Drug Discovery for Diabetic Nephropathy: Trying the Leap From Mouse to Man

被引:11
作者
Breyer, Matthew D. [1 ]
机构
[1] Lilly Res Labs, Biotechnol Discovery Res, Lead Generat Biol, Indianapolis, IN 46285 USA
关键词
Kidney; proteinuria; creatinine; hypertension; mouse; GLOMERULAR-FILTRATION-RATE; STAGE RENAL-DISEASE; SERUM CYSTATIN-C; BARDOXOLONE METHYL; PLASMA CREATININE; TUBULAR SECRETION; KIDNEY-FUNCTION; BLOOD-PRESSURE; MUTANT MICE; ALBUMINURIA;
D O I
10.1016/j.semnephrol.2012.07.007
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
Diabetic nephropathy is the single major cause of kidney failure in the industrialized world and given the emerging global pandemic of diabetes mellitus, its prevalence is expected to only increase. Because of the lack of dynamic biomarkers that define the rate of kidney function loss, there are few proof-of-concept clinical trials for new therapeutics to treat diabetic nephropathy. A molecular understanding of the pathogenesis of diabetic nephropathy also is lacking. These deficiencies are magnified by the fact that most mouse models of diabetic nephropathy fail to show progressive kidney disease. Recently, some mouse models that showed requisite phenotypic changes of diabetic nephropathy have been identified. Validation of results obtained in these experimental models, and showing whether they accurately can predict clinical response to therapeutics in human diabetic nephropathy, must now be established.© 2012 Elsevier Inc.
引用
收藏
页码:445 / 451
页数:7
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