间质性膀胱炎/膀胱疼痛综合征患者尿神经和免疫因子的关系

R. Sholan
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引用次数: 0

摘要

本研究旨在研究间质性膀胱炎/膀胱疼痛综合征(IC/BPS)患者尿细胞因子、肥大细胞和神经生长因子(NGF)之间的关系。68名临床诊断为IC/BPS的女性正在接受研究。平均年龄54.2±12.4岁。采用ELISA法测定尿中白细胞介素(IL-1β、IL-6、IL-8)、肿瘤坏死因子-α(TNFα)和NGF的浓度。肥大细胞在膀胱镜检查期间采集的膀胱粘膜活检中被鉴定。统计评估由微软Excel中的Statistica程序进行。计算Pearson相关商。根据IC/BPS的类型,将患者分为2组:第一组包括36例经典型患者;第二组32例为非溃疡型IC/BPS。两组之间无显著差异。在I组13.9%的患者中,该疾病的临床表现在40岁以下开始出现;在第二组中,28.1%的受检者提到在该年龄出现疾病症状。I组患者的IL-1β水平是对照组的2.4倍(p<0.05),IL-6、IL-8和TNFα浓度分别比对照组高出2.0倍(p<0.05)、2.5倍(p<0.05)和2.0倍(p>0.05)。II组患者IL-1β、IL-6、IL-8和TNFα的含量分别是对照组的2.4倍(p<0.05)、2.0倍(p<0.05)、2.0次(p<0.05)和1.9倍(p>0.05)。I组和II组的IL-1β、IL-6和TNFα水平没有显著差异,但I组女性的IL-8水平比II组高20.3%。IC/BPS患者的尿NGF水平在I组超过对照水平1.6倍(p<0.05),在II组超过1.5倍(p<0.05)。第一组患者的肥大细胞数量显著高于对照组和第二组,分别为1.6倍(p<0.05)和1.4倍(p<0.05)。在大多数情况下,指数之间显示出直接的弱相关性。仅在I组中,IL-1β与肥大细胞之间可检测到中等相关性(r=+0.508)。细胞因子水平的测定可以检测膀胱组织中炎症细胞的激活,并为开发诊断策略提供了机会。肥大细胞数量的增加可能表明这些细胞在疾病进展中的重要性,而尿液中NGF水平的升高表明IC/BPS可能是由慢性炎症引起的。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Relationships between urinary neural and immune factors in the patients with interstitial cystitis/ bladder painful syndrome
The purpose of this work was to study the relationships between urinary cytokines, mast cells and nerve growth factor (NGF) in the patients with interstitial cystitis/bladder pain syndrome (IC/BPS). Sixty-eight women with clinically diagnosed IC/BPS were under study. Their mean age was 54.2±12.4 years. Urinary concentrations of interleukins (IL-1β, IL-6, IL-8), tumor necrosis factor-α (TNFα), and NGF were determined by ELISA technique. Mast cells were identified in biopsies of mucous membranes from urinary bladder harvested during cystoscopy. Statistical evaluation was performed by Statistica program in Microsoft Excel. Pearson correlation quotients were calculated. Depending on the type of IC/BPS, the patients were divided into 2 groups: group I included 36 patients with classic type of disease; group II comprised 32 patients with non-ulcer type of IC/BPS. No significant differences were revealed between the groups. In 13.9% of patients from group I, the onset of clinical manifestations of the disease was observed at the age of less than 40 years; in group II, 28.1% of the examined mentioned appearance of the disease symptoms at this age. The levels of IL-1β in the patients from group I was 2.4 times higher than in controls (p < 0.05). IL-6, IL-8 and TNFα concentrations exceeded control values by 2.0 (p < 0.05), 2.5 (p < 0.05) and 2.0 times (p < 0.05), respectively. In the patients from group II, the content of IL-1β, IL-6, IL-8 and TNFα was 2.4 (p < 0.05), 2.0 (p < 0.05), 2.0 (p < 0.05) and 1.9 (p < 0.05) times higher than in the control group, respectively. There were no significant differences between groups I and II, in IL-1β, IL-6, and TNFα levels, except of IL-8 in women of group I that was 20.3% higher than in group II. The urinary NGF level in the patients with IC/BPS exceeded the control level 1.6 times (p < 0.05) for group I, and 1.5 times (p < 0.05) for group II. The number of mast cells in the patients of group I was significantly higher than in controls and in group II, i.e., 1.6 (p < 0.05) and 1.4 times (p < 0.05), respectively. In most cases, a direct weak correlation was revealed between the indices. Only in group I, a moderate correlation (r = + 0.508) could be detected between IL-1β and mast cells. Determination of cytokine levels allows to detect activation of inflammatory cells in bladder tissue and provides an opportunity for developing diagnostic strategies. Increased numbers of mast cells may indicate the importance of these cells in the disease progression, whereas elevated levels of NGF in urine suggests that IC/BPS may be caused by chronic inflammation.
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