Volume 16, Issue 5 e12745
ORIGINAL RESEARCH

ApoB-lipoprotein remnant dyslipidemia and high-fat meal intolerance is associated with markers of cardiometabolic risk in youth with obesity

Jacqueline A. Krysa

Jacqueline A. Krysa

Division of Nutrition, Metabolic and Cardiovascular Diseases Laboratory, University of Alberta, Edmonton, Alberta, Canada

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Geoff D. C. Ball

Geoff D. C. Ball

Department of Pediatrics, University of Alberta, Edmonton, Alberta, Canada

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Donna F. Vine

Donna F. Vine

Division of Nutrition, Metabolic and Cardiovascular Diseases Laboratory, University of Alberta, Edmonton, Alberta, Canada

Alberta Diabetes Institute, University of Alberta, Edmonton, Alberta, Canada

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Mary Jetha

Mary Jetha

Department of Pediatrics, University of Alberta, Edmonton, Alberta, Canada

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Spencer D. Proctor

Corresponding Author

Spencer D. Proctor

Division of Nutrition, Metabolic and Cardiovascular Diseases Laboratory, University of Alberta, Edmonton, Alberta, Canada

Alberta Diabetes Institute, University of Alberta, Edmonton, Alberta, Canada

Correspondence

Spencer D. Proctor, 4-002J Li Ka Shing Centre for Health Research Innovation, University of Alberta, Edmonton, AB T6G2E1, Canada.

Email: [email protected]

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First published: 04 November 2020
Citations: 6

Funding information: Alberta Health Services Health Outcomes Improvement Fund; Women and Children's Health Research Institute; GDCB was supported by an Alberta Health Services Chair in Obesity Research

Summary

Introduction

Cardiovascular disease (CVD) originates in childhood and risk is exacerbated in obesity. Mechanisms of the etiologic link between early adiposity and CVD-risk remain unclear. Postprandial or non-fasting dyslipidemia is characterized by elevated plasma triglycerides (TG) and intestinal-apolipoprotein(apo)B48-remnants following a high-fat meal and is a known CVD-risk factor in adults. The aim of this study was to determine (a) whether the fasting concentration of apoB48-remnants can predict impaired non-fasting apoB48-lipoprotein metabolism (fat intolerance) and (b) the relationship of these biomarkers with cardiometabolic risk factors in youth with or without obesity.

Methods

We assessed fasting and non-fasting lipids in youth without obesity (n = 22, 10 males, 12 females) and youth with obesity (n = 13, 5 males, 8 females) with a mean BMI Z-score of 0.19 ± 0.70 and 2.25 ± 0.31 (P = .04), respectively.

Results

Fasting and non-fasting apoB48-remnants were elevated in youth with obesity compared to youth without obesity (apoB48: 18.04 ± 1.96 vs 8.09 ± 0.59, P < .0001, and apoB48AUC: 173.0 ± 20.86 vs 61.99 ± 3.44, P < .001). Furthermore, fasting plasma apoB48-remnants were positively correlated with the non-fasting response in apoB48AUC (r = 0.84, P < .0001) as well as other cardiometabolic risk factors including HOMA-IR (r = 0.61, P < .001) and leptin (r = 0.56, P < .0001).

Conclusion

Fasting apoB48-remnants are elevated in youth with obesity and predict apoB48 postprandial dyslipidemia. ApoB48-remnants are associated with the extent of fat intolerance and appear to be potential biomarker of CVD-risk in youth.

CONFLICT OF INTEREST

The authors declare no conflicts of interest.

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