A hypothesis for the etiology of interstitial cystitis.
A hypothesis for the etiology of interstitial cystitis.
复制标题
间质性膀胱炎病因学的假设。
DOI:
10.1007/978-1-4419-8889-8_43
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发表时间:
2003
影响因子:
--
通讯作者:
Elgavish,Ada
中科院分区:
文献类型:
--
作者:
Elgavish,Ada
Interstitial cystitis (IC) is a chronic inflammatory disease of the bladder wall. The etiology is obscure.18,19,35,44,47,56Several theories for the etiology of IC have been proposed over the years, including infection,6,56immunological etiology,1leaky urothelium resulting from a deficiency of its surface coat of glycosaminoglycans,41,42activated mast cells,6,49and neurogenic etiology.6,17However, none of these theories have been proven beyond doubt.6The rapid onset of IC, its appearance in mid-life, and the absence of strong family association have suggested to us8–11and many others6that IC could be an acquired disease, possibly caused by injury. Recurrent exposure to bacterial infection, which is common in the bladder, has been proposed as a putative mechanism of injury.47,56Earlier studies were based on the assumption that the sole avenue for the interaction of noxious agents with the bladder is exposure of terminally differentiated “umbrella” cells to agents in the lumen. However, mere exposure of the superficial layer to injury, such as bacterial infection, may not result in chronic changes in the urothelium. These terminally differentiated cells are often shed in response to infectious agents,2,38and unexposed progenitors of urothelial cells located in the basal layer (stem cells) divide and re-epithelize the injured area.