Phenotypes of responders to mandibular advancement device therapy in obstructive sleep apnea patients: A systematic review and meta-analysis

H. Chen, D.J. Eckert, P.F. van der Stelt, J. Guo, S. Ge, E. Emami, F.R. Almeida, N.T. Huynh

Research output: Contribution to JournalReview articleAcademicpeer-review

Abstract

Mandibular advancement device (MAD) therapy is the most commonly used non-continuous positive airway pressure (CPAP) treatment for obstructive sleep apnea (OSA). Although OSA patients prefer MAD over CPAP, on average over one third have minimal or no major reduction in OSA severity with MAD therapy. Improved understanding of responder characteristics (or “phenotypes”) to MAD may facilitate more efficient use of limited medical resources and optimize treatment efficacy. The aim of this review is to describe the baseline phenotypic characteristics of responders to MAD therapy in OSA patients. Pubmed, Web of Science, EMBASE, Scopus were searched for eligible studies published until Feb 2019. A total of 650 studies were identified. 41 studies were included in this review and meta-analysis. The quality of the studies was assessed using the risk of bias assessment tool for non-randomized studies (RoBANS). Based on meta-analysis, the responders to MAD therapy had certain clinical phenotypic characteristics: lower age (95% CI: −4.55 to −1.62, p < 0.00001), female (95% CI: 0.56 to 0.91, p = 0.006), lower body mass index (95% CI: −2.80 to −1.11, p < 0.00001), smaller neck circumference (95% CI: −1.57 to −0.52, p < 0.00001), lower apnea-hypopnea index (95% CI: −7.23 to −1.89, p < 0.00001), a retracted maxilla and mandible, a narrower airway and a shorter soft palate than non-responders. The above-mentioned phenotypic responder characteristics provides useful information for the clinician when considering prescribing MAD therapy for OSA patients.

Original languageEnglish
Article number101229
Number of pages17
JournalSleep Medicine Reviews
Volume49
DOIs
Publication statusPublished - Feb 2020

Funding

Supported by Canadian Institutes of Health Research (grant number: 325899 ) and Supported by Youth scientific research funds of School of Stomatology, Shandong University (grant number: 2018QNJJ02 ). Appendix A DJE is supported by a National Health and Medical Research Council of Australia Senior Research Fellowship (1116942), has a Cooperative Research Centre (CRC)-P grant: a collaborative grant between the Australian Government, Academia and Industry (Industry partner Oventus Medical), has been a collaborator on research projects in which SomnoMed and Zephyr have provided equipment, has research grants from Apnimed and Bayer and serves on the Scientific Advisory Board for Apnimed. The other authors do not have any conflict of interests to declare.Supported by Canadian Institutes of Health Research (grant number: 325899) and Supported by Youth scientific research funds of School of Stomatology, Shandong University (grant number: 2018QNJJ02). DJE is supported by a National Health and Medical Research Council of Australia Senior Research Fellowship ( 1116942 ), has a Cooperative Research Centre (CRC) -P grant: a collaborative grant between the Australian Government, Academia and Industry (Industry partner Oventus Medical), has been a collaborator on research projects in which SomnoMed and Zephyr have provided equipment, has research grants from Apnimed and Bayer and serves on the Scientific Advisory Board for Apnimed. The other authors do not have any conflict of interests to declare.

FundersFunder number
Academia and Industry
Australian Government, Academia and Industry
Cooperative Research Centre
Oventus Medical
Youth scientific research funds of School of Stomatology
Bayer
Australian Education International, Australian Government
Bushfire Cooperative Research CentreCRC
Shandong University2018QNJJ02
Canadian Institutes of Health Research325899
National Health and Medical Research Council1116942

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