Urinary biomarkers of diabetic kidney disease

医学 蛋白尿 肾脏疾病 疾病 生物标志物 微量白蛋白尿 泌尿系统 生物信息学 糖尿病 肾 糖尿病肾病 肾功能 生物标志物发现 急性肾损伤 内科学 重症监护医学 遗传倾向 肾病科 表观遗传学 终末期肾病 2型糖尿病 蛋白尿
作者
Guido Gembillo,Luca Soraci,Rossella Messina,Lorenzo Lo Cicero,Giuseppe Spadaro,Felicia Cuzzola,Michela Calderone,Maria Federica Ricca,Simona Di Piazza,Flavia Sudano,Luigi Peritore,Domenico Santoro
出处
期刊:World Journal of Diabetes [Baishideng Publishing Group Co (World Journal of Diabetes)]
卷期号:17 (1): 110502-110502 被引量:13
标识
DOI:10.4239/wjd.v17.i1.110502
摘要

Diabetic kidney disease (DKD) represents a significant challenge for diabetes management and public health as it affects the quality of life and metabolic control of millions of people around the world. Characterized by persistent albuminuria and impaired renal function, DKD is an insidious consequence of chronic hyperglycemia and has far-reaching implications for cardiovascular health and mortality. More and more researchers in this field are focusing on the identification of reliable urinary biomarkers that can serve as early indicators of kidney disease progression and enable timely intervention through tailored therapeutic strategies. These biomarkers offer a potential way to improve the diagnosis, monitoring and understanding of kidney disease associated with diabetes, a persistent global health problem. Different types of urinary biomarkers provide insight into the pathophysiological processes involved in DKD. Albumin, for instance, is a crucial biomarker that signals microalbuminuria even before kidney function declines. Other promising candidates include several proteins, such as kidney injury molecule-1, which clearly indicates tubular damage to the kidneys, and neutrophil gelatinase-associated lipocalin, a marker of severe acute kidney injury. In addition, innovations in metabolomics have led to the discovery of certain specific metabolic signatures. These signatures can help distinguish DKD from other forms of kidney disease and show a certain complexity and interconnectivity in overall renal pathology. Finally, the role of many genetic and epigenetic factors is being investigated, highlighting how urinary biomarkers may reflect not only extreme injury but also an individual's genetic predisposition to renal complications. As they become better understood, urinary biomarkers have the potential to significantly improve outcomes and risk stratification for people with DKD. Incorporating biomarker data into routine clinical practice could improve the ability to detect the disease earlier, monitor disease progression more effectively and personalize treatment methods. Moreover, elucidating the mechanisms behind these biomarkers could inspire new treatment approaches that focus on the underlying causes of DKD rather than just treating the symptoms. This will lead to better patient care and improved outcomes for this at-risk group.

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