AI Article Synopsis

  • Accurately measuring added sugars intake and its impact on non-communicable diseases in diverse populations is complex, but using biomarkers can provide a more reliable assessment method.
  • A study on a predominantly Māori population compared sugar intake estimates from a food frequency questionnaire with urinary sugars excretion and carbon stable isotope ratios in red blood cells.
  • The study found significant correlations between biomarkers and sugar intake, suggesting they could enhance monitoring of sugar reduction strategies aimed at reducing health risks, although further validation of the findings is needed.

Article Abstract

Determining the extent to which added sugars intake contribute to non-communicable disease in various populations is challenging because it is difficult to accurately measure intakes. Biomarkers may provide a reliable and easily measured method of assessing intakes. In a predominantly Māori population we compared various sugars intake estimates derived from a 36 item sugar-specific food frequency questionnaire (FFQ) with biomarkers of sugars intake; urinary sugars excretion in random spot collections ( = 153) and carbon stable isotope ratios ( = 36) in red blood cells (RBCs, δC) and in the alanine fraction of the RBCs (δC). Estimated 24 h urinary sucrose+fructose excretion was statistically significantly correlated with intakes of total sugars ( = 0.23), sucrose ( = 0.26) and added sugars from sugar-sweetened beverages (SSBs; = 0.26). δC was correlated with added sugars ( = 0.40). In log linear multiple regression models adjusted with HbA1C and eGFR δC predicted added sugars intakes ( = 0.29) and estimated 24 h urinary sucrose+fructose excretion predicted intakes of total sugars ( = 0.14), sucrose ( = 0.17), added sugars ( = 0.17) and sugars from SSBs ( = 0.14). These biomarkers have potential for improving assessment of sugars intake in New Zealand populations enabling monitoring of the effectiveness of sugar reduction strategies designed to reduce risk of NCDs. However, further validation is required to confirm these preliminary findings.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8278019PMC
http://dx.doi.org/10.3389/fnut.2021.637267DOI Listing

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