Research into the effects of sport activity on platelet and endothelial function and on development of atherosclerosis in children.
Research into the effects of sport activity on platelet and endothelial function and on development of atherosclerosis in children.
批准号:
15500431
负责人:
HORIGOME Hitoshi
金额:
$2.37万
依托单位:
依托单位国家:
日本
项目类别:
Grant-in-Aid for Scientific Research (C)
财政年份:
2003
资助国家:
日本
项目状态:
已结题
起止时间:
2003 至 2005
中文摘要
成人疾病,包括动脉粥样硬化,起源于儿童时期。内皮和血小板功能与动脉粥样硬化的进展有关。虽然体重控制对预防成人疾病很重要,但由于生长或运动引起的内皮和血小板功能的变化尚未阐明。此外,还没有建立从儿童期开始的有效饮食和/或运动干预。我们研究了儿童、成人和紫绀型先天性心脏病(CCHD)患者的血小板活性和凝血纤溶蛋白增强内皮功能。材料与方法:1.测定CCHD患者血浆可溶性P-选择素、β-血小板球蛋白(β-TG)、血小板第4因子(PF 4)、蛋白C和蛋白S水平。2.血浆纤溶酶原激活物抑制剂-1(派-1)活性和组织型纤溶酶原激活物(t-PA)抗纤溶酶原激活物(t-PA)活性的昼夜变化(9:00 am vs 4:00 pm) 关于我们 测定CCHD患者血清en水平。3.比较了肥胖成年人在12周限制热量饮食加或不加有氧运动的情况下,体重减轻对活化血小板释放的血小板衍生微粒(PMP)、派-1活性和t-PA抗原的影响。1.血浆P-选择素、β-TG、PF_4水平显著升高,CCHD患者血清游离蛋白S抗原和蛋白C活性明显低于非紫绀型患者。P-选择素、β-TG与红细胞压积呈正相关,蛋白S、蛋白C与红细胞压积呈负相关。2. CCHD患者派-1活性和t-PA抗原水平晨起升高。CCHD患者上午9时和下午4时血浆t-PA抗原水平均高于非紫绀型患者,且与红细胞增多呈正相关。3.肥胖组与非肥胖组比较,PMP、PAI-1活性和t-PA抗原水平均升高,且与体重指数(BMI)相关。干预显著降低PMP、派-1和t-PA抗原水平。PMP值的变化百分比与BMI、脂肪组织mass.Conclusion的变化百分比之间存在显著相关性:通过改善内皮和血小板功能,体重减轻对于预防成人疾病是必不可少的。慢性低氧暴露的CCHD患者存在血小板和凝血纤溶功能异常。剧烈运动会引起短暂的组织缺氧。建立适当的饮食和运动疗法的年龄可能有助于预防成人疾病从童年。少
英文摘要
Introduction : Adult disease, including atherosclerosis, has its origins in childhood. Endothelial and platelet functions are implicated in progression of atherosclerosis. Although weight control is important for prevention of adult disease, changes in endothelial and platelet function due to growth or to exercise have not been clarified. Moreover, effective diet and/or exercise intervention from childhood has not been established. We investigated platelet activity and coagulofibrinolytic proteins that enhance endothelial function in children, adults and patients with cyanotic congenital heart disease (CCHD). We also assessed the effect of weight reduction on these markers.Materials and Method : 1.Plasma levels of soluble P-selectin, beta-thromboglobulin (beta-TG), platelet factor 4 (PF4), protein C and protein S in CCHD patients were measured. 2.Diurnal changes (9:00 am vs 4:00 pm) in plasminogen activator inhibitor-1 (PAI-1) activity and tissue-type plasminogen activator (t-PA) antig … More en levels in CCHD patients were evaluated. 3.Effects of weight reduction on platelet derived microparticles (PMP) released from activated platelets, PAI-1 activity and t-PA antigen were compared between 12-week calorie restricted diet with or without aerobic exercise in obese adults.Results : 1.Plasma levels of P-selectin, beta-TG,PF4 were significantly high, and those of free protein S antigen and protein C activity were significantly low in CCHD patients compared with acyanotic patients. P-selectin and beta-TG correlated positively, and protein S and protein C correlated negatively with hematocrit. 2.Morning increase of PAI-1 activity and t-PA antigen levels was observed in CCHD patients. Plasma levels of t-PA antigen at 9 am and 4 pm were higher in CCHD patients than those in acyanotic patients, and correlated positively with the levels of erythrocytosis. 3.PMP,PAI-1 activity and t-PA antigen values were elevated in obese adults in comparison with non-obese adults, and these three parameters correlated with body mass index (BMI). The intervention significantly reduced PMP,PAI-1 and t-PA antigen levels. There was a significant correlation between percentages of change in PMP values and those in BMI, fat tissue mass.Conclusion : Weight reduction appears to be essential for prevention of adult disease, through improvement of endothelial and platelet functions. There were platelet and coagulofibrinolytic abnormalities in CCHD patients who were exposed to chronic hypoxia. Strenuous exercise would induce transient tissue hypoxia. Establishment of appropriate diet and exercise therapies for age could contribute to prevention of adult disease from childhood. Less
