Childhood Origins for Cardiac Structure and Function
Childhood Origins for Cardiac Structure and Function
批准号:
8492156
负责人:
SHUMEI S SUN
金额:
$63.81万
依托单位国家:
美国
项目类别:
财政年份:
2012
资助国家:
美国
项目状态:
已结题
起止时间:
2012-07-01 至 2016-05-31
关键词:
AddressAdolescenceAdolescentAdultAffectAgeAppearanceBiological MarkersBirthBlood PressureBody CompositionBody SizeBody fatCardiacCenters for Disease Control and Prevention (U.S.)Central obesityChildChildhoodCongenital Heart DefectsConsentCountryDataData SetDerivation procedureDevelopmentEarly identificationEpidemicFatty acid glycerol estersGrowthHeightHypertensionIndividualInterventionLeadLeftLeft Ventricular Ejection FractionLeft Ventricular MassLifeLife StyleLongitudinal StudiesMeasurementMeasuresMetabolic syndromeModelingNormal RangeObesityParticipantPathologicPhysiologicalPopulation StudyPrevalenceProceduresProcessPublic HealthRelative (related person)RiskShortening FractionStructureThickTimeVentricularage groupbaseboyscationic antimicrobial protein CAP 37experiencefallsgirlshigh riskindexingnormotensiveobesity in childrenpublic health relevancesexsexual dimorphismwaist circumference
中文摘要
描述(申请人提供):影响该国儿童和青少年的儿童肥胖症的流行导致这些年龄段的高血压患病率增加。对FELS纵向研究(FLS)数据集的分析表明,儿童时期的血压升高会准确地跟踪到成年,而童年时期的血压升高,即使在被认为是正常的范围内-从国家疾病控制与预防中心增长图表(2000)的第70%到第95%-准确地预测成年后的高血压和代谢综合征。鉴于肥胖和高血压之间的密切联系,以及高血压与心脏结构和功能异常的关系,确定儿童肥胖是否预示着日后心脏结构和/或功能的异常,这对公共卫生具有重要意义。我们准备询问FLS数据集的一部分来解决这个问题。FLS数据集的相关部分包括从出生到8岁到成年期间对750名同意接受超声心动图研究的参与者进行的一系列人体测量和血压测量。分层和集群纵向建模程序将应用于这组独特的系列测量,以阐明儿童肥胖、血压、成熟速度和心脏结构和功能异常之间的关系。我们计划调查的具体目标包括确定儿童血压、体型和身体成分对(1)血压、(2)心脏结构和(3)成人几十年后相同受试者的心功能的影响。我们有750多项超声心动图研究可供分析,从中可以得出左心室重量指数(LVMI)、室间隔厚度(IVST)和相对室壁厚度(RWT)的结构性测量结果,以及射血分数(EF)和左心室短轴缩短率(LVSF)的功能性测量结果。这些拟议的分析有可能量化成年后高血压和心脏结构和功能异常的风险,给定儿童和青少年时期的身体大小、身体成分和血压的某些值,即使这些值落在目前可接受的正常值范围内。如果我们在儿童中发现预测高血压和/或成人心脏结构和功能异常的生物标志物,那么可以在不可逆转的病理变化发生之前对具有这些生物标志物的儿童进行更彻底的评估,并提供生活方式和/或药物干预。相反,我们提出的分析也有可能确定一组儿童和青少年时期的身体大小、身体成分和血压范围,这些范围与高血压或以后生活中的心脏结构和功能异常无关,可以用来预测成年后血压正常,没有心脏结构或功能异常。
英文摘要
DESCRIPTION (provided by applicant): The epidemic of childhood obesity that has affected children and adolescents in this country has led to an increased prevalence of hypertension in these age groups. Analyses of the Fels Longitudinal Study (FLS) data set have shown that elevated blood pressure in childhood tracks into adulthood with fidelity and that elevated blood pressure in childhood, even within the range considered to be normal---from the 70th to the 95thpercentiles of the National CDC growth charts (2000)---accurately predict hypertension and the metabolic syndrome in adulthood. In view of the close association of obesity and hypertension and of the association of hypertension with abnormalities of cardiac structure and function, it would be of public health importance to ascertain if childhood obesity predicts abnormalities of cardiac structure and/or function later in life. We are poised to interrogate a portion of the FLS data set to address this question. The pertinent portion of the FLS data set includes serial anthropometric and blood pressure measurements from birth---and body composition measurements from age eight years---through adulthood in 750 participants who consented to undergo echocardiographic studies as adults. Hierarchical and cluster longitudinal modeling procedures will be applied to this unique set of serial measurements to elucidate the relationships between childhood obesity, blood pressure, tempo of maturation, and abnormal cardiac structure and function. The specific aims that we plan to investigate include ascertaining the effects of children's blood pressure, body size, and body composition on (1) blood pressure, (2) cardiac structure, and (3) cardiac function in the same subjects decades later as adults. We have available for analysis more than 750 echocardiographic studies from which to derive the structural measurements of left ventricular mass index (LVMI), interventricular septal thickness (IVST), and relative wall thickness (RWT) and the functional measurements of ejection fraction (EF) and left ventricular shortening fraction (LVSF). These proposed analyses have the potential to quantify risk for hypertension and abnormalities of cardiac structure and function in adulthood given certain values for body size, body composition, and blood pressure in childhood and adolescence, even if these values fall within currently accepted normal values. If we identify biomarkers in children that predict hypertension, and/or abnormal cardiac structure and function in adults, then children with these biomarkers can be evaluated more thoroughly and offered lifestyle and/or pharmacologic interventions before irreversible pathologic changes have occurred. Conversely, our proposed analyses also have the potential to identify a set of ranges of body size, body composition, and blood pressure in childhood and adolescence which are not associated with hypertension or abnormal cardiac structure and function later in life and which can be used to predict a normotensive adulthood, free of cardiac structural or functional abnormalities.
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会议论文
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批准号:9026730
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