Background: The prevalence of overweight and obese individuals has dramatically risen over the past 30 years and represents a major threat to public health. Sugars consumed in liquid form (i.e. SSBs) have been targeted as a prominent contributor towards obesity. Pooled analyses of acute preload trials that have assessed food intake as the primary outcome suggest that liquid calories from sugars are more poorly compensated than solid calories. Though tempting, results from these acute studies should not be extrapolated to infer that liquid energy sources lead to weight gain over the long term. A study of long-term randomized controlled trials by Kaiser et al. found that when adults were required to consume sugar sweetened beverages (SSBs) as an additional source of energy, dose-dependent weight gain was observed. However, this weight gain was far less than half the amount one would have predicted to be gained using a mathematical model. This suggests that over extended periods of time, majority of the energy consumed as SSBs is indeed compensated for.
Need for proposed research: To date, it is unknown whether people compensate differently for liquid versus solid sources of calories over the long term.
Objective: To synthesize evidence of the effect of liquid calories versus solid calories on body weight in controlled trials.
Design: This systematic review and meta-analysis will be conducted according to the Cochrane Handbook for Systematic Reviews of Interventions and reported according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA).
Data sources: MEDLINE, EMBASE, and The Cochrane Central Register of Controlled Trials (Clinical Trials; CENTRAL) will be searched using appropriate search terms supplemented by hand searches of references of included studies.
Study selection: The investigators will include controlled trials (randomized and non-randomized) that have compared the effects of liquid sources of calories in isocaloric exchange for solid sources of calories on body weight for \>= 7 days in humans (healthy or non-healthy).
Data extraction: Following systematic exclusion based on title and abstract, 2 reviewers will independently review and extract relevant data from each report that meets the inclusion criteria. Risk of bias will be assessed using the Cochrane Risk of Bias Tool. All disagreements among reviewers were resolved by consensus. Missing variance data will be calculated using standard computations and imputations.
Outcomes: Body weight (kg)
Data synthesis: Pooled analyses of the mean difference will be performed using the generic inverse variance method. Random-effects models will be used even in the absence of statistically significant between-study heterogeneity because they yield more conservative summary effect estimates in the presence of residual heterogeneity. Fixed-effects models will be used only if there are less than 5 included trials. Crossover trials will be assessed via paired analyses. Heterogeneity will be assessed by the Cochran Q statistic and quantified by the I2 statistic. Sensitivity and subgroup analyses will be conducted to identify sources of heterogeneity. Sensitivity analyses will involve an assessment of heterogeneity upon systematic removal of each trial. If there are \>= 10 trials, the study investigators will conduct apriori subgroup analyses by age, health status, comparator, dose, baseline measurements, randomization, study design (parallel, crossover), energy balance (positive, neutral, negative), follow-up (\<= 4 weeks, \> 4 weeks) and risk of bias. Meta-regression analyses will assess the significance of categorical and continuous subgroup analyses. When more than 10 trials are available, publication bias will be investigated by funnel plots and formal testing using Egger and Begg tests. If publication bias is suspected, then the investigators will attempt to adjust for funnel plot asymmetry by imputing the missing study data using the Duval and Tweedie trim and fill method.
Evidence assessment: The strength of the evidence for each outcome will be assessed using the Grading of Recommendations Assessment, Development and Evaluation (GRADE).
Knowledge translation plan: The results will be disseminated through interactive presentations at local, national, and international scientific meetings and publication in high impact factor journals. Target audiences will include the public health and scientific communities with interest in nutrition and obesity. Feedback will be incorporated and used to improve the public health message and key areas for future research will be defined. Applicant/Co-applicant Decision Makers will network among opinion leaders to increase awareness and participate directly as committee members in the development of future guidelines.
Significance: The proposed research will aid in distinguishing the role of liquid calories from solid calories on body weight over the long-term. This will strengthen the evidence-base for guidelines and improve health outcomes by educating healthcare providers and patients, stimulating industry innovation, and guiding future research design.
