Literature DB >> 33536442

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

Kwang Min Kim1, Ji-Hye Roh2, Sangjin Lee3, Jeong-Hyun Yoon4.   

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.

Entities:  

Year:  2021        PMID: 33536442     DOI: 10.1038/s41598-021-81959-1

Source DB:  PubMed          Journal:  Sci Rep        ISSN: 2045-2322            Impact factor:   4.379


  33 in total

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Authors:  Elham Ahmadian; Peter S Pennefather; Aziz Eftekhari; Reza Heidari; Mohammad Ali Eghbal
Journal:  Expert Rev Gastroenterol Hepatol       Date:  2016-07-14       Impact factor: 3.869

Review 2.  NAFLD: a multisystem disease.

Authors:  Christopher D Byrne; Giovanni Targher
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Review 10.  Recent research trends and updates on nonalcoholic fatty liver disease.

Authors:  Jeong-Ju Yoo; Won Kim; Moon Young Kim; Dae Won Jun; Sang Gyune Kim; Jong-Eun Yeon; Jin Woo Lee; Yong Kyun Cho; Sang Hoon Park; Joo Hyun Sohn
Journal:  Clin Mol Hepatol       Date:  2018-08-08
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  4 in total

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2.  Impact of Maternal Obesity on Liver Disease in the Offspring: A Comprehensive Transcriptomic Analysis and Confirmation of Results in a Murine Model.

Authors:  Beat Moeckli; Vaihere Delaune; Julien Prados; Matthieu Tihy; Andrea Peloso; Graziano Oldani; Thomas Delmi; Florence Slits; Quentin Gex; Laura Rubbia-Brandt; Nicolas Goossens; Stéphanie Lacotte; Christian Toso
Journal:  Biomedicines       Date:  2022-01-27

3.  Chrysin Attenuates Fructose-Induced Nonalcoholic Fatty Liver in Rats via Antioxidant and Anti-Inflammatory Effects: The Role of Angiotensin-Converting Enzyme 2/Angiotensin (1-7)/Mas Receptor Axis.

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Journal:  Oxid Med Cell Longev       Date:  2022-06-08       Impact factor: 7.310

4.  Hepatocellular carcinoma chemoprevention by targeting the angiotensin-converting enzyme and EGFR transactivation.

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  4 in total

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