Prenatal Blood Pressure Patterns to Predict Pregnancy-Related Hypertension and Later Life Cardiovascular Risk
产前血压模式可预测妊娠相关高血压和晚年心血管风险
基本信息
- 批准号:10065013
- 负责人:
- 金额:$ 75.39万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2018
- 资助国家:美国
- 起止时间:2018-12-15 至 2022-11-30
- 项目状态:已结题
- 来源:
- 关键词:AddressAdultAdvisory CommitteesAffectAmericanAreaAspirinBiological MarkersBirthBlood PressureCalibrationCaliforniaCardiovascular DiseasesChildChronicClinicalClinical DataClinical Trials DesignCommunitiesData SourcesDiagnosisDiscipline of obstetricsDiseaseDisease OutcomeEarly InterventionEarly identificationEarly treatmentElderlyElectronic Health RecordEtiologyEventFirst Pregnancy TrimesterFollow-Up StudiesFutureGoalsGynecologyHealth BenefitHealthcareHigh Risk WomanHospitalsHypertensionIndividualIntegrated Delivery of Health CareIntervention TrialLaboratoriesLifeLinkMeasurementMeasuresMethodologyMethodsMinorityModelingMonitorMorbidity - disease ratePatternPerinatal mortality demographicsPharmaceutical PreparationsPopulationPre-EclampsiaPregnancyPregnant WomenPreventionPreventive serviceRecording of previous eventsReportingResearchResourcesRetrospective cohort studyRiskRisk FactorsSamplingScanningSecond Pregnancy TrimesterSeveritiesStatistical MethodsSubgroupSystemTechniquesTestingTimeWomanautomated algorithmbasecardiovascular disorder riskcardiovascular risk factorclinical riskclinical translationcohortcollegecongenital heart disorderdesignfetalfollow-uphealth care deliveryhealth care settingshigh riskimprovedimproved outcomeindexinginnovationmaternal morbiditymortalitynovelnovel therapeuticsperinatal morbiditypopulation basedpredictive modelingpregnancy hypertensionprenatalprepregnancy obesitypreventprospectiveresearch clinical testingrisk predictionrisk stratificationroutine careskillssociodemographicsstatisticstherapy designtool
项目摘要
ABSTRACT
Pregnancy-related hypertensive (PRH) disorders, preeclampsia (PE) and gestational hypertension (GH),
complicate up to 10% of all pregnancies and are a leading cause of maternal and perinatal morbidity and
mortality in the U.S. These disorders also have been linked with higher risk of later life hypertension (HTN)
and cardiovascular disease (CVD) in women. In 2013, the American College of Obstetrics and Gynecology
identified the need for early identification of women at risk for PRH disorders because available predictive
models could not demonstrate clinical utility among low risk women. In 2017, the U.S. Preventive Services
Task Force report cited research gaps including the need “to further develop and validate tools for risk
prediction using rigorous methodology, including appropriate calibration statistics and validated models that
use parameters available in routine care (e.g., clinical history and clinical testing).” The proposed study
addresses these gaps utilizing statistical methods designed to identify latent classes of individuals with similar
patterns of blood pressure (BP) change over time. This advanced statistical technique classifies women into
BP trajectory groups that may identify those at higher risk for PE and GH among “low risk” women. We chose
this method because it has already proven to be highly effective for prediction of future CVD in non-pregnant
adults. This study will utilize BP trajectory groups and clinical risk factors to evaluate and validate models for
prediction of PE and GH during the index and subsequent pregnancies, as well as later risk of HTN and CVD.
We propose a retrospective cohort study of pregnancies delivered in 2009-2018 (~330,000) along with
prospective follow up for later life HTN and CVD outcomes in women. This large, community-based, highly
diverse sample from the Kaiser Permanente Northern California (KPNC) integrated healthcare delivery system
leverages the established electronic health record (EHR) since 2008 linking all clinical data sources. The study
will develop prediction models for PE and GH that show high clinical utility across most settings for the early
risk stratification of low risk women, and prediction of new onset HTN and CVD in later life. The specific aims
are: Aim 1: To identify the first 20 wks' gestation BP trajectory groups associated with risk of PE and GH, and
evaluate and validate the BP trajectory model's predictive ability to identify women at risk for PE and GH;
Aim 2: To evaluate and validate the predictive ability of first 20 wks' gestation BP trajectory groups, and the
entire pregnancy BP trajectory groups to each identify women with or without PE and GH who are at risk for
new onset HTN and CVD up to 12 years post-delivery; Aim 3: Among women without PE or GH (Aims 1-2), to
evaluate and validate the entire pregnancy BP trajectory groups ability to predict PE and GH in a subsequent
pregnancy. The clinical translation is to develop an automated algorithm for low risk women with EHR clinical
data to improve early risk stratification for PE and GH, and later life HTN and CVD. The method may
direct clinical monitoring, use of available therapies, and testing of new therapies for early prevention.
