Abstract
Psoriasis is a chronic, relapsing and inflammatory multisystemic disease with bothgenetic predisposition and autoimmune pathogenic traits. Several types of vitamin D receptor (VDR) polymorphisms have been investigated as a predisposing factor for psoriasis susceptibility with controversial results. However, the exact pathophysiological effect ofthe VDR gene on psoriasis susceptibility remains poorly understood.We aimed to determine whetherVDR gene polymorphisms, specificallyrs7975232 (ApaI), afford psoriasis susceptibility in a given community in Saudi Arabia. Also, to assess its possible relation with disease severity. In a comparative case-control study comprising53 psoriatic patients and 41 matched healthy controls, we measured serum ApaIlevels, and the PCR-RFLEP technique detected ApaI genetic polymorphism (rs7975232) for both groups.Serum vitamin D level was measured in both groups. Our results revealed that A/A genotype of ApaI was significantly more predominant in patients than controls, while A/a genotype was more common in healthy subjects. Furthermore, A allele was significantly over-represented in the patients' group compared to the controls (P≤0.001). Serum vitamin D levels were significantly higher in mild psoriatic patients than in those with moderate and severe types (P=0.002). Mild psoriatic patients with a/a genotypes have higher vitamin D levels than severe patients with A/A genotypes and A/a moderate patients (P≤0.001). Our data indicated clearly that VDR gene polymorphism, namely ApaI, is associated with psoriasis susceptibility. Furthermore, serum vitamin D level in psoriatic patients varies among different ApaI genotypes, where it is lowest in AA genotype.
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