Background Vitamin D has pleiotropic actions on many chronic diseases. Multiple studies have confirmed vitamin D deficiency in patients with systemic lupus erythematosus (SLE). Genetic polymorphisms located in VDR gene and low levels of 25-hydroxyvitamin D (25OHD) may increase the risk of cardiovascular event. The relationship of vitamin D with cardiovascular risk factors in SLE patients have been described, but more studies are needed to further clarification.
Objectives To study the influence of vitamin D on cardiovascular disease in SLE patients.
Methods One hundred eighty-one SLE patients previously studied to investigate the influence of BsmI and FokI VDR gene polymorphisms and serum levels of 25OHD were evaluated for the presence of cardiovascular disease (CVD) defined as stroke,transient ischemic attack (TIA), angina pectoris (AP), myocardial infarction (MI) and arterial thrombosis (AT).
Results The mean age and disease duration were 42.0±13.5 and 9.6±7.6 years, respectively. One hundred and seventy (93.9%) patients was female and 134 (74%) was classified as Euro-derived. Eighteen (9.9%) patients had CVD (10 stroke,1 TIA, 3 AP, 3 MI, 1 AT). There was nostatistically significant difference in genotypic and allelic frequencies of BsmI and FokI polymorphisms among patients with CVD and patients without CVD (18.8% vs.13.5% BB, 50% vs. 51.8% Bb, 32.2% vs. 34.7% bb, p=0.618 and 58.8% vs. 47.2% FF, 29.4% vs. 43.7% Ff, 11.8% vs. 9.2% ff, p=0.591, respectively). The mean serum levels of 25OHD were 25.5±11.4 ng/ml. Patients with CVD had 25OHDlevels similar to patients without CVD (24.3±11.6 ng/ml vs. 25.7±11.4 ng/ml, p=0.638). After adjustment for phototype, ethnicity, age, gender, SLEDAI, antiphospholipid syndrome, smoking status, dyslipidemia, hypertension, body mass index, hydroxychloroquine use, current corticosteroids use and vitamin D supplementation, the 25OHD levels remained similar in both groups.
Conclusions Neither the BsmI and FokI polymorphisms nor the levels of vitamin D were associated with presence of CVD in our SLE patients, even after adjusting for possible confounding factors. Additional studies are needed to corroborate our findings.
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Disclosure of Interest None Declared
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