Biomarkers to Diagnose Early Arthritis in Patients With Psoriasis.

Psoriasis forum Pub Date : 2012-01-01
Ya-Hui Grace Chiu, Christopher T Ritchlin
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Abstract

Background: Psoriatic arthritis is a potentially destructive, inflammatory joint disease that affects 20% to 30% of patients with psoriasis. Psoriasis precedes the onset of joint inflammation by approximately 10 years, providing a unique opportunity to intervene and prevent or delay onset of musculoskeletal manifestations. The emergence of sensitive imaging modalities and cellular biomarkers may facilitate early identification of patients with psoriasis who have subclinical joint disease and might help stratify patients with an early onset of arthritis.

Methods: The translational studies described herein are focused on the development of cellular biomarkers identified with flow cytometry and cell culture techniques in patients with psoriasis and psoriatic arthritis.

Results and conclusion: The combination of power Doppler ultrasound imaging and cellular biomarkers (ie, CD16 and dendritic cell specific transmembrane protein) to diagnose early psoriatic arthritis and to stratify patients with established psoriatic arthritis provides a new opportunity to optimize treatment outcomes in this potentially disabling disease.

诊断银屑病患者早期关节炎的生物标志物
背景:银屑病关节炎是一种具有潜在破坏性的炎症性关节疾病,20% 到 30% 的银屑病患者都会患上这种疾病。银屑病比关节炎症发病早约 10 年,这为干预、预防或延迟肌肉骨骼表现的发病提供了独特的机会。灵敏的成像模式和细胞生物标志物的出现可能有助于及早识别患有亚临床关节疾病的银屑病患者,并有助于对早期关节炎患者进行分层:方法:本文所述的转化研究侧重于在银屑病和银屑病性关节炎患者中利用流式细胞术和细胞培养技术开发细胞生物标志物:将功率多普勒超声成像与细胞生物标志物(即 CD16 和树突状细胞特异性跨膜蛋白)相结合,诊断早期银屑病关节炎并对已确诊的银屑病关节炎患者进行分层,为优化这种潜在致残性疾病的治疗效果提供了新的机会。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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