Reduction of De Novo Lipogenesis Mediates Beneficial Effects of Isoenergetic Diets on Fatty Liver: Mechanistic Insights from the MEDEA Randomized Clinical Trial.


Journal

Nutrients
ISSN: 2072-6643
Titre abrégé: Nutrients
Pays: Switzerland
ID NLM: 101521595

Informations de publication

Date de publication:
23 May 2022
Historique:
received: 31 03 2022
revised: 18 05 2022
accepted: 22 05 2022
entrez: 28 5 2022
pubmed: 29 5 2022
medline: 1 6 2022
Statut: epublish

Résumé

Non-alcoholic liver steatosis (NAS) results from an imbalance between hepatic lipid storage, disposal, and partitioning. A multifactorial diet high in fiber, monounsaturated fatty acids (MUFAs), n-6 and n-3 polyunsaturated fatty acids (PUFAs), polyphenols, and vitamins D, E, and C reduces NAS in people with type 2 diabetes (T2D) by 40% compared to a MUFA-rich diet. We evaluated whether dietary effects on NAS are mediated by changes in hepatic de novo lipogenesis (DNL), stearoyl-CoA desaturase (SCD1) activity, and/or β-oxidation. According to a randomized parallel group study design, 37 individuals with T2D completed an 8-week isocaloric intervention with a MUFA diet ( Compared to baseline, mean ± SD DNL significantly decreased after the multifactorial diet (2.2 ± 0.8 vs. 1.5 ± 0.5, A diet rich in multiple beneficial dietary components (fiber, polyphenols, MUFAs, PUFAs, and other antioxidants) compared to a diet rich only in MUFAs further reduces liver fat accumulation through the inhibition of DNL. Registered under ClinicalTrials.gov no. NCT03380416.

Sections du résumé

BACKGROUND BACKGROUND
Non-alcoholic liver steatosis (NAS) results from an imbalance between hepatic lipid storage, disposal, and partitioning. A multifactorial diet high in fiber, monounsaturated fatty acids (MUFAs), n-6 and n-3 polyunsaturated fatty acids (PUFAs), polyphenols, and vitamins D, E, and C reduces NAS in people with type 2 diabetes (T2D) by 40% compared to a MUFA-rich diet. We evaluated whether dietary effects on NAS are mediated by changes in hepatic de novo lipogenesis (DNL), stearoyl-CoA desaturase (SCD1) activity, and/or β-oxidation.
METHODS METHODS
According to a randomized parallel group study design, 37 individuals with T2D completed an 8-week isocaloric intervention with a MUFA diet (
RESULTS RESULTS
Compared to baseline, mean ± SD DNL significantly decreased after the multifactorial diet (2.2 ± 0.8 vs. 1.5 ± 0.5,
CONCLUSIONS CONCLUSIONS
A diet rich in multiple beneficial dietary components (fiber, polyphenols, MUFAs, PUFAs, and other antioxidants) compared to a diet rich only in MUFAs further reduces liver fat accumulation through the inhibition of DNL. Registered under ClinicalTrials.gov no. NCT03380416.

Identifiants

pubmed: 35631319
pii: nu14102178
doi: 10.3390/nu14102178
pmc: PMC9143579
pii:
doi:

Substances chimiques

Polyphenols 0
Palmitic Acid 2V16EO95H1
Stearoyl-CoA Desaturase EC 1.14.19.1
3-Hydroxybutyric Acid TZP1275679

Banques de données

ClinicalTrials.gov
['NCT03380416']

Types de publication

Journal Article Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

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Auteurs

Giuseppina Costabile (G)

Department of Clinical Medicine and Surgery, Federico II University, Via Sergio Pansini 5, 80131 Naples, Italy.
Task Force on Microbiome Studies, University of Naples "Federico II", 80138 Naples, Italy.

Giuseppe Della Pepa (G)

Department of Clinical Medicine and Surgery, Federico II University, Via Sergio Pansini 5, 80131 Naples, Italy.

Dominic Salamone (D)

Department of Clinical Medicine and Surgery, Federico II University, Via Sergio Pansini 5, 80131 Naples, Italy.

Delia Luongo (D)

CNR-Institute of Biostructures and Bioimaging, Naples, Via Mezzocannone 16, 80100 Naples, Italy.

Daniele Naviglio (D)

Department of Chemical Science, Federico II University, Via Cintia 21, 80126 Naples, Italy.

Valentina Brancato (V)

IRCCS Synlab SDN, Via Emanuele Gianturco, 113, 80143 Naples, Italy.

Carlo Cavaliere (C)

IRCCS Synlab SDN, Via Emanuele Gianturco, 113, 80143 Naples, Italy.

Marco Salvatore (M)

IRCCS Synlab SDN, Via Emanuele Gianturco, 113, 80143 Naples, Italy.

Paola Cipriano (P)

Department of Clinical Medicine and Surgery, Federico II University, Via Sergio Pansini 5, 80131 Naples, Italy.

Marilena Vitale (M)

Department of Clinical Medicine and Surgery, Federico II University, Via Sergio Pansini 5, 80131 Naples, Italy.

Alessandra Corrado (A)

Department of Clinical Medicine and Surgery, Federico II University, Via Sergio Pansini 5, 80131 Naples, Italy.

Angela Albarosa Rivellese (AA)

Department of Clinical Medicine and Surgery, Federico II University, Via Sergio Pansini 5, 80131 Naples, Italy.
Task Force on Microbiome Studies, University of Naples "Federico II", 80138 Naples, Italy.

Giovanni Annuzzi (G)

Department of Clinical Medicine and Surgery, Federico II University, Via Sergio Pansini 5, 80131 Naples, Italy.
Task Force on Microbiome Studies, University of Naples "Federico II", 80138 Naples, Italy.

Lutgarda Bozzetto (L)

Department of Clinical Medicine and Surgery, Federico II University, Via Sergio Pansini 5, 80131 Naples, Italy.
Task Force on Microbiome Studies, University of Naples "Federico II", 80138 Naples, Italy.

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Classifications MeSH