Evidence map›Paper›PMID 41776041›Full record

ArticleNPJ cardiovascular health2024

A translational framework of genoproteomic studies for cardiovascular drug discovery.

Zhao Yang, Jie V Zhao, Yue Qi, Xuan Deng, Zhili Ji, Jing Liu

Erratum issuedAbstract read
In one paragraph

Article in NPJ cardiovascular health, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

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

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

6 authors.

Zhao YangCenter for Clinical and Epidemiologic Research, Beijing Anzhen Hospital, Capital Medical University, Beijing Institute of Heart, Lung and Blood Vessel Diseases, Beijing, People's Republic of China.
Jie V ZhaoSchool of Public Health, Li Ka Shing Faculty of Medicine, The University of Hong Kong, 7 Sassoon Road, Pokfulam, Hong Kong SAR, China.
Yue QiCenter for Clinical and Epidemiologic Research, Beijing Anzhen Hospital, Capital Medical University, Beijing Institute of Heart, Lung and Blood Vessel Diseases, Beijing, People's Republic of China.
Xuan DengCenter for Clinical and Epidemiologic Research, Beijing Anzhen Hospital, Capital Medical University, Beijing Institute of Heart, Lung and Blood Vessel Diseases, Beijing, People's Republic of China.
Zhili JiBeijing Anzhen Hospital, Capital Medical University, Beijing, China.
Jing LiuCenter for Clinical and Epidemiologic Research, Beijing Anzhen Hospital, Capital Medical University, Beijing Institute of Heart, Lung and Blood Vessel Diseases, Beijing, People's Republic of China. jingliu@ccmu.edu.cn.

Funding

Beijing Municipal Commission of Health, China 2021-7National Key Research and Development Program of China 2022YFC3602501National Natural Science Foundation of China 12226005
6 · The paper itself

Abstract

Cardiovascular drug development has faced significant challenges in recent decades. The emergence of population-scale genome- and proteome-wide data, alongside sophisticated genetic analytical tools like Mendelian randomization and pragmatic target trials, presents an unprecedented chance to identify and validate drug-targeting proteins for cardiovascular disease. However, how to translate these advances into clinical applications remains to be discovered. This study proposes and validates a translational framework that leverages emerging genoproteomic data and cutting-edge causal analysis techniques to address the intricate benefit-risk concerns associated with cardiovascular drug development. Specifically, the framework elucidates underlying biological mechanisms, identifies and validates potential drug-targeting proteins, and explores the unintended side effects, complementary with pragmatic target trials. Moreover, we illustrate the translational framework via a step-by-step example alongside practical implementation recommendations for cardiovascular drug discovery. We envision this translational framework as a starting point in advancing multi-omics studies, thereby accelerating cardiovascular drug development.

Identifiers

PMID41776041
PMCPMC12912353

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Registered trials

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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.