Evidence map›Paper›PMID 28384193›Full record

ArticlePloS one2017

Metabolically healthy obese women have longer telomere length than obese women with metabolic syndrome.

Andrea E Iglesias Molli, Julieta Panero, Patricia C Dos Santos, Claudio D González, Jorge Vilariño, Marta Sereday, Gloria E Cerrone, Irma Slavutsky, Gustavo D Frechtel

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 17 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
17citing papers in PubMed, 2 pooled it
0.9field-weighted citation impact, top 26% 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

17 citing papers in PubMed, 2 syntheses or guidelines pooled it, 21 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Trial
  4. Review
  5. Review
  6. Article
  7. Review
  8. Article
  9. The consumption ofRedox report : communications in free radical research · 2023
    Article
  10. Article
  11. Review
  12. Review
  13. Article
  14. Association of leukocyte telomere length with metabolic syndrome in type 2 diabetes mellitus.Journal of research in medical sciences : the official journal of Isfahan University of Medical Sciences · 2021
    Article
  15. Article
  16. Observational
  17. 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 4 institutions in 1 country.

Andrea E Iglesias MolliCONICET-Universidad de Buenos Aires. Instituto de Inmunología, Genética y Metabolismo (INIGEM). Laboratorio de Diabetes y Metabolismo. Buenos Aires, Argentina.
Julieta PaneroAcademia Nacional de Medicina. CONICET. Instituto de Medicina experimental (IMEX). Laboratorio de Genética de Neoplasias Linfoides. Buenos Aires, Argentina.
Patricia C Dos SantosAcademia Nacional de Medicina. CONICET. Instituto de Medicina experimental (IMEX). Laboratorio de Genética de Neoplasias Linfoides. Buenos Aires, Argentina.
Claudio D GonzálezUniversidad de Buenos Aires. Facultad de Medicina. Departamento de Farmacología. Cátedra II. Buenos Aires, Argentina.
Jorge VilariñoHospital FLENI. Departamento de Cardiología. Buenos Aires, Argentina.
Marta SeredayHospital Fiorito. Servicio de Endocrinología. Buenos Aires, Argentina.
Gloria E CerroneUniversidad de Buenos Aires. Facultad de Farmacia y Bioquímica. Departamento de Microbiología, Inmunología y Biotecnología. Cátedra de Genética. Buenos Aires, Argentina.
Irma SlavutskyAcademia Nacional de Medicina. CONICET. Instituto de Medicina experimental (IMEX). Laboratorio de Genética de Neoplasias Linfoides. Buenos Aires, Argentina.
Gustavo D FrechtelCONICET-Universidad de Buenos Aires. Instituto de Inmunología, Genética y Metabolismo (INIGEM). Laboratorio de Diabetes y Metabolismo. Buenos Aires, Argentina.
Consejo Nacional de Investigaciones Científicas y Técnicas · ARAcademia Nacional de Medicina · ARUniversity of Buenos Aires · ARFundación para la Lucha contra las Enfermedades Neurológicas de la Infancia · AR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionObesity is the principal component in the Metabolic Syndrome (MetS) that determines the progression of metabolic complications. Metabolically healthy obese (MHO) individuals seem to be protected against those complications. Telomere length (TL) as a novel marker of cellular aging had a complex relationship to the MetS. The principal aim of this study was to investigate the TL in MHO, and to study the association between TL and the worsening of the metabolic condition. MATERIAL AND

methodsWe have determined the absolute TL (aTL) in 400 women (mean age of 46.76 ± 15.47 years; range: 18-86 years), grouped according to the metabolic condition in three groups: metabolically healthy non-obese women (MHNO), MHO and obese women with MetS (MSO); and grouped according to the number of components of MetS.

resultsWe found that MHO displays significantly higher aTL than MSO (p = 0.033; r = -4.63; 95% CI r = -8.89 / -0.37), but did not differ from MHNO. A decrease in aTL with the progressive increase in the number of MetS components was also observed (p < 0.001; r = -2.06; 95% CI r = -3.13 / -0.99). In this way, our results indicate that aTL is influenced by the presence of MetS, but it is not affected by the presence of obesity. DISCUSSION: We found that shorter aTL is not associated with MHO, but is related to MetS and with the increased number of metabolic abnormalities.

Indexed as

TelomereAdolescentAdultAgedAged, 80 and overHumansMetabolic SyndromeMiddle AgedObesity, Metabolically BenignYoung Adult

Identifiers

PMID28384193
PMCPMC5383129
OpenAlexW2604159116

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.