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强直性脊柱炎继发淀粉样变性。

Secondary amyloidosis in ankylosing spondylitis.

机构信息

Department of Rheumatology, Trakya University Medical Faculty, Edirne, Turkey.

出版信息

Rheumatol Int. 2013 Jul;33(7):1725-9. doi: 10.1007/s00296-012-2646-3. Epub 2013 Jan 3.

Abstract

We evaluated the frequency of secondary amyloidosis, associated clinical features, and outcomes in ankylosing spondylitis (AS) patients diagnosed in the last decade. The medical records of AS patients diagnosed at single academic medical center were reviewed for clinical evidence of amyloidosis. During routine follow-up, routine urinalysis was performed at each visit; patients with significant proteinuria underwent rectal biopsy. We diagnosed 8 clinically apparent amyloidosis patients (1.1 %) in our cohort of 730 AS patients (508 males, 222 females). Four patients undergoing hemodialysis were diagnosed secondary amyloidosis. Three patients had nephrotic syndrome and renal dysfunction and one patient had non-nephrotic proteinuria. When AS patients with amyloidosis were compared to AS controls, it was observed that the amyloidosis group was older, had longer disease duration, higher initial BASDAI scores, and ESR values, and more frequent peripheral arthritis (p < 0.05). Logistic regression analysis revealed that the initial BASDAI level was an independent predictor for the development of secondary amyloidosis (OR:2.36). Six patients were administered anti-TNF therapy. The clinical findings resolved in these. In 2 patients with nephrotic syndrome and renal dysfunction, in addition to clinical improvement, there was a decrement in proteinuria; renal function improved or remained stable. Anti-TNF therapy is safe and effective in patients with renal failure, and at an earlier stage, appears effective in improving renal function. The development of proteinuria in AS patients should occasion a search for underlying amyloidosis.

摘要

我们评估了过去十年中诊断的强直性脊柱炎(AS)患者发生继发性淀粉样变性的频率、相关临床特征和结局。我们对单家学术医疗中心诊断的 AS 患者的病历进行了回顾,以寻找淀粉样变性的临床证据。在常规随访中,每次就诊时都会进行常规尿检;有大量蛋白尿的患者会进行直肠活检。在我们的 730 例 AS 患者(508 名男性,222 名女性)队列中,我们诊断出 8 例明显的淀粉样变性患者(1.1%)。4 名接受血液透析的患者被诊断为继发性淀粉样变性。3 名患者患有肾病综合征和肾功能障碍,1 名患者患有非肾病性蛋白尿。当将淀粉样变性的 AS 患者与 AS 对照组进行比较时,观察到淀粉样变性组年龄更大,疾病持续时间更长,初始 BASDAI 评分和 ESR 值更高,外周关节炎更频繁(p<0.05)。Logistic 回归分析显示,初始 BASDAI 水平是发生继发性淀粉样变性的独立预测因子(OR:2.36)。6 名患者接受了抗 TNF 治疗。这些患者的临床发现得到了缓解。在 2 名患有肾病综合征和肾功能障碍的患者中,除了临床改善外,蛋白尿也有所减少;肾功能改善或保持稳定。抗 TNF 治疗在肾衰竭患者中是安全有效的,在早期阶段,似乎对改善肾功能有效。AS 患者出现蛋白尿时应考虑潜在的淀粉样变性。

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