Machine Learning and Network Science for Predicting Kidney Transplant Survival
用于预测肾移植存活率的机器学习和网络科学
基本信息
- 批准号:10221053
- 负责人:
- 金额:$ 27.78万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2019
- 资助国家:美国
- 起止时间:2019-08-01 至 2023-12-31
- 项目状态:已结题
- 来源:
- 关键词:AdultAffectAmino Acid SequenceAntigensAnusBiologicalBone Marrow TransplantationChronic Kidney FailureClassificationClinicalDataDialysis procedureDonor SelectionEnd stage renal failureEpitopesHLA AntigensHeartImmune responseKidney TransplantationLeadLearningLiverLungMachine LearningMethodsModelingOrgan DonorOrgan SurvivalOrgan TransplantationOutcomePancreasPatientsPlantsPopulationQuality of lifeRenal functionResearchScienceSpace ModelsTechniquesTimeTissue TransplantationTransplant RecipientsTransplantationUnited Statesbasecostdiscrete timegraft failurehazardhigh dimensionalityhuman modelimmunogenicityimprovedlearning networkmultitasknovelnovel strategiesprediction algorithmsurvival predictiontransplant modeltreatment comparison
项目摘要
Chronic kidney disease affects about 10% of adults in the United States and 7-12% of the population
worldwide. It may lead to irreversible loss of kidney function, known as end-stage renal disease (ESRD).
For patients with ESRD, kidney transplantation is the preferred treatment compared to dialysis in terms of
patient survival, quality of life and cost. Despite the advantages of kidney transplants, most patients with
ESRD are treated with dialysis primarily because there exist an insufficient number of compatible donors
for patients. The human leukocyte antigens (HLAs) of the organ donor and recipient are known to be a
significant contributing factor to transplanted organ survival times due to immunogenicity, the immune
response of the recipient to the transplanted organ. Mismatches between donor and recipient HLAs are
associated with shorter survival times; however, it is extremely rare to identify donors that have a perfect
match with recipients, so most transplants involve mismatched HLAs.
Our main objective is to accurately predict survival times for kidney transplants by incorporating both data-
driven models of HLA compatibility based on outcomes of past transplants and biologically-driven models
of HLA immunogenicity. Accurate prediction of survival times can improve patient transplant outcomes by
enabling more efficient allocation of donors and recipients, particularly by reducing the number of repeat
transplants due to graft failure with a poorly matched donor. We propose to estimate HLA compatibilities
using high-dimensional variable selection techniques applied to outcomes of past transplants and through a
novel donor-recipient latent space model for the HLA compatibility network. We then propose to incorporate
these predicted compatibilities along with biologically-driven models of HLA immunogenicity using amino
acid sequences and epitopes into a multi-task classification-based survival prediction algorithm. Our
proposed approach for learning integrated data- and biologically-driven models of transplant survival
generalizes broadly to organ transplantation (liver, heart, pancreas, lungs) and possibly to bone marrow
transplantation.
慢性肾脏疾病影响美国约10%的成年人和7-12%的人口
国际吧它可能导致不可逆的肾功能丧失,称为终末期肾病(ESRD)。
对于患有ESRD的患者,在以下方面,与透析相比,肾移植是首选治疗:
患者生存率、生活质量和成本。尽管肾移植有很多优点,但大多数患者
ESRD主要通过透析治疗,因为相容供体数量不足
对患者已知器官供体和受体的人类白细胞抗原(HLA)是一种免疫调节剂。
由于免疫原性,移植器官存活时间的重要影响因素是免疫原性,
受体对移植器官的反应。供体和受体HLA之间的错配是
与较短的生存时间相关;然而,识别具有完美的
所以大多数移植涉及HLA不匹配。
我们的主要目标是准确预测肾移植的存活时间通过整合两个数据-
基于过去移植结果的HLA相容性驱动模型和生物驱动模型
HLA免疫原性。准确预测生存时间可以通过以下方式改善患者移植结果:
更有效地分配捐助者和受援者,特别是通过减少重复捐助的次数,
由于移植失败而导致的器官移植。我们建议评估HLA相容性
使用应用于过去移植结果的高维变量选择技术,
HLA兼容性网络的新的供体-受体潜在空间模型。然后,我们建议将
这些预测的相容性沿着生物驱动的HLA免疫原性模型,
酸序列和表位到一个多任务分类为基础的生存预测算法。我们
用于学习移植存活的集成数据和生物驱动模型的建议方法
广泛地推广到器官移植(肝脏、心脏、胰腺、肺),可能还包括骨髓移植
移植
项目成果
期刊论文数量(4)
专著数量(0)
科研奖励数量(0)
会议论文数量(0)
专利数量(0)
A Latent Space Model for HLA Compatibility Networks in Kidney Transplantation.
