Armijo-Borjon Gwyneth, Miranda-Aguirre Alessandra Irais, Garza-Silva Arnulfo, Fernández-Chau Iván Francisco, Sanz-Sánchez Miguel Ángel, González-Cantú Arnulfo, Romero-Ibarguengoitia Maria Elena
Research Department, Hospital Clínica Nova de Monterrey, San Nicolás de los Garza, Nuevo León, México.
Dermatology Department, Hospital Clínica Nova de Monterrey, San Nicolás de los Garza, Nuevo León, México.
Arch Dermatol Res. 2025 Jan 7;317(1):195. doi: 10.1007/s00403-024-03688-5.
Psoriasis requires a comprehensive assessment of concomitant diseases to make better therapeutic decisions. This study examined the differences in the onset and progression of associated cardiometabolic comorbidities in psoriasis patients based on their treatments.
A retrospective longitudinal study was conducted on patients aged over 13 years with psoriasis seen at a Northern Mexican Hospital between 2012 and 2023. Patients were categorized into three groups according on the type of treatment received: topical, systemic, and biologic. A logistic regression analysis was performed to identify predictors of comorbidity development.
197 patients were included; 52.8% were women, with a mean (SD) age of 54.45 (16.91) years, divided into topical [n = 90 (45.7%)], systemic [n = 57 (29.1%)], and biologic [n = 50 (25.5%)] groups, metabolic dysfunction-associated steatotic liver disease (MASLD) was significantly more prevalent in the biologic group [22 (44%)], p < 0.001. The logistic regression showed that type 2 diabetes mellitus, biological treatments (OR = 5.798, p = 0.001), and body mass index (OR = 1.144, p = 0.002), predicted the development of MASLD with a Nagelkerke's R of 0.400.
Psoriasis patients using biological therapies have a greater predisposition to MASLD. These patients should receive a comprehensive approach to identify metabolic conditions, and screening tests for MASLD are recommended.
银屑病需要对伴发疾病进行全面评估,以做出更好的治疗决策。本研究基于治疗方法,探讨了银屑病患者相关心脏代谢合并症的发病及进展差异。
对2012年至2023年在墨西哥北部一家医院就诊的13岁以上银屑病患者进行回顾性纵向研究。根据接受的治疗类型将患者分为三组:外用治疗组、系统治疗组和生物制剂治疗组。进行逻辑回归分析以确定合并症发生的预测因素。
共纳入197例患者;52.8%为女性,平均(标准差)年龄为54.45(16.91)岁,分为外用治疗组[n = 90(45.7%)]、系统治疗组[n = 57(29.1%)]和生物制剂治疗组[n = 50(25.5%)],代谢功能障碍相关脂肪性肝病(MASLD)在生物制剂治疗组中显著更常见[22例(44%)],p < 0.001。逻辑回归显示,2型糖尿病、生物制剂治疗(比值比 = 5.798,p = 0.001)和体重指数(比值比 = 1.144,p = 0.002)可预测MASLD的发生,Nagelkerke's R为0.400。
使用生物制剂治疗的银屑病患者患MASLD的倾向更大。这些患者应接受全面评估以识别代谢状况,建议进行MASLD筛查。