Left Atrial Phasic Function via Cardiac Magnetic Resonance Imaging in Patients with Duchenne Muscular Dystrophy

被引:0
|
作者
Trussell, Taylor M. [1 ,2 ,3 ]
Brown, Tyler [1 ,2 ,3 ]
Marcuccio, Elisa [1 ,2 ,3 ]
Mullikin, Anna [1 ]
Zang, Huaiyu [1 ]
Ollberding, Nicholas J. [2 ,4 ]
Villa, Chet [1 ,2 ,3 ]
Lang, Sean M. [1 ,2 ,3 ]
机构
[1] Cincinnati Childrens Hosp Med Ctr, Heart Inst, Cincinnati, OH 45229 USA
[2] Univ Cincinnati, Coll Med, Dept Pediat, Cincinnati, OH 45229 USA
[3] Cincinnati Childrens Hosp Med Ctr, Heart Inst Res Core, Cincinnati, OH 45229 USA
[4] Cincinnati Childrens Hosp Med Ctr, Div Biostat & Epidemiol, Cincinnati, OH 45229 USA
关键词
Pediatric cardiology; Cardiac advanced imaging; Atrial strain; Cardiomyopathy; SPECKLE-TRACKING ECHOCARDIOGRAPHY; STRAIN; CARDIOMYOPATHY;
D O I
10.1007/s00246-023-03327-2
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cardiac dysfunction is a leading cause of morbidity and mortality in Duchenne muscular dystrophy (DMD). Left atrial (LA) function is a poorly understood concept in this patient population, and research suggests underlying structural changes that could affect atrial function. Cardiac magnetic resonance (CMR) imaging may provide an important non-invasive approach to evaluating LA function. This study was a single center retrospective review of consecutive CMR studies over a 1 year period comparing LA phasic function within a cohort of DMD patients, and to those with structurally and functionally normal hearts. LA strain measurements including global reservoir, conduit, boost-pump strain, and LA volumes were obtained retrospectively. Spearman correlation analyses were performed on atrial strain measurements. 107 DMD and 79 normal CMR studies were included. The DMD cohort had worse systolic function (p < 0.001), smaller indexed max LA and left ventricular (LV) volumes (p < 0.001), and greater LA emptying fraction (p < 0.001). In the DMD cohort, emptying fraction decreased with advanced patient age (p < 0.001) and diminishing systolic function (p < 0.001). DMD patients with moderate or severe LV dysfunction demonstrated lower LA emptying fraction (p = 0.002), more impaired 2-chamber LA reservoir (p = 0.003), and LA pump (p = 0.006) and conduit strain (p = 0.018). DMD patients with preserved function have lower indexed LA volumes with higher LA emptying fractions than controls. Progression of disease and age is associated with decreased LA emptying fraction with early manifestations in reservoir and conduit strain. These findings suggest that strain markers of LA compliance and early left ventricular relaxation are associated with worsening cardiomyopathy in the DMD population.
引用
收藏
页码:72 / 80
页数:9
相关论文
共 50 条
  • [1] Upper arm and cardiac magnetic resonance imaging in Duchenne muscular dystrophy
    Gaur, Lasya
    Hanna, Alexander
    Bandettini, W. Patricia
    Fischbeck, Kenneth H.
    Arai, Andrew E.
    Mankodi, Ami
    ANNALS OF CLINICAL AND TRANSLATIONAL NEUROLOGY, 2016, 3 (12): : 948 - 955
  • [2] Evaluation of Echocardiographic Measures of Left Ventricular Function in Patients with Duchenne Muscular Dystrophy: Assessment of Reproducibility and Comparison to Cardiac Magnetic Resonance Imaging
    Soslow, Jonathan H.
    Xu, Meng
    Slaughter, James C.
    Stanley, Michael
    Crum, Kimberly
    Markham, Larry W.
    Parra, David A.
    JOURNAL OF THE AMERICAN SOCIETY OF ECHOCARDIOGRAPHY, 2016, 29 (10) : 983 - 991
  • [3] Longitudinal changes in cardiac function in Duchenne muscular dystrophy population as measured by magnetic resonance imaging
    Batra, Abhinandan
    Barnard, Alison M.
    Lott, Donovan J.
    Willcocks, Rebecca J.
    Forbes, Sean C.
    Chakraborty, Saptarshi
    Daniels, Michael J.
    Arbogast, Jannik
    Triplett, William
    Henricson, Erik K.
    Dayan, Jonathan G.
    Schmalfuss, Carsten
    Sweeney, Lee
    Byrne, Barry J.
    McDonald, Craig M.
    Vandenborne, Krista
    Walter, Glenn A.
    BMC CARDIOVASCULAR DISORDERS, 2022, 22 (01)
  • [4] Longitudinal changes in cardiac function in Duchenne muscular dystrophy population as measured by magnetic resonance imaging
    Abhinandan Batra
    Alison M. Barnard
    Donovan J. Lott
    Rebecca J. Willcocks
    Sean C. Forbes
    Saptarshi Chakraborty
    Michael J. Daniels
    Jannik Arbogast
    William Triplett
    Erik K. Henricson
    Jonathan G. Dayan
    Carsten Schmalfuss
    Lee Sweeney
    Barry J. Byrne
    Craig M. McDonald
    Krista Vandenborne
    Glenn A. Walter
    BMC Cardiovascular Disorders, 22
  • [6] Magnetic resonance imaging of masticatory muscles in patients with duchenne muscular dystrophy
    Fuentealba, Carmen Meza
    Arrieta, Cristobal
    Gonzalez, Catalina
    Ortega, Nicolas Aranda
    Salinas, Luis
    Zepeda, Rocio Cortes
    Reyes, Maria de los Angeles Beytia
    Escobar, Raul G.
    Uribe, Sergio
    Avila-Smirnow, Daniela
    EUROPEAN JOURNAL OF PAEDIATRIC NEUROLOGY, 2025, 55 : 47 - 55
  • [7] Delayed enhancement cardiac magnetic resonance imaging in a patient with Duchenne muscular dystrophy
    Guillaume, Melissa D.
    Phoon, Colin K. L.
    Chun, Anne J. L.
    Srichai, Monvadi B.
    TEXAS HEART INSTITUTE JOURNAL, 2008, 35 (03) : 367 - 368
  • [8] Myocardial Fibrosis and Left Ventricular Dysfunction in Duchenne Muscular Dystrophy Carriers Using Cardiac Magnetic Resonance Imaging
    Sean M. Lang
    Svetlana Shugh
    Wojciech Mazur
    Joshua J. Sticka
    Mantosh S. Rattan
    John L. Jefferies
    Michael D. Taylor
    Pediatric Cardiology, 2015, 36 : 1495 - 1501
  • [9] Myocardial Fibrosis and Left Ventricular Dysfunction in Duchenne Muscular Dystrophy Carriers Using Cardiac Magnetic Resonance Imaging
    Lang, Sean M.
    Shugh, Svetlana
    Mazur, Wojciech
    Sticka, Joshua J.
    Rattan, Mantosh S.
    Jefferies, John L.
    Taylor, Michael D.
    PEDIATRIC CARDIOLOGY, 2015, 36 (07) : 1495 - 1501
  • [10] Exercise Cardiac Magnetic Resonance Imaging in Boys With Duchenne Muscular Dystrophy Without Cardiac Disease
    Power, Lisa C.
    Gusso, Silmara
    Hornung, Tim S.
    Jefferies, Craig
    Derraik, Jose G. B.
    Hofman, Paul L.
    O'Grady, Gina L.
    PEDIATRIC NEUROLOGY, 2021, 117 : 35 - 43