Department of Obstetrics and Gynecology, Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands.
Department of Human Genetics, Radboud University Medical Center, 6525 GA Nijmegen, The Netherlands.
Int J Mol Sci. 2022 Mar 21;23(6):3401. doi: 10.3390/ijms23063401.
Stress urinary incontinence (SUI) is a common and burdensome condition. Because of the large knowledge gap around the molecular processes involved in its pathophysiology, the aim of this review was to provide a systematic overview of genetic variants, gene and protein expression changes related to SUI in human and animal studies. On 5 January 2021, a systematic search was performed in Pubmed, Embase, Web of Science, and the Cochrane library. The screening process and quality assessment were performed in duplicate, using predefined inclusion criteria and different quality assessment tools for human and animal studies respectively. The extracted data were grouped in themes per outcome measure, according to their functions in cellular processes, and synthesized in a narrative review. Finally, 107 studies were included, of which 35 used animal models (rats and mice). Resulting from the most examined processes, the evidence suggests that SUI is associated with altered extracellular matrix metabolism, estrogen receptors, oxidative stress, apoptosis, inflammation, neurodegenerative processes, and muscle cell differentiation and contractility. Due to heterogeneity in the studies (e.g., in examined tissues), the precise contribution of the associated genes and proteins in relation to SUI pathophysiology remained unclear. Future research should focus on possible contributors to these alterations.
压力性尿失禁(SUI)是一种常见且令人痛苦的疾病。由于涉及 SUI 病理生理学的分子过程的知识差距较大,因此本综述旨在提供与人类和动物研究中 SUI 相关的遗传变异、基因和蛋白质表达变化的系统概述。2021 年 1 月 5 日,在 Pubmed、Embase、Web of Science 和 Cochrane 图书馆中进行了系统搜索。使用预设的纳入标准和分别用于人类和动物研究的不同质量评估工具,对筛选过程和质量评估进行了重复操作。根据细胞过程的功能,将提取的数据按每个结果测量指标分组,并以叙述性综述的形式进行综合。最终纳入了 107 项研究,其中 35 项使用了动物模型(大鼠和小鼠)。从最受关注的过程来看,有证据表明 SUI 与细胞外基质代谢、雌激素受体、氧化应激、细胞凋亡、炎症、神经退行性过程以及肌肉细胞分化和收缩性改变有关。由于研究中的异质性(例如,在检查的组织中),与 SUI 病理生理学相关的相关基因和蛋白质的确切贡献仍不清楚。未来的研究应集中于这些改变的可能原因。