» Articles » PMID: 35458210

The Dose-Response Effects of Consuming High Fructose Corn Syrup-Sweetened Beverages on Hepatic Lipid Content and Insulin Sensitivity in Young Adults

Abstract

Increased hepatic lipid content and decreased insulin sensitivity have critical roles in the development of cardiometabolic diseases. Therefore, our objective was to investigate the dose-response effects of consuming high fructose corn syrup (HFCS)-sweetened beverages for two weeks on hepatic lipid content and insulin sensitivity in young (18-40 years) adults (BMI 18-35 kg/m). In a parallel, double-blinded study, participants consumed three beverages/day providing 0% (aspartame: = 23), 10% ( = 18), 17.5% ( = 16), or 25% ( = 28) daily energy requirements from HFCS. Magnetic resonance imaging for hepatic lipid content and oral glucose tolerance tests (OGTT) were conducted during 3.5-day inpatient visits at baseline and again at the end of a 15-day intervention. During the 12 intervening outpatient days participants consumed their usual diets with their assigned beverages. Significant linear dose-response effects were observed for increases of hepatic lipid content ( = 0.015) and glucose and insulin AUCs during OGTT (both = 0.0004), and for decreases in the Matsuda ( = 0.0087) and Predicted M ( = 0.0027) indices of insulin sensitivity. These dose-response effects strengthen the mechanistic evidence implicating consumption of HFCS-sweetened beverages as a contributor to the metabolic dysregulation that increases risk for nonalcoholic fatty liver disease and type 2 diabetes.

Citing Articles

Interindividual Variability in Postprandial Plasma Fructose Patterns in Adults.

Gladding M, Shen X, Snyder M, Havel P, Adams S Nutrients. 2024; 16(18).

PMID: 39339679 PMC: 11435096. DOI: 10.3390/nu16183079.


Effects of Consuming Beverages Sweetened with Fructose, Glucose, High-Fructose Corn Syrup, Sucrose, or Aspartame on OGTT-Derived Indices of Insulin Sensitivity in Young Adults.

Hieronimus B, Medici V, Lee V, Nunez M, Sigala D, Bremer A Nutrients. 2024; 16(1).

PMID: 38201980 PMC: 10780640. DOI: 10.3390/nu16010151.


Fructose Metabolism and Metabolic Dysfunction in Adolescents and Young Adults.

Softic S, Lanaspa M, Debosch B Nutrients. 2023; 15(14).

PMID: 37513580 PMC: 10383708. DOI: 10.3390/nu15143162.


Alterations in Oxidative Stress Markers and Na,K-ATPase Enzyme Properties in Kidney after Fructose Intake and Quercetin Intervention in Rats.

Vrbjar N, Vlkovicova J, Snurikova D, Kalocayova B, Zorad S, Culafic T Life (Basel). 2023; 13(4).

PMID: 37109460 PMC: 10142800. DOI: 10.3390/life13040931.


Reply to: 'Guidelines on 'added' sugars are unscientific and unnecessary'.

Stanhope K Nat Rev Cardiol. 2022; 19(12):847-849.

PMID: 36220971 DOI: 10.1038/s41569-022-00794-7.

References
1.
Cook J, Langlet F, Kido Y, Accili D . Pathogenesis of selective insulin resistance in isolated hepatocytes. J Biol Chem. 2015; 290(22):13972-80. PMC: 4447970. DOI: 10.1074/jbc.M115.638197. View

2.
Schwimmer J, Ugalde-Nicalo P, Welsh J, Angeles J, Cordero M, Harlow K . Effect of a Low Free Sugar Diet vs Usual Diet on Nonalcoholic Fatty Liver Disease in Adolescent Boys: A Randomized Clinical Trial. JAMA. 2019; 321(3):256-265. PMC: 6440226. DOI: 10.1001/jama.2018.20579. View

3.
Sigala D, Widaman A, Hieronimus B, Nunez M, Lee V, Benyam Y . Effects of Consuming Sugar-Sweetened Beverages for 2 Weeks on 24-h Circulating Leptin Profiles, Ad Libitum Food Intake and Body Weight in Young Adults. Nutrients. 2020; 12(12). PMC: 7765993. DOI: 10.3390/nu12123893. View

4.
Boren J, Packard C, Taskinen M . The Roles of ApoC-III on the Metabolism of Triglyceride-Rich Lipoproteins in Humans. Front Endocrinol (Lausanne). 2020; 11:474. PMC: 7399058. DOI: 10.3389/fendo.2020.00474. View

5.
Taskinen M, Soderlund S, Bogl L, Hakkarainen A, Matikainen N, Pietilainen K . Adverse effects of fructose on cardiometabolic risk factors and hepatic lipid metabolism in subjects with abdominal obesity. J Intern Med. 2017; 282(2):187-201. DOI: 10.1111/joim.12632. View