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S118 The ventilatory response to CO2 within obstructive sleep apnea patients
  1. CMN Earing1,
  2. JP Moore1,
  3. DJ McKeon2,
  4. H-P Kubis1
  1. 1Bangor University, Bangor, Gwynedd
  2. 2Respiratory Department, Ysbyty Gwynedd, Bangor, Gwynedd

Abstract

Introduction Obstructive Sleep Apnea (OSA) is a condition defined by the collapse of the upper airway and cessation of respiration during sleep. The resulting hypoventilation leads to intermittent nocturnal hypoxia and increased arterial pCO2 (hypercapnia). Control of ventilation is largely dependent on two interactive pathways, the central and peripheral chemoreceptors. Both chemoreceptors’ respond to H+ ions liberated as a result of the presence of CO2. However, the peripheral chemoreceptors also respond to hypoxia particularly when PaO2 falls below 70 Torr. Hypoxia has a synergistic effect on the ventilatory response to CO2. Our study therefore investigated the ventilatory response to CO2 with and without the presence of moderate hypoxia to determine whether the central and/or peripheral chemoreflex response to CO2 is modified with the development of OSA.

Methods The ventilatory response to CO2 amongst 33 newly diagnosed male OSA patients (AHI: 32.6 ± 24.8; age: 53.1 ± 10.3 years, BMI: 36.4 ± 6.8 kg/m2) was measured whilst breathing four different gas mixtures balanced with N2 (Mixture 1: ambient air; mixture 2: 25% O2/6% CO2; mixture 3: 13% O2; mixture 4: 13% O2/6% CO2). The minute ventilation of each participant, normalised by their body surface area (BSA), was recorded with subjects blinded to the order of test gases. Additionally, fasted venous blood samples were taken to assess plasma leptin concentrations.

Results Mild and moderate OSA patients (AHI: 13.76 ± 7.01) revealed a significantly (p <.01) greater change in their ventilatory response to the hyperoxic-hypercapnic gas mixture (5.22 ± 1.95 l x min-1 x BSA-1) compared to severe OSA patients (AHI: 55.31 ± 18.25) (3.26 ± 1.64 l x min-1 x BSA-1). There was no significant change in ventilation between the hyperoxic and hypoxic-hypercapnic conditions in both groups. A significant negative correlation (r = -0.39; p <.05) was found between AHI and ventilation change (l x min-1 x BSA-1) to the hyperoxic-hypercapnic gas mixture.

Conclusion These findings suggest the reduced ventilatory response to hypercapnia amongst severe OSA patients is likely a result of adaptation to the central chemoreceptors.

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