Related Experiment Video
Updated: May 24, 2025

Quantitative Analysis of Chromatin Proteomes in Disease
Published on: December 28, 2012
Exploring Potential Drug Targets in Multiple Cardiovascular Diseases: A Study Based on Proteome-Wide Mendelian
Maoxia Fan1,2, Na Li3, Libin Huang3
1First Clinical Medical College, Shandong University of Traditional Chinese Medicine, Jinan, Shandong Province, China.
Insights
This study identified key plasma proteins causally linked to cardiovascular diseases (CVDs) using proteome-wide Mendelian randomization. Findings highlight novel therapeutic targets and potential drug side effects for CVD treatment.
Area of Science:
- Genetics and Genomics
- Cardiovascular Medicine
- Pharmacology
Background:
- Cardiovascular diseases (CVDs) are the leading cause of global mortality, necessitating the identification of novel therapeutic targets.
- Proteome-wide Mendelian randomization (MR) and colocalization analyses are powerful tools for dissecting causal relationships between proteins and diseases.
Purpose of the Study:
- To identify novel therapeutic protein targets for cardiovascular diseases (CVDs) through proteome-wide Mendelian randomization (MR).
- To evaluate potential drug-related protein side effects associated with identified CVD therapeutic targets.
Main Methods:
- Conducted a proteome-wide MR study using summary-level data for 4907 circulating proteins from a pQTL study (n=35,559).
- Utilized genome-wide association study (GWAS) data for CVDs from UK Biobank and Finnish databases.
- Performed colocalization analysis to identify shared causal variants between plasma proteins and CVDs, followed by phenome-wide association studies (PheWAS) for side effect evaluation.
Main Results:
- Identified specific plasma proteins with significant positive or negative causal relationships with coronary artery disease (CAD), chronic heart failure (CHF), ischemic stroke (IS), and Type 2 diabetes (T2DM).
- Colocalization analysis confirmed shared causal variants for nine proteins (AZGP1, ALDH2, APOE, JAG1, MCL1, PTPN9, PIP4K2A, SNUPN, RAB1A) with CVDs.
- PheWAS revealed potential drug-related side effects for these nine protein targets.
Conclusions:
- This study successfully identified plasma proteins with significant causal associations with various cardiovascular diseases.
- The findings provide a comprehensive understanding of potential therapeutic targets for CVDs and offer insights into underlying mechanisms.
- The identified targets and potential side effects pave the way for developing more effective and safer CVD treatments.
Abstract:
Background: Cardiovascular diseases (CVDs) encompass a group of diseases that affect the heart and/or blood vessels, making them the leading cause of global mortality. In our study, we performed proteome-wide Mendelian randomization (MR) and colocalization analyses to identify novel therapeutic protein targets for CVDs and evaluate the potential drug-related protein side effects. Methods: We conducted a comprehensive proteome-wide MR study to assess the causal relationship between plasma proteins and the risk of CVDs. Summary-level data for 4907 circulating protein levels were extracted from a large-scale protein quantitative trait loci (pQTL) study involving 35,559 individuals. Additionally, genome-wide association study (GWAS) data for CVDs were extracted from the UK Biobank and the Finnish database. Colocalization analysis was utilized to identify causal variants shared between plasma proteins and CVDs. Finally, we conducted a comprehensive phenome-wide association study (PheWAS) using the R10 version of the Finnish database. This study was aimed at examining the potential drug-related protein side effects in the treatment of CVDs. A total of 2408 phenotypes were included in the analysis, categorized into 44 groups. Results: The research findings indicate the following associations: (1) In coronary artery disease (CAD), the plasma proteins A4GNT, COL6A3, KLC1, CALB2, KPNA2, MSMP, and ADH1B showed a positive causal relationship (p-fdr < 0.05). LAYN and GCKR exhibited a negative causal relationship (p-fdr < 0.05). (2) In chronic heart failure (CHF), PLG demonstrated a positive causal relationship (p-fdr < 0.05), while AZGP1 displayed a negative causal relationship (p-fdr < 0.05). (3) In ischemic stroke (IS), ALDH2 exhibited a positive causal relationship (p-fdr < 0.05), while PELO showed a negative causal relationship (p-fdr < 0.05). (4) In Type 2 diabetes (T2DM), the plasma proteins MCL1, SVEP1, PIP4K2A, RFK, HEXIM2, ALDH2, RAB1A, APOE, ANGPTL4, JAG1, FGFR1, and MLN demonstrated a positive causal relationship (p-fdr < 0.05). PTPN9, SNUPN, VAT1, COMT, CCL27, BMP7, and MSMP displayed a negative causal relationship (p-fdr < 0.05). Colocalization analysis conclusively identified that AZGP1, ALDH2, APOE, JAG1, MCL1, PTPN9, PIP4K2A, SNUPN, and RAB1A share a single causal variant with CVDs (PPH3 + PPH4 > 0.8). Further phenotype-wide association studies have shown some potential side effects of these nine targets (p-fdr < 0.05). Conclusions: This study identifies plasma proteins with significant causal associations with CVDs, providing a more comprehensive understanding of potential therapeutic targets. These findings contribute to our knowledge of the underlying mechanisms and offer insights into potential avenues for treatment.
More Related Videos
07:15Determining the Likelihood of Variant Pathogenicity Using Amino Acid-level Signal-to-Noise Analysis of Genetic Variation
Published on: January 16, 2019
09:06Quantitative Analysis of Cellular Composition in Advanced Atherosclerotic Lesions of Smooth Muscle Cell Lineage-Tracing Mice
Published on: February 20, 2019
Related Concept Videos
Genome-wide Association Studies-GWAS
GWAS does not require the identification of the target gene involved in...
Targets for Drug Action: Overview
Receptors are either membrane-spanning or intracellular proteins, which upon binding a ligand, get activated and transmit the signal downstream to elicit a response. Drugs bind receptors, either mimicking the action of endogenous ligands or blocking the receptor activity to bring about a modified response. Nearly 35% of approved drugs target the G...
Cardiovascular Drugs: Classification based on Therapeutic Indications
Heart Failure Drugs: Inhibitors of Renin-Angiotensin System