2015 Fiscal Year Final Research Report
Pathophysiological significance of cathepsin K in dilated cardiomyopathy
Project/Area Number |
25860594
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Research Category |
Grant-in-Aid for Young Scientists (B)
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Allocation Type | Multi-year Fund |
Research Field |
Cardiovascular medicine
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Research Institution | Nagoya University |
Principal Investigator |
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Research Collaborator |
MUROHARA TOYOAKI 名古屋大学, 医学系研究科, 教授 (90299503)
BANDO YASUKO 名古屋大学, 医学部附属病院, 講師 (60452190)
MORIMOTO RYOTA 名古屋大学, 医学系研究科, 寄附講座助教 (00755499)
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Project Period (FY) |
2013-04-01 – 2016-03-31
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Keywords | 拡張型心筋症 / カテプシン |
Outline of Final Research Achievements |
To clarify the pathophysiological role of cathepsin K, we investigated the association between the expression of cathepsin K and pathophysiological index, clinical imaging data, or prognosis in patients with dilated cardiomyopathy (DCM). The results of our studies were as follows; 1) Myocardial fibrosis and impaired left ventricular (LV) relaxation is more serious in late gadolinium enhancement positive group. Unfortunately, the expression of cathepsin K was not associated with the extent of fibrosis. 2) LV phase entropy using 99mTc-sestamibi gated myocardial perfusion SPECT, which may reflect impairment of Ca2+-handling caused by decreased SERCA2a mRNA levels, is a novel prognostic predictor of adverse cardiac events in patients with DCM with a narrow QRS complex. 3) The combined reduction of campesterol and lathosterol that indicated intestinal cholesterol absorption and liver synthesis predicts future cardiac events in patients with early-stage DCM.
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Free Research Field |
医歯薬学
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