Evidence map›Paper›PMID 26275065›Full record

ArticlePloS one2015

Age-Related Left Ventricular Changes and Their Association with Leukocyte Telomere Length in Healthy People.

Dariga U Akasheva, Ekaterina V Plokhova, Olga N Tkacheva, Irina D Strazhesko, Ekaterina N Dudinskaya, Anna S Kruglikova, Valentina S Pykhtina, Natalia V Brailova, Inna A Pokshubina, Natalia V Sharashkina and 3 more

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed
2.3field-weighted citation impact, top 13% 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

21 citing papers in PubMed, 35 citations in OpenAlex.

  1. Trial
  2. Article
  3. Article
  4. Review
  5. Observational
  6. Observational
  7. Immunometabolism in the Aging Heart.Journal of the American Heart Association · 2025
    Review
  8. Article
  9. Review
  10. Article
  11. Article
  12. Article
  13. Review
  14. Left Ventricular Remodeling Patterns in Primary Healthcare.Arquivos brasileiros de cardiologia · 2020
    Article
  15. Article
  16. Article
  17. Senescent cells: a therapeutic target for cardiovascular disease.The Journal of clinical investigation · 2018
    Review
  18. Article
  19. Review
  20. 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

13 authors at 2 institutions in 1 country.

Dariga U AkashevaDepartment of study the ageing and prevent age-associated diseases, National Research Center for Preventive Medicine, Moscow, Russian Federation.
Ekaterina V PlokhovaDepartment of study the ageing and prevent age-associated diseases, National Research Center for Preventive Medicine, Moscow, Russian Federation.
Olga N TkachevaDepartment of study the ageing and prevent age-associated diseases, National Research Center for Preventive Medicine, Moscow, Russian Federation.
Irina D StrazheskoDepartment of study the ageing and prevent age-associated diseases, National Research Center for Preventive Medicine, Moscow, Russian Federation.
Ekaterina N DudinskayaDepartment of study the ageing and prevent age-associated diseases, National Research Center for Preventive Medicine, Moscow, Russian Federation.
Anna S KruglikovaDepartment of study the ageing and prevent age-associated diseases, National Research Center for Preventive Medicine, Moscow, Russian Federation.
Valentina S PykhtinaDepartment of study the ageing and prevent age-associated diseases, National Research Center for Preventive Medicine, Moscow, Russian Federation.
Natalia V BrailovaDepartment of study the ageing and prevent age-associated diseases, National Research Center for Preventive Medicine, Moscow, Russian Federation.
Inna A PokshubinaDepartment of study the ageing and prevent age-associated diseases, National Research Center for Preventive Medicine, Moscow, Russian Federation.
Natalia V SharashkinaDepartment of study the ageing and prevent age-associated diseases, National Research Center for Preventive Medicine, Moscow, Russian Federation.
Mikhail V AgaltsovDepartment of study the ageing and prevent age-associated diseases, National Research Center for Preventive Medicine, Moscow, Russian Federation.
Dmitry SkvortsovDepartment of Chemistry, Lomonosov Moscow State University, Moscow, Russian Federation.
Sergey A BoytsovDepartment of study the ageing and prevent age-associated diseases, National Research Center for Preventive Medicine, Moscow, Russian Federation.
National Research Center for Preventive Medicine · RULomonosov Moscow State University · RU

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionWith advancing age the left ventricle (LV) undergoes structural and functional changes, thereby creating the substrate for the development of diseases. One possible mechanism of the ageing heart is a cellular senescence. Leukocyte telomere length (LTL) is a marker of replicative ageing. The purpose of this study was to evaluate the structure and function of the LV in people of different ages free of cardiovascular diseases (CVD) and regular drug medication and to assess their relationship with LTL. We hypothesized that age-related changes in LV myocardium are associated with telomere length.

methodsThe study population consisted of 150 healthy, non-obese volunteers aged 28 to 78 years without history of CVD, significant deviations by 12-lead electrocardiogram and negative exercise test (treadmill stress test). All the participants underwent standardized transthoracic echocardiography using an available system (iE33; Philips). The LTL was measured by real-time quantitative polymerase chain reaction. We determined the relative ratio of telomere repeat copy number (T) to single-copy gene copy number (S).

resultsIn the older people there was a higher wall thickness than in the younger (1.03 ± 0.09 vs. 0.88 ± 0.10, p<0.01), whereas LV mass index was comparable between them (85.8 ± 15.40 vs. 83.1 ± 11.8, p = 0.20). There was a decrease in LV dimensions with advancing age (p<0.001). Older subjects had impairment in LV relaxation. LTL was associated with decreased E/A, Em/Am ratio (β = -0.323, p = 0.0001) after adjusting for age, sex and risk factors. There is no relation between the LTL and the structure of LV.

conclusionsOur data suggest that the ageing process leads to changes in LV structure and diastolic function and is linked with a phenotype of concentric LV remodeling. Telomere attrition is associated with age-related LV diastolic dysfunction. Telomere length appears to be a biomarker of myocardial ageing.

Indexed as

Telomere HomeostasisVentricular Function, LeftAdultAgedAgingFemaleHeart VentriclesHumansLeukocytesMaleMiddle AgedMyocardium

Identifiers

PMID26275065
PMCPMC4537122
OpenAlexW1807933617

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.