Fry Christopher H, Sahai Arun, Vahabi Bahareh, Kanai Anthony J, Birder Lori A
Department of Biochemistry and Physiology, University of Surrey, Guildford, Surrey, United Kingdom.
Neurourol Urodyn. 2014 Jun;33(5):602-5. doi: 10.1002/nau.22558. Epub 2014 Jan 16.
A biomarker is an entity that measures a normal or pathological process, or the response to an intervention. A biomarker must measure exclusively and be sufficiently sensitive to the process of interest. Alternatively, a biomarker may give clues regarding the underlying pathology of the condition and be a useful research or specialist tool. If a biomarker is to be of practical benefit then it must also be economical and practical to use. This article will consider chemical moieties as biomarkers, although in principle physical markers (e.g., bladder wall thickness) could also be defined as such.
The validation of a biomarker for detrusor overactivity (DO) must appreciate the fact that the condition is likely to multifactorial and thus no single entity may be sufficiently selective and sensitive. However, more specific conditions, such as bladder pain associated with DO, may make the biomarker search easier. Several prospective agents including antiproliferative factor (APF) and epidermal growth factors (EGF) are discussed. Several urinary biomarkers, including neurotrophins (NGF, BDNF) and cytokines, and a serum marker, C-reactive protein, are considered as reaching the above criteria. All suffer from relatively poor lack of discrimination, as they all change in response to other, often inflammatory, conditions; BDNF may offer the highest expectations. Urinary ATP has also been proposed as a DO/OAB biomarker but requires further evaluation. Finally genetic markers offer potential to understand more about the pathophysiology of DO/OAB. The increasing availability of genome-wide association studies and micro-RNA assays offer genetic markers as a new generation of biomarkers. Neurourol. Urodynam. 33:602-605, 2014. © 2014 Wiley Periodicals, Inc.
生物标志物是一种可测量正常或病理过程,或对干预措施反应的实体。生物标志物必须具有专一性测量能力,并且对感兴趣的过程具有足够的敏感性。此外,生物标志物可能会提供有关疾病潜在病理学的线索,是一种有用的研究或专业工具。如果一种生物标志物要具有实际应用价值,那么它还必须经济实用。本文将把化学部分视为生物标志物,尽管原则上物理标志物(如膀胱壁厚度)也可如此定义。
逼尿肌过度活动(DO)生物标志物的验证必须认识到该疾病可能是多因素导致的,因此没有单一实体可能具有足够的选择性和敏感性。然而,更具体的情况,如与DO相关的膀胱疼痛,可能会使生物标志物的寻找更容易。文中讨论了几种前瞻性物质,包括抗增殖因子(APF)和表皮生长因子(EGF)。几种尿液生物标志物,包括神经营养因子(NGF、BDNF)和细胞因子,以及一种血清标志物C反应蛋白,被认为符合上述标准。它们都存在相对较差的鉴别能力不足的问题,因为它们都会因其他(通常是炎症性)情况而发生变化;BDNF可能最具潜力。尿液ATP也被提议作为DO/OAB生物标志物,但需要进一步评估。最后,基因标志物为更深入了解DO/OAB的病理生理学提供了潜力。全基因组关联研究和微小RNA检测的日益普及,为基因标志物作为新一代生物标志物提供了可能。《神经泌尿学与尿动力学》33:602 - 605,2014年。© 2014威利期刊公司