Evidence map›Paper›PMID 29201542›Full record

ArticleBrain and behavior2017

Plasma sphingolipids and depressive symptoms in coronary artery disease.

Adam Dinoff, Mahwesh Saleem, Nathan Herrmann, Michelle M Mielke, Paul I Oh, Swarajya Lakshmi Vattem Venkata, Norman J Haughey, Krista L Lanctôt

Open access · goldAbstract read
In one paragraph

Article in Brain and behavior, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
1.2field-weighted citation impact, top 18% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 28 citations in OpenAlex.

  1. Pooled it
  2. Trial
  3. Trial
  4. Review
  5. Sphingolipids in Emotional Well-Being.Journal of neurochemistry · 2026
    Review
  6. Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Acid Sphingomyelinase Is a Modulator of Contextual Fear.International journal of molecular sciences · 2022
    Article
  12. Article
  13. Article
  14. Article
  15. New Molecular Targets for Antidepressant Drugs.Pharmaceuticals (Basel, Switzerland) · 2021
    Review
  16. mRNA Expression ofInternational journal of molecular sciences · 2021
    Article
  17. Article
  18. Article
  19. Article
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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

8 authors at 3 institutions in 2 countries.

Adam DinoffNeuropsychopharmacology Research Group Hurvitz Brain Sciences Program Sunnybrook Research Institute Toronto ON Canada.
Mahwesh SaleemNeuropsychopharmacology Research Group Hurvitz Brain Sciences Program Sunnybrook Research Institute Toronto ON Canada.
Nathan HerrmannNeuropsychopharmacology Research Group Hurvitz Brain Sciences Program Sunnybrook Research Institute Toronto ON Canada.
Michelle M MielkeDepartment of Neurology Mayo Clinic Rochester MN USA.
Paul I OhDivision of Clinical Pharmacology Sunnybrook Health Sciences Centre Toronto ON Canada.
Swarajya Lakshmi Vattem VenkataDepartment of Neurology Johns Hopkins University School of Medicine Baltimore MD USA.
Norman J HaugheyDepartment of Neurology Johns Hopkins University School of Medicine Baltimore MD USA.
Krista L LanctôtNeuropsychopharmacology Research Group Hurvitz Brain Sciences Program Sunnybrook Research Institute Toronto ON Canada.ORCID 0000-0001-7024-6637
Sunnybrook Health Science Centre · CAJohns Hopkins University · USMayo Clinic in Arizona · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Depression is highly prevalent in individuals with coronary artery disease (CAD) and increases the risk of future cardiac events and mortality. Sphingolipids have been implicated in the pathophysiology of both CAD and depression. This study assessed the association between plasma sphingolipid concentrations and depressive symptoms in CAD subjects. Methods: Depressive symptoms were measured using the depression subscale of the self-reported Hospital Anxiety and Depression Scale (HADS). Sphingolipid concentrations were measured from fasting plasma samples using high-performance liquid chromatography-coupled electrospray ionization tandem mass spectrometry (LC/MS/MS). Linear regression models were used to assess associations between log-transformed concentrations of plasma sphingolipids and depressive symptoms. Results: A total of 111 CAD patients (mean ( Conclusion: Sphingolipids, in particular the ceramide species C16:0 and C18:0 and the sphingomyelin species SM18:1, may be implicated in the pathophysiology of depression in CAD. The association between plasma sphingolipid concentrations and depression should be further examined in CAD patients and in other populations.

Indexed as

Coronary Artery DiseaseDepressionAgedFemaleHumansMaleMiddle AgedPsychiatric Status Rating ScalesSphingolipidsStatistics as TopicTandem Mass SpectrometrySphingolipidscoronary artery diseasedepressive symptomssphingolipid

Identifiers

PMID29201542
PMCPMC5698859
OpenAlexW2759564445

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.