Suppr超能文献

短期碳水化合物过度喂养和长期减肥对超重人群肝脏脂肪的影响。

Effect of short-term carbohydrate overfeeding and long-term weight loss on liver fat in overweight humans.

机构信息

Minerva Foundation Institute for Medical Research, Helsinki, Finland.

出版信息

Am J Clin Nutr. 2012 Oct;96(4):727-34. doi: 10.3945/ajcn.112.038695. Epub 2012 Sep 5.

Abstract

BACKGROUND

Cross-sectional studies have identified a high intake of simple sugars as an important dietary factor predicting nonalcoholic fatty liver disease (NAFLD).

OBJECTIVE

We examined whether overfeeding overweight subjects with simple sugars increases liver fat and de novo lipogenesis (DNL) and whether this is reversible by weight loss.

DESIGN

Sixteen subjects [BMI (kg/m²): 30.6 ± 1.2] were placed on a hypercaloric diet (>1000 kcal simple carbohydrates/d) for 3 wk and, thereafter, on a hypocaloric diet for 6 mo. The subjects were genotyped for rs739409 in the PNPLA3 gene. Before and after overfeeding and after hypocaloric diet, metabolic variables and liver fat (measured by proton magnetic resonance spectroscopy) were measured. The ratio of palmitate (16:0) to linoleate (18:2n-6) in serum and VLDL triglycerides was used as an index of DNL.

RESULTS

Carbohydrate overfeeding increased weight (±SEM) by 2% (1.8 ± 0.3 kg; P < 0.0001) and liver fat by 27% from 9.2 ± 1.9% to 11.7 ± 1.9% (P = 0.005). DNL increased in proportion to the increase in liver fat and serum triglycerides in subjects with PNPLA3-148IIbut not PNPLA3-148MM. During the hypocaloric diet, the subjects lost 4% of their weight (3.2 ± 0.6 kg; P < 0.0001) and 25% of their liver fat content (from 11.7 ± 1.9% to 8.8 ± 1.8%; P < 0.05).

CONCLUSIONS

Carbohydrate overfeeding for 3 wk induced a >10-fold greater relative change in liver fat (27%) than in body weight (2%). The increase in liver fat was proportional to that in DNL. Weight loss restores liver fat to normal. These data indicate that the human fatty liver avidly accumulates fat during carbohydrate overfeeding and support a role for DNL in the pathogenesis of NAFLD. This trial was registered at www.hus.fi as 235780.

摘要

背景

横断面研究已经确定,高摄入量的简单糖是预测非酒精性脂肪性肝病(NAFLD)的一个重要饮食因素。

目的

我们研究了超重者摄入简单糖是否会导致肝脏脂肪和从头脂肪生成(DNL)增加,以及体重减轻是否可以逆转这种情况。

设计

16 名受试者[BMI(kg/m²):30.6±1.2]接受了 3 周的高热量饮食(>1000 千卡简单碳水化合物/天),此后接受了 6 个月的低热量饮食。受试者的 PNPLA3 基因 rs739409 进行了基因分型。在过量喂养前后和低热量饮食后,测量代谢变量和肝脏脂肪(通过质子磁共振波谱法测量)。血清和 VLDL 甘油三酯中棕榈酸(16:0)与亚油酸(18:2n-6)的比值用作 DNL 的指标。

结果

碳水化合物过量喂养使体重增加了 2%(1.8±0.3kg;P<0.0001),肝脏脂肪增加了 27%,从 9.2±1.9%增加到 11.7±1.9%(P=0.005)。在 PNPLA3-148II 但不是 PNPLA3-148MM 受试者中,DNL 与肝脏脂肪和血清甘油三酯的增加成正比。在低热量饮食期间,受试者体重减轻了 4%(3.2±0.6kg;P<0.0001),肝脏脂肪含量减少了 25%(从 11.7±1.9%降至 8.8±1.8%;P<0.05)。

结论

3 周的碳水化合物过量喂养导致肝脏脂肪的相对变化(27%)比体重增加(2%)大 10 倍以上。肝脏脂肪的增加与 DNL 成正比。体重减轻可使肝脏脂肪恢复正常。这些数据表明,人体脂肪肝在碳水化合物过量喂养期间会大量积累脂肪,并支持 DNL 在 NAFLD 发病机制中的作用。该试验在 www.hus.fi 上注册为 235780。

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验