Zbrzeźniak-Suszczewicz Justyna, Winiarska Agata, Perkowska-Ptasińska Agnieszka, Stompór Tomasz
Department of Nephrology, Hypertension and Internal Medicine, University of Warmia and Mazury in Olsztyn, 10-719 Olsztyn, Poland.
Department of Pathology, Medical University of Warsaw, 02-091 Warsaw, Poland.
Int J Mol Sci. 2025 Jun 28;26(13):6247. doi: 10.3390/ijms26136247.
Obesity, hypertension, and chronic kidney disease (CKD) constitute the deadly trinity of modern threats for populations of both developed and developing countries. These diseases (together with type 2 diabetes) are closely linked in their pathophysiology and result in increasing cardiovascular (CV) morbidity and premature death from CV causes. In this review, we focused on the kidney as the target of obesity-related disorders. Obesity-related glomerulosclerosis (ORG) represents a pattern of renal injury caused solely or predominantly by obesity; usually, it is superimposed on chronic kidney disease (CKD) from other causes, such as diabetic kidney disease, hypertensive kidney disease, type 2 cardiorenal syndrome, primary or secondary glomerulopathies, and others. Adipose tissue contributes to kidney injury in several ways: it releases proinflammatory cytokines and growth factors, leading to podocyte and mesangial cell injury and glomerulosclerosis. In particular, perirenal adipose tissue (PRAT), besides exerting paracrine and endocrine effects on the kidney, modifies its function via compression on renal parenchyma and vessels. The intrinsic ability of the kidneys in obesity to increase the reabsorption of sodium warrants intraglomerular hypertension and hyperfiltration, followed by progressive renal injury. Lifestyle interventions and pharmacological agents, as well as metabolic (bariatric) surgery resulting in weight reduction, may also be beneficial for the kidneys. Using GLP1 receptor agonists (with a special focus on subcutaneous semaglutide and tirzepatide) seems to be the most promising treatment strategy for preventing kidney injury in obese individuals.
肥胖、高血压和慢性肾脏病(CKD)构成了发达国家和发展中国家人群面临的现代致命三联症。这些疾病(连同2型糖尿病)在病理生理学上密切相关,会导致心血管(CV)发病率增加以及因心血管原因导致的过早死亡。在本综述中,我们将重点关注肾脏作为肥胖相关疾病的靶器官。肥胖相关肾小球硬化(ORG)代表一种仅由肥胖或主要由肥胖引起的肾损伤模式;通常,它叠加在由其他原因引起的慢性肾脏病(CKD)之上,如糖尿病肾病、高血压肾病、2型心肾综合征、原发性或继发性肾小球病等。脂肪组织通过多种方式导致肾损伤:它释放促炎细胞因子和生长因子,导致足细胞和系膜细胞损伤以及肾小球硬化。特别是肾周脂肪组织(PRAT),除了对肾脏发挥旁分泌和内分泌作用外,还通过对肾实质和血管的压迫来改变其功能。肥胖时肾脏增加钠重吸收的内在能力会导致肾小球内高压和超滤,进而导致进行性肾损伤。生活方式干预、药物治疗以及导致体重减轻的代谢(减肥)手术,对肾脏可能也有益处。使用胰高血糖素样肽1(GLP1)受体激动剂(特别关注皮下注射司美格鲁肽和替尔泊肽)似乎是预防肥胖个体肾损伤最有前景的治疗策略。