Inositol and Non-Alcoholic Fatty Liver Disease: A Systematic Review on Deficiencies and Supplementation.
Arianna PaniRiccardo GiossiDanilo MenichelliVeronica Andrea FittipaldoFrancesca AgnelliElvira IngleseAlessandra RomandiniRossana RoncatoBasilio PintaudiFrancesco Del SoleFrancesco ScaglionePublished in: Nutrients (2020)
Liver lipid accumulation is a hallmark of non-alcoholic fatty liver disease (NAFLD), broadly associated with insulin resistance. Inositols (INS) are ubiquitous polyols implied in many physiological functions. They are produced endogenously, are present in many foods and in dietary supplements. Alterations in INS metabolism seems to play a role in diseases involving insulin resistance such as diabetes and polycystic ovary syndrome. Given its role in other metabolic syndromes, the hypothesis of an INS role as a supplement in NAFLD is intriguing. We performed a systematic review of the literature to find preclinical and clinical evidence of INS supplementation efficacy in NAFLD patients. We retrieved 10 studies on animal models assessing Myoinosiol or Pinitol deficiency or supplementation and one human randomized controlled trial (RCT). Overall, INS deficiency was associated with increased fatty liver in animals. Conversely, INS supplementation in animal models of fatty liver reduced hepatic triglycerides and cholesterol accumulation and maintained a normal ultrastructural liver histopathology. In the one included RCT, Pinitol supplementation obtained similar results. Pinitol significantly reduced liver fat, post-prandial triglycerides, AST levels, lipid peroxidation increasing glutathione peroxidase activity. These results, despite being limited, indicate the need for further evaluation of INS in NAFLD in larger clinical trials.
Keyphrases
- insulin resistance
- polycystic ovary syndrome
- randomized controlled trial
- type diabetes
- adipose tissue
- clinical trial
- endothelial cells
- metabolic syndrome
- skeletal muscle
- end stage renal disease
- study protocol
- newly diagnosed
- cardiovascular disease
- ejection fraction
- systematic review
- stem cells
- mesenchymal stem cells
- bone marrow
- high density