Sandino Justo, Luzardo Leonella, Morales Enrique, Praga Manuel
Department of Nephrology, University Hospital "12 de Octubre", Madrid, Spain.
Nephrology Center, Hospital de Clínicas, Universidad de la República, Montevideo, Uruguay.
Nephron. 2021;145(6):595-603. doi: 10.1159/000513868. Epub 2021 Mar 5.
Obesity-related glomerulopathy (ORG) is an increasingly recognized cause of end-stage kidney disease. The most common clinical presentation is a slowly increasing nonnephrotic proteinuria that is followed by a progressive decline of kidney function. Key histological findings are glomerulomegaly and lesions of focal and segmental glomerulosclerosis. A central pathogenic mechanism is the increased sodium reabsorption by proximal tubules that typically accompanies obesity. This causes a decrease in the offer of sodium to the macula densa in the distal nephron, which results in a vasodilation of afferent glomerular arterioles and glomerular hyperfiltration. From a clinical point of view, it is essential to differentiate focal segmental glomerulosclerosis secondary to obesity from primary glomerular processes, which requires a careful differential diagnosis. Diet-induced weight loss, bariatric surgery, and renin-angiotensin blockers are the fundamental therapeutic measures in ORG. The recently developed sodium-glucose cotransporter 2 inhibitors and glucagon-like peptide 1 agonist represent a significant advance in renal protection and will probably improve clinical kidney outcomes in ORG.
肥胖相关性肾小球病(ORG)是终末期肾病越来越常见的病因。最常见的临床表现是缓慢加重的非肾病性蛋白尿,随后肾功能逐渐下降。关键的组织学表现为肾小球肥大以及局灶节段性肾小球硬化病变。一个核心致病机制是肥胖通常伴随的近端肾小管钠重吸收增加。这导致远端肾单位致密斑处钠供应减少,进而引起肾小球入球小动脉血管舒张和肾小球高滤过。从临床角度来看,将肥胖继发的局灶节段性肾小球硬化与原发性肾小球疾病相鉴别至关重要,这需要仔细的鉴别诊断。饮食诱导的体重减轻、减肥手术以及肾素 - 血管紧张素阻滞剂是ORG的基本治疗措施。最近研发的钠 - 葡萄糖协同转运蛋白2抑制剂和胰高血糖素样肽1激动剂在肾脏保护方面取得了重大进展,可能会改善ORG患者的临床肾脏结局。