Omics research in diabetic kidney disease: new biomarker dimensions and new understandings?

被引:13
|
作者
Tofte, Nete [1 ]
Persson, Frederik [1 ]
Rossing, Peter [1 ,2 ]
机构
[1] Steno Diabet Ctr Copenhagen, Gentofte, Denmark
[2] Univ Copenhagen, Dept Clin Med, Copenhagen, Denmark
关键词
Diabetes; Diabetic kidney disease; Biomarkers; Omics; Proteomics; Metabolomics; STAGE RENAL-DISEASE; URINARY PROTEOMICS; DOUBLE-BLIND; FATTY-ACIDS; NEPHROPATHY; RISK; ALBUMINURIA; PROGRESSION; DIAGNOSIS; COMPLICATIONS;
D O I
10.1007/s40620-020-00759-4
中图分类号
R5 [内科学]; R69 [泌尿科学(泌尿生殖系疾病)];
学科分类号
1002 ; 100201 ;
摘要
The use of "omics" is increasing in research areas looking to identify biomarkers or early preclinical signs of disease or to increase understanding of complex pathological processes that determines prognosis of the disease. Diabetic kidney disease is no exception as it is an area in need of further improvement of both understanding and prognosis. In addition, there is a notion that pretreatment investigations using techniques like proteomics, lipidomics and metabolomics can help individualize therapy thus fulfilling the wish for personalized medicine. An increasing number of cohort studies using these techniques are published, but only few have been validated in external cohorts or even replicated by other groups. In essence, to achieve clinical impact and usefulness, prospective validation is needed. So far, only the urinary proteomics based PRIORITY study has tried to do this, as discussed in this review. Other areas are promising, but are currently lacking such efforts. In this review we report and discuss the current status of urinary proteomics as well as plasma metabolomics and lipidomics with an overview of the results so far, and with some comments and perspectives regarding future developments and implementation. As is evident, these techniques are promising, but there is still some way before widespread clinical use can be foreseen.
引用
收藏
页码:931 / 948
页数:18
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