抽象的
妊娠相关高血压 (PRH) 疾病、先兆子痫 (PE) 和妊娠期高血压 (GH)、
使高达 10% 的妊娠变得复杂,并且是孕产妇和围产期发病率的主要原因
在美国,这些疾病还与晚年高血压 (HTN) 的较高风险有关
2013 年,美国妇产科学会。
确定了早期识别有 PRH 疾病风险的女性的必要性,因为现有的预测
模型无法证明在低风险女性中的临床效用。 2017 年,美国预防服务部门。
特别工作组报告指出了研究差距,包括需要“进一步开发和验证风险工具”
使用严格的方法进行预测,包括适当的校准统计数据和经过验证的模型
使用常规护理中可用的参数(例如临床病史和临床测试)。”
这些地址利用旨在识别具有相似特征的潜在个体类别的统计方法
这种先进的统计技术将女性分为不同的血压模式。
我们选择了可以识别“低风险”女性中 PE 和 GH 风险较高的血压轨迹组。
这种方法已被证明对于预测非怀孕者未来的 CVD 非常有效
本研究将利用血压轨迹组和临床风险因素来评估和验证模型。
预测指数和随后怀孕期间的 PE 和 GH,以及以后发生 HTN 和 CVD 的风险。
我们建议对 2009 年至 2018 年分娩的妊娠(约 330,000 例)进行队列回顾性研究
对女性晚年高血压和心血管疾病结局的前瞻性随访是一项大型、基于社区、高度重视的研究。
来自北加州凯撒医疗机构 (KPNC) 综合医疗服务系统的不同样本
利用自 2008 年以来建立的电子健康记录 (EHR),连接所有临床数据源。
将开发 PE 和 GH 的预测模型,这些模型在早期的大多数情况下都显示出很高的临床实用性
低风险女性的风险分层,以及晚年新发高血压和心血管疾病的预测。
目标 1:确定与 PE 和 GH 风险相关的前 20 周妊娠血压轨迹组,以及
评估和验证血压轨迹模型的预测能力,以识别有 PE 和 GH 风险的女性;
目标 2:评估和验证前 20 周妊娠血压轨迹组的预测能力,以及
整个妊娠期血压轨迹分组,分别识别患有或不患有 PE 和 GH 的女性,这些女性有患 PE 和 GH 的风险
产后 12 年内新发 HTN 和 CVD;目标 3:在没有 PE 或 GH 的女性中(目标 1-2)
评估和验证整个妊娠血压轨迹组在后续预测 PE 和 GH 的能力
临床转化是为具有 EHR 临床的低风险女性开发一种自动化算法。
该方法可以改善 PE 和 GH 的早期风险分层以及晚年 HTN 和 CVD 的数据。
直接临床监测、使用现有疗法以及测试新疗法以进行早期预防。
项目成果
期刊论文数量(0)
专著数量(0)
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会议论文数量(0)
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Erica Pauline Gunderson其他文献
Erica Pauline Gunderson的其他文献
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{{ truncateString('Erica Pauline Gunderson', 18)}}的其他基金
Biomarker of Pancreatic B-cell Loss Predicting Progression to Type 2 Diabetes After Gestational Diabetes
胰腺 B 细胞损失的生物标志物可预测妊娠期糖尿病后进展为 2 型糖尿病
- 批准号:
10583645 - 财政年份:2023
- 资助金额:
$ 75.39万 - 项目类别:
Fetal and Early Postnatal Influences on Child Metabolic Health After Gestational Diabetes
妊娠糖尿病后胎儿和产后早期对儿童代谢健康的影响
- 批准号:
10399625 - 财政年份:2020
- 资助金额:
$ 75.39万 - 项目类别:
Fetal and Early Postnatal Influences on Child Metabolic Health After Gestational Diabetes
妊娠糖尿病后胎儿和产后早期对儿童代谢健康的影响
- 批准号:
10159898 - 财政年份:2020
- 资助金额:
$ 75.39万 - 项目类别:
Fetal and Early Postnatal Influences on Child Metabolic Health After Gestational Diabetes
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10616503 - 财政年份:2020
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$ 75.39万 - 项目类别:
Prenatal Blood Pressure Patterns to Predict Pregnancy-Related Hypertension and Later Life Cardiovascular Risk
产前血压模式可预测妊娠相关高血压和晚年心血管风险
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10398839 - 财政年份:2018
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$ 75.39万 - 项目类别:
Prenatal Blood Pressure Patterns to Predict Pregnancy-Related Hypertension and Later Life Cardiovascular Risk
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