Table 1.
PICOS | Inclusion and exclusion criteria | Data extraction |
---|---|---|
Participants |
Adult population’s ≥ 18 and ≤ 65 y with or without disease. Studies with a median age between these values were eligible. Participants with mean age ≤ 18 y or nonclinical studies were excluded. |
Age, sex, gender, sample size, location, inclusion and exclusion criteria |
Intervention | Resistant Starch defined as “resistant maltodextrin”, “resistant dextrin”, “indigestible starch”, “high amylose starch” or any other compound defined by the author as a resistant starch if justification for the compound fulfilling criteria as a resistant starch were explicitly stated. Resistant starch to be administered at a dose of ≥10 g/day for ≥3 wk. Trials that included other interventions (e.g., drug use) were included if the effect of the resistant sarch alone could be isolated. Multiple intervention arms were eligible. | Resistant Starch type, placebo type, intervention and placebo dosage, duration of intervention |
Comparators |
Only studies with control group were included, The effect of the Resistant starch alone had to be able to be isolated. |
Type and dose of comparator, compliance |
Outcomes | Mean changes and SD in IL-6, CRP, hs-CRP and TNF-α | Outcomes measured, Evaluation methods and side effects. |
Study design | Only randomized controlled trials, where it was possible to extract data on just the resistant starch compared with to placebo. We included both the parallel and crossover design | Design of the study, loss of the study, study quality |
a PICOS, participants, intervention, comparator, outcome, study type