Literature DB >> 21224501

The pilot study of 3-month course of melatonin treatment of patients with nonalcoholic steatohepatitis: effect on plasma levels of liver enzymes, lipids and melatonin.

M Gonciarz1, Z Gonciarz, W Bielanski, A Mularczyk, P C Konturek, T Brzozowski, S J Konturek.   

Abstract

The mechanism by which nonalcoholic fatty liver disease (NAFLD) progresses into nonalcoholic steatohepatitis (NASH) is unknown, however, the major process is oxidative stress with increased production of reactive oxygen species and excessive inflammatory cytokine generation. To date, there are no effective treatments for NASH and the published data with treatment using antioxidants are not satisfactory. Melatonin (MT), the potent endogenous antioxidant secreted in circadian rhythm by pinealocytes and in large amounts in the digestive system, was reported to improve oxidative status and to exert beneficial effects in NASH pathology in experimental animals, but no study attempted to determine the possible effectiveness of MT in humans with NASH. In this study, 42 patients (12 placebo controls and 30 MT-treated) with histological evidence (liver biopsy) of NASH and no history of alcohol abuse, were included. The treatment group took melatonin (2x5 mg/daily orally), while controls were treated with placebo. At baseline no significant differences between the groups were found for age, body mass index (BMI) as well as for plasma alanine aminotransferase (ALT), aspartate aminotransferase (AST), gamma-glutamyl transpeptidase (GGT), alkaline phosphatase (ALP), and concentrations of cholesterol, triglycerides (TG), glucose and MT. During the study period plasma ALT level and cholesterol concentration decreased significantly in both MT-treated and control groups, however AST and GGT levels decreased significantly only in MT-treated groups. Median value of AST level at baseline was 76.5 (64.2-114.2) IU/L and its percentage decrease at 4, 8 and 12 week was 20, 36 and 38%, resp. Baseline GGT median level was 113 (75.7-210.7) IU/L and its mean percentage decrease at week 4, 8 and 12 was 46, 48 and 47%, resp. Plasma ALP levels did not change significantly during MT treatment. Median value of plasma concentrations of MT (pg/mL) in MT-treated group rose from 7.5 (5.0-14.25) at baseline to 35.5(18.8-110.0), 43.5(17.0-102.5) and 49.5(18.0-99.5) at the end of 4, 8 and 12 week of treatment, respectively. Plasma levels of TG and glucose as well as BMI in controls and MT-treated patients were not significantly different from baseline. This study demonstrates for the first time in humans that three months treatment with MT significantly improves plasma liver enzymes in patients with NASH without causing any side-effect. Plasma MT levels during the whole period of MT treatment persisted above that at baseline. Our findings show that treatment with MT significantly improves plasma liver enzymes in NASH patients, but larger cohort trials and longer treatment with MT are required before this indole could be included into the spectrum of the NASH treatment.

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Year:  2010        PMID: 21224501

Source DB:  PubMed          Journal:  J Physiol Pharmacol        ISSN: 0867-5910            Impact factor:   3.011


  19 in total

1.  Fatty liver is associated with recurrent bacterial infections independent of metabolic syndrome.

Authors:  William Nseir; Hussein Taha; Julnar Khateeb; Maria Grosovski; Nimer Assy
Journal:  Dig Dis Sci       Date:  2011-05-12       Impact factor: 3.199

Review 2.  Melatonin, mitochondria, and the metabolic syndrome.

Authors:  Daniel P Cardinali; Daniel E Vigo
Journal:  Cell Mol Life Sci       Date:  2017-08-17       Impact factor: 9.261

Review 3.  Tired of diabetes genetics? Circadian rhythms and diabetes: the MTNR1B story?

Authors:  Cecilia Nagorny; Valeriya Lyssenko
Journal:  Curr Diab Rep       Date:  2012-12       Impact factor: 4.810

Review 4.  Role of the Circadian Clock in the Metabolic Syndrome and Nonalcoholic Fatty Liver Disease.

Authors:  Akshay Shetty; Jennifer W Hsu; Paul P Manka; Wing-Kin Syn
Journal:  Dig Dis Sci       Date:  2018-08-18       Impact factor: 3.199

5.  Melatonin attenuates high fat diet-induced fatty liver disease in rats.

Authors:  Gregorios Hatzis; Panayiotis Ziakas; Nikolaos Kavantzas; Aggeliki Triantafyllou; Panagiotis Sigalas; Ioanna Andreadou; Konstantinos Ioannidis; Stamatios Chatzis; Konstantinos Filis; Alexandros Papalampros; Fragiska Sigala
Journal:  World J Hepatol       Date:  2013-04-27

Review 6.  Possible application of melatonin treatment in human diseases of the biliary tract.

Authors:  Leonardo Baiocchi; Tianhao Zhou; Suthat Liangpunsakul; Lenci Ilaria; Martina Milana; Fanyin Meng; Lindsey Kennedy; Praveen Kusumanchi; Zhihong Yang; Ludovica Ceci; Shannon Glaser; Heather Francis; Gianfranco Alpini
Journal:  Am J Physiol Gastrointest Liver Physiol       Date:  2019-09-11       Impact factor: 4.052

Review 7.  Melatonin in type 2 diabetes mellitus and obesity.

Authors:  Angeliki Karamitri; Ralf Jockers
Journal:  Nat Rev Endocrinol       Date:  2019-02       Impact factor: 43.330

8.  Beneficial effects of melatonin on stroke-induced muscle atrophy in focal cerebral ischemic rats.

Authors:  Seunghoon Lee; Jinhee Shin; Yunkyung Hong; Minkyung Lee; Koo Kim; Sang-Rae Lee; Kyu-Tae Chang; Yonggeun Hong
Journal:  Lab Anim Res       Date:  2012-03-21

9.  Melatonin levels in serum and ascitic fluid of patients with hepatic encephalopathy.

Authors:  Cezary Chojnacki; Marek Romanowski; Katarzyna Winczyk; Janusz Błasiak; Jan Chojnacki
Journal:  Gastroenterol Res Pract       Date:  2012-12-30       Impact factor: 2.260

10.  Sleep Disruption and Daytime Sleepiness Correlating with Disease Severity and Insulin Resistance in Non-Alcoholic Fatty Liver Disease: A Comparison with Healthy Controls.

Authors:  Christine Bernsmeier; Diego M Weisskopf; Marlon O Pflueger; Jan Mosimann; Benedetta Campana; Luigi Terracciano; Christoph Beglinger; Markus H Heim; Christian Cajochen
Journal:  PLoS One       Date:  2015-11-17       Impact factor: 3.240

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