Marie-Joe Dib PhD , Joe David Azzo MD , Lei Zhao MD, PhD , Oday Salman MD , Sushrima Gan PhD , Marc L. De Buyzere MSc , Tim De Meyer PhD , Christina Ebert PhD , Kushan Gunawardhana PhD , Laura Liu PhD , David Gordon PhD , Dietmar Seiffert MD, PhD , Chang Ching-Pin MD, PhD , Payman Zamani MD, MTR , Jordana B. Cohen MD, MSCE , Bianca Pourmussa BA , Seavmeiyin Kun BA , Dipender Gill MD, PhD , Stephen Burgess PhD , Vanessa van Empel MD , Julio A. Chirinos MD, PhD
{"title":"Proteome-Wide Genetic Investigation of Large Artery Stiffness","authors":"Marie-Joe Dib PhD , Joe David Azzo MD , Lei Zhao MD, PhD , Oday Salman MD , Sushrima Gan PhD , Marc L. De Buyzere MSc , Tim De Meyer PhD , Christina Ebert PhD , Kushan Gunawardhana PhD , Laura Liu PhD , David Gordon PhD , Dietmar Seiffert MD, PhD , Chang Ching-Pin MD, PhD , Payman Zamani MD, MTR , Jordana B. Cohen MD, MSCE , Bianca Pourmussa BA , Seavmeiyin Kun BA , Dipender Gill MD, PhD , Stephen Burgess PhD , Vanessa van Empel MD , Julio A. Chirinos MD, PhD","doi":"10.1016/j.jacbts.2024.05.017","DOIUrl":null,"url":null,"abstract":"<div><div>The molecular mechanisms contributing to large artery stiffness (LAS) are not fully understood. The aim of this study was to investigate the association between circulating plasma proteins and LAS using complementary proteomic and genomic analyses. A total of 106 proteins associated with carotid-femoral pulse-wave velocity, a noninvasive measure of LAS, were identified in 1,178 individuals from the Asklepios study cohort. Mendelian randomization analyses revealed causal effects of 13 genetically predicted plasma proteins on pulse pressure, including cartilage intermediate layer protein-2, high-temperature requirement A serine peptidase-1, and neuronal growth factor-1. These findings suggest potential novel therapeutic targets to reduce LAS and its related diseases.</div></div>","PeriodicalId":14831,"journal":{"name":"JACC: Basic to Translational Science","volume":"9 10","pages":"Pages 1178-1191"},"PeriodicalIF":8.4000,"publicationDate":"2024-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"JACC: Basic to Translational Science","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2452302X24002274","RegionNum":1,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CARDIAC & CARDIOVASCULAR SYSTEMS","Score":null,"Total":0}
引用次数: 0
Abstract
The molecular mechanisms contributing to large artery stiffness (LAS) are not fully understood. The aim of this study was to investigate the association between circulating plasma proteins and LAS using complementary proteomic and genomic analyses. A total of 106 proteins associated with carotid-femoral pulse-wave velocity, a noninvasive measure of LAS, were identified in 1,178 individuals from the Asklepios study cohort. Mendelian randomization analyses revealed causal effects of 13 genetically predicted plasma proteins on pulse pressure, including cartilage intermediate layer protein-2, high-temperature requirement A serine peptidase-1, and neuronal growth factor-1. These findings suggest potential novel therapeutic targets to reduce LAS and its related diseases.
期刊介绍:
JACC: Basic to Translational Science is an open access journal that is part of the renowned Journal of the American College of Cardiology (JACC). It focuses on advancing the field of Translational Cardiovascular Medicine and aims to accelerate the translation of new scientific discoveries into therapies that improve outcomes for patients with or at risk for Cardiovascular Disease. The journal covers thematic areas such as pre-clinical research, clinical trials, personalized medicine, novel drugs, devices, and biologics, proteomics, genomics, and metabolomics, as well as early phase clinical trial methodology.