Oralna adjuvantna terapija kurkuminom za postizanje kliničke remisije ulceroznog kolitisa: Sistematski pregled i meta-analiza randomiziranih kontroliranih ispitivanja.
Nutrients
Sažetak istraživanja
Kurkumin je pokazao protuupalna svojstva i istražen je kao pomoćna terapija ulceroznog kolitisa (UC).
Cilj ove studije bio je da sistematski pregleda i meta-analizu efikasnosti oralne primjene kurkumina kao adjuvantne terapije UC. MEDLINE, Cochrane/CENTRAL, ClinicalTrials.gov, WHO-ICT registar, EMBASE i siva literatura su pretraženi za relevantne randomizirane kontrolirane studije (RCT). Primarni ishod je bila klinička remisija (postizanje), a sekundarni ishod je bio klinički odgovor (održavanje/neuspjeh). Rizik od pristrasnosti procijenjen je Cochrane alatom. Odnosi šanse (OR) su izračunati sa Mantel-Haenszelovim (M-H) modelom slučajnih efekata i beta-binomskim (B-B) modelom slučajnih efekata kada se dogodila nula događaja/ćelija. Četiri RCT-a su ispunila kriterije, ali je jedan uklonjen iz analiza zbog nedosljednosti u detaljima protokola. Sa M-H metodom, tretman kurkuminom je bio značajno bolji u odnosu na placebo u postizanju remisije u analizi po protokolu (PP) (OR = 5,83, 95%CI = 1,24⁻27,43), ali ne i u analizi namjere liječenja (ITT) (OR = 4,33, 95,8%CI = 0,40⁻0). Međutim, kod preciznije B-B metode, obje analize su bile beznačajne (za PP OR = 4,26, 95%CI = 0,59⁻31,00, za ITT OR = 3,80, 95%CI = 0,55⁻26,28). Na osnovu trenutno dostupnih dokaza, oralna primjena kurkumina ne izgleda bolja od placeba u postizanju remisije kod pacijenata sa UC. Buduće RCT treba planirati opreznije s dovoljnom veličinom i pridržavati se ITT analize u svim ishodima.
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Oral Adjuvant Curcumin Therapy for Attaining Clinical Remission in Ulcerative Colitis: A Systematic Review and Meta-Analysis of Randomized Controlled Trials.
Curcumin has demonstrated anti-inflammatory properties and has been investigated as an adjuvant therapy of ulcerative colitis (UC). The scope of this study was to systematically review and meta-analyze the efficacy of oral curcumin administration as an adjuvant therapy of UC. MEDLINE, Cochrane/CENTRAL, ClinicalTrials.gov, WHO-ICT Registry, EMBASE and grey literature were searched for relevant randomized controlled trials (RCTs). The primary outcome was clinical remission (attainment) and the secondary outcome was clinical response (maintenance/failure). Risk of bias was assessed with the Cochrane tool. Odds ratios (OR) were calculated with a Mantel-Haenszel (M-H) random effects model and with a beta-binomial (B-B) random effects model when zero events/cells occurred. Four RCTs met the criteria, but one was removed from the analyses due to inconsistency in protocol details. With the M-H method, treatment with curcumin was significantly superior to placebo in attaining remission in the per-protocol (PP) analysis (OR = 5.83, 95%CI = 1.24⁻27.43), but not in the intention-to-treat (ITT) analysis (OR = 4.33, 95%CI = 0.78⁻24.00). However, with the more accurate B-B method, both analyses were insignificant (for PP OR = 4.26, 95%CI = 0.59⁻31.00, for ITT OR = 3.80, 95%CI = 0.55⁻26.28). Based on the current available evidence, oral curcumin administration does not seem superior to placebo in attaining remission in patients with UC. Future RCTs should be planned more cautiously with sufficient size and adhere to the ITT analysis in all outcomes.
Izvorni podaci
- DOI
- 10.3390/nu10111737
- PMID
- 30424514
- PMCID
- PMC6266508
- Provjereno
- 2026-07-26
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