Abstract

BackgroundIntake of high excess free fructose (EFF) beverages, including high fructose corn syrup (HFCS), sweetened soft drinks, fruit drinks, and apple juice, may be associated with childhood asthma, adult idiopathic chronic bronchitis/ COPD, and autoimmune arthritis, possibly due to underlying fructose malabsorption. Fructose malabsorption may contribute to the intestinal in situ formation of advanced glycation end-products (enFruAGEs) that travel to other tissues and promote inflammation. Chronic respiratory conditions and arthritis are comorbidities of coronary heart disease (CHD). The objective of this study was to investigate the association between intake of high EFF beverages and CHD.MethodsIn this cross sectional study (NHANES 2003–2006) of adults, aged 45–59 y, n = 1230, the exposure variables were non-diet soft drinks, and any combination of high EFF beverages including non-diet soft drinks, fruit drinks, and apple juice. Analyses of diet soft drinks, diet fruit drinks, and orange juice (non/low EFF beverages) were included for comparison. The outcome was self-reported history of coronary heart disease and/or angina (CHD). Rao Scott Ҳ2 was used for prevalence differences and logistic regression for associations, adjusted for age, sex, race-ethnicity, BMI, socio-economic status, health insurance coverage, smoking, physical activity level, hypertension, energy intake, fruit and vegetable intake, glycated hemoglobin, pre-diabetes, and diabetes.ResultsIntake of any combination of HFCS sweetened soft drinks, fruit drinks, and apple juice (tEFF) was significantly associated with CHD in adults aged 45–59 y. Adults consuming tEFF ≥5 times/wk. were 2.8 times more likely to report CHD than ≤3 times/mo consumers (OR 2.82; 95% CI 1.16–6.84; P = 0.023), independent of all covariates.ConclusionHFCS sweetened soft drinks, fruit drinks, and apple juice may contribute to CHD, a common comorbidity of chronic respiratory conditions and autoimmune arthritis, possibly due to the high ratio of fructose to glucose in these beverages. Underlying fructose malabsorption may contribute to the intestinal in situ formation of pro-inflammatory enFruAGEs, that are eventually absorbed and induce inflammation of the coronary arteries. Additional research is needed.

Highlights

  • Intake of high excess free fructose (EFF) beverages, including high fructose corn syrup (HFCS), sweetened soft drinks, fruit drinks, and apple juice, may be associated with childhood asthma, adult idiopathic chronic bronchitis/ chronic obstructive pulmonary disease (COPD), and autoimmune arthritis, possibly due to underlying fructose malabsorption

  • This hypothesis is unsupported in epidemiologic research, as large-scale longitudinal studies have shown that adults who regularly consumed sugar sweetened beverages (SSB) had increased risk of coronary heart disease (CHD) [15, 16] and rheumatoid arthritis (RA) [17] that was independent of risk factors known to be associated with CHD and RA, including weight gain, high blood pressure, smoking, and of type 2 diabetes (T2D) [15,16,17]

  • No associations were seen between regular intake of diet soft drinks, diet fruit drinks, or citrus juice and prevalence of CHD (Tables 2, 3 and 4)

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Summary

Introduction

Intake of high excess free fructose (EFF) beverages, including high fructose corn syrup (HFCS), sweetened soft drinks, fruit drinks, and apple juice, may be associated with childhood asthma, adult idiopathic chronic bronchitis/ COPD, and autoimmune arthritis, possibly due to underlying fructose malabsorption. One proposed hypothesis for these associations is that the high dietary glycemic load from SSB leads to chronic inflammation, insulin resistance, and impaired ß-cell function [12,13,14,15,16,17] This hypothesis is unsupported in epidemiologic research, as large-scale longitudinal studies have shown that adults who regularly consumed SSB had increased risk of CHD [15, 16] and RA [17] that was independent of risk factors known to be associated with CHD and RA, including weight gain, high blood pressure, smoking, and of T2D [15,16,17]

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