Sota Jurgen, Vitale Antonio, Rigante Donato, Orlando Ida, Lucherini Orso Maria, Simpatico Antonella, Lopalco Giuseppe, Franceschini Rossella, Galeazzi Mauro, Frediani Bruno, Fabiani Claudia, Tosi Gian Marco, Cantarini Luca
Research Center of Systemic Autoinflammatory Diseases and Behçet's Disease and Rheumatology-Ophthalmology Collaborative Uveitis Center, Department of Medical Sciences, Surgery and Neurosciences, University of Siena, Siena, Italy.
Institute of Pediatrics, Università Cattolica Sacro Cuore, Fondazione Policlinico A. Gemelli, Rome, Italy.
Isr Med Assoc J. 2018 Aug;20(8):517-521.
Behçet's disease (BD) is an inflammatory disorder potentially leading to life- and sight-threatening complications. No laboratory marker correlating with disease activity or predicting the occurrence of disease manifestations is currently available.
To determine an association between serum amyloid-A (SAA) levels and disease activity via the BD Current Activity Form (BDCAF), to evaluate disease activity in relation to different SAA thresholds, to examine the association between single organ involvement and the overall major organ involvement with different SAA thresholds, and to assess the influence of biologic therapy on SAA levels.
We collected 95 serum samples from 64 BD patients. Related demographic, clinical, and therapeutic data were retrospectively gathered.
No association was identified between SAA levels and BD disease activity (Spearman's rho = 0.085, P = 0.411). A significant difference was found in the mean BDCAF score between patients presenting with SAA levels < 200 mg/L and those with SAA levels > 200 mg/L (P = 0.027). SAA levels > 200 mg/L were associated with major organ involvement (P = 0.008). A significant association was found between SAA levels > 150 mg/dl and ocular (P = 0.008), skin (P = 0.002), and mucosal (P = 0.012) manifestations. Patients undergoing biologic therapies displayed more frequently SAA levels < 200 mg/L vs. patients who were not undergoing biologic therapies (P = 0.012).
Although SAA level does not represent a biomarker for disease activity, it might be a predictor of major organ involvement and ocular disease relapse at certain thresholds in patients with BD.
白塞病(BD)是一种炎症性疾病,可能导致危及生命和视力的并发症。目前尚无与疾病活动相关或预测疾病表现发生的实验室标志物。
通过白塞病当前活动形式(BDCAF)确定血清淀粉样蛋白A(SAA)水平与疾病活动之间的关联,评估不同SAA阈值下的疾病活动情况,研究不同SAA阈值下单器官受累与主要器官总体受累之间的关联,并评估生物治疗对SAA水平的影响。
我们收集了64例BD患者的95份血清样本。回顾性收集相关的人口统计学、临床和治疗数据。
未发现SAA水平与BD疾病活动之间存在关联(Spearman等级相关系数=0.085,P=0.411)。SAA水平<200mg/L的患者与SAA水平>200mg/L的患者之间,BDCAF平均得分存在显著差异(P=0.027)。SAA水平>200mg/L与主要器官受累相关(P=0.008)。发现SAA水平>150mg/dl与眼部(P=0.008)、皮肤(P=0.002)和黏膜(P=0.012)表现之间存在显著关联。接受生物治疗的患者SAA水平<200mg/L的频率高于未接受生物治疗的患者(P=0.012)。
虽然SAA水平不代表疾病活动的生物标志物,但在BD患者中,在某些阈值下它可能是主要器官受累和眼部疾病复发的预测指标。