Evidence map›Paper›PMID 38854689›Full record

Trial reportFrontiers in endocrinology2024

Effect of sustained decreases in sedentary time and increases in physical activity on liver enzymes and indices in type 2 diabetes.

Jonida Haxhi, Martina Vitale, Lorenza Mattia, Chiara Giuliani, Massimo Sacchetti, Giorgio Orlando, Carla Iacobini, Stefano Menini, Silvano Zanuso, Antonio Nicolucci and 2 more

Abstract readRandomized Controlled Trial
In one paragraph

Trial report in Frontiers in endocrinology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing 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

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

  1. Pooled it
  2. Review
  3. Review
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.

Jonida Haxhi *Department of Clinical and Molecular Medicine, University of Rome La Sapienza, Rome, Italy.
Martina Vitale *Department of Clinical and Molecular Medicine, University of Rome La Sapienza, Rome, Italy.
Lorenza MattiaDepartment of Clinical and Molecular Medicine, University of Rome La Sapienza, Rome, Italy.
Chiara GiulianiDepartment of Clinical and Molecular Medicine, University of Rome La Sapienza, Rome, Italy.
Massimo SacchettiDepartment of Human Movement and Sport Sciences, University of Rome 'Foro Italico', Rome, Italy.
Giorgio OrlandoDepartment of Human Movement and Sport Sciences, University of Rome 'Foro Italico', Rome, Italy.
Carla IacobiniDepartment of Clinical and Molecular Medicine, University of Rome La Sapienza, Rome, Italy.
Stefano MeniniDepartment of Clinical and Molecular Medicine, University of Rome La Sapienza, Rome, Italy.
Silvano ZanusoCenter for Applied Biological and Exercise Sciences, Faculty of Health and Life Sciences, Coventry University, Coventry, United Kingdom.
Antonio NicolucciCenter for Outcomes Research and Clinical Epidemiology (CORESEARCH), Pescara, Italy.
Stefano BalducciDepartment of Clinical and Molecular Medicine, University of Rome La Sapienza, Rome, Italy.
Giuseppe PuglieseDepartment of Clinical and Molecular Medicine, University of Rome La Sapienza, Rome, Italy.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Current guidelines for nonalcoholic fatty liver disease (NAFLD) recommend high volumes and/or intensities of physical activity (PA), the achievement of which generally requires participation in supervised exercise training programs that however are difficult to implement in routine clinical practice. Conversely, counselling interventions may be more suitable, but result in only modest increases in moderate-to-vigorous-intensity PA (MVPA). This study assessed whether a counseling intervention for increasing PA and decreasing sedentary time (SED-time) is effective in improving NAFLD markers in people with type 2 diabetes. Methods: Three-hundred physically inactive and sedentary patients were randomized 1:1 to receive one-month theoretical and practical counseling once-a-year (intervention group) or standard care (control group) for 3 years. Aspartate aminotransferase (AST), alanine aminotransferase (ALT), and γ-glutamyltranspeptidase (γGT) levels were measured and fatty liver index (FLI), hepatic steatosis index (HSI), and visceral adiposity index (VAI) were calculated. Total PA volume, light-intensity PA (LPA), moderate-to-vigorous-intensity PA (MVPA), and SED-time were objectively measured by an accelerometer. Results: Throughout the 3-year period, NAFLD markers did not change in the control group, whereas ALT, γGT, FLI, and HSI decreased in the intervention group, with significant between-group differences, despite modest MVPA increases, which however were associated with larger decrements in SED-time and reciprocal increments in LPA. Mean changes in NAFLD markers varied according to quartiles of (and correlated with) changes in MVPA (all markers) and SED-time, LPA, and PA volume (ALT, γGT, and HSI). Mean changes in MVPA or PA volume were independent predictors of changes in NAFLD markers. When included in the models, change in cardiorespiratory fitness and lower body muscle strength were independently associated with some NAFLD markers. Conclusion: A behavior change involving all domains of PA lifestyle, even if insufficient to achieve the recommended MVPA target, may provide beneficial effects on NAFLD markers in people with type 2 diabetes.

Indexed as

Alanine TransaminaseAspartate AminotransferasesDiabetes Mellitus, Type 2ExerciseNon-alcoholic Fatty Liver DiseaseSedentary BehaviorAgedBiomarkersFemalegamma-GlutamyltransferaseHumansLiverMaleMiddle AgedAlanine TransaminaseAspartate AminotransferasesBiomarkersgamma-Glutamyltransferaseliver enzymesnonalcoholic fatty liver diseasephysical activitysedentary behaviortype 2 diabetes

Identifiers

PMID38854689
PMCPMC11157683

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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.