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Improvement in Visceral Adipose Tissue and LDL Cholesterol by High PUFA Intake: 1-Year Results of the NutriAct Trial.

Authors :
Meyer, Nina Marie Tosca
Pohrt, Anne
Wernicke, Charlotte
Pletsch-Borba, Laura
Apostolopoulou, Konstantina
Haberbosch, Linus
Machann, Jürgen
Pfeiffer, Andreas F. H.
Spranger, Joachim
Mai, Knut
Source :
Nutrients; Apr2024, Vol. 16 Issue 7, p1057, 16p
Publication Year :
2024

Abstract

We assessed the effect of a dietary pattern rich in unsaturated fatty acids (UFA), protein and fibers, without emphasizing energy restriction, on visceral adipose tissue (VAT) and cardiometabolic risk profile. Within the 36-months randomized controlled NutriAct trial, we randomly assigned 502 participants (50–80 years) to an intervention or control group (IG, CG). The dietary pattern of the IG includes high intake of mono-/polyunsaturated fatty acids (MUFA/PUFA 15–20% E/10–15% E), predominantly plant protein (15–25% E) and fiber (≥30 g/day). The CG followed usual care with intake of 30% E fat, 55% E carbohydrates and 15% E protein. Here, we analyzed VAT in a subgroup of 300 participants via MRI at baseline and after 12 months, and performed further metabolic phenotyping. A small but comparable BMI reduction was seen in both groups (mean difference IG vs. CG: −0.216 kg/m<superscript>2</superscript> [−0.477; 0.045], partial η<superscript>2</superscript> = 0.009, p = 0.105). VAT significantly decreased in the IG but remained unchanged in the CG (mean difference IG vs. CG: −0.162 L [−0.314; −0.011], partial η<superscript>2</superscript> = 0.015, p = 0.036). Change in VAT was mediated by an increase in PUFA intake (ß = −0.03, p = 0.005) and induced a decline in LDL cholesterol (ß = 0.11, p = 0.038). The NutriAct dietary pattern, particularly due to high PUFA content, effectively reduces VAT and cardiometabolic risk markers, independent of body weight loss. [ABSTRACT FROM AUTHOR]

Details

Language :
English
ISSN :
20726643
Volume :
16
Issue :
7
Database :
Complementary Index
Journal :
Nutrients
Publication Type :
Academic Journal
Accession number :
176592770
Full Text :
https://doi.org/10.3390/nu16071057