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Autor(en) / Beteiligte
Titel
Reduction of Some Atherogenic Indices in Patients with Non-Alcoholic Fatty Liver by Vitamin D and Calcium Co-Supplementation: A Double Blind Randomized Controlled Clinical Trial
Ist Teil von
  • Iranian journal of pharmaceutical research : IJPR, 2019-01, Vol.18 (1), p.496-505
Ort / Verlag
Iran: Shaheed Beheshti University of Medical Sciences
Erscheinungsjahr
2019
Quelle
EZB Electronic Journals Library
Beschreibungen/Notizen
  • The role of non-alcoholic fatty liver disease (NAFLD) as a potential independent cardiovascular disease (CVD) risk factor has recently gained considerable attention because CVD is the common cause of death in NAFLD patients. We aimed to estimate the effects of vitamin D supplementation alone or in combination with calcium on atherogenic indices, liver function tests, and grade of disease in patients with NAFLD. One-hundred twenty NAFLD patients were randomized in a double-blind, placebo-controlled clinical trial as follows: D (1000 IU vitamin D), CaD (500 mg as calcium carbonate plus 1000 IU vitamin D) or P (placebo), once daily with meals over 12 weeks. Adjusted for all the baseline measures, reduction in serum ALT, AST, LDL-C/HDL-C, TC/HDL-C, and non-HDL-C were significantly higher in the CaD compared with the P group ( < 0.001, = 0.03, < 0.001, < 0.001, < 0.001 and < 0.001, respectively). Also, mean difference of serum ALT, LDL-C/HDL-C, TC/HDL-C, and TG/HDL-C were significantly higher in the CaD than D group ( < 0.001, = 0.006, < 0.001 and = 0.03, respectively). Serum non-HDL-C was marginally decreased in the CaD compared with the D group ( = 0.06). With considering the BMI changes as covariate, reduction in the grade of fatty liver was significantly higher in the CaD and D groups than the P ( < 0.001). The present study suggests that supplemental calcium combined with vitamin D, but not vitamin D alone, may reduce serum atherogenic indices, liver function tests, and grade of disease in patients with NAFLD.
Sprache
Englisch
Identifikatoren
ISSN: 1735-0328
eISSN: 1726-6890
Titel-ID: cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_6487410
Format
Schlagworte
Original

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