Evidence map›Paper›PMID 25178732›Full record

ReviewNature reviews. Endocrinology2014

Novel metabolic biomarkers of cardiovascular disease.

Majken K Jensen, Monica L Bertoia, Leah E Cahill, Isha Agarwal, Eric B Rimm, Kenneth J Mukamal

Abstract readReview
PubMed Publisher
In one paragraph

Review in Nature reviews. Endocrinology, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed
5.4field-weighted citation impact, top 4% 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

42 citing papers in PubMed, 101 citations in OpenAlex.

  1. Trial
  2. Trial
  3. Article
  4. Pathophysiology of homocysteine: insights into ion channel dysfunction.Pflugers Archiv : European journal of physiology · 2026
    Review
  5. Article
  6. Review
  7. Metabolic theory of preeclampsia: implications for maternal cardiovascular health.American journal of physiology. Heart and circulatory physiology · 2024
    Review
  8. Article
  9. Article
  10. Review
  11. CaBiomolecules · 2023
    Article
  12. Article
  13. Article
  14. Article
  15. Lipoprotein-associated phospholipase AProceedings of the National Academy of Sciences of the United States of America · 2022
    Article
  16. GDF15 and Cardiac Cells: Current Concepts and New Insights.International journal of molecular sciences · 2021
    Review
  17. Review
  18. Article
  19. Article
  20. 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

6 authors at 3 institutions in 1 country.

Majken K JensenDepartment of Nutrition, Harvard School of Public Health, 665 Huntington Avenue, 02115 Boston, MA, USA.
Monica L BertoiaDepartment of Nutrition, Harvard School of Public Health, 665 Huntington Avenue, 02115 Boston, MA, USA.
Leah E CahillDepartment of Nutrition, Harvard School of Public Health, 665 Huntington Avenue, 02115 Boston, MA, USA.
Isha AgarwalDepartment of Nutrition, Harvard School of Public Health, 665 Huntington Avenue, 02115 Boston, MA, USA.
Eric B RimmChanning Division of Network Medicine, Brigham and Women's Hospital, Harvard Medical School, 181 Longwood Avenue, 02115 Boston, MA, USA.
Kenneth J MukamalDepartment of Medicine, Beth Israel Deaconess Medical Centre, 1309 Beacon Street, 02446 Brookline, MA, USA.
Harvard University · USBeth Israel Deaconess Medical Center · USBrigham and Women's Hospital · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Coronary heart disease (CHD) accounts for one in every six deaths in US individuals. Great advances have been made in identifying important risk factors for CHD, such as hypertension, diabetes mellitus, smoking and hypercholesterolaemia, which have led to major developments in therapy. In particular, statins represent one of the greatest successes in the prevention of CHD. While these standard risk factors are important, an obvious opportunity exists to take advantage of ongoing scientific research to better risk-stratify individuals and to identify new treatment targets. In this Review, we summarize ongoing scientific research in a number of metabolic molecules or features, including lipoproteins, homocysteine, calcium metabolism and glycaemic markers. We evaluate the current state of the research and the strength of evidence supporting each emerging biomarker. We also discuss whether the associations with CHD are strong and consistent enough to improve current risk stratification metrics, and whether these markers enhance our understanding of the underlying biology of CHD and thus point towards new treatment options.

Indexed as

1-Alkyl-2-acetylglycerophosphocholine EsteraseAdiponectinBiomarkersCoronary DiseaseFibroblast Growth Factor-23Fibroblast Growth FactorsGlycated HemoglobinHaptoglobinsHomocysteineHumansLipoprotein(a)Lipoproteins, HDLVitamin D1-Alkyl-2-acetylglycerophosphocholine Esterase25-hydroxyvitamin DAdiponectinBiomarkersFibroblast Growth Factor-23Fibroblast Growth FactorsGlycated HemoglobinHaptoglobinshemoglobin A1c protein, humanHomocysteineLipoprotein(a)Lipoproteins, HDLVitamin D

Identifiers

PMID25178732
OpenAlexW1994628779

What OpenQuestion holds

Textmetadata
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.