Objective Classification of Lupus Nephritis
Objective Classification of Lupus Nephritis
批准号:
10683624
负责人:
CHANDRA MOHAN
金额:
$66.94万
依托单位:
依托单位国家:
美国
项目类别:
财政年份:
2023
资助国家:
美国
项目状态:
未结题
起止时间:
2023-08-20 至 2028-05-31
关键词:
AdultAlgorithmsAutomobile DrivingCellsChildChronicClassificationComputer Vision SystemsDiagnosisDiagnosticEducational process of instructingEnd stage renal failureFeedbackHistologicHumanImageKidneyLupusLupus ErythematosusLupus NephritisMachine LearningNephritisOutcomeOutcome StudyPathologistPathologyPatientsPerformancePhenotypePrediction of Response to TherapyReadingReportingReproducibilityRetrievalStructureSystemic Lupus ErythematosusTestingTissuesTrainingUncertaintyaccurate diagnosisconvolutional neural networkdeep learningdiagnosis standarddiagnostic criteriafallsimprovedindexinginnovationkidney biopsyneural networknovelpredict clinical outcometime intervaltooltreatment responseuser-friendlyweb portal
中文摘要
高达60%的成人和80%的儿童系统性红斑狼疮(SLE)
肾炎(LN),10%-30%进展为终末期肾病(ESRD)。金本位
诊断狼疮性肾炎的方法是肾活检。组织学参数仍然是最好的预测因子
ESRD。尽管组织学诊断是LN的金标准,但它也有几个缺点。
在迄今为止报道的多项观察者间肾脏病理评估研究中,
病理学家在评估大多数组织学参数时的相关系数或一致性
都不是最优的。这为当前的提议提供了动力。
我们建议利用计算机视觉和深度学习的力量来构建一个分类器,
与训练有素的肾脏病理学家竞争,使用CURRENT进行LN的组织学诊断
诊断标准。我们建议训练一个深度卷积神经网络来区分
不同的LN类型,并确定对诊断有用的全谱组织学属性。
我们将比较新生成的神经网络在评分中的性能
肾小球/肾小管间质的特征和LN类型,与人肾面板对照
病理学家。最后,我们建议建立一个可以预测临床结果的神经网络。
根据基线肾脏病理。可靠和可重复的LN分类可以
显著改善患者管理以及肾脏和患者的长期存活率。
英文摘要
Up to 60% of adults and 80% of children with systemic lupus erythematosus (SLE) develop
nephritis (LN), with 10–30% progressing to end-stage renal disease (ESRD). The gold standard
for diagnosis of LN is a renal biopsy. Histological parameters remain the best predictors of
ESRD. Despite being the gold standard, histological diagnosis of LN has several shortcomings.
In multiple inter-observer renal pathology assessment studies reported thus far, the inter-
pathologist correlation coefficients, or concordance, in assessing most histological parameters
have been sub-optimal. This has provided the impetus for the current proposal.
We propose to leverage the power of computer vision and deep learning to build a classifier that
rivals the best-trained renal pathologists in making a histological diagnosis of LN using current
diagnostic criteria. We propose to train a deep convolutional neural network to distinguish the
different LN classes, and to identify a full spectrum of histological attributes useful for diagnosis.
We will compare the performance of the newly generated neural network in scoring
glomerular/tubulo-interstitial features and LN classes, against a panel of human renal
pathologists. Finally, we propose to build a neural network that can predict clinical outcome
based on baseline renal pathology. Reliable and reproducible classification of LN could
dramatically improve patient management and long-term renal and patient survival.
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会议论文
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海外基金