Abstract

This study assessed the effects of curcumin intake on psychological status, markers of inflammation and oxidative damage in patients with type 2 diabetes mellitus (T2DM) and coronary heart disease (CHD). This randomized, double-blind, placebo-controlled trial was performed in 60 patients with T2DM and CHD, aged 45-85 years with 2- and 3-vessel CHD. Patients were randomized into two groups to receive either 1000mg/day curcumin (n=30) or placebo (n=30) for 12 weeks. Using RT-PCR method, gene expression related to insulin metabolism and inflammatory markers on mononuclear cells from peripheral blood was evaluated. Curcumin intake significantly decreased Pittsburgh Sleep Quality Index (PSQI) (β-1.27; 95% CI,-2.27,-0.31; P=0.01) compared to the placebo group. Curcumin intake caused a significant reduction in malondialdehyde (MDA) (β-0.20μmol/L; 95% CI,-0.36,-0.04; P=0.01), significant increase in total antioxidant capacity (TAC) (β 75.82mmol/L; 95% CI, 3.400, 148.25; P=0.04) and glutathione (GSH) levels (β 63.48μmol/L; 95% CI, 26.58, 100.37; P=0.001) when compared with the placebo. Additionally, curcumin intake upregulated peroxisome proliferator-activated receptor gamma (PPAR-γ) (P=0.01). Curcumin intake for 12 weeks in patients with T2DM and CHD had beneficial effects on PSQI, TAC, GSH, MDA values, and gene expression of PPAR-γ. This study was retrospectively registered in the Iranian website (www.irct.ir) for registration of clinical trials (http://www.irct.ir: IRCT20170513033941N63).

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