Evidence map›Paper›PMID 27020448›Full record

ArticleDiabetologia2016

A short leucocyte telomere length is associated with development of insulin resistance.

Simon Verhulst, Christine Dalgård, Carlos Labat, Jeremy D Kark, Masayuki Kimura, Kaare Christensen, Simon Toupance, Abraham Aviv, Kirsten O Kyvik, Athanase Benetos

Abstract read
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In one paragraph

Article in Diabetologia, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 54 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
54citing papers in PubMed, 1 pooled it
–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

54 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Association between telomere length and diabetes mellitus: A meta-analysis.The Journal of international medical research · 2016
    Pooled it
  2. Trial
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  13. Insulin and aging - a disappointing relationship.Frontiers in endocrinology · 2023
    Review
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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

10 authors.

Simon VerhulstGroningen Institute for Evolutionary Life Sciences, University of Groningen, Groningen, the Netherlands.
Christine DalgårdDepartment of Public Health, Environmental Medicine, University of Southern Denmark, Odense, Denmark.
Carlos LabatINSERM, U1116, Vandoeuvre-les-Nancy, France.
Jeremy D KarkHebrew University-Hadassah School of Public Health and Community Medicine, Jerusalem, Israel.
Masayuki KimuraCenter of Human Development and Aging, Rutgers, The State University of New Jersey, New Jersey Medical School, Newark, NJ, USA.
Kaare ChristensenThe Danish Twin Registry, University of Southern Denmark, Odense, Denmark.
Simon ToupanceINSERM, U1116, Vandoeuvre-les-Nancy, France.
Abraham AvivCenter of Human Development and Aging, Rutgers, The State University of New Jersey, New Jersey Medical School, Newark, NJ, USA.
Kirsten O KyvikDepartment of Clinical Research, University of Southern Denmark and Odense Patient data Explorative Network (OPEN), Odense University Hospital, Odense, Denmark.
Athanase BenetosINSERM, U1116, Vandoeuvre-les-Nancy, France. a.benetos@chu-nancy.fr.

Funding

Determinants of Leukocyte Telomere Length at BirthR01HD071180 · NICHD · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI AVIV, ABRAHAM, FACTOR-LITVAK, PAM R · 2012 to 2016
$3.3M
Leukocyte TelomerE Dynamics, Gender, Menopause, Insulin Resistance and SurvivalR01AG030678 · NIA · UNIV OF MED/DENT OF NJ-NJ MEDICAL SCHOOL · PI AVIV, ABRAHAM · 2009 to 2013
$2.2M
NIA NIH HHS R01 AG030678NICHD NIH HHS R01 HD071180
6 · The paper itself

Abstract

aims/hypothesisA number of studies have shown that leucocyte telomere length (LTL) is inversely associated with insulin resistance and type 2 diabetes mellitus. The aim of the present longitudinal cohort study, utilising a twin design, was to assess whether shorter LTL predicts insulin resistance or is a consequence thereof.

methodsParticipants were recruited between 1997 and 2000 through the population-based national Danish Twin Registry to participate in the GEMINAKAR study, a longitudinal evaluation of metabolic disorders and cardiovascular risk factors. Baseline and follow-up measurements of LTL and insulin resistance over an average of 12 years were performed in a subset of the Registry consisting of 338 (184 monozygotic and 154 dizygotic) same-sex twin pairs.

resultsAge at baseline examination was 37.4 ± 9.6 (mean ± SD) years. Baseline insulin resistance was not associated with age-dependent changes in LTL (attrition) over the follow-up period, whereas baseline LTL was associated with changes in insulin resistance during this period. The shorter the LTL at baseline, the more pronounced was the increase in insulin resistance over the follow-up period (p < 0.001); this effect was additive to that of BMI. The co-twin with the shorter baseline LTL displayed higher insulin resistance at follow-up than the co-twin with the longer LTL. CONCLUSIONS/

interpretationThese findings suggest that individuals with short LTL are more likely to develop insulin resistance later in life. By contrast, presence of insulin resistance does not accelerate LTL attrition.

Indexed as

AdultAge FactorsBody Mass IndexCardiovascular DiseasesFemaleHumansInsulin ResistanceLeukocytesMaleMiddle AgedRisk FactorsSex FactorsTelomereGenetics/epidemiology (all)HumanInsulin sensitivity and resistance

Identifiers

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Textmetadata
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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.