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Nutrigenetic Interaction Between Apolipoprotein C3 Polymorphism and Fat Intake in People with Nonalcoholic Fatty Liver Disease

BACKGROUND: Recent genome-wide association studies have revealed that nonalcoholic fatty liver disease (NAFLD) is correlated with genetic polymorphisms. However, the effects of genetic variation on nutritional metabolism and NAFLD are complex and further studies are still needed. OBJECTIVES: This st...

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Autores principales: Yamamoto, Reina, Takeshita, Yumie, Tsujiguchi, Hiromasa, Kannon, Takayuki, Sato, Takehiro, Hosomichi, Kazuyoshi, Suzuki, Keita, Kita, Yuki, Tanaka, Takeo, Goto, Hisanori, Nakano, Yujiro, Yamashita, Tatsuya, Kaneko, Shuichi, Tajima, Atsushi, Nakamura, Hiroyuki, Takamura, Toshinari
Formato: Online Artículo Texto
Lenguaje:English
Publicado: American Society for Nutrition 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10257212/
https://www.ncbi.nlm.nih.gov/pubmed/37304843
http://dx.doi.org/10.1016/j.cdnut.2023.100051
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author Yamamoto, Reina
Takeshita, Yumie
Tsujiguchi, Hiromasa
Kannon, Takayuki
Sato, Takehiro
Hosomichi, Kazuyoshi
Suzuki, Keita
Kita, Yuki
Tanaka, Takeo
Goto, Hisanori
Nakano, Yujiro
Yamashita, Tatsuya
Kaneko, Shuichi
Tajima, Atsushi
Nakamura, Hiroyuki
Takamura, Toshinari
author_facet Yamamoto, Reina
Takeshita, Yumie
Tsujiguchi, Hiromasa
Kannon, Takayuki
Sato, Takehiro
Hosomichi, Kazuyoshi
Suzuki, Keita
Kita, Yuki
Tanaka, Takeo
Goto, Hisanori
Nakano, Yujiro
Yamashita, Tatsuya
Kaneko, Shuichi
Tajima, Atsushi
Nakamura, Hiroyuki
Takamura, Toshinari
author_sort Yamamoto, Reina
collection PubMed
description BACKGROUND: Recent genome-wide association studies have revealed that nonalcoholic fatty liver disease (NAFLD) is correlated with genetic polymorphisms. However, the effects of genetic variation on nutritional metabolism and NAFLD are complex and further studies are still needed. OBJECTIVES: This study aimed to assess the nutritional characteristics interacting with the correlation between genetic predisposition and NAFLD. METHODS: We assessed the 2013–2017 health examination data of 1191 adults aged ≥40 y living in Shika town, Ishikawa Prefecture, Japan. Adults with moderate or heavy alcohol consumption and hepatitis were excluded, and 464 participants who underwent genetic analyses were included in the study. Abdominal echography was performed to diagnose fatty liver condition, and dietary intake and nutritional balance were evaluated using the brief self-administered diet history questionnaire. NAFLD-related gene polymorphisms were identified using Japonica Array v2 (Toshiba). RESULTS: Among the 31 single nucleotide polymorphisms, only the polymorphism T-455C in the apolipoprotein C3 (APOC3) gene (rs2854116) was significantly associated with fatty liver condition. The condition was more common in participants with heterozygotes of the APOC3 gene (rs2854116) than in those with the TT and CC genotypes. Significant interactions were observed between NAFLD and the intake of fat, vegetable fat, MUFAs, PUFAs, cholesterol, n-3 FAs, and n-6 FAs. Moreover, participants with NAFLD who presented with the TT genotype had a significantly higher fat intake than those without NAFLD. CONCLUSIONS: The polymorphism T-455C in the APOC3 gene (rs2854116) and fat intake are associated with the NAFLD risk in Japanese adults. Participants with a fatty liver who presented with the TT genotype of rs2854116 had a higher fat intake. Such nutrigenetic interaction can deepen our understanding of the NAFLD pathology. Moreover, in clinical settings, the correlation between genetic factors and nutrition intake should be considered in personalized nutritional interventions against NAFLD. Curr Dev Nutr 2023;xx:xx. The study was registered in the University Hospital Medical Information Network Clinical Trials Registry as UMIN 000024915.
