Nüsken Eva, Dötsch Jörg, Weber Lutz T, Nüsken Kai-Dietrich
Pediatric Nephrology, Department of Pediatrics, Medical Faculty, University of Cologne, Cologne, Germany.
Front Pediatr. 2018 Feb 27;6:36. doi: 10.3389/fped.2018.00036. eCollection 2018.
Chronic kidney disease affects more than 10% of the population. Programming studies have examined the interrelationship between environmental factors in early life and differences in morbidity and mortality between individuals. A number of important principles has been identified, namely permanent structural modifications of organs and cells, long-lasting adjustments of endocrine regulatory circuits, as well as altered gene transcription. Risk factors include intrauterine deficiencies by disturbed placental function or maternal malnutrition, prematurity, intrauterine and postnatal stress, intrauterine and postnatal overnutrition, as well as dietary dysbalances in postnatal life. This mini-review discusses critical developmental periods and long-term sequelae of renal programming in humans and presents studies examining the underlying mechanisms as well as interventional approaches to "re-program" renal susceptibility toward disease. Clinical manifestations of programmed kidney disease include arterial hypertension, proteinuria, aggravation of inflammatory glomerular disease, and loss of kidney function. Nephron number, regulation of the renin-angiotensin-aldosterone system, renal sodium transport, vasomotor and endothelial function, myogenic response, and tubuloglomerular feedback have been identified as being vulnerable to environmental factors. Oxidative stress levels, metabolic pathways, including insulin, leptin, steroids, and arachidonic acid, DNA methylation, and histone configuration may be significantly altered by adverse environmental conditions. Studies on re-programming interventions focused on dietary or anti-oxidative approaches so far. Further studies that broaden our understanding of renal programming mechanisms are needed to ultimately develop preventive strategies. Targeted re-programming interventions in animal models focusing on known mechanisms will contribute to new concepts which finally will have to be translated to human application. Early nutritional concepts with specific modifications in macro- or micronutrients are among the most promising approaches to improve future renal health.
慢性肾脏病影响着超过10%的人口。编程研究已经探讨了生命早期环境因素与个体发病率和死亡率差异之间的相互关系。已经确定了一些重要原则,即器官和细胞的永久性结构改变、内分泌调节回路的长期调整以及基因转录的改变。风险因素包括胎盘功能紊乱或母亲营养不良导致的宫内营养缺乏、早产、宫内和产后应激、宫内和产后营养过剩以及出生后生活中的饮食失衡。这篇小型综述讨论了人类肾脏编程的关键发育时期和长期后遗症,并介绍了研究潜在机制以及“重新编程”肾脏疾病易感性的干预方法。编程性肾脏疾病的临床表现包括动脉高血压、蛋白尿、炎症性肾小球疾病加重以及肾功能丧失。肾单位数量、肾素 - 血管紧张素 - 醛固酮系统的调节、肾钠转运、血管舒缩和内皮功能、肌源性反应以及肾小管 - 肾小球反馈已被确定为易受环境因素影响。氧化应激水平、代谢途径,包括胰岛素、瘦素、类固醇和花生四烯酸、DNA甲基化以及组蛋白构型可能会因不利的环境条件而发生显著改变。到目前为止,关于重新编程干预的研究集中在饮食或抗氧化方法上。需要进一步开展研究以拓宽我们对肾脏编程机制的理解,从而最终制定预防策略。针对动物模型中已知机制的靶向重新编程干预将有助于形成新的概念,这些概念最终必须转化为人类应用。对常量或微量营养素进行特定调整的早期营养理念是改善未来肾脏健康最有前景的方法之一。