Effects of a four-week very low-carbohydrate high-fat diet on biomarkers of inflammation: Non-randomised parallel-group study
Jazyk angličtina Země Velká Británie, Anglie Médium print-electronic
Typ dokumentu časopisecké články
PubMed
32000572
DOI
10.1177/0260106020903206
Knihovny.cz E-zdroje
- Klíčová slova
- Ketogenic diet, adiponectin, interleukin-6, leptin,
- MeSH
- adiponektin krev MeSH
- biologické markery krev MeSH
- dieta s omezením sacharidů metody MeSH
- dieta s vysokým obsahem tuků metody MeSH
- dietní tuky MeSH
- dospělí MeSH
- interleukin-6 krev MeSH
- ketogenní dieta metody MeSH
- krevní glukóza analýza MeSH
- leptin krev MeSH
- lidé MeSH
- mladý dospělý MeSH
- resistin krev MeSH
- triglyceridy krev MeSH
- zánět krev dietoterapie MeSH
- Check Tag
- dospělí MeSH
- lidé MeSH
- mladý dospělý MeSH
- mužské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- Názvy látek
- adiponektin MeSH
- ADIPOQ protein, human MeSH Prohlížeč
- biologické markery MeSH
- dietní tuky MeSH
- interleukin-6 MeSH
- krevní glukóza MeSH
- leptin MeSH
- resistin MeSH
- RETN protein, human MeSH Prohlížeč
- triglyceridy MeSH
BACKGROUND: It is commonly assumed that increased dietary fat and/or caloric excess induces chronic inflammatory processes, since the association between obesity and chronic adipose tissue with systemic inflammation has been shown previously. As far as we know, the reported health benefits of a VLCHF or ketogenic diet have not adequately involved an evaluation of biomarkers of inflammation. AIM: This study investigated the effects of a four-week very low-carbohydrate high-fat (VLCHF) diet in healthy young individuals on biomarkers of inflammation. METHODS: Eighteen moderately trained males (age 23.8 ± 2.1 years) were assigned to two groups. One group switched to a non-standardised VLCHF diet for four weeks, while the second group remained consuming their normal habitual diet (HD). Biomarkers of inflammation (adiponectin, leptin, resistin and interleukin-6) and substrate metabolism (fasting glucose and triacylglyceride concentrations) were analysed from blood at baseline and after four weeks. RESULTS: There was moderate evidence for substantial changes in leptin serum concentrations in the VLCHF group, with small to large decreases compared to the HD group after four weeks (effect size = 0.78, 95% CI 0.42, 0.93, p = 0.008; Bayes Factor10 = 5.70). No substantial between-group change differences over time were found across any other biomarkers. CONCLUSIONS: A four-week period of consuming a VLCHF diet in healthy young men was not associated with any considerable changes in markers of inflammation but showed evidence for lowered serum leptin concentrations relative to the HD group.
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