Assessing effects of adverse Social Determinants of Health (SDOH) in TTR V122l carriers via Structured data and Natural Language Processing (NLP) extraction, a comparison
通过结构化数据和自然语言处理 (NLP) 提取评估 TTR V122l 携带者健康不良社会决定因素 (SDOH) 的影响,比较
基本信息
- 批准号:10830156
- 负责人:
- 金额:$ 12.72万
- 依托单位:
- 依托单位国家:美国
- 项目类别:
- 财政年份:2021
- 资助国家:美国
- 起止时间:2021-02-15 至 2025-01-31
- 项目状态:未结题
- 来源:
- 关键词:AddressClinicalCodeComplexDNA Sequence AlterationDataDevelopmentDisease ProgressionDisease modelExhibitsFutureGenesGoalsHealthMedicalMethodologyMethodsMutationNatural Language ProcessingOutcomePatientsPenetranceProcessResearch PersonnelResearch Project Grantsimprovedinnovationpatient health informationpoor health outcomesocial factorssocial health determinantsstructured datatool
项目摘要
The research project has two goals. The first is to use natural language processing (NLP) to
improve the identification of adverse social determinants of health (SDOH) in patients with a
specific genetic mutation. This is important because many social factors are only captured in
unstructured medical narratives, and NLP can help identify these factors more accurately than
the current method of using specific codes. The second goal is to investigate whether adverse
SDOH are associated with poor health outcomes in patients with this mutation. The researchers
will look at patients' medical records to identify adverse SDOH and compare their health
outcomes to those without adverse SDOH. The researchers hypothesize that adverse SDOH will
be associated with worse outcomes, and that more adverse SDOH will be associated with even
worse outcomes. However, the study has limitations, including relying on only one NLP tool and
using a binary definition of adverse SDOH. Future studies may address these limitations by
using different methodologies and more granular data.
该研究项目有两个目标。第一种是使用自然语言处理(NLP),
改善对健康不良社会决定因素(SDOH)的识别,
特定的基因突变。这一点很重要,因为许多社会因素只在
非结构化的医疗叙述,NLP可以帮助更准确地识别这些因素,
使用特定代码的当前方法。第二个目标是调查是否不利
SDOH与携带该突变的患者的不良健康结局相关。研究人员
我将查看病人的医疗记录,以确定不利的SDOH和比较他们的健康
对那些没有不利的SDOH的结果。研究人员假设,不利的SDOH将
与更糟糕的结果相关,并且更不利的SDOH将与甚至
更糟糕的结果。然而,该研究存在局限性,包括仅依赖一种NLP工具,
使用不利SDOH的二元定义。未来的研究可能会解决这些限制,
使用不同的方法和更精细的数据。
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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Ron Do其他文献
Ron Do的其他文献
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{{ truncateString('Ron Do', 18)}}的其他基金
Elucidating hereditary transthyretin-mediated heart failure risk using machine learning, polygenic risk and recall by genotype approaches in African ancestry individuals
利用机器学习、多基因风险和非洲血统个体基因型记忆方法阐明遗传性转甲状腺素蛋白介导的心力衰竭风险
- 批准号:
10563131 - 财政年份:2021
- 资助金额:
$ 12.72万 - 项目类别:
Elucidating hereditary transthyretin-mediated heart failure risk using machine learning, polygenic risk and recall by genotype approaches in African ancestry individuals
利用机器学习、多基因风险和非洲血统个体基因型记忆方法阐明遗传性转甲状腺素蛋白介导的心力衰竭风险
- 批准号:
10348687 - 财政年份:2021
- 资助金额:
$ 12.72万 - 项目类别:
Resolving Causal Influences Among Correlated Risk Biomarkers for Coronary Artery Disease
解决冠状动脉疾病相关风险生物标志物之间的因果影响
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10088462 - 财政年份:2018
- 资助金额:
$ 12.72万 - 项目类别:
Towards an integrated map of causal connections for common, complex diseases
绘制常见、复杂疾病因果关系的综合图
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10263329 - 财政年份:2017
- 资助金额:
$ 12.72万 - 项目类别:
Towards an integrated map of causal connections for common, complex diseases
绘制常见、复杂疾病因果关系的综合图
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9381896 - 财政年份:2017
- 资助金额:
$ 12.72万 - 项目类别:
Towards an integrated map of causal connections for common, complex diseases
绘制常见、复杂疾病因果关系的综合图
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10004664 - 财政年份:2017
- 资助金额:
$ 12.72万 - 项目类别:
Computational approaches to advance genomic, biological and clinical understandings of human disease
促进对人类疾病的基因组、生物学和临床理解的计算方法
- 批准号:
10552389 - 财政年份:2017
- 资助金额:
$ 12.72万 - 项目类别:
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