Solak Berna, Karkucak Mutlu, Turan Hakan, Ocakoğlu Gökhan, Özemri Sağ Şebnem, Uslu Esma, Yakut Tahsin, Erdem Teoman
Department of Dermatology, School of Medicine, Sakarya University, Sakarya, Turkey.
Med Princ Pract. 2016;25(2):155-8. doi: 10.1159/000442165. Epub 2015 Nov 4.
To determine the role of glutathione S-transferase (GST) isoenzyme polymorphisms as susceptibility factors in patients with psoriasis in a Turkish cohort.
In this case-control study, 105 patients with plaque-type psoriasis and 102 healthy controls were recruited from the dermatology outpatient clinics of two university hospitals. Genomic DNA was extracted from whole blood using a DZ DNA isolation kit. Multiplex PCR was used to determine GSTM1 and GSTT1 polymorphisms in the isolated DNAs.
Of the 150 patients with psoriasis, 83 (79%) were identified with the GSTT1 genotype and 22 (21%) with the null genotype. Of the 102 patients in the control group, 69 (67.6%) subjects were identified with the GSTT1 genotype and 33 (32.4%) with the null genotype. There was no significant difference between the patient and control groups (p = 0.063). Regarding the GSTM1 polymorphism, 54 (51.4%) patients were identified with this genotype and 51 (48.6%) with the null genotype; in the control group, 50 (49%) were identified with this genotype and 52 (51%) with the null genotype. Again there was no statistically significant difference between the groups (p = 0.957).
In this Turkish cohort of patients with psoriasis, neither GSTT1 nor GSTM1 polymorphisms were associated with disease susceptibility. Larger studies with a wider range of GST isoenzyme are needed.
确定谷胱甘肽S-转移酶(GST)同工酶多态性作为土耳其人群中银屑病患者易感性因素的作用。
在这项病例对照研究中,从两家大学医院的皮肤科门诊招募了105例斑块型银屑病患者和102名健康对照者。使用DZ DNA分离试剂盒从全血中提取基因组DNA。采用多重聚合酶链反应(PCR)检测分离DNA中的GSTM1和GSTT1多态性。
在150例银屑病患者中,83例(79%)为GSTT1基因型,22例(21%)为无效基因型。在102例对照组患者中,69例(67.6%)为GSTT1基因型,33例(32.4%)为无效基因型。患者组和对照组之间无显著差异(p = 0.063)。关于GSTM1多态性,54例(51.4%)患者为该基因型,51例(48.6%)为无效基因型;在对照组中,50例(49%)为该基因型,52例(51%)为无效基因型。两组之间同样无统计学显著差异(p = 0.957)。
在这个土耳其银屑病患者队列中,GSTT1和GSTM1多态性均与疾病易感性无关。需要对更广泛的GST同工酶进行更大规模的研究。