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Novel Phospholipid Signature of Depressive Symptoms in Patients With Coronary Artery Disease

BACKGROUND: Depression in patients with coronary artery disease (CAD) is associated with increased cardiovascular morbidity. Given the proinflammatory actions of phospholipids, aberrant phospholipid metabolism may be an etiological mechanism linking CAD and depression. Our primary objective was to i...

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Autores principales: Chan, Parco, Suridjan, Ivonne, Mohammad, Dana, Herrmann, Nathan, Mazereeuw, Graham, Hillyer, Lyn M., Ma, David W. L., Oh, Paul I., Lanctôt, Krista L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6015327/
https://www.ncbi.nlm.nih.gov/pubmed/29730646
http://dx.doi.org/10.1161/JAHA.117.008278
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author Chan, Parco
Suridjan, Ivonne
Mohammad, Dana
Herrmann, Nathan
Mazereeuw, Graham
Hillyer, Lyn M.
Ma, David W. L.
Oh, Paul I.
Lanctôt, Krista L.
author_facet Chan, Parco
Suridjan, Ivonne
Mohammad, Dana
Herrmann, Nathan
Mazereeuw, Graham
Hillyer, Lyn M.
Ma, David W. L.
Oh, Paul I.
Lanctôt, Krista L.
author_sort Chan, Parco
collection PubMed
description BACKGROUND: Depression in patients with coronary artery disease (CAD) is associated with increased cardiovascular morbidity. Given the proinflammatory actions of phospholipids, aberrant phospholipid metabolism may be an etiological mechanism linking CAD and depression. Our primary objective was to identify a phospholipid biomarker panel that characterizes CAD patients with significant depressive symptoms from those without. METHODS AND RESULTS: We performed a targeted lipidomic analysis on CAD patients with significant depressive symptoms (n=37, Center for Epidemiologic Studies Depression score ≥16) and those without (n=49). Phospholipid species were selected using partial least‐square discriminant analysis, and the ability of the resulting model to discriminate between groups was evaluated using receiver operator characteristic curves. Biosignature scores were calculated from this model, and analyses of covariance were performed to compare intergroup differences in biosignature scores, with adjustment for clinical differences between patients. Those with significant depressive symptoms had lower cardiopulmonary fitness, more prevalent history of depression, and a greater number of vascular risk factors. A model of 10 phospholipid species had an area under the curve value of 0.84 (95% confidence interval 0.72‐0.95), sensitivity of 0.73, and specificity of 0.71. This model passed permutation testing (n=1000, P<0.001). Biosignature scores were higher in those with significant depressive symptoms after adjustment for potential confounders (F[1.86]=14.39, P<0.0005). CONCLUSIONS: The present findings support the role of proinflammatory phospholipid species in the presence of depression in CAD patients from the CAROTID trial (Coronary Artery Disease Randomized Omega‐3 Trial in Depression). Future investigations should aim to replicate findings in larger data sets and clarify possible pathophysiological mechanisms. CLINICAL TRIAL REGISTRATION: URL: https://www.clinicaltrials.gov. Unique identifier: NCT00981383.
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spelling pubmed-60153272018-07-05 Novel Phospholipid Signature of Depressive Symptoms in Patients With Coronary Artery Disease Chan, Parco Suridjan, Ivonne Mohammad, Dana Herrmann, Nathan Mazereeuw, Graham Hillyer, Lyn M. Ma, David W. L. Oh, Paul I. Lanctôt, Krista L. J Am Heart Assoc Original Research BACKGROUND: Depression in patients with coronary artery disease (CAD) is associated with increased cardiovascular morbidity. Given the proinflammatory actions of phospholipids, aberrant phospholipid metabolism may be an etiological mechanism linking CAD and depression. Our primary objective was to identify a phospholipid biomarker panel that characterizes CAD patients with significant depressive symptoms from those without. METHODS AND RESULTS: We performed a targeted lipidomic analysis on CAD patients with significant depressive symptoms (n=37, Center for Epidemiologic Studies Depression score ≥16) and those without (n=49). Phospholipid species were selected using partial least‐square discriminant analysis, and the ability of the resulting model to discriminate between groups was evaluated using receiver operator characteristic curves. Biosignature scores were calculated from this model, and analyses of covariance were performed to compare intergroup differences in biosignature scores, with adjustment for clinical differences between patients. Those with significant depressive symptoms had lower cardiopulmonary fitness, more prevalent history of depression, and a greater number of vascular risk factors. A model of 10 phospholipid species had an area under the curve value of 0.84 (95% confidence interval 0.72‐0.95), sensitivity of 0.73, and specificity of 0.71. This model passed permutation testing (n=1000, P<0.001). Biosignature scores were higher in those with significant depressive symptoms after adjustment for potential confounders (F[1.86]=14.39, P<0.0005). CONCLUSIONS: The present findings support the role of proinflammatory phospholipid species in the presence of depression in CAD patients from the CAROTID trial (Coronary Artery Disease Randomized Omega‐3 Trial in Depression). Future investigations should aim to replicate findings in larger data sets and clarify possible pathophysiological mechanisms. CLINICAL TRIAL REGISTRATION: URL: https://www.clinicaltrials.gov. Unique identifier: NCT00981383. John Wiley and Sons Inc. 2018-05-05 /pmc/articles/PMC6015327/ /pubmed/29730646 http://dx.doi.org/10.1161/JAHA.117.008278 Text en © 2018 The Authors. Published on behalf of the American Heart Association, Inc., by Wiley. This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc-nd/4.0/ License, which permits use and distribution in any medium, provided the original work is properly cited, the use is non‐commercial and no modifications or adaptations are made.
spellingShingle Original Research
Chan, Parco
Suridjan, Ivonne
Mohammad, Dana
Herrmann, Nathan
Mazereeuw, Graham
Hillyer, Lyn M.
Ma, David W. L.
Oh, Paul I.
Lanctôt, Krista L.
Novel Phospholipid Signature of Depressive Symptoms in Patients With Coronary Artery Disease
title Novel Phospholipid Signature of Depressive Symptoms in Patients With Coronary Artery Disease
title_full Novel Phospholipid Signature of Depressive Symptoms in Patients With Coronary Artery Disease
title_fullStr Novel Phospholipid Signature of Depressive Symptoms in Patients With Coronary Artery Disease
title_full_unstemmed Novel Phospholipid Signature of Depressive Symptoms in Patients With Coronary Artery Disease
title_short Novel Phospholipid Signature of Depressive Symptoms in Patients With Coronary Artery Disease
title_sort novel phospholipid signature of depressive symptoms in patients with coronary artery disease
topic Original Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6015327/
https://www.ncbi.nlm.nih.gov/pubmed/29730646
http://dx.doi.org/10.1161/JAHA.117.008278
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