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Minerva Gastroenterologica e Dietologica 2016-Mar

Supplementary management of functional, temporary alcoholic hepatic damage with Robuvit® (French oak wood extract).

Csak regisztrált felhasználók fordíthatnak cikkeket
Belépés Regisztrálás
A hivatkozás a vágólapra kerül
Luciano Pellegrini
Gianni Belcaro
Mark Dugall
Marcello Corsi
Roberta Luzzi
Masayuki Hosoi

Kulcsszavak

Absztrakt

The aim of this registry study was to evaluate Robuvit® (quercus robur wood extract) supplementation in the evolution of moderate functional hepatic failure (MTHF) due to alcohol. Recent studies have indicated the protective effect of oak wood (QR) extracts on liver injury. This registry included patients with MTHF characterized by: decreased albumin levels; increased total bilirubin, altered hepatic functions enzymes, increased oxidative stress, negative viral hepatitis markers.

RESULTS

The two groups resulted divided into a best management (BM) group and a comparative group (BM+ Robuvit ® were comparable): 23 Robuvit® patients and 21 comparable controls completed the 12-week registry. At inclusion, blood parameters in the two groups were comparable. At the end of the observation period, the increase in albumin levels was significantly (P<0.05 at 12 weeks) faster and higher in the Robuvit® group. The decreasee in ALT-SGPT and AST-ASAT were significantly larger in the supplement group (P<0.05 at 6 and 12 weeks). Alkaline phosphatase was reduced more, at 6 and 12 weeks in Robuvit® patients; (Robuvit® group's values were significantly better; P<0.05). Total bilirubin improved better in Robuvit® subjects at 6 and 12 weeks. Results were significantly better in comparison with controls (P<0.05). Also, direct bilirubin values increased more in the Robuvit® group at 6 and 12 weeks (P<0.05). Gamma GT values were normalized at 6 and 12 weeks in the Robuvit® group. There was a less important decrease in controls (P<0.05) without normalization at 12 weeks. Plasma free radicals, increased at inclusion, showed a more significant decrease in Robuvit® subject (at 6 and 12 weeks), with normalization at 12 weeks. Persisting, elevated values in controls were observed even at 12 weeks (P<0.05). ESR decreased in both groups with a more important decrease in the Robuvit® group (P<0.05). Hepatitis markers were negative when repeated at 6 and 12 weeks. In conclusion, observations from this pilot, supplement registry study indicate a significant protective activity of the supplementation with Robuvit®, associated with a very good safety profile, in patients with temporary hepatic failure. The activity of Robuvit ® seems to be mediated by its anti-inflammatory activity associated to its important action on oxidative stress.

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