Evidence map›Paper›PMID 24376531›Full record

ArticlePloS one2013

Clustering of the metabolic syndrome components in adolescence: role of visceral fat.

Melkaye G Melka, Michal Abrahamowicz, Gabriel T Leonard, Michel Perron, Louis Richer, Suzanne Veillette, Daniel Gaudet, Tomáš Paus, Zdenka Pausova

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
2.6field-weighted citation impact, top 11% 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

7 citing papers in PubMed, 20 citations in OpenAlex.

  1. Trial
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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

9 authors at 6 institutions in 1 country.

Melkaye G MelkaThe Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.
Michal AbrahamowiczDepartment of Epidemiology, Biostatistics and Occupational Health, McGill University, Montreal, Quebec, Canada.
Gabriel T LeonardMontreal Neurological Institute, McGill University, Montreal, Quebec, Canada.
Michel PerronÉCOBES, Recherche et transfert, Cégep de Jonquière, Jonquière, Quebec, Canada ; Department of Human Sciences, Université du Québec à Chicoutimi, Chicoutimi, Quebec, Canada.
Louis RicherDepartment of Psychology, Université du Québec à Chicoutimi, Chicoutimi, Quebec, Canada.
Suzanne VeilletteÉCOBES, Recherche et transfert, Cégep de Jonquière, Jonquière, Quebec, Canada ; Department of Human Sciences, Université du Québec à Chicoutimi, Chicoutimi, Quebec, Canada.
Daniel GaudetCommunity Genomic Centre, Université de Montréal, Chicoutimi, Quebec, Canada.
Tomáš PausRotman Research Institute, University of Toronto, Toronto, Ontario, Canada.
Zdenka PausovaThe Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada.
Hospital for Sick Children · CAMcGill University · CAUniversité du Québec à Chicoutimi · CACégep de Jonquière · CAUniversité de Montréal · CAUniversity of Toronto · CA

Funding

Canadian Institutes of Health Research
6 · The paper itself

Abstract

Visceral fat (VF) promotes the development of metabolic syndrome (MetS), which emerges as early as in adolescence. The clustering of MetS components suggests shared etiologies, but these are largely unknown and may vary between males and females. Here, we investigated the latent structure of pre-clinical MetS in a community-based sample of 286 male and 312 female adolescents, assessing their abdominal adiposity (VF) directly with magnetic resonance imaging. Principal component analysis of the five MetS-defining variables (VF, blood pressure [BP], fasting serum triglycerides, HDL-cholesterol and glucose) identified two independent components in both males and females. The first component was sex-similar; it explained >30% of variance and was loaded by all but BP variables. The second component explained >20% of variance; it was loaded by BP similarly in both sexes but additional loading by metabolic variables was sex-specific. This sex-specificity was not detected in analyses that used waist circumference instead of VF. In adolescence, MetS-defining variables cluster into at least two sub-syndromes: (1) sex-similar metabolic abnormalities of obesity-induced insulin resistance and (2) sex-specific metabolic abnormalities associated with BP elevation. These results suggest that the etiology of MetS may involve more than one pathway and that some of the pathways may differ between males and females. Further, the sex-specific metabolic abnormalities associated with BP elevation suggest the need for sex-specific prevention and treatment strategies of MetS.

Indexed as

AdolescentChildCluster AnalysisFemaleHumansIntra-Abdominal FatMaleMetabolic SyndromePrincipal Component AnalysisWaist Circumference

Identifiers

PMID24376531
PMCPMC3869691
OpenAlexW2029187537

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.