Biomedical Institute for Global Health Research and Technology (BIGHEART), National University of Singapore (NUS), Singapore, Singapore.
National University of Singapore, Singapore, Singapore.
Front Immunol. 2018 Jun 4;9:1208. doi: 10.3389/fimmu.2018.01208. eCollection 2018.
The immune system is highly dynamic and regulated by many baseline characteristic factors. As such, significant variability may exist among different patient groups suffering from the same autoimmune disease (AD). However, contemporary research practices tend to take the reductionist aggregate approach: they do not segment AD patients before embarking on biomarker discovery. This approach has been productive: many novel AD biomarkers have recently been discovered. Yet, subsequent validation studies of these biomarkers tend to suffer from a lack of specificity, sensitivity, and reproducibility which hamper their translation for clinical use. To enhance reproducibility in validation studies, an optimal discovery-phase study design is paramount: one which takes into account different parameters affecting the immune system biology. In this systematic review, we highlight need for stratification in one such parameter, i.e., sex stratification. We will first explore sex differences in immune system biology and AD prevalence, followed by reported sex-bias in the clinical phenotypes of two ADs-one which more commonly affects females: systemic lupus erythematosus, and one which more commonly affects males: ankylosing spondylitis. The practice of sex stratification in biomarker research may not only advance the discovery of sex-specific AD biomarkers but more importantly, promote reproducibility in subsequent validation studies, thus easing the translation of these novel biomarkers from bench to bedside to improve AD diagnosis. In addition, such practice will also promote deeper understanding for differential AD pathophysiology in males and females, which will be useful for the development of more effective interventions for each sex type.
免疫系统具有高度的动态性,并受许多基线特征因素的调节。因此,患有同种自身免疫性疾病 (AD) 的不同患者群体之间可能存在显著的可变性。然而,当代研究实践往往采用还原论的综合方法:在开始发现生物标志物之前,他们不会对 AD 患者进行细分。这种方法已经取得了成效:最近发现了许多新的 AD 生物标志物。然而,这些生物标志物的后续验证研究往往存在特异性、敏感性和可重复性的缺乏,这阻碍了它们在临床上的应用。为了提高验证研究的可重复性,最佳的发现阶段研究设计至关重要:该设计需要考虑影响免疫系统生物学的不同参数。在本系统评价中,我们强调需要对一个这样的参数进行分层,即性别分层。我们将首先探讨免疫系统生物学和 AD 患病率中的性别差异,然后报告两种 AD 的临床表型中的性别偏见:一种更常见于女性的疾病:系统性红斑狼疮,另一种更常见于男性的疾病:强直性脊柱炎。在生物标志物研究中进行性别分层的做法不仅可能推进发现特定于性别的 AD 生物标志物,而且更重要的是,促进后续验证研究的可重复性,从而将这些新的生物标志物从实验室推向床边,以改善 AD 的诊断。此外,这种做法还将促进对男性和女性 AD 病理生理学差异的更深入理解,这对于为每种性别类型开发更有效的干预措施将是有用的。