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Treatment of sleep-disordered breathing in heart failure impacts cardiac remodeling: Insights from the CAT-HF Trial - 18/06/18

Doi : 10.1016/j.ahj.2018.03.026 
Melissa A. Daubert, MD a, , David J. Whellan, MD b, Holger Woehrle, MD c, Gudaye Tasissa, PhD a, Kevin J. Anstrom, PhD a, JoAnn Lindenfeld, MD d, Adam Benjafield, PhD c, Amy Blase, CCRA c, Naresh Punjabi, MD, PhD e, Mona Fiuzat, PharmD a, Olaf Oldenburg, MD f, Christopher M. O'Connor, MD a, g
a Duke University and Duke Clinical Research Institute, Durham, NC 
b Thomas Jefferson University, Philadelphia, PA 
c ResMed Science Center ResMed Corp, San Diego, CA 
d Vanderbilt University, Nashville, TN 
e Johns Hopkins University, Baltimore, MD 
f Ruhr University Bochum, Bad Oeynhausen, Germany 
g Inova Heart and Vascular Institute, Falls Church, VA 

Reprint requests: Melissa A. Daubert, MD, 2400 Pratt St, Room 0311 Terrace Level, Durham, NC 27705.2400 Pratt St, Room 0311 Terrace LevelDurhamNC27705

Abstract

Background

Sleep-disordered breathing (SDB), including central and obstructive sleep apnea, is a marker of poor prognosis in heart failure (HF) and may worsen cardiac dysfunction over time. Treatment of SDB with adaptive servoventilation (ASV) may reverse pathologic cardiac remodeling in HF patients.

Methods

The Cardiovascular Improvements with Minute Ventilation-targeted Adaptive Servo-Ventilation Therapy in Heart Failure (CAT-HF) trial randomized patients with acute decompensated HF and confirmed SDB to either optimal medical therapy (OMT) or treatment with ASV and OMT. Patients with reduced ejection fraction (HFrEF) or preserved EF (HFpEF) were included. Echocardiograms, performed at baseline and 6 months, assessed cardiac size and function and evaluated cardiac remodeling over time. The CAT-HF trial was stopped early in response to the SERVE-HF trial, which found increased mortality among HFrEF patients with central sleep apnea treated with ASV.

Results

Of the 126 patients enrolled prior to trial cessation, 95 had both baseline and 6-month echocardiograms (77 HFrEF and 18 HFpEF). Among HFrEF patients, both treatment arms demonstrated a significant increase in EF: +4.3% in the ASV group (.0004) and +4.6% in OMT alone (P = .007) and a significant decrease in LV end-systolic volume index: −9.4 mL/m2 in the ASV group (P = .01) and −8.6 mL/m2 in OMT alone (P = .003). Reductions in left atrial (LA) volume and E/e’ were greater in the ASV arm, whereas patients receiving OMT alone demonstrated more improvement in right ventricular function. HFpEF patients treated with ASV also had a decrease in LA size that was greater than those receiving OMT alone. Although there were significant intragroup changes within the ASV + OMT and OMT-alone groups, there were no significant intergroup differences at 6 months.

Conclusions

Significant reverse LV remodeling was seen among HFrEF patients with SDB regardless of treatment allocation. Substantial reductions in LA volume among HFrEF and HFpEF patients receiving ASV suggest that ASV treatment may also improve diastolic function and warrant further investigation.

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 Larry A. Allen, MD, MHS, served as guest editor for this article.
 Clinical Trial Registration: ClinicalTrials.gov Identifier: NCT01953874
 Funding sources: The CAT-HF Trial was funded by ResMed Corp.
 Relationships with Industry: Duke Clinical Research Institute was the recipient of research grants from ResMed Corp. M. Daubert has received research support from ResMed Corp. D. Whellan has received consulting fees and research support from ResMed Corp. H. Woehrle was employed by ResMed and has received consulting fees and research support from ResMed Corp. K. Anstrom has received research support from ResMed Corp. J. Lindenfeld has received consulting fees and research support from ResMed Corp. A. Blase is employed by ResMed. A. Benjafield is employed by ResMed. M. Fiuzat has received consulting fees and research support from ResMed Corp. O. Oldenburg has received consulting fees and research support from ResMed Corp. C. O'Connor has received consulting fees and research support from ResMed Corp. The other authors report no relevant relationships with industry to disclose.


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Vol 201

P. 40-48 - juillet 2018 Retour au numéro
Article précédent Article précédent
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