@article{e031b30ca5594b50bb14ea75348ca555,
title = "Ertugliflozin and incident obstructive sleep apnea: an analysis from the VERTIS CV trial",
abstract = "Purpose: The sodium-glucose transporter 2 inhibitor (SGLT2i) empagliflozin may reduce the incidence of obstructive sleep apnea (OSA) in patients with type 2 diabetes (T2D) and cardiovascular (CV) disease. This analysis of VERTIS CV, the CV outcome trial for the SGLT2i ertugliflozin conducted in a similar group of patients, explored the effects of ertugliflozin on reported incident OSA. Methods: In VERTIS CV, patients ≥ 40 years with T2D and atherosclerotic CV disease (ASCVD) were randomized to ertugliflozin 5 or 15 mg or placebo. The primary endpoint was the composite of major adverse CV events. This exploratory analysis evaluated the impact of ertugliflozin (5 and 15 mg pooled) on incident OSA. Patients with prevalent OSA were excluded. Incident OSA events were based on investigator-reported events using the MedDRA SMQ term “sleep apnea syndrome.” A multivariable Cox proportional hazards regression model was constructed to assess the association between ertugliflozin and incident OSA. Results: Of 8246 patients enrolled, 7697 (93.3%) were without baseline OSA (placebo, n = 2561; ertugliflozin, n = 5136; mean age 64.4 years; BMI 31.7 kg/m2; HbA1c, 8.2%; 69.2% male; 88.3% White). The OSA incidence rate was 1.44 per 1000 person-years versus 2.61 per 1000 person-years among patients treated with ertugliflozin versus placebo, respectively, corresponding to a 48% relative risk reduction (HR 0.52; 95% CI 0.28–0.96; P = 0.04). Conclusions: In VERTIS CV, ertugliflozin reduced by nearly half the incidence of OSA in patients with T2D and ASCVD. These data contribute to the literature that SGLT2is may have a significant beneficial impact on OSA. Trial registration. ClinicalTrials.gov identifier: NCT01986881.",
keywords = "OSA, SGLT2, Sleep apnea, Sleep disordered breathing, Sodium glucose transporter type 2 inhibitor",
author = "Wojeck, {Brian S.} and Inzucchi, {Silvio E.} and Neeland, {Ian J.} and Mancuso, {James P.} and Robert Frederich and Urszula Masiukiewicz and Cater, {Nilo B.} and McGuire, {Darren K.} and Cannon, {Christopher P.} and Yaggi, {Henry Klar}",
note = "Funding Information: B.S.W. declares no conflicts of interest. S.E.I. has participated on clinical trial executive/steering/publications committees and/or served as an adviser for Abbott, AstraZeneca, Boehringer Ingelheim, Esperion, Novo Nordisk, and VTV Therapeutics; has delivered lectures supported by AstraZeneca, Boehringer Ingelheim, and Merck; and has received support for attending meetings from AstraZeneca, Boehringer Ingelheim, and Novo Nordisk. I.J.N. has received a grant (directed to his institution) from the National Institutes of Health, consulting fees from Boehringer Ingelheim/Lilly Alliance, and Merck & Co., and has delivered lectures supported by Nestl{\'e} Health Sciences. H.K.Y. declares no conflicts of interest. D.K.M. has received consulting fees from AstraZeneca, Boehringer Ingelheim, Lexicon, Merck Sharp & Dohme, and Pfizer Inc. and has received payment for expert testimony from Kirkland & Ellis on behalf of Boehringer Ingelheim. C.P.C. has received research grants from Amgen, Better Therapeutics, Boehringer Ingelheim, Bristol-Myers Squibb, Daiichi Sankyo, Janssen, Merck, Novo Nordisk, and Pfizer; fees from Aegerion/Amryt, Alnylam, Amarin, Amgen, Applied Therapeutics, Ascendia, Boehringer Ingelheim, Bristol-Myers Squibb, Eli Lilly, Janssen, Lexicon, Merck, Pfizer, Rhoshan, and Sanofi; and has served on Data and Safety Monitoring Boards for the Veteran{\textquoteright}s Administration, Applied Therapeutics, and NovoNordisk. J.P.M., R.F., U.M., and N.B.C. are employees and shareholders of Pfizer Inc. Funding Information: This study was sponsored by Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc., Kenilworth, NJ, USA in collaboration with Pfizer Inc., New York, NY, USA. The support provided by Engage Scientific Solutions, funded by Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc., Kenilworth, NJ, USA, and Pfizer, New York, NY, USA, consisted solely of copyediting and formatting for submission; no contribution was made to content. Publisher Copyright: {\textcopyright} 2022, Pfizer Inc. and The Author(s).",
year = "2022",
doi = "10.1007/s11325-022-02594-2",
language = "English (US)",
journal = "Sleep and Breathing",
issn = "1520-9512",
publisher = "Springer Verlag",
}