Pan · Frontiers in nutrition 2026 · systematic review of randomized controlled trials · n=20 studies

Curcumin-piperine supplementation modulates inflammation, oxidative stress, and cardiometabolic risk: a systematic review of randomized controlled trials.

Cited 0 times in the scientific literature.

Level 1 - systematic review of randomized trials

Systematic review of randomized controlled trials

PubMed 42232574 · doi:10.3389/fnut.2026.1814168 · record verified 2026-08-28

What was done

A systematic review was conducted across major electronic databases through 2026 to evaluate randomized controlled trials (RCTs) assessing oral curcumin in combination with piperine. Eligible studies reported outcomes related to oxidative stress, inflammation, metabolism, cardiovascular disease, or clinical symptoms across various health conditions. Methodological risk of bias was assessed for all included studies.

What was found

Twenty RCTs were included, with sample sizes ranging from 8 to 117 participants and study durations ranging from 1 to 12 weeks. Dosages ranged from 500 to 1,500 mg/day for curcumin and 5 to 15 mg/day for piperine. Significant reductions in inflammatory markers (CRP, hs-CRP, IL-6) were reported in 15 of 20 trials, and improvements in oxidative stress markers (SOD, TAC, MDA) were observed in 12 of 15 trials. Fasting blood glucose, HbA1c, and HOMA-IR decreased in metabolic syndrome and type 2 diabetes populations, while 14 of 18 trials reported reductions in lipid markers. Decreases in cardiac biomarkers (CK-MB, AST, ALT) occurred in post-CABG and acute myocardial infarction cohorts, and symptom improvements were reported for COVID-19, PMS, dysmenorrhea, and chronic pulmonary disease. No significant adverse events were reported. Thirteen trials had low risk of bias and 6 had moderate risk. The abstract provided no pooled effect sizes or confidence intervals.

Why it matters

Co-administration with piperine overcomes curcumin's low bioavailability, providing consistent multi-system biomarker improvements across diverse inflammatory and cardiometabolic conditions in short-term randomized trials.

Limits

Individual included trials were small (maximum 117 participants, minimum 8) and brief (1 to 12 weeks). Dosages and patient populations were heterogeneous, outcomes relied heavily on surrogate laboratory markers rather than hard clinical endpoints, and findings in the abstract are presented via vote counting rather than quantitative meta-analysis.

Cited by