首页> 外文期刊>Journal of Diabetes and Metabolic Disorders >Lifestyle and silymarin: a fight against liver damage in NAFLD associated - prediabetic disease
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Lifestyle and silymarin: a fight against liver damage in NAFLD associated - prediabetic disease

机译:生活方式和西里马林:反对肝脏损伤的抗肝脏损伤 - 预脂肪疾病

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BackgroundNonalcoholic fatty liver disease (NAFLD) is common in both prediabetic patients and healthy overweight individuals, yet it remains understudied. This study investigates the effects of hepatic steatosis on fibrosis and evaluates the major predictors of liver injury in prediabetes and whether this damage is reversible with Mediterranean diet and administration of the nutraceutical silymarin.MethodsFirst, a case-control study was conducted in which 212 patients with prediabetes, not known to have NAFLD, and 126 healthy controls underwent clinical evaluation, transient elastography with measurement of liver stiffness (LS) and controlled attenuation parameter (CAP). Subsequently, the 212 prediabetic patients were enrolled into a prospective randomized interventional study: 104 were allocated to Mediterranean diet alone while 108 followed Mediterranean diet plus supplementation with silymarin (a flavonolignan complex isolated from Silybum marianum and Morus alba ). The administered silymarin dose was 210?mg twice daily for 6?months. Clinical and instrumental evaluations were repeated at the end of the 6?month-study period. Prediabetics were genotyped for patatin like phospholipase domain containing 3 (PNPLA3).ResultsIn the case-control study, 29% of prediabetic patients have significant fibrosis defined as LS?≥?7.9?kPa vs only 3% of controls ( p ?0.001). PNPLA3 genotype CG/GG are significantly associated with significant fibrosis LS?≥?7.9 relative to CC genotype χ2(1)?=?76.466, p ?0.001. Binomial regression analysis shows that increase in BMI, ALT and AST are significantly associated with increased likelihood of significant fibrosis (χ2(7)?=?191.9, p ?.001) prior to intervention. In the randomized interventional study, prediabetics following Mediterranean diet alone (group 1) experienced a significant regression of fibrosis and decrease in ALT, HbA1c, FBS after 6?months ( p ?0.001); similar findings were observed in patients following Mediterranean diet plus silymarin regimen (group 2); group 2 had a significant decrease in HbA1c relative to group 1 (95% CI: 37.8–38.6 vs 39.5–40.3, p ?0.001).ConclusionPNPLA3 genotype CG/GG and elevated BMI are the major predictors of significant fibrosis in prediabetic patients prior to intervention in this study. Mediterranean diet either alone or with silymarin treatment for 6?months leads to significant regression of liver damage and improvement of the glycemic profile in prediabetic patients. Yet, as combination treatment of silymarin with Mediterranean diet shows significant reduction of HbA1c when compared to diet alone, this suggests that silymarin may exert an independent anti-glycemic action.
机译:背景下酒精性脂肪性肝病(NAFLD)在预先奶油病患者和健康的超重个体中是常见的,但它仍然被解读。本研究调查了肝脏脂肪变性对纤维化的影响,并评估肝损伤的主要预测因子,以及这种损害是否与地中海饮食和Nutraceutical Silymarin的施用是可逆的。方法对案例对照研究,其中212例患者进行了一种案例对照研究PrediaBetes,未知有NAFLD,126个健康对照接受临床评价,瞬态弹性显影,测量肝硬化(LS)和受控衰减参数(帽)。随后,212名预奶脂乳患者注册到前瞻性随机介入研究中:104单独分配给地中海饮食,而108次遵循地中海饮食加上西米林(来自Silvonolignan综合的黄酮醇和Morus Alba分离)。施用的体米素剂量为210μm,每天两次,6?个月。在6个月级研究期结束时重复临床和乐器评估。 ProTiaBetics对含有3(PNPLA3)的磷脂酶结构域等磷脂酶结构域进行基因分型。案例对照研究,29%的预奶粉患者具有显着的纤维化,定义为LS?≥?7.9?KPA仅3%的控制(P <0.001) 。 pnpla3基因型cg / gg与显着的纤维化Ls有显着相关,相对于Cc基因型χ2(1)?=α76.466,p <0.001。二项式回归分析显示BMI,ALT和AST的增加与在干预之前的显着纤维化的可能性增加(χ2(7)?= 191.9,P <β.001)。在随机介入研究中,单独的地中海饮食后的前脂肪病(第1组)在6?月后纤维化和ALT,HBA1C,FBS减少的显着回归(P <0.001);在地中海饮食加上西米蓟素方案(第2组)后患者观察到类似的发现;第2组相对于第1组的HBA1C的显着降低(95%CI:37.8-38.6 Vs 39.5-40.3,P <0.001).Conclusionpnpla3基因型CG / GG和升高的BMI是预先抗脂患者的主要纤维化的主要预测因子干预本研究。地中海饮食单独或用西米兰林治疗6?个月导致肝脏损伤的显着回归和预先奶油病患者的血糖性概况。然而,随着Silymarin的组合治疗与地中海饮食的表现出与单独的饮食相比,HBA1C的显着减少,这表明西米兰林可能施加独立的抗血糖作用。

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