Purpose: Cardiac involvement in limb-girdle muscular dystrophy (LGMD)2A and LGMD2B, the most common subgroups of LGMD, is controversial. Our study aims to determine whether myocardial dysfunction develops in LGMD2A and LGMD2B patients.

Methods: The study included 16 LGMD2A, 12 LGMD2B patients, and 48 healthy individuals. Comparisons included demographic, clinical, and laboratory parameters of LGMD2A and LGMD2B subgroups and traditional echocardiography and two-dimensional speckle tracking echocardiography (2D-STE) parameters with the normal population.

Results: The median age was 33 (22-39 interquartile range [IQR]) in the LGMD2A group, 33 (27-38 IQR) in the LGMD2B group, and 28 (25-35 IQR) in the control group. The left ventricular (LV) ejection fraction of both LGMD2A and LGMD2B groups was similar to the control group (p = 0.296 and p = 0.918). Apical 4-chamber longitudinal strain (LS), Apical 2-chamber LS, Apical 3-chamber LS, left ventricular global longitudinal strain (LVGLS)-mid-myocardial, LVGLS-endocardium, and LVGLS-epicardium were lower (less negative) in the LGMD2B group compared to the control group (p = 0.006, p = 0.001, p < 0.001, p < 0.001, p < 0.001, and p < 0.001, respectively).

Conclusion: LV 2D-STE parameters of LGMD2A patients were similar to the control group, while they decreased significantly (less negative) in LGMD2B patients, indicating that LV subclinical myocardial dysfunction may develop in LGMD2B patients.

Download full-text PDF

Source
http://dx.doi.org/10.1002/jcu.23323DOI Listing

Publication Analysis

Top Keywords

lgmd2a lgmd2b
20
control group
12
two-dimensional speckle
8
speckle tracking
8
tracking echocardiography
8
limb-girdle muscular
8
muscular dystrophy
8
lgmd2b group
8
left ventricular
8
longitudinal strain
8

Similar Publications

Article Synopsis
  • Limb-girdle muscular dystrophies (LGMDs) are inherited disorders that primarily lead to muscle weakness and vary in subtype prevalence across different regions and ethnic groups in China, with common types identified among patients in Southeast China.
  • In a study of 81 patients from 62 families, the most frequent LGMD subtypes were LGMD-R2 (LGMD2B) and LGMD-R1 (LGMD2A), along with specific genetic mutations being more prevalent in certain subtypes, particularly those affecting childhood-onset cases.
  • Patients exhibited various clinical issues, including cardiac problems and respiratory insufficiency, while muscle imaging revealed distinct patterns of fatty infiltration and edema based on the LGMD subtype.
View Article and Find Full Text PDF

Limb-girdle muscular dystrophy (LGMD) is a genetic muscle disorder causing weakness and wasting of the proximal limb musculature. When ambulation is lost, the attention must be shifted to the upper limb muscles' function. We studied the upper limb muscle strength and the corresponding function in 15 LGMDR1/LGMD2A and 13 LGMDR2/LGMD2B, through the Performance of Upper Limb scale and the MRC score of upper limbs.

View Article and Find Full Text PDF

Purpose: Cardiac involvement in limb-girdle muscular dystrophy (LGMD)2A and LGMD2B, the most common subgroups of LGMD, is controversial. Our study aims to determine whether myocardial dysfunction develops in LGMD2A and LGMD2B patients.

Methods: The study included 16 LGMD2A, 12 LGMD2B patients, and 48 healthy individuals.

View Article and Find Full Text PDF

Limb-girdle muscle dystrophy (LGMD) is the fourth most common genetic cause of muscle weakness, with LGMD type 2A (LGMD2A) being one of the most common adult-onset muscular dystrophies presenting with limb-girdle weakness, while LGMD type 2B (LGMD2B) being the most common distal myopathy. This study includes two cases. The first case is a 13-year-old male, with no family history of similar symptoms, who presented with lower extremity weakness at the age of nine, starting with proximal weakness of the lower extremities, progressively involving the upper extremities.

View Article and Find Full Text PDF

Diagnostic yield of multi-gene panel for muscular dystrophies and other hereditary myopathies.

Neurol Sci

July 2022

Graduate Program in Medicine: Medical Sciences, Universidade Federal Do Rio Grande Do Sul (UFRGS), Porto Alegre, Brazil.

Genetic testing is being considered the first-step in the investigation of hereditary myopathies. However, the performance of the different testing approaches is little known. The aims of the present study were to evaluate the diagnostic yield of a next-generation sequencing panel comprising 39 genes as the first-tier test for genetic myopathies diagnosis and to characterize clinical and molecular findings of families from southern Brazil.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!