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Analysis of the SYSDIET Healthy Nordic Diet randomized trial based on metabolic profiling reveal beneficial effects on glucose metabolism and blood lipids

Oresic Matej; Cloetens Lieselotte; Ulven Stine Marie; Rosqvist Fredrik; Gürdeniz Gözde; Herzig Karl-Heinz; Åkesson Björn; Uusitupa Matti; Gunnarsdóttir Ingibjörg; Dragsted Lars Ove; Risérus U; Brader Lea; Hukkanen Janne; Thorsdottir Inga; Schwab Ursula; Savolainen Markku J; Poutanen Kaisa S; Hermansen Kjeld; Kolehmainen Marjukka

Analysis of the SYSDIET Healthy Nordic Diet randomized trial based on metabolic profiling reveal beneficial effects on glucose metabolism and blood lipids

Oresic Matej
Cloetens Lieselotte
Ulven Stine Marie
Rosqvist Fredrik
Gürdeniz Gözde
Herzig Karl-Heinz
Åkesson Björn
Uusitupa Matti
Gunnarsdóttir Ingibjörg
Dragsted Lars Ove
Risérus U
Brader Lea
Hukkanen Janne
Thorsdottir Inga
Schwab Ursula
Savolainen Markku J
Poutanen Kaisa S
Hermansen Kjeld
Kolehmainen Marjukka
Katso/Avaa
1-s2.0-S0261561421005963-main.pdf (1.067Mb)
Lataukset: 

CHURCHILL LIVINGSTONE
doi:10.1016/j.clnu.2021.12.031
URI
https://doi.org/10.1016/j.clnu.2021.12.031
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Julkaisun pysyvä osoite on:
https://urn.fi/URN:NBN:fi-fe2022081154816
Tiivistelmä

Background & aims 

Intake assessment in multicenter trials is challenging, yet important for accurate outcome evaluation. The present study aimed to characterize a multicenter randomized controlled trial with a healthy Nordic diet (HND) compared to a Control diet (CD) by plasma and urine metabolic profiles and to associate them with cardiometabolic markers.

Methods

During 18-24 weeks of intervention, 200 participants with metabolic syndrome were advised at six centres to eat either HND (e.g. whole-grain products, berries, rapeseed oil, fish and low-fat dairy) or CD while being weight stable. Of these 166/159 completers delivered blood/urine samples. Metabolic profiles of fasting plasma and 24 h pooled urine were analysed to identify characteristic diet-related patterns. Principal components analysis (PCA) scores (i.e. PC1 and PC2 scores) were used to test their combined effect on blood glucose response (primary endpoint), serum lipoproteins, triglycerides, and inflammatory markers.

Results

The profiles distinguished HND and CD with AUC of 0.96 ± 0.03 and 0.93 ± 0.02 for plasma and urine, respectively, with limited heterogeneity between centers, reflecting markers of key foods. Markers of fish, whole grain and polyunsaturated lipids characterized HND, while CD was reflected by lipids containing palmitoleic acid. The PC1 scores of plasma metabolites characterizing the intervention is associated with HDL (β = 0.05; 95% CI: 0.02, 0.08; P = 0.001) and triglycerides (β = -0.06; 95% CI: -0.09, -0.03; P < 0.001). PC2 scores were related with glucose metabolism (2 h Glucose, β = 0.1; 95% CI: 0.05, 0.15; P < 0.001), LDL (β = 0.06; 95% CI: 0.01, 0.1; P = 0.02) and triglycerides (β = 0.11; 95% CI: 0.06, 0.15; P < 0.001). For urine, the scores were related with LDL cholesterol.

Conclusions

Plasma and urine metabolite profiles from SYSDIET reflected good compliance with dietary recommendations across the region. The scores of metabolites characterizing the diets associated with outcomes related with cardio-metabolic risk. Our analysis therefore offers a novel way to approach a per protocol analysis with a balanced compliance assessment in larger multicentre dietary trials.

The study was registered at clinicaltrials.gov with NCT00992641.

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