Outcomes of Japanese patients with non-alcoholic fatty liver disease according to genetic background and lifestyle-related diseases
Introduction and objectives: Genetic background may be involved in the mechanisms of liver injury and the development of non-alcoholic fatty liver disease (NAFLD). However, its contributions to the long-term outcome of NAFLD have been unclear. Methods: We enrolled 314 Japanese patients with biopsy-c...
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doaj-1ecbe33477f64747aca5bb6679156a202021-06-09T05:57:15ZengElsevierAnnals of Hepatology1665-26812021-03-0121100260Outcomes of Japanese patients with non-alcoholic fatty liver disease according to genetic background and lifestyle-related diseasesTomomi Kogiso0Takaomi Sagawa1Kazuhisa Kodama2Makiko Taniai3Etsuko Hashimoto4Katsutoshi Tokushige5Institute of Gastroenterology, Department of Internal Medicine, Tokyo Women’s Medical University, 8-1 Kawada-cho, Shinjuku-ku, Tokyo 162-8666, Japan; Corresponding author.Institute of Gastroenterology, Department of Internal Medicine, Tokyo Women’s Medical University, 8-1 Kawada-cho, Shinjuku-ku, Tokyo 162-8666, JapanInstitute of Gastroenterology, Department of Internal Medicine, Tokyo Women’s Medical University, 8-1 Kawada-cho, Shinjuku-ku, Tokyo 162-8666, JapanInstitute of Gastroenterology, Department of Internal Medicine, Tokyo Women’s Medical University, 8-1 Kawada-cho, Shinjuku-ku, Tokyo 162-8666, JapanSeibu Railway Health Support Center, 1-11-2 Seibu Second Building 7th Floor, Kusunoki-dai, Tokorozawa-shi, Saitama, 359-0037, JapanInstitute of Gastroenterology, Department of Internal Medicine, Tokyo Women’s Medical University, 8-1 Kawada-cho, Shinjuku-ku, Tokyo 162-8666, JapanIntroduction and objectives: Genetic background may be involved in the mechanisms of liver injury and the development of non-alcoholic fatty liver disease (NAFLD). However, its contributions to the long-term outcome of NAFLD have been unclear. Methods: We enrolled 314 Japanese patients with biopsy-confirmed NAFLD from 2000 to 2018 (161 men [51.3%]; median age, 53 [14–84] years; 114 with advanced fibrosis [37.5%]) in the patients without hepatocellular carcinoma at diagnosis. Genomic DNA was extracted from peripheral blood and single nucleotide polymorphisms (SNPs) were analyzed. Associations of mortality with patatin-like phospholipase 3 (PNPLA3) and aldehyde dehydrogenase 2 (ALDH2) were analyzed. Finally, a subgroup analysis according to lifestyle-related disease was performed. Results: During the median 7 years of follow-up, 20 patients (6.4%) died (13 liver-related [4.1%] and 7 non-liver-related deaths [2.2%]). Patients with ALDH2 (non-GG genotype) who had reduced alcohol metabolism tended to have a poor prognosis (p = 0.06). Patients carrying both risk SNPs of PNPLA3 (GG) and ALDH2 (non-GG) had a significantly poor prognosis (p = 0.01). In the subgroup analysis, patients with PNPLA3 (GG) who were non-diabetics (p = 0.06) or non-dyslipidemic (p = 0.03), with ALDH2 (non-GG) who were non-dyslipidemic (p = 0.01) or hypertensive (p = 0.03), also had a poor prognosis. The Cox analysis revealed that ALDH2 (non-GG) was associated with a poor prognosis (Hazard ratio: 4.568, 95% Confidence Interval: 1.294–16.131, p = 0.02) similar to the liver function tests. Conclusions: Genetic background may affect NAFLD prognosis and ALDH2 SNP could predict the outcome.http://www.sciencedirect.com/science/article/pii/S1665268120301757Non-alcoholic fatty liver disease (NAFLD)MortalitySingle nucleotide polymorphism (SNP)Patatin-like phospholipase 3 (PNPLA3)Aldehyde dehydrogenase 2 (ALDH2) |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Tomomi Kogiso Takaomi Sagawa Kazuhisa Kodama Makiko Taniai Etsuko Hashimoto Katsutoshi Tokushige |
