The RETN gene rs1862513 polymorphism as a novel predisposing marker for familial Acne vulgaris in a Pakistani population

Authors

  • Ahmad Faraz Department of surgery, Government Post Graduate Medical Institute, Lady Reading Hospital, Peshawar, Pakistan
  • Sabir Hussain Department of Biosciences, COMSATS Institute of Information Technology, Islamabad-46000, Pakistan
  • Tahir Iqbal Department of Internal Medicine, Shifa College of Medicine, Shifa International Hospital, H-8/4, Islamabad, Pakistan
Abstract:

Resistin (RETN), recently found to be relevant to inflammation and inflammatory disorders. We, therefore, aimed to investigate the potential role of RETN gene polymorphism in pathogenesis of acne vulgaris with familial history. We investigated the RETN-420C/G polymorphism in 180 patients with acne vulgaris and 180 healthy individuals in a case-control association analysis. In this study, we also investigated the heritability of the RETN susceptible allele from 140 trio families with acne affected offspring. The genotyping was performed by polymerase chain reaction and direct DNA sequencing.The RETN-420C/G polymorphism was significantly associated with acne in patients compared with healthy controls (P=0.014). The minor allele G at -420 was more prevalent in cases vs. controls (P=0.002). The RETN-420C/G polymorphism was significantly associated with severity of acne vulgaris in patients (P=0.0097). The results of a transmission disequilibrium test revealed a significant association between the RETN-420C/G polymorphism and acne vulgaris (P

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Journal title

volume 18  issue 5

pages  526- 528

publication date 2015-05-01

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