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Takamune Takahashi
Personal Information
Title
Associate Professor
Expertise
Nephropathy
Institution
Vanderbilt University
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1
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2
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2
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Noninvasive evaluation of diabetic nephropathy using magnetization transfer MRI
Diabetic nephropathy (DN) is a major diabetic complication that determines the morbidity and mortality of the diabetic patients. However, currently available clinical tests or risk factors do not reliably assess its severity or progression in individual patients, making it difficult to do the targeted and intensified treatment to high-risk patient populations. One of the major limitations of current tests is their inability to reliably assess the extent of renal fibrosis in the affected kidney, even though renal fibrosis is the most important pathological change to evaluate or predict the long-term outcome of the patient. Although renal biopsy can diagnose fibrosis, it is invasive and prone to sampling errors, and does not reliably measure renal fibrosis in the affected kidney. Thus, a non-invasive test that better evaluate renal fibrosis in diabetic kidney should greatly improve the assessment of this disease, enabling better treatment protocol and prognosis.In recent decade, a variety of magnetic resonance imaging (MRI) methods have been developed andapplied to human disease including cancer and brain disorders. These techniques have enabled us toassess the pathological changes in disease organ at molecular and cellular levels. Magnetization transfer(MT) imaging is a MRI technique that evaluates large and immobile macromolecules distributed within thetissue and could provide a means to evaluate the pathological events that are accompanied by the changes of macromolecular components, such as fibrosis and apoptosis. However, this method is poorly applied to kidney disease including DN. Therefore, here we will evaluate the utility of MT imaging in measuring renal fibrosis in diabetic kidney using a mouse model of progressive DN (db/db eNOS -/- mice). The aims of thisstudy are: 1) To optimize and establish the MT protocol for mouse kidney imaging; 2) To examine the correlation between MT data and histological or biochemical measures of renal fibrosis. Thus, thisapplication explores a new MRI test to assess renal fibrosis in DN. Given the fact that this MRI technique can be translated to clinics, the present work should efficiently improve the outcome of the patients with DN.
Progress Reports
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Noninvasive evaluation of diabetic nephropathy using magnetization transfer MRI (Takahashi, Takamune)
3/27/2017
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PubMed ID
Status
Year: 2009; Items: 1
Reduction of renal superoxide dismutase in progressive diabetic nephropathy.
Fujita H, Fujishima H, Chida S, Takahashi K, Qi Z, Kanetsuna Y, Breyer MD, Harris RC, Yamada Y, Takahashi T
Journal of the American Society of Nephrology : JASN
, 2009 (20(6)), 1303 - 1313
Takahashi, Takamune
19470681
Published
Year: 2007; Items: 1
Deficiency of endothelial nitric-oxide synthase confers susceptibility to diabetic nephropathy in nephropathy-resistant inbred mice.
Kanetsuna Y, Takahashi K, Nagata M, Gannon MA, Breyer MD, Harris RC, Takahashi T
The American journal of pathology
, 2007 (170), 1473 - 1484
Takahashi, Takamune
17456755
Published
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Steering Committee
The DiaComp Steering Committee is the governing body of the consortium. The principle function of this committee is to guide the scientific direction of the consortium. This is accomplished by creating various subcommittees necessary to advance the scientific goals and providing guidance to the broader complications research community. Policies for the consortium are developed through consultation with the
External Evaluation Committee
Nephropathy
The DiaComp Nephropathy Committee has the principal function of furthering the mission of the consortium with regard to diabetic kidney disease.
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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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