Division of Kidney Diseases, Department of Pediatrics, Feinberg School of Medicine, Northwestern University, Chicago, IL, USA.
Pediatr Nephrol. 2010 Nov;25(11):2223-30. doi: 10.1007/s00467-010-1503-4. Epub 2010 Mar 30.
The data regarding the pathogenesis of progressive kidney disease implicate cytokine effects, physiological factors, and myriad examples of relatively nonspecific cellular dysfunction. The sheer volume of information being generated on this topic threatens to overwhelm our efforts to understand progression in chronic kidney disease or to derive rational strategies to treat it. Here, a conceptual framework is offered for organizing and considering these data. Disease is initiated by an injury that evokes a tissue-specific cellular response. Subsequent structural repair may be effective, or the new structure may be sufficiently changed that it requires an adaptive physiological response. If this adaptation is not successful, subsequent cycles of misdirected repair or maladaptation may lead to progressive nephron loss. To illustrate how this framework can be used to organize our approach to disease pathogenesis, the role of cytokines in proteinuria and progressive glomerular disease is discussed. Finally, this theoretical framework is reconsidered to examine its implications for the diagnosis and treatment of clinical conditions. Application of this schema could have significant relevance to both research inquiry and clinical practice.
有关进行性肾病发病机制的数据提示细胞因子的作用、生理因素和大量相对非特异性细胞功能障碍的例子。关于这一主题所产生的信息量之大,可能使我们努力了解慢性肾病的进展或制定合理的治疗策略受到阻碍。本文提出了一个概念框架,用于组织和考虑这些数据。疾病由损伤引发,引起组织特异性的细胞反应。随后的结构修复可能有效,或者新的结构可能发生了足够的改变,需要适应性的生理反应。如果这种适应不成功,随后的错误修复或适应不良循环可能导致进行性肾单位损失。为了说明如何使用该框架来组织我们对疾病发病机制的方法,讨论了细胞因子在蛋白尿和进行性肾小球疾病中的作用。最后,重新考虑这个理论框架,以检验其对临床疾病诊断和治疗的意义。应用该方案可能对研究和临床实践都具有重要意义。