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间质性膀胱炎的挑战:现状与未来展望。

The Challenges of Interstitial Cystitis: Current Status and Future Prospects.

机构信息

Department of Urology, University of Kentucky College of Medicine, 800 Rose St., MS-269, Lexington, KY, 40536-0298, USA.

Department of Pharmacology and Nutritional Sciences, University of Kentucky College of Medicine, Lexington, KY, USA.

出版信息

Drugs. 2015 Dec;75(18):2057-63. doi: 10.1007/s40265-015-0504-9.

DOI:10.1007/s40265-015-0504-9
PMID:26603875
Abstract

Interstitial cystitis/bladder pain syndrome (IC/BPS) is a syndrome of unpleasant bladder sensations and lower urinary tract symptoms. The three main proposed etiologies are bladder urothelial dysfunction, bladder inflammation (possible neurogenic), and neuropathic pain. Despite decades of basic and clinical research, IC/BPS remains difficult to treat. A variety of treatments are used, each aimed towards one etiology. For example, glycosaminoglycans are thought to improve the urothelial permeability barrier, anti-inflammatory agents are used to decrease general inflammation, and mast cell stabilizers and/or antagonists of mast cell products are used in the treatment of neurogenic inflammation. In the (unfortunately frequent) event that a treatment fails, possible reasons are that (1) the clinician is aiming towards the wrong etiology for that patient (i.e., the treatment is off target) or (2) the correct etiology is being targeted, but the treatment is not ameliorating it (i.e., the treatment is sub-therapeutic). This is a crucial distinction, because an off-target treatment should be abandoned, but a sub-therapeutic treatment should be escalated. Currently, our inability to make this crucial distinction is the greatest obstacle to effective treatment. An important future advance would be to identify urine or serum biomarkers specific to each etiologic target. Then, each biomarker could be used to select appropriate patients for each treatment and monitor the treatment's effect on its intended target.

摘要

间质性膀胱炎/膀胱疼痛综合征(IC/BPS)是一种令人不适的膀胱感觉和下尿路症状的综合征。三个主要的发病机制是膀胱尿路上皮功能障碍、膀胱炎症(可能是神经源性的)和神经性疼痛。尽管经过几十年的基础和临床研究,IC/BPS 仍然难以治疗。有多种治疗方法被用于治疗不同的发病机制,例如,糖胺聚糖被认为可以改善尿路上皮的通透性屏障,抗炎药物用于减轻一般炎症,肥大细胞稳定剂和/或肥大细胞产物的拮抗剂用于治疗神经源性炎症。在(不幸的是经常发生的)治疗失败的情况下,可能的原因是(1)临床医生针对该患者的目标病因不正确(即治疗目标错误),或者(2)正确的病因被针对,但治疗没有改善它(即治疗效果不佳)。这是一个至关重要的区别,因为针对错误目标的治疗应该被放弃,但治疗效果不佳的治疗应该被升级。目前,我们无法做出这种关键区别是有效治疗的最大障碍。未来的一个重要进展将是确定针对每个病因靶点的尿液或血清生物标志物。然后,每个生物标志物都可以用于选择适合每种治疗方法的患者,并监测治疗对其预期目标的效果。

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本文引用的文献

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Urinary Nerve Growth Factor Levels in Urinary Tract Diseases With or Without Frequency Urgency Symptoms.伴有或不伴有尿频尿急症状的泌尿系统疾病患者尿液中神经生长因子水平
Low Urin Tract Symptoms. 2010 Sep;2(2):88-94. doi: 10.1111/j.1757-5672.2010.00065.x. Epub 2010 May 3.
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Have we been led astray by the NGF biomarker data?我们是否被神经生长因子生物标志物数据引入歧途了?
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A Case Control Study Reveals that Polyomaviruria Is Significantly Associated with Interstitial Cystitis and Vesical Ulceration.
Acyloxyacyl hydrolase regulates microglia-mediated pelvic pain.
酰氧基酰基水解酶调节小胶质细胞介导的盆腔疼痛。
PLoS One. 2022 Aug 18;17(8):e0269140. doi: 10.1371/journal.pone.0269140. eCollection 2022.
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Peptidomics analysis reveals changes in small urinary peptides in patients with interstitial cystitis/bladder pain syndrome.肽组学分析揭示了间质性膀胱炎/膀胱疼痛综合征患者中小尿肽的变化。
Sci Rep. 2022 May 18;12(1):8289. doi: 10.1038/s41598-022-12197-2.
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Comparison of deep phenotyping features of UCPPS with and without Hunner lesion: A MAPP-II Research Network Study.UCPPS 伴有和不伴有 Hunner 病变的深度表型特征比较:MAPP-II 研究网络研究。
Neurourol Urodyn. 2021 Mar;40(3):810-818. doi: 10.1002/nau.24623. Epub 2021 Feb 19.
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Application of Adult and Pluripotent Stem Cells in Interstitial Cystitis/Bladder Pain Syndrome Therapy: Methods and Perspectives.成人及多能干细胞在间质性膀胱炎/膀胱疼痛综合征治疗中的应用:方法与展望
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