2017
DOI: 10.1016/j.cgh.2017.04.016
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A Randomized Trial of Silymarin for the Treatment of Nonalcoholic Steatohepatitis

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Cited by 180 publications
(170 citation statements)
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“…In contrast to the previously mentioned study, a randomized, double blind, placebo‐controlled trial used higher doses of silymarin (700 mg, trice daily for 48 weeks) in patients diagnosed with NASH and a NAFLD activity score (NAS) of ≥4. Despite improvement in fibrosis, no significant reduction was observed either in NAS or in the liver function tests compared to that of the placebo …”
Section: Human Studiesmentioning
confidence: 82%
“…In contrast to the previously mentioned study, a randomized, double blind, placebo‐controlled trial used higher doses of silymarin (700 mg, trice daily for 48 weeks) in patients diagnosed with NASH and a NAFLD activity score (NAS) of ≥4. Despite improvement in fibrosis, no significant reduction was observed either in NAS or in the liver function tests compared to that of the placebo …”
Section: Human Studiesmentioning
confidence: 82%
“…Two studies36 133 considered decrease in ALT without specifying as the response. One study each has defined the response rate as the end of treatment fibrosis stage less than baseline,39 decrease in 30% NAS,134 decrease in ALT by at least 0.3 times the upper limit of normal reference range,77 decrease in steatosis >30% compared with baseline,48 at least 50% decrease in aminotransferases83 and one did not have any specific definition of responders 69. For studies (877 patients) with the criterion of NAS improvement by at least two points, elafibranor (OR 2.37; 95% CI 1.2 to 4.7), obeticholic acid (OR 3.12; 95% CI 1.7 to 5.6), pentoxifylline (OR 4.3; 95% CI 1.4 to 13.6), telmisartan (OR 7.4; 95% CI 1.2 to 45) and vitamin E (OR 3.5; 95% CI 1.5 to 6.9) were observed to perform better than standard of care (online supplementary figure S4).…”
Section: Resultsmentioning
confidence: 99%
“…The PO bioavailability of silymarin is low (30%‐50%) and the half‐life short (4‐6 hours), meaning high doses and repeated administration are necessary to obtain therapeutic concentrations . Studies of silymarin in humans, including National Institutes of Health‐sponsored clinical trials using highly standardized preparations, have failed to achieve projected therapeutic endpoints …”
Section: Treatmentmentioning
confidence: 99%