Monash Centre for Health Research and Implementation, School of Public Health and Preventive Medicine, Monash University, Melbourne, VIC 3168, Australia; Diabetes and Vascular Medicine Unit, Monash Health, Melbourne, VIC 3168, Australia.
Monash Centre for Health Research and Implementation, School of Public Health and Preventive Medicine, Monash University, Melbourne, VIC 3168, Australia.
J Steroid Biochem Mol Biol. 2018 Mar;177:193-199. doi: 10.1016/j.jsbmb.2017.09.009. Epub 2017 Sep 9.
Vitamin D deficiency is prevalent in individuals with non-alcoholic fatty liver disease (NAFLD) and non-alcoholic steatohepatitis. However, there is limited and inconsistent data on the effect of vitamin D supplementation on liver function. Hepatic enzymes have been used as surrogate markers for NAFLD and have been associated with metabolic syndrome. We examined the relationships between 25-hydroxyvitamin D (25(OH)D) and γ-glutamyl transferase (GGT), alanine aminotransferase (ALT), alkaline phosphatase (ALP) in 120 drug-naïve individuals with no history of liver disease. In addition, the effect of vitamin D supplementation (100,000 loading dose of cholecalciferol followed by 4000IU daily for 16 weeks) on hepatic enzymes was investigated in a subgroup of 54 vitamin D-deficient overweight or obese individuals (28 randomised to cholecalciferol and 26 to placebo). Hepatic enzymes, anthropometric parameters, lipid profile, insulin sensitivity (hyperinsulinaemic-euglycaemic clamp, M value) and high sensitivity C-reactive protein (hs-CRP) were measured before and after the intervention. In the cross-sectional study, levels of GGT and ALT were higher in men compared to women (both p=0.001). There were no significant differences in GGT, ALT and ALP between vitamin D categories (25(OH)D<25nmol/L, 25-50nmol/L, and >50nmol/L) and no relationships were found between the three enzymes and 25(OH)D before and after adjustment for age, sex, BMI, WHR, and insulin sensitivity (all p>0.5). In the randomised trial, 25(OH)D concentrations increased in the vitamin D group (mean change 57.0±21.3nmol/L) compared to the placebo group (mean change 1.9±15.1nmol/L). Mean changes in GGT, ALT and ALP were not significantly different between vitamin D and placebo groups (all p>0.2). Change in 25(OH)D concentration was not correlated with changes in GGT, ALT and ALP before and after adjustments for age and sex (all p>0.1). In summary, 25(OH)D concentrations were not related to hepatic enzymes in drug-naive adults with no history of liver disease, and vitamin D supplementation had no effect on the serum levels of hepatic enzymes in vitamin D-deficient and overweight or obese, otherwise healthy individuals. Hence, vitamin D supplementation is unlikely to prevent incident NAFLD.
维生素 D 缺乏症在非酒精性脂肪性肝病(NAFLD)和非酒精性脂肪性肝炎患者中很常见。然而,关于维生素 D 补充对肝功能的影响的数据有限且不一致。肝酶已被用作 NAFLD 的替代标志物,并与代谢综合征相关。我们在 120 名无肝病病史的药物未治疗的个体中检查了 25-羟维生素 D(25(OH)D)和γ-谷氨酰转移酶(GGT)、丙氨酸氨基转移酶(ALT)、碱性磷酸酶(ALP)之间的关系。此外,在 54 名维生素 D 缺乏症超重或肥胖个体(28 名随机分配接受胆钙化醇治疗,26 名接受安慰剂治疗)的亚组中,研究了维生素 D 补充(100,000 单位胆钙化醇负荷剂量,随后每天 4000IU,持续 16 周)对肝酶的影响。在干预前后测量了肝酶、人体测量参数、血脂谱、胰岛素敏感性(高胰岛素-正常血糖钳夹,M 值)和高敏 C 反应蛋白(hs-CRP)。在横断面研究中,男性的 GGT 和 ALT 水平高于女性(均 p=0.001)。25(OH)D 水平<25nmol/L、25-50nmol/L 和>50nmol/L 三组之间的 GGT、ALT 和 ALP 无显著差异,且在调整年龄、性别、BMI、腰臀比和胰岛素敏感性后,三种酶与 25(OH)D 之间无相关性(均 p>0.5)。在随机试验中,与安慰剂组相比,维生素 D 组 25(OH)D 浓度升高(平均变化 57.0±21.3nmol/L),而安慰剂组(平均变化 1.9±15.1nmol/L)。维生素 D 组和安慰剂组的 GGT、ALT 和 ALP 变化无显著差异(均 p>0.2)。在调整年龄和性别后,25(OH)D 浓度的变化与 GGT、ALT 和 ALP 的变化无相关性(均 p>0.1)。总之,在无肝病病史的药物未治疗的成年患者中,25(OH)D 浓度与肝酶无关,维生素 D 补充对维生素 D 缺乏症和超重或肥胖的健康个体的血清肝酶水平没有影响。因此,维生素 D 补充不太可能预防非酒精性脂肪性肝病的发生。