肾移植中 HLA 相容性网络的潜在空间模型。
- DOI:10.1109/bibm55620.2022.9995514
- 发表时间:2022
- 期刊:
- 影响因子:0
- 作者:Huang,Zhipeng;Xu,KevinS
- 通讯作者:Xu,KevinS
Predicting Kidney Transplant Survival using Multiple Feature Representations for HLAs
使用 HLA 的多个特征表示预测肾移植存活率
- DOI:10.1007/978-3-030-77211-6_6
- 发表时间:2021
- 期刊:
- 影响因子:0
- 作者:Mohammadreza Nemati;Haonan Zhang;Michael Sloma;D. Bekbolsynov;Hong Wang;S. Stepkowski;Kevin S. Xu
- 通讯作者:Kevin S. Xu
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Stanislaw M Stepkowski其他文献
Functional quartet by CD4+ T cells: a concerto of multiple cytokines
CD4 T 细胞的功能四重奏:多种细胞因子的协奏曲
- DOI:
- 发表时间:
2008 - 期刊:
- 影响因子:4.4
- 作者:
Stanislaw M Stepkowski;Wenhao Chen - 通讯作者:
Wenhao Chen
Cytokine Expression in Cardiac Allograft Tissue Using Mice Deficient in Intercellular Adhesion Molecule-1 (ICAM-1) as Transplant Donors or Recipients♦ 139
以缺乏细胞间黏附分子-1(ICAM-1)的小鼠作为移植供体或受体时心脏移植物组织中的细胞因子表达♦ 139
- DOI:
10.1203/00006450-199704001-00159 - 发表时间:
1997-04-01 - 期刊:
- 影响因子:3.100
- 作者:
Kenneth O Schowengerdt;Zhihong Chen;Jeffrey A Towbin;Stanislaw M Stepkowski;M E Wang;Christie M Ballantyne - 通讯作者:
Christie M Ballantyne
Differences in Fas and Fas-Ligand Expression in Cardiac Allograft Tissue Using Mice Deficient in Intercellular Adhesion Molecule-1 (ICAM-1) As Donors or Recipients • 138
使用缺乏细胞间黏附分子-1(ICAM-1)的小鼠作为供体或受体时,心脏移植组织中 Fas 和 Fas 配体表达的差异 • 138
- DOI:
10.1203/00006450-199704001-00158 - 发表时间:
1997-04-01 - 期刊:
- 影响因子:3.100
- 作者:
Kenneth O Schowengerdt;Zhihong Chen;Jeffrey A Towbin;Stanislaw M Stepkowski;M E Wang;Christie M Ballantyne - 通讯作者:
Christie M Ballantyne
Stanislaw M Stepkowski的其他文献
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{{ truncateString('Stanislaw M Stepkowski', 18)}}的其他基金
Risk stratification for sensitized patients in Kidney Paired Donation program
肾脏配对捐赠计划中敏感患者的风险分层
- 批准号:
8876574 - 财政年份:2014
- 资助金额:
$ 27.78万 - 项目类别:
Deletion of T and B Cells to Induce Tolerance
删除 T 和 B 细胞以诱导耐受
- 批准号:
7083650 - 财政年份:2004
- 资助金额:
$ 27.78万 - 项目类别:
Deletion of T and B Cells to Induce Tolerance
删除 T 和 B 细胞以诱导耐受
- 批准号:
7249386 - 财政年份:2004
- 资助金额:
$ 27.78万 - 项目类别:
Deletion of T and B Cells to Induce Tolerance
删除 T 和 B 细胞以诱导耐受
- 批准号:
7630785 - 财政年份:2004
- 资助金额:
$ 27.78万 - 项目类别:
Role of SOCS in Regulation of Transplantation Tolerance
SOCS 在移植耐受调节中的作用
- 批准号:
6727883 - 财政年份:2004
- 资助金额:
$ 27.78万 - 项目类别:
Deletion of T and B Cells to Induce Tolerance
删除 T 和 B 细胞以诱导耐受
- 批准号:
6913679 - 财政年份:2004
- 资助金额:
$ 27.78万 - 项目类别:
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