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临床试验/NCT04133805
NCT04133805Unknown不适用

The Effect of Viscous Dietary Fibers on LDL-cholesterol: A Systematic Review and Meta-analysis of Randomized Controlled Trials

Unity Health Toronto1 个研究点 分布在 1 个国家目标入组 7,845 人开始时间: 2018年9月17日最近更新:
适应症

试验速览

阶段
不适用
入组人数
7,845
试验地点
1
主要终点
LDL-Cholesterol

研究概览

简要总结

This systematic review and meta-analysis is aimed to assess the effect of commonly consumed viscous fibers on blood lipids including LDL-C, non-HDL-C, and ApoB.

详细描述

Medline, Embase, CINAHL, and the Cochrane Central databases were searched through May 13, 2019. Three independent reviews extracted data and assessed risk of bias. Randomized controlled trials that assessed the effect of barley b-glucan, oat b-glucan, konjac glucomannan (KJM), psyllium, guar gum, and pectin, with a study duration of ≥ 3 weeks, in adults with or without hypercholesterolemia were included. Data were pooled using the generic inverse variance method with random effects models and expressed as mean differences with 95% confidence intervals. Heterogeneity was assessed by the Cochran Q statistic and quantified by I2 statistic. Overall quality of the evidence was assessed using the GRADE (Grading of Recommendations Assessment, Development, and Evaluation) approach.

研究设计

研究类型
Observational
观察模型
Other
时间视角
Other

入排标准

年龄范围
18 Years 至 —(Adult, Older Adult)
性别
All
接受健康志愿者

入选标准

  • Must be a randomized controlled clinical trial with either a parallel or cross-over design
  • have a treatment period of at least 3 weeks
  • Hypercholesterolemic or normocholesterolemic adults, overweight and obese individuals or individuals with diabetes were all acceptable
  • Sources from β-glucan oats, β-glucan barley, konjac, psyllium, guar gum, and pectin were accepted
  • The amount of soluble fiber must be reported or measured or must be computable.
  • Must be appropriately controlled.
  • Must measure one of LDL-C, non-HDL-C or ApoB. These lipid measures can be either primary or secondary outcomes.
  • Enough information must be provided to calculate the magnitude of effect, i.e. end of treatment measures and/or change from baseline measures

排除标准

  • If the study was insufficiently controlled, i.e. the control was another soluble fiber
  • If the soluble fiber was a combination supplement or in whole food sources where the amount of soluble fiber could not be isolated
  • If the outcome measures did not include LDL-C, non-HDL-C or ApoB
  • If the treatment period was less than 3 weeks
  • If the study was from a non-adult population
  • If the study provided insufficient information to calculate a magnitude of effect
  • Secondary information such as reviews, editorials, commentaries, were excluded
  • If the dose was less than 0.4g/day

结局指标

主要结局

LDL-Cholesterol

时间窗: ≥ 3 weeks

次要结局

  • ApoB(≥ 3 weeks)
  • non-HDL-Cholesterol(≥ 3 weeks)

研究者

申办方类型
Other
责任方
Sponsor

研究点 (1)

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