Musumeci Antonino, Vinci Mirella, Treccarichi Simone, Ragalmuto Alda, Bruno Giuseppe, Tinniriello Giordana, Farina Jessica, Federico Concetta, Saccone Salvatore, Calì Francesco, Porru Daniele
Oasi Research Institute-IRCCS, 94018 Troina, Italy.
Department of Medical and Surgical Sciences and Advanced Technologies "G.F. Ingrassia", Anatomic Pathology, University of Catania, 95131 Catania, Italy.
Genes (Basel). 2025 Feb 26;16(3):281. doi: 10.3390/genes16030281.
BACKGROUND/OBJECTIVES: Symptoms of pudendal nerve neuropathy may overlap with various symptoms of interstitial cystitis (IC). As documented, there is a well-established correlation between the genes involved in ATP metabolism, neuropathy, and IC. ATP-binding cassette (ABC) transporters genes, in fact, are vital for ATP signaling. This study aims to associate the gene with a suspected pudendal nerve neuropathy and IC.
Histological analysis was conducted for diagnosing IC while the genetic variant was identified by whole exome sequencing (WES) Trio and confirmed through Sanger.
We report a patient with IC, confirmed by histological examination, presenting with a suspected bladder and pudendal nerve neuropathy, though not analytically confirmed. Histological analysis revealed urothelial detachment caused by a dense subepithelial lymphocytic infiltrate, predominantly composed of mast cells, which serve as key diagnostic markers for interstitial cystitis (IC). WES analysis identified the heterozygous genetic variant c.1253T>G p.Phe418Cys within gene, precisely in its functional domain which actively operates in the hydrolysis of ATP energizing various biological systems. As reported, this gene displays high expression patterns in bladder tissue. The variant, absent in the healthy brother, was inherited from the father which presents mosaicism. The in silico prediction analyses classified this variant as pathogenic, identifying potential alterations in the protein structure.
Although the precise role of should be supported by further studies, we hypothesize that its disruption might impair ATP metabolism, likely altering the nociceptive response and leading to the patient's neuropathy. Further analyses are imperative to validate this research, for laying the groundwork for a specific therapy targeting the genetic dysregulation involved in this condition.
背景/目的:阴部神经病变的症状可能与间质性膀胱炎(IC)的各种症状重叠。据记载,参与ATP代谢、神经病变和IC的基因之间存在明确的相关性。事实上,ATP结合盒(ABC)转运蛋白基因对ATP信号传导至关重要。本研究旨在将该基因与疑似阴部神经病变和IC联系起来。
进行组织学分析以诊断IC,同时通过全外显子组测序(WES)三联体鉴定基因变异,并通过桑格测序进行确认。
我们报告了一名经组织学检查确诊为IC的患者,该患者表现出疑似膀胱和阴部神经病变,尽管未经分析证实。组织学分析显示,上皮下密集的淋巴细胞浸润导致尿路上皮脱离,主要由肥大细胞组成,肥大细胞是间质性膀胱炎(IC)的关键诊断标志物。WES分析在该基因内精确地在其功能域中鉴定出杂合基因变异c.125³T>G p.Phe418Cys,该功能域在为各种生物系统提供能量的ATP水解中起积极作用。据报道,该基因在膀胱组织中显示出高表达模式。该变异在健康的兄弟中不存在,是从呈现嵌合体的父亲那里遗传而来的。计算机预测分析将该变异分类为致病性变异,确定了蛋白质结构中的潜在改变。
尽管该基因的确切作用应通过进一步研究来支持,但我们假设其破坏可能会损害ATP代谢,可能改变伤害性反应并导致患者的神经病变。必须进行进一步分析以验证本研究,为针对这种情况所涉及的基因失调的特定治疗奠定基础。