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spelling pubmed-102572122023-06-11 Nutrigenetic Interaction Between Apolipoprotein C3 Polymorphism and Fat Intake in People with Nonalcoholic Fatty Liver Disease Yamamoto, Reina Takeshita, Yumie Tsujiguchi, Hiromasa Kannon, Takayuki Sato, Takehiro Hosomichi, Kazuyoshi Suzuki, Keita Kita, Yuki Tanaka, Takeo Goto, Hisanori Nakano, Yujiro Yamashita, Tatsuya Kaneko, Shuichi Tajima, Atsushi Nakamura, Hiroyuki Takamura, Toshinari Curr Dev Nutr Original Research BACKGROUND: Recent genome-wide association studies have revealed that nonalcoholic fatty liver disease (NAFLD) is correlated with genetic polymorphisms. However, the effects of genetic variation on nutritional metabolism and NAFLD are complex and further studies are still needed. OBJECTIVES: This study aimed to assess the nutritional characteristics interacting with the correlation between genetic predisposition and NAFLD. METHODS: We assessed the 2013–2017 health examination data of 1191 adults aged ≥40 y living in Shika town, Ishikawa Prefecture, Japan. Adults with moderate or heavy alcohol consumption and hepatitis were excluded, and 464 participants who underwent genetic analyses were included in the study. Abdominal echography was performed to diagnose fatty liver condition, and dietary intake and nutritional balance were evaluated using the brief self-administered diet history questionnaire. NAFLD-related gene polymorphisms were identified using Japonica Array v2 (Toshiba). RESULTS: Among the 31 single nucleotide polymorphisms, only the polymorphism T-455C in the apolipoprotein C3 (APOC3) gene (rs2854116) was significantly associated with fatty liver condition. The condition was more common in participants with heterozygotes of the APOC3 gene (rs2854116) than in those with the TT and CC genotypes. Significant interactions were observed between NAFLD and the intake of fat, vegetable fat, MUFAs, PUFAs, cholesterol, n-3 FAs, and n-6 FAs. Moreover, participants with NAFLD who presented with the TT genotype had a significantly higher fat intake than those without NAFLD. CONCLUSIONS: The polymorphism T-455C in the APOC3 gene (rs2854116) and fat intake are associated with the NAFLD risk in Japanese adults. Participants with a fatty liver who presented with the TT genotype of rs2854116 had a higher fat intake. Such nutrigenetic interaction can deepen our understanding of the NAFLD pathology. Moreover, in clinical settings, the correlation between genetic factors and nutrition intake should be considered in personalized nutritional interventions against NAFLD. Curr Dev Nutr 2023;xx:xx. The study was registered in the University Hospital Medical Information Network Clinical Trials Registry as UMIN 000024915. American Society for Nutrition 2023-03-02 /pmc/articles/PMC10257212/ /pubmed/37304843 http://dx.doi.org/10.1016/j.cdnut.2023.100051 Text en © 2023 The Authors https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Original Research
Yamamoto, Reina
Takeshita, Yumie
Tsujiguchi, Hiromasa
Kannon, Takayuki
Sato, Takehiro
Hosomichi, Kazuyoshi
Suzuki, Keita
Kita, Yuki
Tanaka, Takeo
Goto, Hisanori
Nakano, Yujiro
Yamashita, Tatsuya
Kaneko, Shuichi
Tajima, Atsushi
Nakamura, Hiroyuki
Takamura, Toshinari
Nutrigenetic Interaction Between Apolipoprotein C3 Polymorphism and Fat Intake in People with Nonalcoholic Fatty Liver Disease
title Nutrigenetic Interaction Between Apolipoprotein C3 Polymorphism and Fat Intake in People with Nonalcoholic Fatty Liver Disease
title_full Nutrigenetic Interaction Between Apolipoprotein C3 Polymorphism and Fat Intake in People with Nonalcoholic Fatty Liver Disease
title_fullStr Nutrigenetic Interaction Between Apolipoprotein C3 Polymorphism and Fat Intake in People with Nonalcoholic Fatty Liver Disease
title_full_unstemmed Nutrigenetic Interaction Between Apolipoprotein C3 Polymorphism and Fat Intake in People with Nonalcoholic Fatty Liver Disease
title_short Nutrigenetic Interaction Between Apolipoprotein C3 Polymorphism and Fat Intake in People with Nonalcoholic Fatty Liver Disease
title_sort nutrigenetic interaction between apolipoprotein c3 polymorphism and fat intake in people with nonalcoholic fatty liver disease
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10257212/
https://www.ncbi.nlm.nih.gov/pubmed/37304843
http://dx.doi.org/10.1016/j.cdnut.2023.100051
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