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Ensayo controlado aleatorizado2025Financiación no declarada

Six weeks of time-restricted eating improves basal fat oxidation and body composition but not fat oxidation during exercise in young males

Aktaş H, Atakan MM, Aktitiz S, Ergün Z, Koşar ŞN, Astorino TA, Turnagöl HH

Clinical nutrition (Edinburgh, Scotland) · 4 citas

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Cómo se estudió

Diseño
Ensayo controlado aleatorizado (indexado por PubMed)
Estudiado en
Personas
Resultado principal
Marcadores de salud y funcionamiento

Quién lo pagó

Financiación
Financiación no declarada

Publicación

Publicado
2025-04-30 · Clin Nutr · vol. 50 · págs. 92–103
Editorial
Elsevier BV
Citado
4 citas · más que el 87% de estudios similares · 2.2× el promedio de su campo
Referencias
70 trabajos
Acceso
De pago
Áreas de investigación
Dietary Effects on Health · Diet and metabolism studies · Muscle metabolism and nutrition
Palabras clave
time-restricted eating, fat oxidation, basal metabolic rate, respiratory exchange ratio, body composition, fat mass, cardiometabolic health, young men, fasting blood glucose, insulin, lipids
MeSH
adipose tissue, humans, insulin, blood glucose, exercise, body composition, oxidation-reduction, oxygen consumption, adult, male, lipid metabolism, young adult, intermittent fasting

7 autores

  • Hale Aktaş🇹🇷Hacettepe University
  • Muhammed Mustafa ATAKAN🇹🇷Hacettepe University
  • Selin Aktitiz🇹🇷Hacettepe University
  • Zeynep Ergün🇹🇷Hacettepe University
  • Şükran Nazan Koşar🇹🇷Hacettepe University
  • Todd Anthony Astorino🇺🇸California State University, San Marcos
  • Hüseyin Hüsrev Turnagöl🇹🇷Hacettepe University

Resumen

El texto original del estudio, en el idioma en que se publicó.

Background & aims

Time-restricted eating (TRE) is a type of intermittent fasting, requiring individuals to limit their eating timeframe to specific hours in the day, while maintaining a fasting period greater than 12 h. Fat oxidation (FOx) is a critical determinant in the pathophysiology of metabolic diseases, with impaired FOx contributing to conditions such as insulin resistance and obesity, whereas enhanced FOx is associated with improved metabolic health. However, the impact of the 16:8 TRE model on FOx remains largely unexplored. The aim of this study was to determine the effect of a 6-week TRE on resting and exercise substrate oxidation, body composition, and blood markers related to metabolic health.

Methods

Thirty-three healthy, young males (age: 27.5 ± 6 years, body mass: 76.5 ± 8.4 kg, maximal oxygen uptake [V˙O2max]: 43.9 ± 6.6 mL·kg-1·min-1) were assigned to either TRE (n = 16) or control group (n = 17), with efforts to match baseline characteristics, including V˙O2max and body composition. The TRE group followed a 16:8 program for 6 weeks, while controls maintained their existing dietary habits. Body composition, blood glucose, insulin, blood lipids, resting substrate oxidation, and FOx during cycling at 40 % V˙O2max were assessed before and after the 6-week period. Data were analyzed using both intention-to-treat (ITT) and per-protocol approaches.

Results

Thirty-three participants were included in the ITT analysis, while 31 participants were included in the per-protocol analysis. Compared to baseline, results showed a significant difference (p -1·min-1versus Δ = -0.37 mg·kg FFM-1·min-1; p = 0.007), and carbohydrate oxidation (Δ = -0.39 mg·kg FFM-1·min-1versus Δ = 0.45 mg·kg FFM-1·min-1; p = 0.037) after the 6-week period. Exercise substrate oxidation and fasting blood glucose, insulin, triglycerides, total cholesterol, and high-density lipoprotein cholesterol did not significantly change over time in either group (p > 0.05).

Conclusions

In summary, a 6-week TRE significantly reduces body mass, fat mass, and resting RER as well as increases resting FOx in young, healthy males. However, it does not affect blood markers related to cardiometabolic health or exercise substrate oxidation. This trial was registered at https://clinicaltrials.gov/study/NCT06498102asNCT06498102.

Resumen vía Europe PMC. Los derechos de autor siguen siendo de los autores o la editorial.

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