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PREVALENCE AND PROGRESSION OF DM2 RISK IN MA YOUTH

PREVALENCE AND PROGRESSION OF DM2 RISK IN MA YOUTH
MA 青年中 DM2 风险的患病率和进展
批准号:
6635343
负责人:
DANIEL ESTEN HALE
金额:
$32.63万
依托单位国家:
美国
项目类别:
财政年份:
2001
资助国家:
美国
项目状态:
已结题
起止时间:
2001-06-01 至 2005-02-28

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中文摘要
翻译
在过去的5年里,美国少数民族儿童中有2型糖尿病(DM2)的报道,包括墨西哥裔美国人(MA)。局部来看,在过去3年中,患DM2的MA儿童多于患1型糖尿病(DM1)的儿童,尽管DM1的发病率并没有下降。虽然在MA成人中DM2的高流行率和发病率上升、相关危险因素和合并症有广泛的文献记载,但在具有相同遗传遗传和生活在相同环境中的MA儿童中,这些问题的流行率或发病率的信息很少。关于儿童从遗传风险到显性疾病的自然进展,人们所知的就更少了。因此,本建议的具体目的是:1。确定大约2000名同质组(4年级,9岁和10岁)MA儿童的危险因素,高胰岛素血症,空腹血糖受损和糖尿病的患病率(1期)2。通过详细的临床评估和广泛的生化调查,探讨约300名MA儿童的危险因素与葡萄糖稳态异常之间的关系。这些儿童将分为3个亚群:空腹血糖受损、高风险和低风险。(第二阶段);检查3个亚组在4年内物理和生化参数的时间变化(第3阶段)。每年都会看到孩子们,因为这是一个身体动态变化的时期。这些研究的完成将提供对MA儿童中葡萄糖稳态异常患病率的估计,增加对相对早期和早期代谢异常的理解,允许检查这些异常的自然进展,并提供新的美国糖尿病协会筛查MA儿童指南的适用性评估。
英文摘要
Over the past 5 years there have been reports of type 2 diabetes (DM2) in minority children in the U.S., including Mexican Americans (MA). Locally, in the past 3 years more MA children were seen with DM2 than type 1 diabetes (DM1), although the incidence of DM1 has not decreased. While the high prevalence and rising incidence of DM2, related risk factors and co-morbidities in MA adults is extensively documented, minimal information is available on the prevalence or incidence of these problems in MA children who share the same genetic heritage and live in the same environment. Even less is known about the natural progression from genetic risk to overt disease in children. Therefore, the specific aims of this proposal are to: 1. Determine the prevalence of risk factors, hyperinsulinism, impaired fasting glucose and diabetes in a homogenous group of approximately 2000 MA children 4th grade, 9 and 10 years of age) (Phase 1) 2. Explore the relationship between risk factors and glucose homeostasis abnormalities in approximately 300 MA children using a detailed clinical assessment and extensive biochemical investigations. The children will be in 3 subsets: impaired fasting glucose, high-risk, and low risk. (Phase 2). 3. Examine the temporal change in physical and biochemical parameters in the 3 subsets over 4-years (Phase 3). Children will be seen annually, because this is a period of dynamic physical change. Completion of the proposed studies will provide an estimate of the prevalence of glucose homeostasis abnormalities in MA children, increase understanding of the metabolic abnormalities at a relatively early age and stage, permit an examination of the natural progression of these abnormalities, and provide an assessment of the applicability of the new American Diabetes Association guidelines for screening MA children.
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