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Publication
Insight into the genetics of diabetic nephropathy through the study of mice.
Authors
Breyer MD, Qi Z, Tchekneva EE, Harris RC
Submitted By
Raymond Harris on 2/8/2009
Status
Published
Journal
Current opinion in nephrology and hypertension
Year
2008
Date Published
1/1/2008
Volume : Pages
17(1) : 82 - 86
PubMed Reference
18090675
Abstract
PURPOSE OF REVIEW: To discuss mouse models of diabetic nephropathy and their use
in discovering genetic risk factors predisposing to diabetic nephropathy. RECENT
FINDINGS: Despite occurring in only 10-40% of diabetic patients, diabetic
nephropathy is the largest single cause of end stage renal disease in the USA.
Accumulated evidence points to critical genetic factors that predispose a subset
of diabetic patients to nephropathy.Defining the genes that confer risk for
nephropathy in human populations has proven challenging. The use of robust
genetic reagents available in the laboratory mouse provides a complementary
approach to defining genes that predispose to diabetic nephropathy in mice and
humans. These findings support the existence of dominant mutations predisposing
to diabetic nephropathy in mice as well as substantiating an important role for
eNOS in forestalling the development of diabetic nephropathy. SUMMARY: When
studied for a sufficient duration of diabetic hyperglycemia, some strains of
mice exhibit changes similar to those of human diabetic nephropathy. The unique
genetic reagents in mice should help accelerate the identification of genes
predisposing to diabetic nephropathy.
Investigators with authorship
Name
Institution
Matthew Breyer
Johnson & Johnson
Raymond Harris
Vanderbilt University
Complications
All Complications
Bioinformatics
Bone
Cardiomyopathy
Cardiovascular
Gastro-Intestinal (GI)
Nephropathy
Neuropathy & Neurocognition
Pediatric Endocrinology
Retinopathy
Uropathy
Wound Healing
Genes
Symbol
Description
Nos3
nitric oxide synthase 3, endothelial cell
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Please acknowledge all posters, manuscripts or scientific materials that were generated in part or whole using funds from the Diabetic Complications Consortium(DiaComp) using the following text:
Financial support for this work provided by the NIDDK Diabetic Complications Consortium (RRID:SCR_001415, www.diacomp.org), grants DK076169 and DK115255
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