Abstract

There is evidence that hypopneas are more common than apneas in obstructive sleep apnea (OSA) related to idiopathic pulmonary fibrosis (IPF). We investigated the frequency distribution of hypopneas in 100 patients with interstitial lung diseases (ILDs) (mean age 69 yrs ± 7.8; 70% males), including 54 IPF cases, screened for OSA by home sleep testing. Fifty age- and sex-matched pure OSA patients were included as controls. In ILD-OSA patients the sleep breathing pattern was characterized by a high prevalence of hypopneas that were preceded by hyperpnea events configuring a sort of periodic pattern. This finding, we arbitrarily defined hyperpnea–hypopnea periodic breathing (HHPB), was likely reflecting a central event and was completely absent in control OSA. Also, the HHPB was highly responsive to oxygen but not to the continuous positive pressure support. Thirty-three ILD-OSA patients (42%) with a HHPB associated with a hypopnea/apnea ratio ≥3 had the best response to oxygen with a median residual AHI of 2.6 (1.8–5.6) vs. 28.3 (20.7–37.8) at baseline (p < 0.0001). ILD-OSA patients with these characteristics were similarly distributed in IPF (54.5%) and no-IPF cases (45.5%), the most of them being affected by moderate–severe OSA (p = 0.027). Future studies addressing the pathogenesis and therapy management of the HHPB should be encouraged in ILD-OSA patients.

Highlights

  • Interstitial lung diseases (ILDs) include more than 200 disorders with considerable variation of clinical course, treatment, and prognosis

  • interstitial lung diseases (ILDs) patients were sub-divided in two groups (i.e., idiopathic pulmonary fibrosis (IPF) and no-IPF)

  • We found that in ILD-obstructive sleep apnea (OSA) patients the respiratory sleep pattern was characterized by a high prevalence of hypopneas over apneas, and that most hypopneas were preceded by a sequence of hyperpnea events with evidence of a sort of periodic pattern

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Summary

Introduction

Interstitial lung diseases (ILDs) include more than 200 disorders with considerable variation of clinical course, treatment, and prognosis. Two-thirds do not have a known cause, the others resulting from environmental/occupational exposure, infections, drugs, and radiation [1]. Despite recent advances in pharmacotherapy [2], many ILDs have limited treatment options. Among the idiopathic interstitial pneumonia, idiopathic pulmonary fibrosis (IPF) is the most common form affecting. Res. Public Health 2019, 16, 4712; doi:10.3390/ijerph16234712 www.mdpi.com/journal/ijerph

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