Evidence map›Paper›PMID 29730646›Full record

ArticleJournal of the American Heart Association2018

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

Parco Chan, Ivonne Suridjan, Dana Mohammad, Nathan Herrmann, Graham Mazereeuw, Lyn M Hillyer, David W L Ma, Paul I Oh, Krista L Lanctôt

Registry-linked trialOpen access · goldAbstract readValidation Study
In one paragraph

Article in Journal of the American Heart Association, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00981383 (CAROTID), which is not on this map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.0field-weighted citation impact, top 22% of its field
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.

NCT00981383 phase3completednot on this map

CAROTID: CAD Randomized Omega-3 Trial In Depression

TypeinterventionalSponsorSunnybrook Health Sciences CentreRan2010 to 2016Enrolled92ConditionsCoronary Artery Disease, DepressionArmsOmega-3 Fatty Acid Supplement, Placebo
3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 15 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Article
  8. Review
  9. Article
  10. Review
  11. Lipidomics in Major Depressive Disorder.Frontiers in psychiatry · 2018
    Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 5 institutions in 1 country.

Parco ChanSunnybrook Research Institute, Toronto, Ontario, Canada.
Ivonne SuridjanSunnybrook Research Institute, Toronto, Ontario, Canada.
Dana MohammadSunnybrook Research Institute, Toronto, Ontario, Canada.
Nathan HerrmannSunnybrook Research Institute, Toronto, Ontario, Canada.
Graham MazereeuwSunnybrook Research Institute, Toronto, Ontario, Canada.
Lyn M HillyerDepartment of Human Health and Nutritional Sciences, University of Guelph, Ontario, Canada.
David W L MaDepartment of Human Health and Nutritional Sciences, University of Guelph, Ontario, Canada.
Paul I OhSunnybrook Research Institute, Toronto, Ontario, Canada.
Krista L LanctôtSunnybrook Research Institute, Toronto, Ontario, Canada Krista.Lanctot@sunnybrook.ca.
Sunnybrook Health Science Centre · CAUniversity of Guelph · CAUniversity of Toronto · CASunnybrook Research InstituteToronto Rehabilitation Institute · CA

Funding

CIHR MOP 114913
6 · The paper itself

Abstract

backgroundDepression 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

resultsWe 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,

conclusionsThe 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 registrationURL: https://www.clinicaltrials.gov. Unique identifier: NCT00981383.

Indexed as

AffectAgedAged, 80 and overBiomarkersCase-Control StudiesCoronary Artery DiseaseCross-Sectional StudiesDepressionFemaleHumansInflammation MediatorsMaleMetabolomicsMiddle AgedPhospholipidsPredictive Value of TestsBiomarkersInflammation MediatorsPhospholipidscardiac rehabilitationcoronary artery diseasedepressioninflammationlipidomicslipids

Identifiers

PMID29730646
PMCPMC6015327
OpenAlexW2802241866

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

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.