Lau Wei Ling, Kalantar-Zadeh Kamyar, Vaziri Nosratola D
Division of Nephrology and Hypertension, University of California Irvine, Orange, Calif., USA.
Nephron. 2015;130(2):92-8. doi: 10.1159/000381990. Epub 2015 May 9.
Chronic inflammation is a non-traditional risk factor for cardiovascular mortality in the chronic kidney disease (CKD) population. In recent years, the gastrointestinal tract has emerged as a major instigator of systemic inflammation in CKD. Postmortem studies previously discovered gut wall inflammation throughout the digestive tract in chronic dialysis patients. In CKD animals, colon wall inflammation is associated with breakdown of the epithelial tight junction barrier ('leaky gut') and translocation of bacterial DNA and endotoxin into the bloodstream. Gut bacterial DNA and endotoxin have also been detected in the serum from CKD and dialysis patients, whereby endotoxin levels increase with the CKD stage and correlate with the severity of systemic inflammation in the dialysis population. The CKD diet that is low in plant fiber and symbiotic organisms (in adherence with low potassium, low phosphorus intake) can alter the normal gut microbiome, leading to overgrowth of bacteria that produce uremic toxins such as cresyl and indoxyl molecules. The translocation of these toxins from the 'leaky gut' into the bloodstream further promotes systemic inflammation, adverse cardiovascular outcomes and CKD progression. Data are lacking on optimal fiber and yogurt consumption in CKD that would favor growth of a more symbiotic microbiome while avoiding potassium and phosphorus overload. Prebiotic and probiotic formulations have shown promise in small clinical trials, in terms of lowering serum levels of uremic toxins and improving quality of life. The evidence points to a strong relationship between intestinal inflammation and adverse outcomes in CKD, and more trials investigating gut-targeted therapeutics are needed.
慢性炎症是慢性肾脏病(CKD)人群心血管死亡的非传统危险因素。近年来,胃肠道已成为CKD全身性炎症的主要诱因。尸检研究先前发现慢性透析患者整个消化道存在肠壁炎症。在CKD动物中,结肠壁炎症与上皮紧密连接屏障的破坏(“肠漏”)以及细菌DNA和内毒素向血液中的移位有关。在CKD患者和透析患者的血清中也检测到了肠道细菌DNA和内毒素,其中内毒素水平随CKD分期增加,并与透析人群全身性炎症的严重程度相关。低植物纤维和共生生物的CKD饮食(符合低钾、低磷摄入)会改变正常的肠道微生物群,导致产生甲酚和吲哚等尿毒症毒素的细菌过度生长。这些毒素从“肠漏”向血液中的移位进一步促进了全身性炎症、不良心血管结局和CKD进展。关于CKD中最佳纤维和酸奶摄入量的数据尚缺,这些摄入量应有利于更具共生性的微生物群生长,同时避免钾和磷过载。益生元和益生菌制剂在小型临床试验中已显示出前景,可降低血清尿毒症毒素水平并改善生活质量。证据表明肠道炎症与CKD不良结局之间存在密切关系,需要更多试验来研究针对肠道的治疗方法。