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Horigome H, et al.: "P-selectin and thrombomodulin-protein C-protein S pathway in cyanotic congenital heart disease with secondary erythrocytosis"Thrombosis Research. 112(4). 223-227 (2003)
Horigome H等人:“P-选择素和血栓调节蛋白-蛋白C-蛋白S途径在紫绀型先天性心脏病伴继发性红细胞增多症中的作用”血栓形成研究。
DOI:
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发表时间:
期刊:
影响因子:
--
作者:
[]
通讯作者:
Replacement of the common atrioventricular valve with floating annuloplasty in a patient with univentricular physiology.
对单心室生理患者采用浮动瓣环成形术置换普通房室瓣。
DOI:
--
发表时间:
2006
期刊:
Jpn Thorac Cardiovasc Surg. 54(2)
影响因子:
--
作者:
[Sato M, et al.]
通讯作者:
et al.
Who is at risk for cardiac events in young patients with long QT syndrome?
长 QT 综合征年轻患者中谁有发生心脏事件的风险?
DOI:
--
发表时间:
2003
期刊:
Circ J. 67(12)
影响因子:
--
作者:
[Horigome H, et al., Shiono J. et al., Shiono J. et al., Yoshinaga M. et al.]
通讯作者:
Yoshinaga M. et al.
DOI:
10.1007/s00380-004-0786-4
发表时间:
2005-05-01
期刊:
HEART AND VESSELS
影响因子:
1.5
作者:
[Horigome, H, Sumazaki, R, Matsui, A]
通讯作者:
Matsui, A
A pitfall in ligation of intrahepatic shunting after fontan type operation.
Fontan型手术后肝内分流结扎的陷阱。
DOI:
--
发表时间:
2006
期刊:
Asian Cardiovasc Thorac Ann. 14(1)
影响因子:
--
作者:
[Ikeda A, et al.]
通讯作者:
et al.
共 20 条
Establishment of treatment strategies for early-onset inherited arrhythmias based on genotype-phenotype relationships
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批准号:15K09680
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$3.16万
-
财政年份:2015
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负责人:HORIGOME Hitoshi
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依托单位:
Investigation of the correlation between genetic background and clinical phenotype in congenital long QT syndrome diagnosed in fetal and neonatal life
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批准号:24591599
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$3.41万
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财政年份:2012
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负责人:HORIGOME Hitoshi
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依托单位:
血液凝固線溶系を指標とした幼児期からのメタボリックシンドロームの予防に関する研究
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批准号:21500680
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$2.83万
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财政年份:2009
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负责人:HORIGOME Hitoshi
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依托单位:
A Study on Coagulation and Fibrinolytic Characteristics and Effective Interventions for Childhood Metabolic Syndrome
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批准号:19500591
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$3.0万
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财政年份:2007
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负责人:HORIGOME Hitoshi
-
依托单位:
Research on the developmental changes of central nervous system in the fetus using magnetocardiography and magnetoencephalography
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批准号:12671061
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项目类别:Grant-in-Aid for Scientific Research (C)
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资助金额:$2.11万
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财政年份:2000
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负责人:HORIGOME Hitoshi
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依托单位:
海外基金