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Licensed Unlicensed Requires Authentication Published by De Gruyter January 5, 2018

Associations of leptin, insulin and lipids with retinal microvasculature in children and adolescents

  • Carola J.C. van Aart EMAIL logo , Nathalie Michels , Isabelle Sioen , Annelies De Decker , Tim S. Nawrot and Stefaan De Henauw

Abstract

Background:

We investigated whether cardiometabolic risk factors measured in serum (total cholesterol [TC], high-density lipoprotein [HDL], triglyceride, leptin, insulin, glucose and insulin resistance) are associated with the retinal microvasculature, a marker of cardiovascular aging, in healthy children and adolescents. Moreover, we tested whether these associations are due to direct biological effects or more indirectly due to adiposity-related side effects.

Methods:

We recruited 168 healthy Flemish children (7–16 years old, 54.8% boys). Blood samples and retinal photographs were taken during clinical examinations. Arteriolar and venular vessel calibers were calculated using a semi-automated computer program. Multivariable regression models were used and adjusted for age, sex, mean arterial pressure (MAP) and alternate retinal caliber. In a second step, we adjusted for body mass index z-score (zBMI).

Results:

Only continuous serum leptin was associated with retinal parameters, i.e. wider arterioles; however, this disappeared after adjustment for zBMI. Children with high cardiometabolic risk factors (>90th percentile for serum leptin, insulin and insulin resistance) had wider arterioles compared to children with lower concentrations, even after additional adjustment for zBMI. No significant associations were found with lipids.

Conclusions:

In this healthy population of children and adolescents, the hormones insulin and leptin and insulin resistance were associated with retinal microvasculature alterations, mainly in children with high cardiometabolic factors (>90th percentile), while lipids were not. These associations were independent of zBMI.


Corresponding author: Carola J.C. van Aart, MSc, Department of Public Health, Faculty of Medicine and Health Sciences, Ghent University, De Pintelaan 185 4K3, 9000 Ghent, Belgium, Phone: 0032 9 332 3685, Fax: 0032 9 332 4994

Acknowledgments

The authors would like to thank all children and their parents for their voluntary participation. We acknowledge the Bimetra biobank UGent for sample storage.

  1. Author contributions: All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.

  2. Research funding: This work was supported by the Research Foundation – Flanders, Belgium (funder id: 10.13039/501100003130, project number G073315N).

  3. Employment or leadership: None declared.

  4. Honorarium: None declared.

  5. Competing interests: The funding organization(s) played no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the report for publication.

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Supplemental Material:

The online version of this article offers supplementary material (https://doi.org/10.1515/jpem-2017-0374).


Received: 2017-9-20
Accepted: 2017-11-16
Published Online: 2018-1-5
Published in Print: 2018-1-26

©2018 Walter de Gruyter GmbH, Berlin/Boston

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