2017
DOI: 10.3390/nu9091015
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Vitamin D Supplementation and Non-Alcoholic Fatty Liver Disease: Present and Future

Abstract: Non-alcoholic fatty liver disease (NAFLD) is the most common chronic hepatic disease throughout the Western world and is recognized as the main cause of cryptogenic cirrhosis; however, the identification of an effective therapy for NAFLD is still a major challenge. Vitamin D deficiency is a wide-spread condition which reaches epidemic proportions in industrialized countries, mainly in relation to current lifestyle and limited dietary sources. Epidemiological studies point towards an association between hypovit… Show more

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Cited by 59 publications
(25 citation statements)
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“…Several observational studies reported a link between low 25(OH)D plasma levels and fatty liver diseases [13,[47][48][49]. If the causality is still not clearly demonstrated in humans [50], observations on animal models, including the present study, tend to confirm such an assumption.…”
Section: Discussionsupporting
confidence: 56%
“…Several observational studies reported a link between low 25(OH)D plasma levels and fatty liver diseases [13,[47][48][49]. If the causality is still not clearly demonstrated in humans [50], observations on animal models, including the present study, tend to confirm such an assumption.…”
Section: Discussionsupporting
confidence: 56%
“…9, 10-Secoergosta-7, 10 (19), 22-triene-3, 5, 6-triol is one form of dehydrocalciferol from vitamin D 31 . Hydroxyvitamin D form in the body will affect the health of a human's liver 32 .…”
Section: Gracilismentioning
confidence: 99%
“…Vitamin D knockout mice spontaneously developed liver fibrosis, while mice fed a vitamin D‐deficient diet developed severe hepatic steatosis and inflammation,82, 83 demonstrating that NAFLD may be associated with vitamin D deficiency. However, clinical studies on vitamin D supplementation on NAFLD pathogenesis have been limited; thus, more studies are needed to provide conclusive results 84. On the other hand, studies have shown that PXR can activate de novo lipogenesis in an SREPB1c‐dependent manner.…”
Section: Nuclear Receptors As Therapeutic Targetsmentioning
confidence: 99%