@article{d95287dda41841dab15dd178a381c82b,
title = "Metabolic profiling of intra- and extracranial carotid artery atherosclerosis",
abstract = "Background and aims: Increasing evidence shows that intracranial carotid artery atherosclerosis may develop under the influence of a differential metabolic risk factor profile than atherosclerosis in the extracranial part of the carotid artery. To further elucidate these differences, we investigated associations of a wide range of circulating metabolites with intracranial and extracranial carotid artery atherosclerosis. Methods: From the population-based Rotterdam Study, blood samples from 1111 participants were used to determine a wide range of metabolites by proton nuclear magnetic resonance (NMR). Moreover, these participants underwent non-contrast computed tomography of the neck and head to quantify the amount of extra- and intracranial carotid artery calcification (ECAC and ICAC), as a proxy of atherosclerosis. We assessed associations of the metabolites with ICAC and ECAC and compared the metabolic association patterns of the two. Results: We found that one standard deviation (SD) increase in concentration of 3-hydroxybutyrate, a ketone body, was significantly associated with a 0.11 SD increase in ICAC volume (p = 1.8 × 10−4). When we compared the metabolic association pattern of ICAC with that of ECAC, we observed differences in glycolysis-related metabolite measures, lipoprotein subfractions, and amino acids. Interestingly, glycoprotein acetyls were associated with calcification in both studied vessel beds. These associations were most prominent in men. Conclusions: We found that a higher circulating level of 3-hydroxybutyrate was associated with an increase in ICAC. Furthermore, we found differences in metabolic association patterns of ICAC and ECAC, providing further evidence for location-specific differences in the etiology of atherosclerosis.",
keywords = "Atherosclerosis, Carotid artery, Metabolomics",
author = "Dina Vojinovic and {van der Lee}, {Sven J.} and {van Duijn}, {Cornelia M.} and Vernooij, {Meike W.} and Maryam Kavousi and Najaf Amin and Ay{\c s}e Demirkan and Ikram, {M. Arfan} and {van der Lugt}, Aad and Daniel Bos",
note = "Funding Information: The Rotterdam Study is supported by the Erasmus MC University Medical Center and Erasmus University Rotterdam ; The Netherlands Organisation for Scientific Research (NWO); The Netherlands Organisation for Health Research and Development (ZonMw); the Research Institute for Diseases in the Elderly (RIDE); The Netherlands Genomics Initiative (NGI); the Ministry of Education, Culture and Science ; the Ministry of Health, Welfare and Sports ; the European Commission (DG XII); and the Municipality of Rotterdam. Metabolomics measurements were funded by Biobanking and Biomolecular Resources Research Infrastructure (BBMRI)–NL ( 184.021.007 ) and the JNPD under the project PERADES (grant number 733051021 , Defining Genetic, Polygenic and Environmental Risk for Alzheimer's Disease using multiple powerful cohorts, focused Epigenetics and Stem cell metabolomics). This work has been performed as part of the CoSTREAM project ( www.costream.eu ) and has received funding from the European Union's Horizon 2020 research and innovation programme under grant agreement No 667375. This work has been performed as part of the CardioVasculair Onderzoek Nederland (CVON 2012-03) . Ayse Demirkan, Dina Vojinovic, and Cornelia van Duijn have used exchange grants from Personalized pREvention of Chronic DIseases consortium (PRECeDI) ( H2020-MSCA-RISE-2014 ). Ay{\c s}e Demirkan is supported by the NWO VENI grant (VENI, 91616165 ). Maryam Kavousi is supported by the NWO VENI grant (VENI, 91616079 ). Publisher Copyright: {\textcopyright} 2018 Elsevier B.V.",
year = "2018",
month = may,
doi = "https://doi.org/10.1016/j.atherosclerosis.2018.03.015",
language = "English",
volume = "272",
pages = "60--65",
journal = "Atherosclerosis",
issn = "0021-9150",
publisher = "Elsevier Ireland Ltd",
}