Allergology International (Apr 2024)

Role of bronchial hyperresponsiveness in patients with obstructive sleep apnea with asthma-like symptoms

  • Akiko Sano,
  • Takenori Kozuka,
  • Nanase Watatani,
  • Yuuki Kunita,
  • Yoshiyuki Kawabata,
  • Kyuya Gose,
  • Ken Shirahase,
  • Kazuya Yoshikawa,
  • Ryo Yamazaki,
  • Yusaku Nishikawa,
  • Takashi Omori,
  • Osamu Nishiyama,
  • Takashi Iwanaga,
  • Hiroyuki Sano,
  • Ryuta Haraguchi,
  • Yuji Tohda,
  • Hisako Matsumoto

Journal volume & issue
Vol. 73, no. 2
pp. 231 – 235

Abstract

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Background: Obstructive sleep apnea (OSA) is one of the major co-morbidities and aggravating factors of asthma. In OSA-complicated asthma, obesity, visceral fat, and systemic inflammation are associated with its severity, but the role of bronchial hyperresponsiveness (BHR) is unclear. We investigated the involvement of BHR and mediastinal fat width, as a measure of visceral fat, with OSA severity in patients with OSA and asthma-like symptoms. Methods: Patients with OSA who underwent BHR test and chest computed tomography scan for asthma-like symptoms were retrospectively enrolled. We evaluated the relationship between apnea–hypopnea index (AHI) and PC20 or anterior mediastinal fat width, stratified by the presence or absence of BHR. Results: OSA patients with BHR (n = 29) showed more obstructive airways and frequent low arousal threshold and lower mediastinal fat width, and tended to show fewer AHI than those without BHR (n = 25). In the overall analysis, mediastinal fat width was significantly positively correlated with AHI, which was significant even after adjustment with age and gender. This was especially significant in patients without BHR, while in OSA patients with BHR, there were significant negative associations between apnea index and airflow limitation, and hypopnea index and PC20. Conclusions: Risk factors for greater AHI differed depending on the presence or absence of BHR in OSA patients with asthma-like symptoms. In the presence of BHR, severity of asthma may determine the severity of concomitant OSA.

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