Stanich Jessica A, Carter John D, Whittum-Hudson Judith, Hudson Alan P
Department of Immunology and Microbiology, Wayne State University School of Medicine, Detroit, MI, USA.
Division of Rheumatology, Department of Internal Medicine, University of South Florida School of Medicine, Tampa, FL, USA.
Open Access Rheumatol. 2009 Dec 8;1:179-192. doi: 10.2147/oarrr.s7680. eCollection 2009.
Rheumatoid arthritis (RA) has been described in the medical literature for over two hundred years, but its etiology remains unknown. RA displays phenotypic heterogeneity, and it is a relatively prevalent clinical entity: it affects approximately 1% of the population, resulting in enormous pathologic sequelae. Earlier studies targeting the cause(s) of RA suggested potential infectious involvement, whereas more recent reports have focused on a genetic origin of the disease. However, neither infection nor genetics, nor any other single factor is currently accepted as causative of RA. In this article we review studies relating to the etiology of RA, and those of several related matters, and we conclude that the literature indeed does provide insight into the causes underlying the initiation of RA pathogenesis. Briefly, given the remarkable phenotypic variation of RA, especially in its early stages, as well as a number of other characteristics of the condition, we contend that RA is not a discrete clinical entity with a single etiological source. Rather, we argue that it represents a common clinical endpoint for various starting points, each of which is largely guided by as yet poorly understood aspects of the genetic background of the affected individual. Adoption of this alternative view of the origin of RA will have significant consequences for future research and for development of new therapeutic interventions for this burdensome condition.
类风湿性关节炎(RA)在医学文献中的记载已有两百多年,但它的病因仍然不明。RA表现出表型异质性,是一种相对常见的临床病症:它影响着约1%的人口,会导致严重的病理后遗症。早期针对RA病因的研究表明可能存在感染因素,而最近的报告则聚焦于该疾病的遗传起源。然而,目前无论是感染、遗传,还是任何其他单一因素都未被确认为RA的病因。在本文中,我们回顾了与RA病因及一些相关问题有关的研究,并得出结论,文献确实为RA发病机制起始的潜在原因提供了见解。简而言之,鉴于RA显著的表型变异,尤其是在其早期阶段,以及该病症的一些其他特征,我们认为RA并非具有单一病因的离散临床实体。相反,我们认为它代表了多种起始点的共同临床终点,其中每个起始点在很大程度上都受受影响个体遗传背景中尚未充分了解的方面所引导。采用这种关于RA起源的不同观点将对未来研究以及针对这种疑难病症的新治疗干预措施的开发产生重大影响。