Khanam Afreen, Ahmad Saheem, Husain Arbab
Department of Biotechnology & Life Science, Institute of Biomedical Education & Research, Mangalayatan University, Aligarh, Uttar Pradesh, India.
Department of Medical Laboratory Sciences, College of Applied Medical Sciences, University of Hail, Hail-2440, Saudi Arabia.
Curr Protein Pept Sci. 2023;24(1):2-6. doi: 10.2174/1389203724666221108120715.
In 2007, diabetes affected around 244 million people across the globe. The number of diabetics worldwide is projected to reach 370 million by 2030. With diabetes incidence reaching epidemic proportions globally, diabetic nephropathy (DN) has emerged as one of the most difficult health conditions. Although therapeutic approaches such as rigorous blood glucose and blood pressure management are successful in preventing DN, they are far from ideal, and the number of diabetic patients with endstage renal disease continues to grow. As a result, a unique treatment approach for DN should be devised. There is mounting evidence that advanced glycation end products (AGEs), senescent macro protein derivatives generated at an accelerated pace in DN, contribute to DN by generating oxidative stress. The purpose of this article is to discuss the pathophysiological significance of AGEs and their receptor in DN.
2007年,全球约有2.44亿人患有糖尿病。预计到2030年,全球糖尿病患者人数将达到3.7亿。随着糖尿病发病率在全球达到流行程度,糖尿病肾病(DN)已成为最棘手的健康问题之一。尽管严格控制血糖和血压等治疗方法在预防DN方面取得了成功,但它们远非理想方案,终末期肾病糖尿病患者的数量仍在持续增加。因此,应设计一种独特的DN治疗方法。越来越多的证据表明,晚期糖基化终产物(AGEs)是在DN中加速生成的衰老大分子蛋白质衍生物,通过产生氧化应激导致DN。本文旨在探讨AGEs及其受体在DN中的病理生理意义。