Evidence map›Paper›PMID 41527552›Full record

ArticleACM-BCB ... ... : the ... ACM Conference on Bioinformatics, Computational Biology and Biomedicine. ACM Conference on Bioinformatics, Computational Biology and Biomedicine2023

Evaluating Drug Effectiveness for Antihypertensives in Heart Failure Prognosis: Leveraging Composite Clinical Endpoints and Biomarkers from Electronic Health Records.

Shaika Chowdhury, Yongbin Chen, Xiao Ma, Qiying Dai, Yue Yu, Nansu Zong

Abstract read
In one paragraph

Article in ACM-BCB ... ... : the ... ACM Conference on Bioinformatics, Computational Biology and Biomedicine. ACM Conference on Bioinformatics, Computational Biology and Biomedicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Shaika ChowdhuryDepartment of Artificial Intelligence and Informatics Research, Mayo Clinic, Rochester, MN, USA.
Yongbin ChenDepartment of Biochemistry and Molecular Biology, Mayo Clinic, Rochester, MN, USA.
Xiao MaDepartment of Cardiovascular Medicine Mayo Clinic, Rochester, MN, USA.
Qiying DaiDepartment of Cardiovascular Medicine, Mayo Clinic, Rochester, MN, USA.
Yue YuDepartment of Health Sciences Research, Mayo Clinic, Rochester, MN, USA.
Nansu ZongDepartment of Artificial Intelligence and Informatics Research, Mayo Clinic, Rochester, MN, USA.

Funding

BOND: Benchmarking based on heterogeneous biOmedical Network and Deep learning novel drug-target associationsR00GM135488 · NIGMS · MAYO CLINIC ROCHESTER · PI ZONG, NANSU · 2021 to 2023
$747k
BOND: Benchmarking based on heterogeneous biOmedical Network and Deep learning novel drug-target associationsK99GM135488 · NIGMS · MAYO CLINIC ROCHESTER · PI ZONG, NANSU · 2020 to 2021
$108k
NIGMS NIH HHS K99 GM135488NIGMS NIH HHS R00 GM135488
6 · The paper itself

Abstract

Arterial hypertension is a major risk factor for heart failure and antihypertensives such as angiotensin converting enzyme (ACE) inhibitors and β-blockers are considered as its first-line treatment. Drug response prediction models designed to determine the most effective antihypertensive drug for a patient are hindered by the interpatient response variability. Although typically pharmacogenetic data have been used to investigate the association of genetic variants with the antihypertensive response, genomewide association studies are currently expensive and the translation of genotype guided antihypertensive therapy to clinical practice is challenging. With the generation of electronic health records (EHR) data summarized over the patient's disease prognosis and interventions, it is still an underused resource for antihypertensive effectiveness studies in heart failure management. In this study, we first use the clinical events in the EHR related to the patient's hard clinical endpoints and biomarkers associated with the heart failure condition to design selection strategies that determine the antihypertensive effectiveness, then develop annotated corpora using the strategies and eventually evaluate supervised deep learning classifiers on the annotated data. We annotated the EHR sequences of approximately 9500 patients with binary labels corresponding to the drug effectiveness across two different antihypertensive classes and our trained classifier was able to obtain the best F1 performance of 0.97.

Indexed as

AnnotationDeep learningDrug effectivenessElectronic health recordsHeart failure

Identifiers

PMID41527552
PMCPMC12790705

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.