Rate of Change in Cardiac Magnetic Resonance Imaging Measures Is Associated With Death in Duchenne Muscular Dystrophy

Author:

Starnes Joseph R.1ORCID,Xu Meng2,George‐Durrett Kristen1ORCID,Crum Kimberly1ORCID,Raucci Frank J.3ORCID,Spurney Christopher F.4ORCID,Hor Kan N.5ORCID,Cripe Linda H.5ORCID,Husain Nazia6ORCID,Buddhe Sujatha7,Gambetta Katheryn6,Tamaroff Jaclyn8ORCID,Slaughter James C.2ORCID,Markham Larry W.9ORCID,Soslow Jonathan H.1ORCID

Affiliation:

1. Division of Cardiology, Department of Pediatrics Vanderbilt University Medical Center Nashville TN USA

2. Department of Biostatistics Vanderbilt University Nashville TN USA

3. Division of Cardiology, Department of Pediatrics Children’s Hospital of Richmond at Virginia Commonwealth University Richmond VA USA

4. Children’s National Heart Institute Children’s National Hospital Washington DC USA

5. Division of Cardiology, Department of Pediatrics Nationwide Children’s Hospital, Ohio State University Columbus OH USA

6. Division of Cardiology, Department of Pediatrics Ann & Robert H. Lurie Children’s Hospital of Chicago, Northwestern University Feinberg School of Medicine Chicago IL USA

7. Division of Cardiology, Department of Pediatrics Stanford University School of Medicine Stanford CA USA

8. Division of Endocrinology and Diabetes, Department of Pediatrics Vanderbilt University Medical Center Nashville TN USA

9. Division of Cardiology, Department of Pediatrics Riley Hospital for Children at Indiana University Health Indianapolis IN USA

Abstract

Background Cardiovascular disease is the leading cause of death among patients with Duchenne muscular dystrophy (DMD). Identifying patients at risk of early death could allow for increased monitoring and more intensive therapy. Measures that associate with death could serve as surrogate outcomes in clinical trials. Methods and Results Duchenne muscular dystrophy subjects prospectively enrolled in observational studies were included. Models using generalized least squares were used to assess the difference of cardiac magnetic resonance measurements between deceased and alive subjects. A total of 63 participants underwent multiple cardiac magnetic resonance imaging and were included in the analyses. Twelve subjects (19.1%) died over a median follow‐up of 5 years (interquartile range, 3.1–7.0). Rate of decline in left ventricular ejection fraction was faster in deceased than alive subjects ( P <0.0001). Rate of increase in indexed left ventricular end‐diastolic ( P =0.0132) and systolic ( P <0.0001) volumes were higher in deceased subjects. Faster worsening in midcircumferential strain was seen in deceased subjects ( P =0.049) while no difference in global circumferential strain was seen. The rate of increase in late gadolinium enhancement, base T1, and mid T1 did not differ between groups. Conclusions Duchenne muscular dystrophy death is associated with the rate of change in left ventricular ejection fraction, midcircumferential strain, and ventricular volumes. Aggressive medical therapy to decrease the rate of progression may improve the mortality rate in this population. A decrease in the rate of progression may serve as a valid surrogate outcome for therapeutic trials.

Publisher

Ovid Technologies (Wolters Kluwer Health)

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