Cardiovascular Risk after Preeclampsia - The CRISP study
Cardiovascular Risk after Preeclampsia - The CRISP study
批准号:
9769190
负责人:
LISA Danielle LEVINE
金额:
$74.01万
依托单位国家:
美国
项目类别:
财政年份:
2018
资助国家:
美国
项目状态:
已结题
起止时间:
2018-09-15 至 2021-02-28
关键词:
AddressAffectAfrican AmericanAmerican Heart AssociationBiological MarkersBloodBlood VesselsCardiacCardiovascular DiseasesCardiovascular systemCessation of lifeChronicClinicalCollaborationsComputer Retrieval of Information on Scientific Projects DatabaseCross-Sectional StudiesDevelopmentDiabetes MellitusDiagnosisDiseaseDyslipidemiasEarly InterventionEchocardiographyEnrollmentEpidemiologistEventExposure toFeasibility StudiesFutureGoalsHigh PrevalenceHigh Risk WomanHypertensionIndividualInstitutionKnowledgeMaternal MortalityMaternal-fetal medicineMetabolic syndromeMetadataMorbidity - disease ratePhenotypePhysiologic pulsePopulationPositioning AttributePre-EclampsiaPregnancyPrevalenceProspective StudiesRecording of previous eventsResearchResearch PersonnelRiskRisk FactorsSmokingSpecialistTelephoneTherapeuticTimeTroponinUnited StatesVascular DiseasesVisitWomanWomen&aposs Groupcardiovascular disorder riskcardiovascular healthcardiovascular risk factorcare seekingcase controlcohorthigh riskmaternal morbiditymortalitymultidisciplinarypersonalized carestudy population
中文摘要
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英文摘要
PROJECT SUMMARY/ABSTRACT
Cardiovascular disease (CVD) is responsible for the annual death of 8.6 million women worldwide and
disproportionally affects African American women. Preeclampsia (PEC) affects 3-8% of all pregnancies and is
now recognized by the American Heart Association as a potent independent risk factor for CVD. The increased
cardiovascular (CV) risk in women with a remote history of PEC is posited to be from the vascular dysfunction
that is the hallmark feature of the disease.
The development of CVD typically occurs 20-30 years after the exposure to PEC. However, there is a
paucity of research investigating the presence of cardiac risk factors in the decade after exposure to PEC – an
intermediate time period between the development of PEC disease and overt CVD, when women are young
(30-40's) and might not otherwise be seeking care. Our overarching goal is to understand how a history of PEC
modifies a woman's long-term CV health. The first step in this goal is to evaluate whether there are risk factors
that identify a woman previously exposed to PEC as high risk for CVD, prior to an overt CV event in order to
target early intervention and therapeutic strategies. The fundamental premise of our proposal is that
women with a history of PEC will have a higher prevalence of traditional risk factors for CVD and a
higher prevalence of an intermediate CV phenotype compared to women without a history of PEC.
Women from this study will be followed long-term in order to correlate these risk factors with future CV events.
We are uniquely positioned to address this important clinical question. We have a group of women with
(n=441) and without PEC (n=591) that were previously enrolled in a prospective study conducted at our
institution from 2005-2007. An exceptional advantage to this cohort is that cases and controls were evaluated
and well-phenotyped at the time of enrollment by specialized Obstetricians, allowing us to have limited bias
regarding initial diagnosis of PEC as well as the ability to control for a large amount of metadata that was
collected at the time of enrollment. Adding to the richness of this cohort, more than 75% of these women are
African American, providing a unique opportunity to study a high risk yet typically understudied population, in
whom PEC and CVD are both more prevalent and more severe. This cohort will serve as the study population
for our current proposal. We have a multidisciplinary team of obstetricians, cardiologists, vascular researchers
and epidemiologists and are well poised to complete the study given our expertise and prior collaboration.
Together, in a feasibility study of 150 women, we demonstrated that 57% of women from the original study,
now 10 (+/-1) years from their initial exposure to PEC, can be contacted, agree to participate and present for a
study visit. Completion of this study will address significant gaps in knowledge regarding the association
between PEC and CVD.
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Enhance Trial-Enriched Holistic Care to Eradicate Maternal Morbidity
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批准号:10604899
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项目类别:
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资助金额:$80.68万
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财政年份:2023
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负责人:LISA Danielle LEVINE
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依托单位:
海外基金