Mount Sinai Health System Kidney Precision Medicine Project

西奈山卫生系统肾脏精准医学项目

基本信息

项目摘要

Project Summary Forty million Americans live with kidney disease and this number is projected to increase with rising rates of CKD comorbid conditions, including diabetes, obesity, and hypertension, superimposed on an aging patient population. A tremendous financial burden is imparted by dialysis therapy and kidney transplantation for end- stage CKD. At present, however, there are limited tools in existence to predict the progression of AKI and CKD, and development of therapies has been disappointingly restricted. The overall objective of this application is to establish the Mount Sinai Kidney Precision Medicine Project (KPMP) recruitment site in support of the larger consortium’s tissue interrogation and phenotyping activities. There is a tremendous need to utilize human kidney tissue as a research tool for the identification of AKI and CKD disease markers to elucidate molecular pathways that contribute to kidney disease development and progression. We have proposed three Specific Aims: Aim 1 will establish a robust system of patient centered oversight to recruit diverse patients into a kidney biopsy cohort while maintaining the highest standards of safety, quality and ethical research conduct. In Aim 2 we will recruit and retain a spectrum of patients with CKD in response to KPMP priorities. This includes leveraging existing institutional risk stratification tools and resources to identify and recall patients at risk for CKD progression due to diabetes, hypertension, prior COVID-19 infection and apolipoprotein L1 associated disease. Aim 3 will recruit and retain patients with AKI as well as those at high risk for AKI identified by a machine learning algorithm. These Aims overseen by a stakeholder board and executed by an experienced multidisciplinary team, will integrate with the KPMP consortium to accomplish its transformative aims.
项目概要 四千万美国人患有肾病,预计这个数字会随着肾病发病率的上升而增加 老年患者患有 CKD 合并症,包括糖尿病、肥胖和高血压 透析治疗和肾移植给最终人口带来了巨大的经济负担。 然而,目前预测 AKI 进展和进展的工具有限。 令人失望的是,CKD 及其疗法的开发受到了限制。 申请旨在建立西奈山肾脏精准医学项目(KPMP)招募站点 迫切需要支持更大联盟的组织询问和表型分析活动。 利用人体肾脏组织作为识别 AKI 和 CKD 疾病标志物的研究工具 我们已经阐明了导致肾脏疾病发生和进展的分子途径。 提出了三个具体目标: 目标 1 将建立一个以患者为中心的强大监督体系,以招募 将不同的患者纳入肾活检队列,同时保持最高的安全性、质量和标准 在目标 2 中,我们将招募并保留一系列 CKD 患者,以应对以下情况。 KPMP 的优先事项包括利用现有的机构风险分层工具和资源来识别 并回顾因糖尿病、高血压、既往感染过 COVID-19 且有 CKD 进展风险的患者 目标 3 将招募并保留 AKI 患者以及高危患者。 由机器学习算法识别的 AKI 风险。这些目标由利益相关者委员会监督,并且 由经验丰富的多学科团队执行,将与 KPMP 财团整合以完成其 变革性目标。

项目成果

期刊论文数量(0)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)

