Clinical implications of renin–angiotensin system inhibitors for development and progression of non-alcoholic fatty liver disease

Abstract Recently, there has been an increasing interest in the therapeutic efficacy of RAS inhibitors (RASi) in patients with non-alcoholic fatty liver disease (NAFLD) because they may reduce oxidative stress, inflammatory markers, and enhanced fibrosis. An objective of this study was to investigat...

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Main Authors: Kwang Min Kim, Ji-Hye Roh, Sangjin Lee, Jeong-Hyun Yoon
Format: Article
Language:English
Published: Nature Portfolio 2021-02-01
Series:Scientific Reports
Online Access:https://doi.org/10.1038/s41598-021-81959-1
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author Kwang Min Kim
Ji-Hye Roh
Sangjin Lee
Jeong-Hyun Yoon
author_facet Kwang Min Kim
Ji-Hye Roh
Sangjin Lee
Jeong-Hyun Yoon
author_sort Kwang Min Kim
collection DOAJ
description Abstract Recently, there has been an increasing interest in the therapeutic efficacy of RAS inhibitors (RASi) in patients with non-alcoholic fatty liver disease (NAFLD) because they may reduce oxidative stress, inflammatory markers, and enhanced fibrosis. An objective of this study was to investigate the role of RASi on NAFLD development and progression in a large cohort. We conducted a nested case–control study. Study subjects were classified into two study cohorts according to baseline NAFLD status: non-NAFLD (n = 184,581) and established NALFD (n = 27,565). An NAFLD development or progression case was defined as a patient with newly developed NAFLD or new progression of advanced fibrosis from non-NAFLD and established NALFD cohorts, respectively. A conditional logistic regression analysis was conducted to estimate the associations between RASi exposure and NAFLD development/progression. Overall, no significant association was evident between RASi use and NAFLD development or progression (NAFLD development; ever-user vs. never-user: OR 1.017; 95% CI 0.842–1.230, NAFLD progression; ever-user vs. never-user: aOR 0.942; 95% CI 0.803–1.105). RASi ever-use in cases of individuals who were obese or who had normal fasting plasma glucose (FPG) was associated with reduced risk of both NAFLD development (body mass index (BMI) ≥ 25 kg/m2: 0.708 [95% confidence interval (CI) 0.535–0.937], FPG of < 100 mg/mL: 0.774 [95% CI 0.606–0.987]) and progression (BMI ≥ 25 kg/m2: 0.668 [95% CI 0.568–0.784], FPG of < 100 mg/mL: 0.732 [95% CI 0.582–0.921]). The present study did not verify a significant overall association between RASi use and NAFLD development/progression but suggested that RASi might prevent NAFLD development and progression among specific subjects.
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spelling doaj.art-648294fd0b844a61a38cb4f6b5afa69b2022-12-21T20:35:20ZengNature PortfolioScientific Reports2045-23222021-02-0111111210.1038/s41598-021-81959-1Clinical implications of renin–angiotensin system inhibitors for development and progression of non-alcoholic fatty liver diseaseKwang Min Kim0Ji-Hye Roh1Sangjin Lee2Jeong-Hyun Yoon3Department of Medicine, Samsung Changwon Hospital, Sungkyunkwan University School of MedicineCollege of Pharmacy, Pusan National UniversityDepartment of Statistics, College of Natural Science, Pusan National UniversityCollege of Pharmacy, Pusan National UniversityAbstract Recently, there has been an increasing interest in the therapeutic efficacy of RAS inhibitors (RASi) in patients with non-alcoholic fatty liver disease (NAFLD) because they may reduce oxidative stress, inflammatory markers, and enhanced fibrosis. An objective of this study was to investigate the role of RASi on NAFLD development and progression in a large cohort. We conducted a nested case–control study. Study subjects were classified into two study cohorts according to baseline NAFLD status: non-NAFLD (n = 184,581) and established NALFD (n = 27,565). An NAFLD development or progression case was defined as a patient with newly developed NAFLD or new progression of advanced fibrosis from non-NAFLD and established NALFD cohorts, respectively. A conditional logistic regression analysis was conducted to estimate the associations between RASi exposure and NAFLD development/progression. Overall, no significant association was evident between RASi use and NAFLD development or progression (NAFLD development; ever-user vs. never-user: OR 1.017; 95% CI 0.842–1.230, NAFLD progression; ever-user vs. never-user: aOR 0.942; 95% CI 0.803–1.105). RASi ever-use in cases of individuals who were obese or who had normal fasting plasma glucose (FPG) was associated with reduced risk of both NAFLD development (body mass index (BMI) ≥ 25 kg/m2: 0.708 [95% confidence interval (CI) 0.535–0.937], FPG of < 100 mg/mL: 0.774 [95% CI 0.606–0.987]) and progression (BMI ≥ 25 kg/m2: 0.668 [95% CI 0.568–0.784], FPG of < 100 mg/mL: 0.732 [95% CI 0.582–0.921]). The present study did not verify a significant overall association between RASi use and NAFLD development/progression but suggested that RASi might prevent NAFLD development and progression among specific subjects.https://doi.org/10.1038/s41598-021-81959-1
spellingShingle Kwang Min Kim
Ji-Hye Roh
Sangjin Lee
Jeong-Hyun Yoon
Clinical implications of renin–angiotensin system inhibitors for development and progression of non-alcoholic fatty liver disease
Scientific Reports
title Clinical implications of renin–angiotensin system inhibitors for development and progression of non-alcoholic fatty liver disease
title_full Clinical implications of renin–angiotensin system inhibitors for development and progression of non-alcoholic fatty liver disease
title_fullStr Clinical implications of renin–angiotensin system inhibitors for development and progression of non-alcoholic fatty liver disease
title_full_unstemmed Clinical implications of renin–angiotensin system inhibitors for development and progression of non-alcoholic fatty liver disease
title_short Clinical implications of renin–angiotensin system inhibitors for development and progression of non-alcoholic fatty liver disease
title_sort clinical implications of renin angiotensin system inhibitors for development and progression of non alcoholic fatty liver disease
url https://doi.org/10.1038/s41598-021-81959-1
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