spellingShingle |
Tomomi Kogiso Takaomi Sagawa Kazuhisa Kodama Makiko Taniai Etsuko Hashimoto Katsutoshi Tokushige Outcomes of Japanese patients with non-alcoholic fatty liver disease according to genetic background and lifestyle-related diseases Annals of Hepatology Non-alcoholic fatty liver disease (NAFLD) Mortality Single nucleotide polymorphism (SNP) Patatin-like phospholipase 3 (PNPLA3) Aldehyde dehydrogenase 2 (ALDH2) |
author_facet |
Tomomi Kogiso Takaomi Sagawa Kazuhisa Kodama Makiko Taniai Etsuko Hashimoto Katsutoshi Tokushige |
author_sort |
Tomomi Kogiso |
title |
Outcomes of Japanese patients with non-alcoholic fatty liver disease according to genetic background and lifestyle-related diseases |
title_short |
Outcomes of Japanese patients with non-alcoholic fatty liver disease according to genetic background and lifestyle-related diseases |
title_full |
Outcomes of Japanese patients with non-alcoholic fatty liver disease according to genetic background and lifestyle-related diseases |
title_fullStr |
Outcomes of Japanese patients with non-alcoholic fatty liver disease according to genetic background and lifestyle-related diseases |
title_full_unstemmed |
Outcomes of Japanese patients with non-alcoholic fatty liver disease according to genetic background and lifestyle-related diseases |
title_sort |
outcomes of japanese patients with non-alcoholic fatty liver disease according to genetic background and lifestyle-related diseases |
publisher |
Elsevier |
series |
Annals of Hepatology |
issn |
1665-2681 |
publishDate |
2021-03-01 |
description |
Introduction and objectives: Genetic background may be involved in the mechanisms of liver injury and the development of non-alcoholic fatty liver disease (NAFLD). However, its contributions to the long-term outcome of NAFLD have been unclear. Methods: We enrolled 314 Japanese patients with biopsy-confirmed NAFLD from 2000 to 2018 (161 men [51.3%]; median age, 53 [14–84] years; 114 with advanced fibrosis [37.5%]) in the patients without hepatocellular carcinoma at diagnosis. Genomic DNA was extracted from peripheral blood and single nucleotide polymorphisms (SNPs) were analyzed. Associations of mortality with patatin-like phospholipase 3 (PNPLA3) and aldehyde dehydrogenase 2 (ALDH2) were analyzed. Finally, a subgroup analysis according to lifestyle-related disease was performed. Results: During the median 7 years of follow-up, 20 patients (6.4%) died (13 liver-related [4.1%] and 7 non-liver-related deaths [2.2%]). Patients with ALDH2 (non-GG genotype) who had reduced alcohol metabolism tended to have a poor prognosis (p = 0.06). Patients carrying both risk SNPs of PNPLA3 (GG) and ALDH2 (non-GG) had a significantly poor prognosis (p = 0.01). In the subgroup analysis, patients with PNPLA3 (GG) who were non-diabetics (p = 0.06) or non-dyslipidemic (p = 0.03), with ALDH2 (non-GG) who were non-dyslipidemic (p = 0.01) or hypertensive (p = 0.03), also had a poor prognosis. The Cox analysis revealed that ALDH2 (non-GG) was associated with a poor prognosis (Hazard ratio: 4.568, 95% Confidence Interval: 1.294–16.131, p = 0.02) similar to the liver function tests. Conclusions: Genetic background may affect NAFLD prognosis and ALDH2 SNP could predict the outcome. |
topic |
Non-alcoholic fatty liver disease (NAFLD) Mortality Single nucleotide polymorphism (SNP) Patatin-like phospholipase 3 (PNPLA3) Aldehyde dehydrogenase 2 (ALDH2) |
url |
http://www.sciencedirect.com/science/article/pii/S1665268120301757 |
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