Department of Dermatology, Hospital Sultanah Aminah Johor Bahru, Johor Bahru, Malaysia.
Clinical School Johor Bahru, Jeffrey Cheah School of Medicine & Health Sciences, Monash University, Kuala Lumpur, Malaysia.
Exp Dermatol. 2023 Aug;32(8):1263-1271. doi: 10.1111/exd.14776. Epub 2023 Mar 3.
Generalized Pustular psoriasis (GPP), a rare and potentially life-threatening auto-inflammatory disease, is associated with IL36RN mutations. Here, we analyse the prevalence of IL36RN mutations in our multi-ethnic GPP cohort and assess differences in the clinical profile of patients with (IL36RN-positive) and without (IL36RN-negative) mutations. IL36RN mutations were present in 17.7% of 137 GPP patients (29.7% of Chinese cases, 17.3% of Malay cases, but 0% of Indian patients). 92% of these individuals carried the c.115 + 6 T > C mutation. Male: female ratio was 1:2.3. Females predominate in both groups with no significant difference between IL36RN-positive and IL36RN-negative individuals. The overall mean age (±SD) at disease onset for GPP was 37.6 ± 17.2 years, but disease onset was significantly earlier in IL36RN-positive vs IL36RN-negative cases (mean age:30.6 ± 18.92 vs. 39.2 ± 16.49 years, p = 0.027). IL36RN-positive patients were less likely to have associated plaque psoriasis (52.4% vs. 83.5%, p-value = 0.002). There was no difference in the common clinical and laboratory manifestations or triggers of GPP between IL36RN-positive and -negative patients, except for geographic tongue which was significantly more common in IL36RN-positive patients (41.7% vs. 11.9%, p-value = 0.002). Annual flare rate was significantly higher in IL36RN-positive compared to IL36RN-negative (mean ± SD of 1.92 ± 1.32 vs. 1.46 ± 0.90, p = 0.041) cases. However, no significant difference in the rate of hospitalization and length of hospital stay was observed between the two groups. These observations demonstrate that IL36RN disease alleles occur with varying frequencies among Asian populations and are associated with a severe, early-onset clinical phenotype.
全身性脓疱型银屑病(GPP)是一种罕见且可能危及生命的自身炎症性疾病,与 IL36RN 突变有关。在此,我们分析了我们的多民族 GPP 队列中 IL36RN 突变的患病率,并评估了具有(IL36RN 阳性)和不具有(IL36RN 阴性)突变的患者在临床特征方面的差异。在 137 例 GPP 患者中,IL36RN 突变的存在率为 17.7%(中国病例为 29.7%,马来病例为 17.3%,但印度患者中无突变)。这些人中的 92%携带 c.115 + 6 T > C 突变。男性与女性的比例为 1:2.3。两组均以女性为主,IL36RN 阳性与 IL36RN 阴性个体之间无显著差异。GPP 的总体平均发病年龄(±SD)为 37.6 ± 17.2 岁,但 IL36RN 阳性病例的发病年龄明显更早(平均年龄:30.6 ± 18.92 岁 vs. 39.2 ± 16.49 岁,p = 0.027)。IL36RN 阳性患者更不可能同时患有斑块型银屑病(52.4% vs. 83.5%,p 值=0.002)。IL36RN 阳性和阴性患者之间的 GPP 常见临床表现和实验室指标或诱因没有差异,除了地理舌,其在 IL36RN 阳性患者中更为常见(41.7% vs. 11.9%,p 值=0.002)。与 IL36RN 阴性患者相比,IL36RN 阳性患者的年发病频率显著更高(平均 ± SD 为 1.92 ± 1.32 比 1.46 ± 0.90,p = 0.041)。然而,两组之间的住院率和住院时间无显著差异。这些观察结果表明,IL36RN 疾病等位基因在亚洲人群中的发生频率不同,并与严重的早发型临床表型相关。