Tier 4 — mechanistic

Dietary patterns, food groups, and nutrients as predictors of plasma choline and betaine in middle-aged and elderly men and women

Svetlana V Konstantinova, Grethe S Tell, Stein E Vollset, Arve Ulvik, Christian A Drevon, Per M Ueland
The American journal of clinical nutrition 2008 88(6):1663-1669

Bibliography

PubMed
PMID 19064529
Funding
Funding was not specified in the indexed record or accessible funding metadata.
Competing interests
A competing-interest declaration was not available in the indexed record or accessible disclosure metadata.

Study snapshot

DesignCross-sectional cohort analysis
ModelHuman participants
Sample5812 Hordaland Health Study participants
InterventionHabitual food intake and plasma choline/betaine
DurationSingle observational assessment
EndpointsFood patterns; Plasma betaine

What the study showed, in plain terms

Published in 2008, this source examined food sources, absorption and nutrient metabolism. Design: Cross-sectional cohort analysis. Sample/model: 5812 Hordaland Health Study participants. The exposure or intervention was Habitual food intake and plasma choline/betaine. Follow-up or treatment period: Single observational assessment.

High-fiber bread and several related nutrients predicted higher circulating betaine, whereas a Western dietary pattern predicted lower concentrations.

Associations reflect diet and metabolism together; blood betaine is not a simple measure of supplement intake.

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Key findings

  • High-fiber bread and several related nutrients predicted higher circulating betaine, whereas a Western dietary pattern predicted lower concentrations.
  • The recorded outcome domains were Food patterns; Plasma betaine.
  • The exposure was observed rather than assigned as an isolated supplement treatment.

What this study can and cannot tell us

  • Associations reflect diet and metabolism together; blood betaine is not a simple measure of supplement intake.
  • Confounding, dietary patterns, illness, medication use and reverse causation can influence an association. Blood or dietary concentrations do not identify the effect of starting a capsule.
  • Source basis: Indexed abstract and bibliographic data. Missing method details, funding information or participant denominators are not inferred.

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