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Kirk N Campbell其他文献

Urinary Plasminogen as a Marker of Disease Progression in Human Glomerular Disease.
尿纤溶酶原作为人类肾小球疾病进展的标志物。
  • DOI:
    10.1053/j.ajkd.2024.01.520
  • 发表时间:
    2024-03-01
  • 期刊:
  • 影响因子:
    0
  • 作者:
    Marina de Cos;Gohar Mosoyan;K. Chauhan;J. Troost;Jenny S. Wong;Sean Lefferts;Paul Morgan;K. Meliambro;Marc A. Egerman;Justina Ray;Tom Parker;Daniel Levine;Surya Seshan;Yoni Bardash;Benjamin Horowitz;C;ice Kent;ice;Melissa M. Shaw;Alan Perlman;D. Moledina;Steven G Coca;Kirk N Campbell
  • 通讯作者:
    Kirk N Campbell
Practical Considerations for the Use of Sparsentan in the Treatment of Patients with IgAN in Clinical Practice
临床实践中使用 Sparsentan 治疗 IgAN 患者的实际考虑
Plasminogenuria is associated with podocyte injury, edema, and kidney dysfunction in incident glomerular disease
纤溶酶原尿与肾小球疾病中的足细胞损伤、水肿和肾功能障碍有关
  • DOI:
    10.1101/19006809
  • 发表时间:
    2019-09-16
  • 期刊:
  • 影响因子:
    0
  • 作者:
    Marc A. Egerman;Jenny S. Wong;Runxia Tian;Gohar Mosoyan;K. Chauhan;Fadi El Salem;K. Meliambro;Hong Li;E. Azeloglu;Steven G Coca;Kirk N Campbell;Leopoldo Raij
  • 通讯作者:
    Leopoldo Raij
Podocyte-targeted therapies - progress and future directions.
足细胞靶向治疗 - 进展和未来方向。
  • DOI:
    10.1038/s41581-024-00843-z
  • 发表时间:
    2024-05-09
  • 期刊:
  • 影响因子:
    0
  • 作者:
    K. Meliambro;John C. He;Kirk N Campbell
  • 通讯作者:
    Kirk N Campbell

Kirk N Campbell的其他文献

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{{ truncateString('Kirk N Campbell', 18)}}的其他基金

Mount Sinai Health System Kidney Precision Medicine Project
西奈山卫生系统肾脏精准医学项目
  • 批准号:
    10703420
  • 财政年份:
    2022
  • 资助金额:
    $ 37.49万
  • 项目类别:
Plasminogen in glomerular disease progression
肾小球疾病进展中的纤溶酶原
  • 批准号:
    10410524
  • 财政年份:
    2020
  • 资助金额:
    $ 37.49万
  • 项目类别:
Plasminogen in glomerular disease progression
肾小球疾病进展中的纤溶酶原
  • 批准号:
    10183244
  • 财政年份:
    2020
  • 资助金额:
    $ 37.49万
  • 项目类别:
Plasminogen in glomerular disease progression
肾小球疾病进展中的纤溶酶原
  • 批准号:
    10620244
  • 财政年份:
    2020
  • 资助金额:
    $ 37.49万
  • 项目类别:
Hippo-YAP in podocyte health and disease
Hippo-YAP 在足细胞健康和疾病中的作用
  • 批准号:
    9917038
  • 财政年份:
    2019
  • 资助金额:
    $ 37.49万
  • 项目类别:
Hippo-YAP in podocyte health and disease
Hippo-YAP 在足细胞健康和疾病中的作用
  • 批准号:
    10006878
  • 财政年份:
    2019
  • 资助金额:
    $ 37.49万
  • 项目类别:
Hippo-YAP in podocyte health and disease
Hippo-YAP 在足细胞健康和疾病中的作用
  • 批准号:
    10433862
  • 财政年份:
    2019
  • 资助金额:
    $ 37.49万
  • 项目类别:
Hippo-YAP in podocyte health and disease
Hippo-YAP 在足细胞健康和疾病中的作用
  • 批准号:
    10188524
  • 财政年份:
    2019
  • 资助金额:
    $ 37.49万
  • 项目类别:
Hippo-YAP in podocyte health and disease
Hippo-YAP 在足细胞健康和疾病中的作用
  • 批准号:
    10618369
  • 财政年份:
    2019
  • 资助金额:
    $ 37.49万
  • 项目类别:
The role of dendrin in glomerular disease progression
树突蛋白在肾小球疾病进展中的作用
  • 批准号:
    8963906
  • 财政年份:
    2015
  • 资助金额:
    $ 37.49万
  • 项目类别:

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SCH:人工智能支持的多模式传感器平台,用于患者的家庭健康监测
  • 批准号:
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肾脏和心血管疾病交叉领域的指导研究
  • 批准号:
    10795588
  • 财政年份:
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AKI 后女性亚临床肾损伤的机制:对不良妊娠结局的影响
  • 批准号:
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