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Cardiac and vascular disease prevention after hypertensive pregnancy: insights from AI-derived, multi-organ, hypertensive disease progression models

Cardiac and vascular disease prevention after hypertensive pregnancy: insights from AI-derived, multi-organ, hypertensive disease progression models
高血压妊娠后心脏和血管疾病的预防:来自人工智能的多器官高血压疾病进展模型的见解
批准号:
MR/W003686/1
负责人:
Paul Leeson
金额:
$252.43万
依托单位:
依托单位国家:
英国
项目类别:
Research Grant
财政年份:
2022
资助国家:
英国
项目状态:
未结题
起止时间:
2022 至 --

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英文摘要
Women who develop blood pressure problems during pregnancy are more likely to have high blood pressure in later life as well as heart attacks or strokes. The children born to the pregnancy also tend to have higher blood pressure and are more likely to have problems during their own pregnancies. Our work has shown that the children and mothers have changes in their blood vessels, heart and brain that can be identified long before they develop high blood pressure or suffer the severe complications. We think these changes in the body develop slowly throughout their life and the progression of these changes is establishing their risk for later disease. By understanding the pattern of changes across multiple parts of the body, over a lifetime, we think we can identify how advanced the underlying disease is for an individual and how their disease is likely to develop over the next few years. Furthermore, as the rate of change is likely to differ between parts of the body, and a change in one area of the body could drive development of disease elsewhere, we can also use this information to decide on optimal treatments. Certain treatments may be required to slow down the development of disease in a particular area and the selection of interventions may need to change at different stages of life and disease.To test these ideas, we are going use large datasets we have acquired over the years based on imaging studies of women and children after a hypertensive pregnancy. The data includes information on the structure and function of several important organs such as the heart, brain and blood vessels. We will also expand these datasets by undertaking additional studies in older women, women who have grown up in different environments and in young adults. In all these studies, the same approaches have been used for the imaging and we will harmonise all the datasets so that we can study how this early underlying disease progression in different organs varies with their pregnancy history, age and their current health. The initial analysis will focus on assessing changes in specific organs, but we also want to know how the patterns emerge across the whole body. To do this we will need to combine information from many different measures at the same time and use some of the latest advances in artificial intelligence (AI) to analyse the data collected in our studies, as well as other large studies of people within the UK. The computer will learn the multi-dimensional patterns of changes to the organs that occur as someone progresses from 'health' to a 'disease' state. From this information we will discover the unique patterns of hypertensive disease development, and with that hope to open the door to better interventions and therapies tailored to each person. For example, specific stages of disease could be identified based on a particular combination of complex imaging markers. From this, we could then use the computer to learn the combination of simple measures that best approximate to the more complex pattern to generate tools that can be used in any hospital or community to manage and track disease development for an individual patient. At the end of this programme of work we will understand how the body changes in mothers who have a hypertensive pregnancy, and their children, over the life course of their disease. This knowledge, enhanced by AI technology, has the potential to lead to simple tests that can be used in the clinic to determine the stage of disease for an individual. The results of these tests could then advise on the best preventive intervention (e.g. lifestyle choice) or treatment strategy that protect the woman or child from developing disease.
期刊论文(10)
专著(0)
科研奖励(0)
会议论文
DOI: 10.3389/fendo.2022.868441
发表时间: 2022
期刊: Frontiers in endocrinology
影响因子: 5.2
作者: []
通讯作者:
DOI: 10.1136/bmjopen-2023-076950
发表时间: 2023-12-11
期刊: BMJ open
影响因子: 2.9
作者: []
通讯作者:
Modelling relations between blood pressure, cardiovascular phenotype, and clinical factors using large scale imaging data.
使用大规模成像数据对血压、心血管表型和临床因素之间的关系进行建模。
DOI: 10.1093/ehjci/jead161
发表时间: 2023
期刊: European heart journal. Cardiovascular Imaging
影响因子: --
作者: [Kart T]
通讯作者: Kart T
Focused Cardiac Ultrasound to Guide the Diagnosis of Heart Failure in Pregnant Women in India.
聚焦心脏超声指导印度孕妇心力衰竭的诊断。
DOI: 10.1016/j.echo.2022.07.014
发表时间: 2022
期刊: official publication of the American Society of Echocardiography
影响因子: --
作者: [Alsharqi M]
通讯作者: Alsharqi M
国内基金
海外基金
环境抗雄激素干预AR/TGFB1I1致尿道下裂血管内皮细胞发育异常的机制及其“预警信号”在早期诊断中的价值
  • 批准号:
    82371605
  • 项目类别:
    面上项目
  • 资助金额:
    46.00万元
  • 批准年份:
    2023
  • 负责人:
    蒋君涛
  • 依托单位:
尾加压素II介导血管外膜氧化应激促进血管重构的作用研究
  • 批准号:
    81141003
  • 项目类别:
    专项基金项目
  • 资助金额:
    10.0万元
  • 批准年份:
    2011
  • 负责人:
    丁文惠
  • 依托单位:
核素靶向示踪肿瘤新生血管作用位点研究
  • 批准号:
    81071183
  • 项目类别:
    面上项目
  • 资助金额:
    32.0万元
  • 批准年份:
    2010
  • 负责人:
    王荣福
  • 依托单位:
硫化氢通过核转录因子-kB信号途径调节高血压大鼠血管平滑肌细胞增殖的研究
  • 批准号:
    81070212
  • 项目类别:
    面上项目
  • 资助金额:
    33.0万元
  • 批准年份:
    2010
  • 负责人:
    金红芳
  • 依托单位: