a Department of Nephropathy , Lanzhou University Second Hospital , Lanzhou , PR China.
b Thinks People's Hospital , Gan Su , PR China.
Autoimmunity. 2017 Dec;50(8):476-480. doi: 10.1080/08916934.2017.1402302.
This study aims to evaluate the role of FEN1 E160D mutation in lupus nephritis (LN) patients with cell apoptosis dysfunction.
(1) Cell apoptosis was detected from 50 paraffin samples obtained from renal biopsies of patients with Class IV LN by TUNEL method and the relationship of the systemic lupus erythematosus disease activity index 2000 (SLEDAI 2000) and renal tissue cell apoptotic index (AI) was discussed. (2) FEN1 gene 61563142-61563342 containing E160D were analysed by extracting genomic DNA from peripheral blood collected from the above 50 LN patients and 25 patients with nephrectomy caused by renal trauma. The difference between these two groups was statistically significant.
Cell apoptosis was detected in all patients with LN, and correlation analysis results revealed a positive relationship between SLEDAI 2000 and AI (r = 0.39, p = .032). The FEN1 gene 61563142-61563342 fragment had site mutations at C/- (+61563189), A/T (+61563198), A/- (+61563204), G/T (+61563303), and T/C (+61563304). However, no statistical significance was found between LN patients detected with cell apoptosis and healthy individuals.
This study revealed that cell apoptosis dysfunction plays a key role in the pathogenesis of LN, even though the difference in FEN1 gene 61563142-61563342 between LN patients and healthy individuals was not statistically significant. Larger sample size studies or genome-wide association studies are needed.
本研究旨在评估 FEN1 E160D 突变在细胞凋亡功能障碍的狼疮肾炎(LN)患者中的作用。
(1)通过 TUNEL 法检测 50 例 LN 患者肾活检组织中细胞凋亡情况,并探讨系统性红斑狼疮疾病活动指数 2000(SLEDAI 2000)与肾组织细胞凋亡指数(AI)的关系。(2)提取 50 例 LN 患者和 25 例因肾外伤行肾切除术患者外周血基因组 DNA,分析 FEN1 基因 61563142-61563342 内含子 E160D,两组间差异有统计学意义。
所有 LN 患者均检测到细胞凋亡,相关性分析结果显示 SLEDAI 2000 与 AI 呈正相关(r=0.39,p=0.032)。FEN1 基因 61563142-61563342 片段在 C/-(+61563189)、A/T(+61563198)、A/-(+61563204)、G/T(+61563303)和 T/C(+61563304)位点发生突变,但细胞凋亡检测的 LN 患者与健康个体之间无统计学差异。
本研究表明,细胞凋亡功能障碍在 LN 的发病机制中起关键作用,尽管 LN 患者和健康个体之间 FEN1 基因 61563142-61563342 无统计学差异。需要更大的样本量研究或全基因组关联研究。