Evidence map›Paper›PMID 42369048›Full record

ArticleFrontiers in endocrinology2026

Time-restricted eating versus calorie restriction for improving biomarkers of age in adults with overweight or obesity and incipient fatty liver disease: protocol for the ENSATI randomized controlled parallel groups trial.

José A Celada-Guerrero, Laura Rubio-Gordón, Yolanda Jiménez-Perez, Lorena López-Lora, Andrés López-González, Sara Delbuono, Ana Huertas, Diego Martínez-Urbistondo, José Ma Ordovás, Víctor de la O and 1 more

Abstract readClinical Trial Protocol
In one paragraph

Article in Frontiers in endocrinology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

11 authors.

José A Celada-GuerreroNutritional Control of the Epigenome (NUCONEP), Precision Nutrition and Obesity Program, IMDEA Nutrition. CEI UAM + CSIC., Madrid, Spain.
Laura Rubio-GordónCIBER de Fisiopatología de la Obesidad y Nutrición, Instituto de Salud Carlos III, Madrid, Spain.
Yolanda Jiménez-PerezNutritional Control of the Epigenome (NUCONEP), Precision Nutrition and Obesity Program, IMDEA Nutrition. CEI UAM + CSIC., Madrid, Spain.
Lorena López-LoraNutritional Control of the Epigenome (NUCONEP), Precision Nutrition and Obesity Program, IMDEA Nutrition. CEI UAM + CSIC., Madrid, Spain.
Andrés López-GonzálezNutritional Control of the Epigenome (NUCONEP), Precision Nutrition and Obesity Program, IMDEA Nutrition. CEI UAM + CSIC., Madrid, Spain.
Sara DelbuonoNutritional Control of the Epigenome (NUCONEP), Precision Nutrition and Obesity Program, IMDEA Nutrition. CEI UAM + CSIC., Madrid, Spain.
Ana HuertasDepartment of Endocrinology, Clínica Universidad de Navarra, Madrid, Spain.
Diego Martínez-UrbistondoDepartment of Endocrinology, Clínica Universidad de Navarra, Madrid, Spain.
José Ma OrdovásCIBER de Fisiopatología de la Obesidad y Nutrición, Instituto de Salud Carlos III, Madrid, Spain.
Víctor de la ONutritional Control of the Epigenome (NUCONEP), Precision Nutrition and Obesity Program, IMDEA Nutrition. CEI UAM + CSIC., Madrid, Spain.
Lidia DaimielNutritional Control of the Epigenome (NUCONEP), Precision Nutrition and Obesity Program, IMDEA Nutrition. CEI UAM + CSIC., Madrid, Spain.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: The increasing global lifespan has shifted the primary objective of geroscience from merely extending lifespan to maximizing health span. Biological aging is a gradual, time-dependent process marked by progressive cellular deterioration that culminates in increased vulnerability, frailty, morbidity, and mortality. Understanding the mechanisms that accelerate or decelerate this deterioration is crucial for developing effective interventions. Diet is recognized as the leading modifiable behavioral risk factor influencing the global burden of noncommunicable diseases and mortality. Therefore, nutritional interventions constitute a highly practical and scalable strategy for promoting healthy aging. Methods: The ENSATI trial is a randomized, open-label, controlled study with three parallel arms: active dietary counseling control, 25% calorie restriction, and time-restricted eating (14-hour fasting/10-hour eating window) over six months, followed by six months of post-intervention monitoring. A total of 177 adults aged 50-70 years with overweight/obesity and incipient fatty liver disease will be enrolled. Analyses: Primary outcomes include changes in body composition (dual X ray densitometry), hepatic fat (elastography) and metabolism (indirect calorimetry). Secondary outcomes encompass glucose regulation (continuous glucose monitoring), gut microbiome profiles, molecular biomarkers of aging (epigenetics, autophagy, immunosenescence), alongside psychological, cognitive, sleep, and dietary assessments using validated tools. Analyses will follow an intention-to-treat approach, with per-protocol sensitivity analyses and sex-stratified models. Mixed-effects models adjusted for potential confounders will assess intervention effects. Discussion: Current TRE and caloric restriction studies are limited by short durations, small samples, and poor control of energy intake, often lacking molecular biomarkers of aging. ENSATI overcomes these gaps through a 12-month, adequately powered, randomized, multi-arm design with rigorous dietary monitoring and comprehensive molecular and physiological profiling, enabling a more rigorous exploration of the relative contributions of caloric intake versus chronobiological effects on obesity and aging. Ethics and dissemination: This study was approved by IMDEA Ethics Committee (IMF PI-057). All participants will provide written informed consent. The findings will be disseminated in peer-reviewed scientific journals and at scientific conferences.

Indexed as

AgingBiomarkersCaloric RestrictionObesityOverweightAgedFemaleHumansIntermittent FastingMaleMiddle AgedRandomized Controlled Trials as TopicBiomarkersbiological age (BA)biomarkers of agingcalorie restriction (CR)epigenetic clockfatty liver disease associated with metabolic dysfunctiongeroscienceobesitytime-restricted eating

Identifiers

PMID42369048
PMCPMC13303218

What Socratic holds

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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 Socratic graph.