Evidence map›Paper›PMID 37964387›Full record

ArticleImmunity & ageing : I & A2023

Aging and the impact of global DNA methylation, telomere shortening, and total oxidative status on sarcopenia and frailty syndrome.

Tomasz Kmiołek, Gabriela Filipowicz, Diana Bogucka, Anna Wajda, Adam Ejma-Multański, Barbara Stypińska, Ewa Modzelewska, Yana Kaliberda, Marcin Radkowski, Tomasz Targowski and 2 more

Open access · goldAbstract read
In one paragraph

Article in Immunity & ageing : I & A, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.0field-weighted citation impact, top 14% 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

8 citing papers in PubMed, 11 citations in OpenAlex.

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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

12 authors at 2 institutions in 1 country.

Tomasz KmiołekDepartment of Molecular Biology, National Institute of Geriatrics, Rheumatology and Rehabilitation, 02-637, Warsawm, Poland. tomekkmiolek@gmail.com.
Gabriela FilipowiczDepartment of Molecular Biology, National Institute of Geriatrics, Rheumatology and Rehabilitation, 02-637, Warsawm, Poland.
Diana BoguckaDepartment of Molecular Biology, National Institute of Geriatrics, Rheumatology and Rehabilitation, 02-637, Warsawm, Poland.
Anna WajdaDepartment of Molecular Biology, National Institute of Geriatrics, Rheumatology and Rehabilitation, 02-637, Warsawm, Poland.
Adam Ejma-MultańskiDepartment of Molecular Biology, National Institute of Geriatrics, Rheumatology and Rehabilitation, 02-637, Warsawm, Poland.
Barbara StypińskaDepartment of Molecular Biology, National Institute of Geriatrics, Rheumatology and Rehabilitation, 02-637, Warsawm, Poland.
Ewa ModzelewskaDepartment of Molecular Biology, National Institute of Geriatrics, Rheumatology and Rehabilitation, 02-637, Warsawm, Poland.
Yana KaliberdaDepartment of Molecular Biology, National Institute of Geriatrics, Rheumatology and Rehabilitation, 02-637, Warsawm, Poland.
Marcin RadkowskiDepartment of Pathophysiology and Immunology, National Institute of Geriatrics, Rheumatology and Rehabilitation, 02-637, Warsaw, Poland.
Tomasz TargowskiDepartment of Pathophysiology and Immunology, National Institute of Geriatrics, Rheumatology and Rehabilitation, 02-637, Warsaw, Poland.
Julia WronaCollegium Medicum University of Jan Kochanowski, 25-317, Kielce, Poland.
Agnieszka Paradowska-GoryckaDepartment of Molecular Biology, National Institute of Geriatrics, Rheumatology and Rehabilitation, 02-637, Warsawm, Poland.
National Institute of Geriatrics, Rheumatology and Rehabilitation · PLJan Kochanowski University · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aging is a biological event that influences many organs and systems. Both sarcopenia and frailty syndrome refer to geriatric conditions with overlapping phenotypes. Many mechanisms are involved in the aging process such as DNA methylation telomeres which are susceptible to oxidative stress, and inflammations which result in telomere shortening, leading to chromosomal instability. The study aimed to determine the associations between these processes, frailty and sarcopenia syndrome. Global DNA methylation was analyzed using the ELISA method. Telomere length was analyzed using qPCR. Total oxidative status (TOS) was analyzed using a colorimetric method. The present study revealed that the main factor affecting methylation, telomeres length and level of total oxidant stress was age.

Indexed as

AgingDNA methylationFrailty syndromeSarcopeniaTelomere lengthTotal oxidative stress

Identifiers

PMID37964387
PMCPMC10644469
OpenAlexW4388667795

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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.