Evidence map›Paper›PMID 27598908›Full record

ArticlePloS one2016

A Global View of the Relationships between the Main Behavioural and Clinical Cardiovascular Risk Factors in the GAZEL Prospective Cohort.

Pierre Meneton, Cédric Lemogne, Eléonore Herquelot, Sébastien Bonenfant, Martin G Larson, Ramachandran S Vasan, Joël Ménard, Marcel Goldberg, Marie Zins

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 2 pooled it
2.4field-weighted citation impact, top 10% 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

6 citing papers in PubMed, 2 syntheses or guidelines pooled it, 20 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Article
  6. 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 6 institutions in 2 countries.

Pierre MenetonINSERM U1142 LIMICS, UMR_S 1142 Sorbonne Université, UPMC Université Paris 06, Université Paris 13, Paris, France.
Cédric LemogneCentre Psychiatrie et Neurosciences, INSERM U894, Université Paris Descartes, AP-HP Hôpitaux Universitaires Paris Ouest, Paris, France.
Eléonore HerquelotINSERM UVSQ UMS 011 and UMR-S 1168 VIMA, Villejuif, France.
Sébastien BonenfantINSERM UVSQ UMS 011 and UMR-S 1168 VIMA, Villejuif, France.
Martin G LarsonDepartment of Biostatistics, Department of Mathematics and Statistics, Boston University, Boston, MA, United States of America.
Ramachandran S VasanFramingham Heart Study, Department of Medicine, Boston University, Boston, MA, United States of America.
Joël MénardINSERM/AP-HP CIC1418, Université Paris Descartes, AP-HP Hôpitaux Universitaires Paris Ouest, Paris, France.
Marcel GoldbergINSERM UVSQ UMS 011 and UMR-S 1168 VIMA, Villejuif, France.
Marie ZinsINSERM UVSQ UMS 011 and UMR-S 1168 VIMA, Villejuif, France.
Boston University · USUniversité de Versailles Saint-Quentin-en-Yvelines · FRUniversité Paris Cité · FRHôpitaux Universitaires Paris-Ouest · FRInserm · FRVieillissement et Maladies Chroniques. Approches Epidémiologiques et de santé publique · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Although it has been recognized for a long time that the predisposition to cardiovascular diseases (CVD) is determined by many risk factors and despite the common use of algorithms incorporating several of these factors to predict the overall risk, there has yet been no global description of the complex way in which CVD risk factors interact with each other. This is the aim of the present study which investigated all existing relationships between the main CVD risk factors in a well-characterized occupational cohort. Prospective associations between 12 behavioural and clinical risk factors (gender, age, parental history of CVD, non-moderate alcohol consumption, smoking, physical inactivity, obesity, hypertension, dyslipidemia, diabetes, sleep disorder, depression) were systematically tested using Cox regression in 10,736 middle-aged individuals free of CVD at baseline and followed over 20 years. In addition to independently predicting CVD risk (HRs from 1.18 to 1.97 in multivariable models), these factors form a vast network of associations where each factor predicts, and/or is predicted by, several other factors (n = 47 with p<0.05, n = 37 with p<0.01, n = 28 with p<0.001, n = 22 with p<0.0001). Both the number of factors associated with a given factor (1 to 9) and the strength of the associations (HRs from 1.10 to 6.12 in multivariable models) are very variable, suggesting that all the factors do not have the same influence within this network. These results show that there is a remarkably extensive network of relationships between the main CVD risk factors which may have not been sufficiently taken into account, notably in preventive strategies aiming to lower CVD risk.

Indexed as

AdultAgedAge FactorsAlcohol DrinkingCardiovascular DiseasesDepressionDiabetes ComplicationsDiabetes MellitusDyslipidemiasFemaleHeredityHumansHypertensionLongitudinal StudiesMaleMiddle Aged

Identifiers

PMID27598908
PMCPMC5012694
OpenAlexW2520154016

What OpenQuestion holds

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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.