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Sureillance and Epidemiologic Research of Duchenne and Becker Muscular Dystrophy

Sureillance and Epidemiologic Research of Duchenne and Becker Muscular Dystrophy
杜氏肌营养不良症和贝克肌营养不良症的可信度和流行病学研究
批准号:
7231276
负责人:
LISA Ann MILLER
金额:
$47.3万
依托单位国家:
美国
项目类别:
财政年份:
2006
资助国家:
美国
项目状态:
已结题
起止时间:
2006-09-01 至 2011-08-31

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中文摘要
翻译
描述(由申请人提供):Duchenne和Becker肌营养不良症(DBMD)是x连锁疾病,据推测每3500名男婴中就有1人患病。这些情况都是随着肌肉无力的进展而发生的,最终会在十几岁到二十岁之间死亡。因此,这些疾病对医疗系统、社区和家庭的影响是巨大的。通过《2001年肌肉萎缩症社区援助、研究和教育修正案》,美国国会颁布了立法,为各种形式的肌肉萎缩症(包括DBMD)提供研究。本法案的一部分授权建立国家肌萎缩症流行病学计划,部长通过疾病控制和预防中心(CDC)主任制定国家肌萎缩症监测计划,以开展流行病学活动,包括收集和分析有关肌萎缩症患者数量、发病率、相关性和症状的信息。为了完成这项任务,2002年,美国疾病控制与预防中心授予亚利桑那州、科罗拉多州、爱荷华州和纽约州四个地点合作协议,以建立一个监测网络,即肌肉萎缩症监测跟踪和研究网络(MD STARnet)。在过去的四年里,MD STARnet网站一直在开发和实施流行病学方法,这些方法将有助于更好地了解DBMD。对于目前的项目,科罗拉多州公共卫生和环境部建议继续作为MD STARnet的一个参与站点,以便:1)在美国产生基于人群的DBMD患病率和发病率,特别注意发病率随时间和种族/民族的差异;2)识别DBMD的早期体征和症状;3)描述DBMD患者家庭接受的医疗和社会服务以及生活质量,以及这些是否因种族/民族和社会经济地位而异;4)调查DBMD的严重程度或病程是否受到所接受治疗类型的变化和所确定的突变类型的影响。我们相信上述目标和活动的实现将对临床医生和家庭都有意义,并将有助于指导肌萎缩症护理标准的发展。
英文摘要
DESCRIPTION (provided by applicant): Duchenne and Becker muscular dystrophies (DBMD) are X-linked disorders presumed to affect 1 in 3,500 male births. These conditions follow a course of progressive muscle weakness leading to death in the late teens to early twenties. As such, the impact of these conditions on medical systems, communities, and families is significant. Through the 'Muscular Dystrophy Community Assistance, Research and Education Amendments of 2001', the United States Congress enacted legislation to provide for research with respect to various forms of muscular dystrophy, including DBMD. A part of this Act authorized the creation of a National Muscular Dystrophy Epidemiology Program, in which the Secretary, acting through the Director of the Centers for Disease Control and Prevention (CDC), provided for a national surveillance program for DBMD for the purpose of carrying out epidemiological activities, including collecting and analyzing information on the number, incidence, correlates, and symptoms of those individuals with DBMD. To fulfill this mandate, in 2002, the CDC awarded four sites - Arizona, Colorado, Iowa and New York - cooperative agreements to develop a surveillance network, the Muscular Dystrophy Surveillance Tracking and Research Network (MD STARnet). MD STARnet sites have been developing and implementing epidemiologic methods that will lead to a better understanding of DBMD over the past four years. For the current project, the Colorado Department of Public Health and Environment proposes to continue as a participating MD STARnet site to: 1) Generate population-based prevalence and incidence rates for DBMD in the United States with particular attention to differences in rates over time and by race/ethnicity; 2) Identify the early signs and symptoms of DBMD; 3) Describe the medical and social services received and quality of life of families of patients with DBMD and whether these vary by race/ethnicity and socioeconomic status; and 4) Investigate whether the severity or course of DBMD is influenced by variation in type of care received and by type of mutation identified. We believe that the accomplishment of the objectives and activities above will be meaningful to both clinicians and families and will help to guide the development of standards of care for muscular dystrophy.
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