Division of Rheumatology, Department of Medicine, The Second Hospital of Shanxi Medical University, Taiyuan, Shanxi 030001, China.
Division of Nephrology, Department of Medicine, The Second Hospital of Shanxi Medical University, Taiyuan, Shanxi 030001, China.
J Immunol Res. 2019 Feb 17;2019:3952392. doi: 10.1155/2019/3952392. eCollection 2019.
A retrospective analysis of clinical characteristics and immunological manifestations of primary Sjogren's syndrome (pSS) patients with or without renal involvement was conducted in order to elucidate the potential risk factors of renal damage in pSS and evaluate the condition.
A total of 1002 patients, who fulfilled the 2002 classification criteria for pSS from the Second Affiliated Hospital of Shanxi Medical University, were enrolled in the cross-sectional study. Clinical, immunological, and histological characteristics were compared between pSS patients with and without renal involvement, and potential risk factors of renal involvements in pSS patients were examined by multivariate analysis.
Among these pSS patients, there were 162 cases (16.17%) with and 840 cases (83.83%) without renal damage. Serious edema of both lower limbs, interstitial nephritis, and renal tubular acidosis were found in the pSS with renal damage group. Compared with simple pSS patients, the levels of creatinine, cystatin C, and alpha-1-microglobulin ( -MG) in the pSS with renal damage group were significantly increased. The difference between the two groups was statistically significant ( < 0.05). The AUC of the combination of creatinine and -MG and creatinine, -MG, and creatinine was statistically larger than that of creatinine, and the biomarker of the biggest AUC is the combination of creatinine and -MG.
The main clinical manifestations of pSS with renal damage were edema of the lower limbs, interstitial nephritis, and renal tubular acidosis. Creatinine and -MG are effective indicators for renal function in pSS, which may provide a better understanding for clinical decision-making.
回顾性分析原发性干燥综合征(pSS)患者是否存在肾损害的临床特征和免疫学表现,以阐明pSS 患者发生肾损害的潜在危险因素并评估病情。
本横断面研究纳入了山西医科大学第二附属医院满足 2002 年 pSS 分类标准的 1002 例患者。比较了有肾损害和无肾损害的 pSS 患者的临床、免疫学和组织学特征,并通过多因素分析检查了 pSS 患者发生肾损害的潜在危险因素。
在这些 pSS 患者中,有 162 例(16.17%)存在肾损害,840 例(83.83%)无肾损害。pSS 合并肾损害组出现双下肢严重水肿、间质性肾炎和肾小管性酸中毒。与单纯 pSS 患者相比,pSS 合并肾损害组的肌酐、胱抑素 C 和α-1-微球蛋白( -MG)水平明显升高,两组差异有统计学意义( < 0.05)。肌酐和 -MG 以及肌酐、 -MG 和肌酐联合的 AUC 均大于肌酐,且 AUC 最大的标志物是肌酐和 -MG 的联合。
pSS 合并肾损害的主要临床表现为下肢水肿、间质性肾炎和肾小管性酸中毒。肌酐和 -MG 是 pSS 患者肾功能的有效指标,可能为临床决策提供更好的依据。