Literature DB >> 23607264

Efficacy of probucol for the treatment of non-alcoholic steatohepatitis with dyslipidemia: An open-label pilot study.

Tomokazu Ishitobi1, Hideyuki Hyogo1, Hironori Tokumo2, Koji Arihiro3, Kazuaki Chayama1.   

Abstract

AIM: Oxidative stress plays a pivotal role in the transition from simple steatosis to non-alcoholic steatohepatitis (NASH). Probucol is a lipid-lowering agent with strong antioxidant properties, and is reported to be effective for the treatment of NASH in several studies. The aim of the present study was to evaluate the efficacy of probucol for the treatment of NASH with dyslipidemia.
METHODS: Twenty-six patients with biopsy-proven NASH accompanied by dyslipidemia were treated with 500 mg of probucol daily for 48 weeks. Body mass index, visceral fat area, liver function tests, serum lipids, fibrosis markers, ferritin, adiponectin, leptin, urinary 8-hydroxy-2'-deoxyguanosine (U-8OHdG) and elasticity were measured periodically during the study. Follow-up liver biopsy was performed in 18 patients.
RESULTS: Serum levels of aminotransferases, total cholesterol and U-8OHdG significantly decreased (P < 0.01). Levels of hemoglobin A1c (HbA1c), the Homeostasis Model of Assessment - Insulin Resistance index and serum levels of ferritin, type IV collagen 7S and hyaluronic acid significantly decreased (P < 0.05). The serum levels of adiponectin tended to be increased. Liver stiffness significantly decreased from 8.8 ± 6.8 to 6.6 ± 4.0 kPa (P < 0.01). Non-alcoholic fatty liver disease activity scores were significantly improved from 4.2 ± 1.4 to 3.4 ± 1.6 (P < 0.05) and fibrotic stages tended to be improved from 1.6 ± 0.8 to 1.3 ± 1.1, respectively. No adverse effects of this treatment were noted.
CONCLUSION: Probucol improved clinical and histological findings probably through its ability to reduce insulin resistance and oxidative stress. Probucol therapy was safe and effective for Japanese NASH patients with dyslipidemia.
© 2013 The Japan Society of Hepatology.

Entities:  

Keywords:  dyslipidemia; non-alcoholic steatohepatitis; oxidative stress; probucol

Year:  2013        PMID: 23607264     DOI: 10.1111/hepr.12135

Source DB:  PubMed          Journal:  Hepatol Res        ISSN: 1386-6346            Impact factor:   4.288


  5 in total

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Journal:  World J Hepatol       Date:  2014-10-27

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Journal:  World J Gastroenterol       Date:  2014-09-28       Impact factor: 5.742

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Journal:  Drug Saf       Date:  2014-04       Impact factor: 5.606

4.  Effect of probucol on insulin resistance in patients with non-diabetic chronic kidney disease.

Authors:  Rui Wang; Ri-Bao Wei; Yue Yang; Na Wang; Meng-Jie Huang; Cui-Ming Cao; Zi-Cheng Wang; Guang-Yan Cai; Xiang-Mei Chen
Journal:  J Geriatr Cardiol       Date:  2015-09       Impact factor: 3.327

5.  Improved dissolution and oral absorption by co-grinding active drug probucol and ternary stabilizers mixtures with planetary beads-milling method.

Authors:  Fang Li; Linsen Li; Shaoning Wang; Yan Yang; Jia Li; Dongchun Liu; Sijie Zhang; Siling Wang; Hui Xu
Journal:  Asian J Pharm Sci       Date:  2018-12-12       Impact factor: 6.598

  5 in total

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