Fatty acid profiles in erythrocyte membranes following the Mediterranean diet - data from a multicenter lifestyle intervention study in women with hereditary breast cancer (LIBRE).


Journal

Clinical nutrition (Edinburgh, Scotland)
ISSN: 1532-1983
Titre abrégé: Clin Nutr
Pays: England
ID NLM: 8309603

Informations de publication

Date de publication:
08 2020
Historique:
received: 22 04 2019
revised: 21 10 2019
accepted: 24 10 2019
pubmed: 19 11 2019
medline: 19 8 2021
entrez: 19 11 2019
Statut: ppublish

Résumé

Evidence-based concepts to prevent breast cancer in women with BRCA1/2 mutations are limited. Adherence to a Mediterranean diet (MedD) has been associated with a lower risk for breast cancer, possibly due to a favorable fatty acid (FA) intake. Here, we studied in an at-risk population the effect of a lifestyle intervention that included the MedD on FA composition in red blood cell membranes (RBCM). Data derived from the German multicenter trial LIBRE, from which 68 women were randomized into an intervention group (IG) trained for MedD and increased physical activity for 12 months, and a usual care control group (CG). Adherence to the diet was assessed after 3 and 12 months using the validated Mediterranean Diet Adherence Screener (MEDAS) and a food frequency questionnaire. RBCM FA were analyzed by gas chromatography with mass spectrometry. The MEDAS was increased in both groups after 3 months (IG: P < 0.001; CG: P = 0.004), and remained increased only in the IG after 12 months (P < 0.001). The food frequency questionnaire revealed an increased intake of omega-3 (n-3) FA at month 3 and month 12 in the IG (both P < 0.01), but not in the CG, in which intake of energy, protein and saturated FA decreased. In both groups n-6 FA in the RBCM decreased (P < 0.001), while n-9 FA increased (P < 0.001) and n-3 FA were unchanged. Women with higher consumption of fish had higher amounts of n-3 fatty acids in the RBCM. The MEDAS was inversely correlated with n-6 fatty acids. The RBCM FA composition was associated with dietetic parameters related to the MedD. Adherence to the MedD resulted in an altered, likely favorable FA composition. Our data suggest selected FA as biomarkers to monitor compliance to a dietetic intervention such as the MedD. The trial is registered at ClinicalTrials.gov (reference: NCT02087592).

Sections du résumé

BACKGROUND & AIMS
Evidence-based concepts to prevent breast cancer in women with BRCA1/2 mutations are limited. Adherence to a Mediterranean diet (MedD) has been associated with a lower risk for breast cancer, possibly due to a favorable fatty acid (FA) intake. Here, we studied in an at-risk population the effect of a lifestyle intervention that included the MedD on FA composition in red blood cell membranes (RBCM).
METHODS
Data derived from the German multicenter trial LIBRE, from which 68 women were randomized into an intervention group (IG) trained for MedD and increased physical activity for 12 months, and a usual care control group (CG). Adherence to the diet was assessed after 3 and 12 months using the validated Mediterranean Diet Adherence Screener (MEDAS) and a food frequency questionnaire. RBCM FA were analyzed by gas chromatography with mass spectrometry.
RESULTS
The MEDAS was increased in both groups after 3 months (IG: P < 0.001; CG: P = 0.004), and remained increased only in the IG after 12 months (P < 0.001). The food frequency questionnaire revealed an increased intake of omega-3 (n-3) FA at month 3 and month 12 in the IG (both P < 0.01), but not in the CG, in which intake of energy, protein and saturated FA decreased. In both groups n-6 FA in the RBCM decreased (P < 0.001), while n-9 FA increased (P < 0.001) and n-3 FA were unchanged. Women with higher consumption of fish had higher amounts of n-3 fatty acids in the RBCM. The MEDAS was inversely correlated with n-6 fatty acids.
CONCLUSIONS
The RBCM FA composition was associated with dietetic parameters related to the MedD. Adherence to the MedD resulted in an altered, likely favorable FA composition. Our data suggest selected FA as biomarkers to monitor compliance to a dietetic intervention such as the MedD.
CLINICAL TRIAL REGISTRY
The trial is registered at ClinicalTrials.gov (reference: NCT02087592).

Identifiants

pubmed: 31735538
pii: S0261-5614(19)33126-7
doi: 10.1016/j.clnu.2019.10.033
pii:
doi:

Substances chimiques

Biomarkers 0
Fatty Acids 0
Fatty Acids, Omega-3 0
Fatty Acids, Omega-6 0

Banques de données

ClinicalTrials.gov
['NCT02087592']

Types de publication

Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

2389-2398

Informations de copyright

Copyright © 2019 Elsevier Ltd and European Society for Clinical Nutrition and Metabolism. All rights reserved.

Déclaration de conflit d'intérêts

Conflict of interest None of the authors report a conflict of interest related to the study.

Auteurs

Benjamin Seethaler (B)

Institute of Nutritional Medicine, University of Hohenheim, Fruwirthstr. 12, 70593, Stuttgart, Germany. Electronic address: b.seethaler@uni-hohenheim.de.

Maryam Basrai (M)

Institute of Nutritional Medicine, University of Hohenheim, Fruwirthstr. 12, 70593, Stuttgart, Germany. Electronic address: m.basrai@uni-hohenheim.de.

Walter Vetter (W)

Institute of Food Chemistry, University of Hohenheim, Garbenstr. 28, 70593, Stuttgart, Germany. Electronic address: w-vetter@uni-hohenheim.de.

Katja Lehnert (K)

Institute of Food Chemistry, University of Hohenheim, Garbenstr. 28, 70593, Stuttgart, Germany. Electronic address: Katja.Lehnert@uni-hohenheim.de.

Christoph Engel (C)

Institute for Medical Informatics, Statistics and Epidemiology, University of Leipzig, Haertelstrasse 16-18, 04107, Leipzig, Germany. Electronic address: christoph.engel@imise.uni-leipzig.de.

Michael Siniatchkin (M)

Institute for Medical Psychology and Sociology, University Hospital Schleswig-Holstein, Campus Kiel, Preusserstr. 1 - 9, 24105, Kiel, Germany. Electronic address: siniatchkin@med-psych.uni-kiel.de.

Martin Halle (M)

Department of Prevention and Sports Medicine, Klinikum Rechts der Isar, 6 Technical University Munich (TUM), Ismaninger Str. 22, 81675, Munich, Germany. Electronic address: Martin.Halle@mri.tum.de.

Marion Kiechle (M)

Department of Gynecology, Center for Hereditary Breast and Ovarian Cancer, Klinikum Rechts Der Isar, Technical University Munich (TUM) and Comprehensive Cancer Center Munich (CCCM), Ismaninger Str. 22, 81675, München, Germany. Electronic address: Marion.Kiechle@mri.tum.de.

Stephan C Bischoff (SC)

Institute of Nutritional Medicine, University of Hohenheim, Fruwirthstr. 12, 70593, Stuttgart, Germany. Electronic address: bischoff.stephan@uni-hohenheim.de.

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