4.3 Article

Increased systemic inflammation overnight correlates with insulin resistance among children evaluated for obstructive sleep apnea

Journal

SLEEP AND BREATHING
Volume 16, Issue 2, Pages 349-354

Publisher

SPRINGER HEIDELBERG
DOI: 10.1007/s11325-011-0499-8

Keywords

Obstructive sleep apnea; Inflammation; hsCRP; Obesity; Insulin resistance; Oxygen desaturation; Adolescents

Funding

  1. University of Virginia Children's Hospital [NIH 5K08HD060739-02, 5R01HL059337-11, 5R01NS054117-04, 5M01RR000847-37]

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Obstructive sleep apnea (OSA) in children is associated with obesity, insulin resistance, and elevated baseline inflammation as measured by high-sensitivity C-reactive protein (hsCRP). Our goal was to evaluate whether inflammation increases overnight among children suspected of having OSA and to determine whether worsened inflammation is associated with the degree of OSA severity, obesity, and/or insulin resistance. Twenty-three children with clinical suspicion of OSA underwent a sleep study. Levels of hsCRP were tested the evening before and morning after the sleep study. Fasting insulin and glucose levels were measured from which the homeostasis model of insulin resistance (HOMA-IR) was calculated. Linear correlations were performed to evaluate relationships between hsCRP levels at baseline and change overnight (Delta hsCRP) vs. HOMA-IR, body mass index (BMI) z-score, and sleep study parameters related to O-2 saturation and the apnea-hypopnea index (AHI). Among children with OSA and the entire cohort, hsCRP values were correlated with HOMA-IR and BMI z-scores. HOMA-IR but not BMI z-score correlated with Delta hsCRP overnight in the entire cohort. Sleep study parameters, including AHI mean O-2 saturation overnight, REM O-2 nadir, and non-REM O-2 nadir were not correlated with hsCRP or Delta hsCRP overnight. Among children being evaluated for OSA, degree of insulin resistance may be an important determinant of increased systemic inflammation overnight. Sleep study markers did not correlate with Delta hsCRP, leaving uncertain the role of OSA in increasing inflammation overnight. Further studies are needed to explore these associations and their potential mechanisms.

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