Sorour Neveen Emad, Abd El-Kareem Heba Mohamed, Ibrahim Asmaa Em, Salem Rehab Mohammed
Drs. Sorour and Salem are with the Dermatology Department, Faculty of Medicine, Benha University in Benha, Egypt.
Dr. Abd El-Kareem is with the Medical Biochemistry Department, Faculty of Medicine, Benha University in Benha, Egypt.
J Clin Aesthet Dermatol. 2021 Jun;14(6):14-17. Epub 2021 Jun 1.
Oxidative stress is now one of the accepted theories of vitiligo development. Nuclear factor erythroid-2-related factor 2 (Nrf2) regulates the expression of antioxidant proteins.
This work aimed to evaluate the association of Nrf2 gene polymorphisms with the susceptibility to vitiligo among a sample of Egyptian patients with vitiligo.
This case-control study included 100 patients with vitiligo and 50 healthy matched volunteers serving as a control group. Genotyping was carried out by real-time polymerase chain reaction.
The frequencies of TT, CT, and combined (TT+CT) genotypes and the T allele of Nrf2 (rs35652124) were significantly increased in the studied patients with vitiligo relative to the healthy controls (<0.001, =0.012, <0.001 and <0.001, respectively). There was a nonsignificant difference between patients and controls regarding Nrf2 (rs6721961) genotypes. However, the T allele of Nrf2 (rs6721961) was significantly predominant in the studied patients compared to in the controls (=0.029). Among the studied criteria, the T allele of Nrf2 (rs6721961) was predominant in patients with a marginal type of repigmentation (=0.022), while the G allele of the same single-nucleotide polymorphism was associated with a higher body mass index value (=0.034). One hundred percent of patients with vitiligo with the Nrf2 (rs6721961) GT genotype had a progressive disease course (=0.015).
Nrf2 (-617 T/G) and (-653 T/C) polymorphism might play a role in patient susceptibility to vitiligo and modify the clinical presentation of the disease.
氧化应激是目前公认的白癜风发病理论之一。核因子红细胞2相关因子2(Nrf2)调节抗氧化蛋白的表达。
本研究旨在评估埃及白癜风患者样本中Nrf2基因多态性与白癜风易感性的关联。
本病例对照研究纳入100例白癜风患者和50名健康匹配志愿者作为对照组。采用实时聚合酶链反应进行基因分型。
与健康对照组相比,白癜风患者中Nrf2(rs35652124)的TT、CT及合并(TT + CT)基因型频率和T等位基因频率显著升高(分别为<0.001、=0.012、<0.001和<0.001)。白癜风患者和对照组在Nrf2(rs6721961)基因型方面无显著差异。然而,与对照组相比,Nrf2(rs6721961)的T等位基因在研究患者中显著占优势(=0.029)。在研究的标准中,Nrf2(rs6721961)的T等位基因在边缘性色素再生型患者中占优势(=0.022),而同一单核苷酸多态性的G等位基因与较高的体重指数值相关(=0.034)。Nrf2(rs6721961)GT基因型的白癜风患者中有100%病程呈进行性(=0.015)。
Nrf2(-617 T/G)和(-653 T/C)多态性可能在患者对白癜风的易感性中起作用,并改变疾病的临床表现。