Evidence map›Paper›PMID 26180744›Full record

ArticleSpringerPlus2015

Dissecting metabolic syndrome components: data from an epidemiologic survey in a genetic isolate.

Ginevra Biino, Maria Pina Concas, Hellas Cena, Debora Parracciani, Simona Vaccargiu, Massimiliano Cosso, Francesca Marras, Vittoria D'Esposito, Francesco Beguinot, Mario Pirastu

Abstract read
In one paragraph

Article in SpringerPlus, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
–field-weighted citation impact
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

4 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
  4. Metabolic Syndrome Presenting as Abdominal Pain.Saudi journal of medicine & medical sciences
    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

10 authors.

Ginevra BiinoInstitute of Molecular Genetics-CNR, National Research Council of Italy, Via Abbiategrasso 207, 27100 Pavia, Italy.
Maria Pina ConcasInstitute of Population Genetics, National Research Council of Italy, Sassari, Italy.
Hellas CenaUnit of Human Nutrition, Department of Public Health, Experimental and Forensic Medicine, University of Pavia, Pavia, Italy.
Debora ParraccianiOgliastra Genetic Park, Perdasdefogu, Italy.
Simona VaccargiuInstitute of Population Genetics, National Research Council of Italy, Sassari, Italy.
Massimiliano CossoInstitute of Population Genetics, National Research Council of Italy, Sassari, Italy.
Francesca MarrasInstitute of Population Genetics, National Research Council of Italy, Sassari, Italy.
Vittoria D'EspositoDipartimento di Scienze Mediche Traslazionali, Università degli Studi di Napoli "Federico II", Naples, Italy.
Francesco BeguinotDipartimento di Scienze Mediche Traslazionali, Università degli Studi di Napoli "Federico II", Naples, Italy ; Istituto di Endocrinologia ed Oncologia Sperimentale (IEOS-CNR), Naples, Italy.
Mario PirastuInstitute of Population Genetics, National Research Council of Italy, Sassari, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

The metabolic syndrome (MetS) is a large-scale and expanding public-health and clinical threat worldwide. We investigated the determinants of MetS, assessed its prevalence and components and, estimated their genetic contribution, taking advantage of the special characteristics of Sardinian isolated populations. Inhabitants of 10 villages in Ogliastra region participated in a cross-sectional survey in 2002-2008 (n = 9,647). Blood samples, blood pressure (BP), anthropometry and, data from a standardized interview were collected. Prevalence of MetS was estimated by the direct method of standardization. Variables associated with the MetS were identified using multilevel logistic regression. Heritability was determined using variance component models. MetS Prevalence was 19.6% (95% CI 18.9-20.4%) according to NCEP-ATPIII, 24.8% (95% CI 24.0-25.6%) according to IDF and, 29% (95% CI 28.1-29.8%) according to AHA/NHLBI harmonized criteria, ranging from 9 to 26% among villages. The most prevalent combination was BP + HDL-cholesterol (HDL) + triglycerides (TRIG) (19%), followed by BP + HDL + waist circumference (WAIST) (17%) and, BP + HDL + TRIG + WAIST (13.6%). Heritability of MetS was 48% (p = 1.62 × 10(-25)), as the two most common combinations (BP + HDL + TRIG and BP + HDL + WAIST) showed heritability of 53 and 52%, respectively. The larger genetic components of the two most frequent combinations determining MetS deserve greater investigation in order to understand the underlying mechanisms. Besides, further studies are warranted to confirm these findings both in isolated and outbred populations.

Indexed as

ComponentEnvironmentalGeneticMetabolic syndromePrevalence

Identifiers

PMID26180744
PMCPMC4493262

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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.