Long-term vitamin D and high-dose n-3 fatty acids’ supplementation improve markers of cardiometabolic risk in type 2 diabetic patients with CHD
What this study found
Co-supplementation with vitamin D and n-3 fatty acids produced beneficial effects on cardiometabolic risk markers. Compared with placebo, carotid intima-media thickness decreased on the left mean (P = 0.01) and maximum (P = 0.004) and on the right mean (P = 0.02) and maximum (P = 0.003). Serum 25(OH)D increased (P < 0.001), while fasting plasma glucose (P = 0.03), insulin (P < 0.001), HOMA-IR (P < 0.001), LDL-cholesterol (P = 0.04), total-/HDL-cholesterol (P = 0.01), and hs-CRP (P = 0.005) decreased; QUICKI (P = 0.001) and HDL-cholesterol (P = 0.02) increased. Plasma total nitrite did not…
- Study & population
- Single-center randomized placebo-controlled trial in vitamin D-deficient adults with type 2 diabetes mellitus and coronary heart disease in Kashan, Iran.
- Intervention
- The active regimen combined vitamin D 50,000 IU every 2 weeks with n-3 fatty acids from flaxseed oil, 2 capsules daily of 1000 mg each for a total of 2000 mg/day.
- Key limitation
- The trial was small, single-center, and only 6 months long, which limits precision and long-term interpretation.
Original abstract
Abstract This study was performed to evaluate the effects of vitamin D and n-3 fatty acids’ co-supplementation on markers of cardiometabolic risk in diabetic patients with CHD. This randomised, double-blinded, placebo-controlled trial was conducted among sixty-one vitamin D-deficient diabetic patients with CHD. At baseline, the range of serum 25-hydroxyvitamin D levels in study participants was 6·3–19·9 ng/ml. Subjects were randomly assigned into two groups either taking 50 000 IU vitamin D supplements every 2 weeks plus 2× 1000 mg/d n-3 fatty acids from flaxseed oil (n 30) or placebo (n 31) for 6 months. Vitamin D and n-3 fatty acids’ co-supplementation significantly reduced mean (P = 0·01) and maximum levels of left carotid intima–media thickness (CIMT) (P = 0·004), and mean (P = 0·02) and maximum levels of right CIMT (P = 0·003) compared with the placebo. In addition, co-supplementation led to a significant reduction in fasting plasma glucose (β −0·40 mmol/l; 95 % CI −0·77, −0·03; P = 0·03), insulin (β −1·66 μIU/ml; 95 % CI −2·43, −0·89; P < 0·001), insulin resistance (β −0·49; 95 % CI −0·72, −0·25; P < 0·001) and LDL-cholesterol (β −0·21 mmol/l; 95 % CI −0·41, −0·01; P = 0·04), and a significant increase in insulin sensitivity (β +0·008; 95 % CI 0·004, 0·01; P = 0·001) and HDL-cholesterol (β +0·09 mmol/l; 95 % CI 0·01, 0·17; P = 0·02) compared with the placebo. Additionally, high-sensitivity C-reactive protein (β −1·56 mg/l; 95 % CI −2·65, −0·48; P = 0·005) was reduced in the supplemented group compared with the placebo group. Overall, vitamin D and n-3 fatty acids’ co-supplementation had beneficial effects on markers of cardiometabolic risk.