《绿茶对肥胖人群脂质代谢的影响》

  • 来源专题:食物与营养
  • 编译者: lixiaoman
  • 发布时间:2017-07-05
  • 范围:绿茶对脂质代谢的影响不一致。荟萃分析的目的是评估绿茶对肥胖人群脂质代谢的影响。

    方法和结果:我们搜索比较了PUBMED和WEB OF SCIENCE(1990年1月至2016年9月)、COCHRANE和EMBASE(2016年10月更新)和中国数据库CNKI、万方和中国数据库关于绿茶的随机对照试验的文章。选择了21篇研究1704例超重或肥胖受试者的文章进行荟萃分析。结果表明,绿茶显着降低超重或肥胖人群的血浆总胆固醇(TC)和低密度脂蛋白胆固醇(LDL)水平。

    结论:荟萃分析显示饮用绿茶可以显着降低血浆TC和LDL水平。然而,绿茶对血浆TG和HDL的影响必须通过额外的高质量和大规模的实验进一步评估。

相关报告
  • 《肥胖和脂代谢性别差异的遗传基础》

    • 来源专题:食物与营养
    • 编译者:niexiuping
    • 发布时间:2017-11-30
    • 男性和女性在肥胖,心血管疾病和糖尿病方面表现出显着差异。为了给两性提供更好的诊断和治疗,重要的是确定观察到的性别差异的基础因素。传统上,性别差异归因于男性和女性性腺分泌物(通常称为性激素)的不同作用,这实质上影响代谢和相关疾病的许多方面。作为性别差异的贡献者,较少被赞赏是男性和女性之间基本的遗传差异,其最终由存在XX或XY性染色体补体决定。在这里,我们回顾了性腺激素和性染色体补体各自有助于脂质代谢和相关疾病的机制,以及目前用于研究它们的方法。我们特别关注遗传方法,包括人类和小鼠的全基因组关联研究,组织学和系统遗传学方法,以及独特的实验性小鼠模型,可以区分性腺和性染色体的影响
  • 《对超重和肥胖的绝经后妇女随机对照试验证明,绿茶提取物和COMT基因型可改变空腹血清胰岛素和血浆脂联素浓度》

    • 来源专题:食物与营养
    • 编译者:潘淑春
    • 发布时间:2016-03-23
    • Abstract. Background: Green tea consumption has been associated with favorable changes in body weight and obesity-related hormones, although it is not known whether these changes result from green tea polyphenols or caffeine. Objective: We examined the impact of decaffeinated green tea extract (GTE) containing 843 mg of (−)-epigallocatechin-3-gallate on anthropometric variables, obesity-associated hormones, and glucose homeostasis. Methods: The Minnesota Green Tea Trial was a 12-mo randomized, double-blind, placebo-controlled clinical trial of 937 healthy postmenopausal women assigned to either decaffeinated GTE (1315 mg total catechins/d) or a placebo, stratified by catechol-O-methyltransferase (COMT) genotype. This study was conducted in a subset of 237 overweight and obese participants [body mass index (BMI) ≥25 kg/m2]. Results: No changes in energy intake, body weight, BMI, or waist circumference (WC) were observed over 12 mo in women taking GTE (n = 117) or placebo (n = 120). No differences were seen in circulating leptin, ghrelin, adiponectin, or glucose concentrations at month 12. Participants randomly assigned to GTE with baseline insulin ≥10 μIU/mL (n = 23) had a decrease in fasting serum insulin from baseline to month 12 (−1.43 ± 0.59 μIU/mL), whereas those randomly assigned to placebo with baseline insulin ≥10 μIU/mL (n = 19) had an increase in insulin over 12 mo (0.55 ± 0.64 μIU/mL, P < 0.01). Participants with the homozygous high-activity (G/G) form of COMT had significantly lower adiponectin (5.97 ± 0.50 compared with 7.58 ± 0.53 μg/mL, P = 0.03) and greater insulin concentrations (7.63 ± 0.53 compared with 6.18 ± 0.36 μIU/mL, P = 0.02) at month 12 compared with those with the low-activity (A/A) genotype, regardless of treatment group. Conclusions: Decaffeinated GTE was not associated with reductions in body weight, BMI, or WC and did not alter energy intake or mean hormone concentrations in healthy postmenopausal women over 12 mo. GTE decreased fasting insulin concentrations in those with elevated baseline fasting concentrations. The high-activity form of the COMT enzyme may be associated with elevations in insulin and a reduction in adiponectin concentrations over time. This trial was registered at http://www.clinicaltrials.gov as NCT00917735. .