Abstract
Background: Curcumin-piperine might synergise with vitamin D to induce clinical remission in patients with systemic lupus erythematosus (SLE).
Objective: To observe the improvement of patients with SLE clinically and the levels of inflammatory cytokines after receiving supplements of curcumin-piperine and cholecalciferol (Vitamin D3).
Methods: Forty-five female SLE patients were included in a three-month double-blind, randomized controlled trial. Participants were classified into: Group I (400 IU cholecalciferol + placebo three times daily, n = 15), Group II (600 mg curcumin + 15,800 m piperine once daily and three times daily placebo, n = 15), and Group III (cholecalciferol 400 IU three times and 600 mg curcumin + 15,800 mg piperine once a day, n = 15). Mexican SLE disease activity score (Mex- SLEDAI), fatigue severity scale (FSS), TGF-β, and IL-6 levels were measured from all patients before and after the treatments.
Results: Mex-SLEDAI, FSS, and IL-6 were reduced significantly, while TGF-β serum levels were increased in all groups after the treatments (p <0.05). Changes in Mex-SLEDAI score (p = 0.003 and p = 0.008), FSS (p = 0.001 and p <0.001), and TGF-β (p = 0.003 and p = 0.004) serum levels were significantly higher in group III compared to the group I or group II. On the other hand, changes in Mex-SLEDAI, FSS, IL-6, and TGF-β serum levels were similar between groups I and II.
Conclusion: Although vitamin D or curcumin-piperine alone could improve the clinical outcome and cytokines levels in SLE, curcumin-piperine combined with vitamin D had the best outcome in improving the disease activity and cytokines levels among patients with SLE. (ClinicalTrials.gov number, NCT05430087).
Graphical Abstract
[http://dx.doi.org/10.1177/0961203319878499] [PMID: 31566078]
[http://dx.doi.org/10.1016/j.autrev.2019.102392] [PMID: 31520805]
[http://dx.doi.org/10.1017/S0029665111001613] [PMID: 21861947]
[http://dx.doi.org/10.3390/ijms21249626] [PMID: 33348854]
[http://dx.doi.org/10.12659/MSM.882131] [PMID: 22129903]
[http://dx.doi.org/10.1186/ar4060] [PMID: 23075451]
[http://dx.doi.org/10.1002/art.39108] [PMID: 25777546]
[http://dx.doi.org/10.5935/0101-2800.20140062] [PMID: 25517270]
[http://dx.doi.org/10.1093/rheumatology/ker212] [PMID: 21719424]
[http://dx.doi.org/10.1177/1099800420983596] [PMID: 33380211]
[http://dx.doi.org/10.1016/j.amjms.2019.04.020] [PMID: 31331447]
[http://dx.doi.org/10.1016/j.intimp.2019.01.046] [PMID: 30738291]
[http://dx.doi.org/10.1016/j.autrev.2017.11.016] [PMID: 29180127]
[http://dx.doi.org/10.3390/app10124096]
[http://dx.doi.org/10.1016/j.jnutbio.2009.09.012] [PMID: 20153625]
[http://dx.doi.org/10.1177/1179573520924311] [PMID: 32528227]
[http://dx.doi.org/10.1186/s12906-022-03515-2] [PMID: 35065636]
[http://dx.doi.org/10.1155/2017/7687053] [PMID: 29445400]
[http://dx.doi.org/10.3109/1061186X.2016.1157883] [PMID: 26942997]
[http://dx.doi.org/10.1002/ptr.6855] [PMID: 32929825]
[http://dx.doi.org/10.1055/s-2006-957450] [PMID: 9619120]
[http://dx.doi.org/10.1136/annrheumdis-2018-214819] [PMID: 31383717]
[PMID: 15468356]
[http://dx.doi.org/10.1186/s41927-021-00223-1] [PMID: 34857051]
[http://dx.doi.org/10.55374/jseamed.v4i1.57]
[http://dx.doi.org/10.4103/1735-1995.199089] [PMID: 28400826]
[http://dx.doi.org/10.3390/nu10101553] [PMID: 30347782]
[http://dx.doi.org/10.1177/0961203311425530] [PMID: 22004972]
[http://dx.doi.org/10.1111/1756-185X.14505]
[http://dx.doi.org/10.1002/acr.22621] [PMID: 25988278]
[PMID: 25071589]
[http://dx.doi.org/10.2147/DDDT.S327378] [PMID: 34754179]
[http://dx.doi.org/10.1007/s12026-016-8829-3] [PMID: 27423437]
[http://dx.doi.org/10.5114/ceji.2015.56970] [PMID: 26862311]
[http://dx.doi.org/10.4103/injr.injr_95_16]
[http://dx.doi.org/10.1007/s00784-018-2755-9] [PMID: 30498979]