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本文引用的文献

1
Can we improve our management of dysfunctional voiding in children and adults: International Consultation on Incontinence Research Society; ICI-RS2018?我们能否改善儿童和成人排尿功能障碍的管理:国际尿控协会;ICI-RS2018?
Neurourol Urodyn. 2019 Dec;38 Suppl 5:S82-S89. doi: 10.1002/nau.24088.
2
Oxidative stress and lower urinary tract symptoms: cause or consequence?氧化应激与下尿路症状:原因还是结果?
BJU Int. 2019 May;123(5):749-750. doi: 10.1111/bju.14633.
3
Is bladder blood flow an etiologic factor for the bladder pain syndrome?膀胱血流是否为膀胱疼痛综合征的病因?
Neurourol Urodyn. 2019 Apr;38(4):1135-1141. doi: 10.1002/nau.23969. Epub 2019 Mar 7.
4
Mitochondria, Oxidative Stress and Innate Immunity.线粒体、氧化应激与固有免疫
Front Physiol. 2018 Oct 18;9:1487. doi: 10.3389/fphys.2018.01487. eCollection 2018.
5
The Impact of Chronic Pelvic Ischemia on LUTS and Urinary Levels of Neuroinflammatory, Inflammatory, and Oxidative Stress Markers in Elderly Men: A Case-control Study.慢性盆腔缺血对老年男性下尿路症状及神经炎症、炎症和氧化应激标志物尿水平的影响:一项病例对照研究。
Urology. 2019 Jan;123:230-234. doi: 10.1016/j.urology.2018.09.004. Epub 2018 Sep 13.
6
Do the definitions of the underactive bladder and detrusor underactivity help in managing patients: International Consultation on Incontinence Research Society (ICI-RS) Think Tank 2017?下尿路症状和逼尿肌活动低下的定义是否有助于管理患者:国际尿控协会(ICI-RS)2017 年研究小组座谈会?
Neurourol Urodyn. 2018 Jun;37(S4):S60-S68. doi: 10.1002/nau.23570.
7
Potential vascular mechanisms in an ex vivo functional pig bladder model.在体外功能性猪膀胱模型中的潜在血管机制。
Neurourol Urodyn. 2018 Nov;37(8):2425-2433. doi: 10.1002/nau.23710. Epub 2018 May 19.
8
Occurrence of nocturia is not mediated by nocturnal hypoxia length and severity in patients with sleep-disordered breathing.夜尿症的发生与睡眠呼吸障碍患者夜间低氧长度和严重程度无关。
Sleep Med. 2018 May;45:69-73. doi: 10.1016/j.sleep.2018.01.009. Epub 2018 Feb 7.
9
Is overactive bladder microvasculature disease a component of systemic atheroscleorosis?膀胱过度活动症的微血管病变是否是系统性动脉粥样硬化的一个组成部分?
Neurourol Urodyn. 2018 Apr;37(4):1372-1379. doi: 10.1002/nau.23452. Epub 2017 Nov 15.
10
Mitochondrial stress and activation of PI3K and Akt survival pathway in bladder ischemia.膀胱缺血中线粒体应激与PI3K和Akt生存通路的激活
Res Rep Urol. 2017 Jun 10;9:93-100. doi: 10.2147/RRU.S132082. eCollection 2017.

氧化应激和缺血是否是导致下尿路功能障碍的膀胱损伤的重要原因?来自 2019 年国际尿控协会的报告。

Are oxidative stress and ischemia significant causes of bladder damage leading to lower urinary tract dysfunction? Report from the ICI-RS 2019.

机构信息

Department of Mechanical and Nuclear Engineering, Virginia Commonwealth University, Richmond, Virginia.

Department of Urology, School of Medicine, Koç University, Istanbul, Turkey.

出版信息

Neurourol Urodyn. 2020 Jul;39 Suppl 3(Suppl 3):S16-S22. doi: 10.1002/nau.24313. Epub 2020 Feb 14.

DOI:10.1002/nau.24313
PMID:32056281
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9794413/
Abstract

Several studies indicate that pelvic ischemia and oxidative stress may play a significant role in lower urinary tract dysfunction (LUTD), including detrusor overactivity (DO)/overactive bladder (OAB) and detrusor underactivity (DU)/underactive bladder (UAB). The present article addresses proposal 1: "Are oxidative stress and ischemia significant causes of bladder damage leading to LUTD?" from the 2019 International Consultation on Incontinence-Research Society (ICI-RS) meeting. Bladder ischemia in animals and humans is briefly described, along with the proposed progression from ischemia to LUTD. Bladder ischemia is compared with ischemia of other organs, and the ongoing development of pelvic ischemia animal models is discussed. In addition, the distribution of blood within the bladder during filling and voiding and the challenges of quantification of blood flow in vivo are described. Furthermore, oxidative stress, including potential biomarkers and treatments, and challenges regarding antioxidant therapy for the treatment of LUTD are discussed. Finally, seven critical research questions and proposed studies to answer those questions were identified as priorities that would lead to major advances in the understanding and treatment of lower urinary tract symptoms (LUTS)/LUTD associated with pelvic ischemia and oxidative stress.

摘要

多项研究表明,盆腔缺血和氧化应激可能在下尿路功能障碍(LUTD)中发挥重要作用,包括逼尿肌过度活动(DO)/膀胱过度活动症(OAB)和逼尿肌活动不足(DU)/膀胱活动不足(UAB)。本文探讨了 2019 年国际尿控协会(ICI-RS)会议上提出的问题 1:“氧化应激和缺血是否是导致 LUTD 的膀胱损伤的重要原因?”。简要描述了动物和人类的膀胱缺血,并提出了从缺血到 LUTD 的进展过程。将膀胱缺血与其他器官的缺血进行了比较,并讨论了目前正在开发的盆腔缺血动物模型。此外,还描述了膀胱在充盈和排空过程中血液的分布以及体内血流定量的挑战。此外,还讨论了氧化应激,包括潜在的生物标志物和治疗方法,以及抗氧化治疗治疗 LUTD 的挑战。最后,确定了七个关键的研究问题和拟议的研究,以回答这些问题,这些问题将是理解和治疗与盆腔缺血和氧化应激相关的下尿路症状(LUTS)/LUTD 的主要进展的优先事项。