Department of Laboratory Medicine and Department of Dermatology, Huashan Hospital, Fudan University, Shanghai, China.
Department of Information, Huashan Hospital, Fudan University, Shanghai, China.
Dermatology. 2021;237(4):579-587. doi: 10.1159/000514072. Epub 2021 Feb 12.
There are great interindividual variations in the clinical efficacy of methotrexate (MTX) treatment and patients' genetic background seems promising in its explanation.
The study aimed to test whether the polymorphism of annexin A6 (ANxA6) gene, a susceptibility factor for psoriasis, was associated with the clinical response to MTX therapy.
A total of 325 patients enrolled in the study received oral MTX treatment, of whom 310 completed the 1-year study and performed the genotype analysis. They were defined as responders (a reduction of Psoriasis Area and Severity Index [PASI] score ≥75%) and nonresponders (a reduction of PASI <50%) compared to baseline after 12 weeks of short-time therapy. On 1-year treatment, they were defined as responders if they achieved PASI75 and absolute PASI ≤3, otherwise as nonresponders. The genotypes of 4 single-nucleotide polymorphisms (SNPs) in the ANxA6 gene were verified using the Sequenom platform. Potential predictors associated with the treatment outcome of MTX were assessed by binary logistic regression.
We found significant associations for the ANxA6 SNPs of rs11960458, rs960709, and rs13168551 with psoriasis severity. Patients with rs11960458 CC genotype and rs960709 GG genotype showed higher percentages of PASI75 and improvement rates of PASI at 12 weeks. And on 1-year treatment, statistical difference occurred in rs11960458 rather than other SNPs compared between responders and nonresponders that the frequency of CC genotype was higher in responders (p = 0.019). After adjustment for potential confounders, patients with rs11960458 TT/CT genotype (at 12 weeks: OR 0.483, 95% CI 0.245-0.951, p = 0.035; at 1 year: OR 0.483, 95% CI 0.280-0.833, p = 0.009) were significantly more likely to not respond to MTX both on the short-term and long-term treatment, while rs960709 and rs13168551 polymorphisms were only associated with the short-term efficacy of MTX (p = 0.018 and p = 0.036, respectively).
The CC ge-notype of ANxA6 (rs11960458) was significantly associated with a better response when compared to those patients with the TT/CT genotype, thus being a potential predictor for the clinical efficacy of MTX.
甲氨蝶呤(MTX)治疗的临床疗效存在很大的个体间差异,患者的遗传背景似乎是其解释的一个有希望的因素。
本研究旨在检测银屑病易感因素-膜联蛋白 A6(ANxA6)基因的多态性是否与 MTX 治疗的临床反应相关。
共有 325 名患者入组本研究,接受口服 MTX 治疗,其中 310 名完成了 1 年的研究并进行了基因型分析。根据 12 周短期治疗后 PASI 评分较基线下降≥75%(应答者)和<50%(无应答者),将患者定义为应答者和无应答者。在 1 年治疗时,如果患者达到 PASI75 且绝对 PASI≤3,则定义为应答者,否则为无应答者。采用Sequenom 平台验证 ANxA6 基因中 4 个单核苷酸多态性(SNPs)的基因型。采用二项逻辑回归评估与 MTX 治疗结果相关的潜在预测因素。
我们发现 ANxA6 基因 rs11960458、rs960709 和 rs13168551 的 SNP 与银屑病严重程度显著相关。rs11960458 CC 基因型和 rs960709 GG 基因型的患者在 12 周时 PASI75 百分比和 PASI 改善率更高。在 1 年治疗时,与应答者和无应答者相比,rs11960458 而非其他 SNPs 在统计学上存在差异,即 CC 基因型在应答者中更为常见(p=0.019)。在调整了潜在混杂因素后,rs11960458 TT/CT 基因型(12 周:OR 0.483,95%CI 0.245-0.951,p=0.035;1 年:OR 0.483,95%CI 0.280-0.833,p=0.009)的患者在短期和长期治疗中均不太可能对 MTX 无反应,而 rs960709 和 rs13168551 多态性仅与 MTX 的短期疗效相关(p=0.018 和 p=0.036)。
与 TT/CT 基因型相比,ANxA6(rs11960458)的 CC 基因型与更好的反应显著相关,因此是 MTX 临床疗效的潜在预测因素。