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Abstract Background: Acne vulgaris is a disease of the pilosebaceous unit with predominance at the face, neck, upper chest and back. Sebocytes were identified as 1, 25 (OH) 2 D responsive target cells. This theory confirms that vitamin D exerts an immune regulatory function in sebocytes, which supports it's the anti-inflammatory effects in acne patients. Objectives: To assess the role of vitamin D in treatment of acne vulgaris and to study its relation to VDR Apa 1,Taq 1,Fok 1 and Cdx 2 polymorphisms. Methods: This randomized control study included 300 acne patients. Group 1 received cholecalciferol 8,000 IU/day for three months. group 2 applied 1-2gm of topical vitamin D analogue for three months. group 3 had no treatment. VDR gene Apa 1, Taq 1, Fok 1 & Cdx 2 polymorphisms were examined by real time PCR with Taq Man allelic discrimination assay. Serum 25(OH) D 3 was measured in all participants before and after treatment by ELISA. Results: Acne patients showed more significant decrease in serum 25(OH) D 3 concentration (9.7ng/ml) than controls (26ng/ml). Systemic cholecalciferol and topical vitamin D analogue had significantly decreased GAGS by 21.88% & 38.75% respectively after treatment. Patients had significant decrease in Taq 1 A-allele & AA genotype (47.5%, 10%) than controls (80%, 60%) respectively. Conclusion: vitamin D deficiency and VDR polymorphisms of Taq 1and Apa 1 may increase the risk for AV. Systemic and topical vitamin D can be used as a complementary therapy for AV. Keywords: Acne vulgaris – vitamin D - VDR polymorphism. |