Hypercholesterolemia Clinical Trial
Official title:
The Effect of Psyllium Fibre (Plantago Ovata) on LDL-cholesterol and Emerging Lipid Targets, Non-HDL-cholesterol and Apolioprotein-B: A Systematic Review and Meta-analysis of Randomized Controlled Trials
Serum cholesterol is a major modifiable risk factor for cardiovascular disease, which despite considerable reduction in prevalence, remains the leading cause of premature mortality worldwide. Although LDL-C continues to be recognized as the primary therapeutic target, accumulating evidence suggests that alternative lipid parameters, non-HDL-C and apoB, may provide predictive value beyond that of LDL-C alone, in most population categories. Numerous lifestyle strategies have been developed to manage elevated cholesterol concentrations, of which viscous fibre is often encouraged for its beneficial effects on LDL-C reduction. Conversely, the effects of viscous fibre on new lipid markers, non-HDL and apoB, have yet to be defined. Therefore, this study seeks to elucidate the therapeutic potential of psyllium fibre on totality of atherogenic cholesterol and lipoprotein particles in a systematic review and meta-analysis of randomized controlled trials.
Background: Studies have identified viscous dietary fibre as potentially attenuating
cholesterol, including psyllium husk that reduces LDL-cholesterol (LDL-C) thus, may alleviate
cardiovascular disease (CVD) treatment.
Objective: To update evidence on the effect of psyllium on LDL-C, and provide assessment of
its impact on new lipid markers: non-HDL cholesterol (non-HDL-C) and apolipoprotein-B (apoB).
Design: Conduct of the systematic review and meta-analysis will follow the Cochrane handbook
for systematic reviews of interventions. The reporting will follow the Preferred Reporting
Items for Systematic reviews and Meta-Analyses (PRISMA) guidelines.
Data Sources & Study Selection: MEDLINE, EMBASE, CINAHL and The Cochrane Central Register of
Controlled Trials will be searched using appropriate search terms. Independent reviewers will
extract information about study design, sample size, subject characteristics, dose,
follow-up, and placebo/compare. RCTs that investigate the effect of psyllium fibre on LDL-C,
non-HDL-C or apoB will be included with a minimum follow-up period ≥ 3 weeks. The amount of
psyllium fibre must be reported and effects on outcomes LDL-C, non-HDL-C or apoB must be
isolatable. Studies detailing sufficient information for non-HDL-C calculation will also be
considered. Unpublished trials are considered and no restriction placed on language.
Outcomes: LDL-C, non-HDL-C, apoB
Data Extraction: Mean±SEM values will be extracted for all outcomes. Standard computations
and imputations will be used to derive missing variance data. Risk of bias and overall study
quality will be assessed using the Cochrane Risk of Bias tool and GRADE approach.
Data Synthesis: Data will be pooled using the generic inverse variance method with random
effects models. Heterogeneity assessed by the Cochran Q-statistic and quantified by I2.
Sensitivity analysis and a priori subgroup analyses will be performed to explore sources of
heterogeneity. A spline curve model (MKSPLINE procedure) will be utilized to illustrate a
non-linear dose-response curve. Publication bias will be investigated by visual inspection of
funnel plots and formally tested using Egger's and Begg's tests. If significant, a Trim and
Fill analyses will be performed.
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