Evidence map›Paper›PMID 34535961›Full record

Trial reportAging cell2021

DNA methylation-based biomarkers of aging were slowed down in a two-year diet and physical activity intervention trial: the DAMA study.

Giovanni Fiorito, Saverio Caini, Domenico Palli, Benedetta Bendinelli, Calogero Saieva, Ilaria Ermini, Virginia Valentini, Melania Assedi, Piera Rizzolo, Daniela Ambrogetti and 2 more

Open access · goldAbstract readRandomized Controlled Trial
In one paragraph

Trial report in Aging cell, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 127 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
127citing papers in PubMed, 2 pooled it
9.6field-weighted citation impact, top 1% 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

127 citing papers in PubMed, 2 syntheses or guidelines pooled it, 182 citations in OpenAlex.

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67 more citing papers are in PubMed but not listed here.

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 3 institutions in 3 countries.

Giovanni FioritoLaboratory of Biostatistics, Department of Biomedical Sciences, University of Sassari, Sassari, Italy.ORCID 0000-0002-7651-5452
Saverio CainiInstitute for Cancer Research, Prevention and Clinical Network - ISPRO, Florence, Italy.
Domenico PalliInstitute for Cancer Research, Prevention and Clinical Network - ISPRO, Florence, Italy.ORCID 0000-0002-5558-2437
Benedetta BendinelliInstitute for Cancer Research, Prevention and Clinical Network - ISPRO, Florence, Italy.
Calogero SaievaInstitute for Cancer Research, Prevention and Clinical Network - ISPRO, Florence, Italy.
Ilaria ErminiInstitute for Cancer Research, Prevention and Clinical Network - ISPRO, Florence, Italy.
Virginia ValentiniDepartment of Molecular Medicine, Sapienza University of Rome, Rome, Italy.
Melania AssediInstitute for Cancer Research, Prevention and Clinical Network - ISPRO, Florence, Italy.
Piera RizzoloDepartment of Molecular Medicine, Sapienza University of Rome, Rome, Italy.
Daniela AmbrogettiInstitute for Cancer Research, Prevention and Clinical Network - ISPRO, Florence, Italy.
Laura OttiniDepartment of Molecular Medicine, Sapienza University of Rome, Rome, Italy.
Giovanna MasalaInstitute for Cancer Research, Prevention and Clinical Network - ISPRO, Florence, Italy.
Prevention Institute · USSapienza University of Rome · ITUniversity of Sassari · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Several biomarkers of healthy aging have been proposed in recent years, including the epigenetic clocks, based on DNA methylation (DNAm) measures, which are getting increasingly accurate in predicting the individual biological age. The recently developed "next-generation clock" DNAmGrimAge outperforms "first-generation clocks" in predicting longevity and the onset of many age-related pathological conditions and diseases. Additionally, the total number of stochastic epigenetic mutations (SEMs), also known as the epigenetic mutation load (EML), has been proposed as a complementary DNAm-based biomarker of healthy aging. A fundamental biological property of epigenetic, and in particular DNAm modifications, is the potential reversibility of the effect, raising questions about the possible slowdown of epigenetic aging by modifying one's lifestyle. Here, we investigated whether improved dietary habits and increased physical activity have favorable effects on aging biomarkers in healthy postmenopausal women. The study sample consists of 219 women from the "Diet, Physical Activity, and Mammography" (DAMA) study: a 24-month randomized factorial intervention trial with DNAm measured twice, at baseline and the end of the trial. Women who participated in the dietary intervention had a significant slowing of the DNAmGrimAge clock, whereas increasing physical activity led to a significant reduction of SEMs in crucial cancer-related pathways. Our study provides strong evidence of a causal association between lifestyle modification and slowing down of DNAm aging biomarkers. This randomized trial elucidates the causal relationship between lifestyle and healthy aging-related epigenetic mechanisms.

Indexed as

AgingDiet TherapyDNA MethylationExerciseFemaleHumansMaleTime Factorsdietary habitsDNA methylationepigenetic clockepigenetic mutation loadphysical activitypostmenopausal womenprimary prevention trial

Identifiers

PMID34535961
PMCPMC8520727
OpenAlexW3201585688

What OpenQuestion holds

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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.