection by their entry to the liver through the LDLR.
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spelling doaj.art-05affeb4464e47dc8286b7cfdd978d552022-12-21T22:48:44ZengBMCBMC Gastroenterology1471-230X2018-01-011811810.1186/s12876-018-0747-5APOB codon 4311 polymorphism is associated with hepatitis C virus infection through altered lipid metabolismRie Harada0Masako Kimura1Yasushi Sato2Tatsuya Taniguchi3Tetsu Tomonari4Takahiro Tanaka5Hironori Tanaka6Naoki Muguruma7Hirohiko Shinomiya8Hirohito Honda9Issei Imoto10Masahiro Sogabe11Toshiya Okahisa12Tetsuji Takayama13Department of Gastroenterology and Oncology, Tokushima University Graduate School of Biomedical SciencesDepartment of Gastroenterology and Oncology, Tokushima University Graduate School of Biomedical SciencesDepartment of Gastroenterology and Oncology, Tokushima University Graduate School of Biomedical SciencesDepartment of Gastroenterology and Oncology, Tokushima University Graduate School of Biomedical SciencesDepartment of Gastroenterology and Oncology, Tokushima University Graduate School of Biomedical SciencesDepartment of Gastroenterology and Oncology, Tokushima University Graduate School of Biomedical SciencesDepartment of Gastroenterology and Oncology, Tokushima University Graduate School of Biomedical SciencesDepartment of Gastroenterology and Oncology, Tokushima University Graduate School of Biomedical SciencesDepartment of Gastroenterology, Yoshinogawa Medical CenterDepartment of Internal Medicine, Tokushima Health Screening CenterDepartment of Human Genetics, Tokushima University Graduate School of Biomedical SciencesDepartment of General Medicine and Community Health Science, Tokushima University Graduate School of Biomedical SciencesDepartment of General Medicine and Community Health Science, Tokushima University Graduate School of Biomedical SciencesDepartment of Gastroenterology and Oncology, Tokushima University Graduate School of Biomedical SciencesAbstract Background It has been reported that some single-nucleotide polymorphisms (SNPs) in lipid regulators such as apolipoproteins and cell surface molecules for hepatitis C virus (HCV) entry into hepatocytes are associated with HCV infection. However, it is unknown how HCV infection is affected by altered lipid metabolism resulting from the SNPs. We investigated the relationship between these SNPs and HCV infection status, and also analyzed the mechanism by which these SNPs mediate HCV infection via lipid metabolism alterations. Methods Serum lipid and apolipoprotein profiles were tested in 158 HCV-positive and 220 HCV-negative subjects. We selected 22 SNPs in five lipid regulator genes which were related to HCV entry into hepatocytes and to lipid metabolism (APOA1, APOB, SR-B1, LDLR, and APOE), and their polymorphisms were analyzed using the PCR-sequence-specific oligonucleotide probe-Luminex method. Results An APOB N4311S (g.41553a > g) SNP, rs1042034, was significantly associated with HCV positivity; the HCV positivity rate for the minor allele AA genotype was significantly higher than for genotype AG + GG (P = 0.016). Other SNPs except for APOB P2712L SNP rs676210, which is in linkage disequilibrium with rs1042034, showed no significant difference in genotype distribution. The serum level of low density lipoprotein-cholesterol (LDL-C) in the genotype AA group was significantly lower than in the genotype non-AA group (P = 0.032), whereas the triglyceride (TG) level was significantly higher (P = 0.007). Conclusion An APOB SNP, rs1042034, is closely associated with HCV infection through lipid metabolism alteration. The minor allele AA genotype might contribute to facilitating serum LDL uptake into hepatocytes via LDLR by modifying their affinity and interaction and may have an influence on HCV infection by their entry to the liver through the LDLR.http://link.springer.com/article/10.1186/s12876-018-0747-5Hepatitis C virusLipid metabolismSNPsApoB
spellingShingle Rie Harada
Masako Kimura
Yasushi Sato
Tatsuya Taniguchi
Tetsu Tomonari
Takahiro Tanaka
Hironori Tanaka
Naoki Muguruma
Hirohiko Shinomiya
Hirohito Honda
Issei Imoto
Masahiro Sogabe
Toshiya Okahisa
Tetsuji Takayama
APOB codon 4311 polymorphism is associated with hepatitis C virus infection through altered lipid metabolism
BMC Gastroenterology
Hepatitis C virus
Lipid metabolism
SNPs
ApoB
title APOB codon 4311 polymorphism is associated with hepatitis C virus infection through altered lipid metabolism
title_full APOB codon 4311 polymorphism is associated with hepatitis C virus infection through altered lipid metabolism
title_fullStr APOB codon 4311 polymorphism is associated with hepatitis C virus infection through altered lipid metabolism
title_full_unstemmed APOB codon 4311 polymorphism is associated with hepatitis C virus infection through altered lipid metabolism
title_short APOB codon 4311 polymorphism is associated with hepatitis C virus infection through altered lipid metabolism
title_sort apob codon 4311 polymorphism is associated with hepatitis c virus infection through altered lipid metabolism
topic Hepatitis C virus
Lipid metabolism
SNPs
ApoB
url http://link.springer.com/article/10.1186/s12876-018-0747-5
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