Atorvastatin and Vitamin E Accelerates NASH Resolution by Dietary Intervention in a Preclinical Guinea Pig Model.
Julie Hviid KlaebelMia SkjødtJosephine Skat-RørdamGünaj RakipovskiDavid H IpsenAnne Marie V Schou-PedersenJens LykkesfeldtPernille Tveden-NyborgPublished in: Nutrients (2019)
Despite affecting millions of patients worldwide, no pharmacological treatment has yet proved effective against non-alcoholic steatohepatitis (NASH) induced liver fibrosis. Current guidelines recommend lifestyle modifications including reductions in dietary energy intake. Recently, therapy with atorvastatin and vitamin E (vitE) has been recommended, although clinical studies on the resolution of hepatic fibrosis are inconclusive. Targeting NASH-induced hepatic end-points, this study evaluated the effects of atorvastatin and vitE alone or in combination with a dietary intervention in the guinea pig NASH model. Guinea pigs (n = 72) received 20 weeks of high fat feeding before allocating to four groups: continued HF feeding (HF), HF diet with atorvastatin and vitE (HF+), low-fat diet (LF) and low-fat with atorvastatin and vitE (LF+), for four or eight weeks of intervention. Both LF and LF+ decreased liver weight, cholesterol and plasma dyslipidemia. LF+ further improved hepatic histopathological hallmarks (p < 0.05), liver injury markers aspartate aminotransferase (AST) and alanine aminotransferase (ALT) (p < 0.05) and reduced the expression of target genes of hepatic inflammation and fibrosis (p < 0.05), underlining an increased effect on NASH resolution in this group. Collectively, the data support an overall beneficial effect of diet change, and indicate that atorvastatin and vitE therapy combined with a diet change act synergistically in improving NASH-induced endpoints.
Keyphrases
- liver injury
- drug induced
- weight loss
- physical activity
- liver fibrosis
- randomized controlled trial
- high glucose
- diabetic rats
- adipose tissue
- poor prognosis
- end stage renal disease
- chronic kidney disease
- cardiovascular disease
- ejection fraction
- single molecule
- newly diagnosed
- type diabetes
- metabolic syndrome
- gene expression
- fatty acid
- weight gain
- heart failure
- gestational age
- patient reported outcomes
- artificial intelligence
- clinical practice
- bone marrow
- cancer therapy
- low density lipoprotein
- genome wide identification