Key result
LV GLS detects LV dysfunction ~29% more often than LVEF in Becker muscular dystrophy.
Why the study?
Cardiac involvement is the main cause of death in Becker muscular dystrophy, but standard echocardiographic measurements like LVEF might not be sensitive enough to detect early myocardial dysfunction.
Does LV GLS improve the identification and monitoring of left ventricular dysfunction compared to LVEF in patients with Becker muscular dystrophy?
Cohort (n=61)
Does LV GLS improve the identification and monitoring of left ventricular dysfunction compared to LVEF in patients with Becker muscular dystrophy?
Absolute Event Rate: 77.5% vs 60%
LV GLS is a more sensitive echocardiographic parameter than LVEF for identifying and monitoring early left ventricular dysfunction in patients with Becker muscular dystrophy.
May support GLS for earlier LV monitoring in Becker MD; hypothesis-generating and should not yet change practice.
Cardiac involvement is the main cause of death in Becker muscular dystrophy (BMD). Identification of left ventricular (LV) function is crucial, but standard echocardiographic measurements such as LV ejection fraction (LVEF) might not be sensitive enough to detect early myocardial dysfunction. We explored the value of LV global longitudinal strain (GLS) as a more accurate echocardiographic parameter to detect and monitor LV dysfunction in BMD. Furthermore, we studied possible factors associated with LV dysfunction and progression. A total of 40 patients with BMD (age 39.0 ± 13.2 years) and 21 matched controls were included. Clinical variables, pulmonary tests, serum biomarkers, and echocardiograms were collected at baseline and after 2 years. LV systolic function was assessed by LVEF and LV GLS; a significant progression in LV dysfunction was defined as an absolute LV GLS deterioration ≥15%. Responsiveness to cardiac disease progression was determined using standardized response means. Patients showed impaired LVEF and LV GLS compared with controls (p <0.001). Of interest, 31 patients (77.5%) showed impaired LV GLS (defined as greater than -18%), whereas only 24 patients (60%) had reduced LVEF. LV GLS and LVEF correlated with troponin I (ρ = 0.553 and -0.523) and N-terminal pro-b-type natriuretic peptide (ρ = 0.506 and -0.585), but not with skeletal muscle or pulmonary function. At follow-up (2.0 ± 0.5 years, n = 29), LV GLS worsened significantly (-1.3 ± 0.8%, p = 0.002, standardized response mean = 0.70, annually = 0.60%), whereas LVEF remained stable. No risk factors for LV dysfunction progression were identified. In BMD, LV GLS is frequently impaired and shows deterioration over time compared with LVEF. LV GLS could be used as a more sensitive parameter to identify and monitor LV dysfunction.
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Velde et al. (2021) conducted a cohort in Becker muscular dystrophy (n=61). Left ventricular global longitudinal strain (LV GLS) vs. Left ventricular ejection fraction (LVEF) was evaluated on Detection of impaired left ventricular function at baseline. In patients with Becker muscular dystrophy, LV GLS detected impaired left ventricular function more frequently than LVEF (77.5% vs 60%) and worsened significantly over 2 years (p=0.002).
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