Key result
NEB was the most frequent causative gene (73.33%) in a cohort of 15 Chinese patients with nemaline myopathy, with the splicing mutation c.21522+3A>G identified as a potential hotspot.
Why the study?
Nemaline myopathy is the most common congenital myopathy and is caused by various genetic mutations, warranting investigation into its clinical, pathological, and genetic features.
Observational (n=15)
No
In a Chinese cohort of 15 patients with nemaline myopathy, NEB was the most common causative gene, and muscle pathology consistently showed nemaline body aggregation.
Case series expands nemaline myopathy phenotypes; leaves open need for larger genotype-phenotype studies.
BACKGROUND: Nemaline myopathy, the most common of the congenital myopathies, is caused by various genetic mutations. In this study, we attempted to investigate the clinical features, muscle pathology and genetic features of 15 patients with nemaline myopathy. RESULTS: Among the 15 patients, there were 9 (60.00%) males and 6 (40.00%) females, and 9 (60.00%) of them came from three families respectively. The age of seeing a doctor ranged from 9 to 52 years old, the age of onset was from 5 to 23 years old, and the duration of disease ranged from 3 to 35 years. Ten out of the 15 patients had high arched palate and elongated face. Only one patient had mild respiratory muscle involvement and none had dysphagia. Muscle biopsies were performed in 9 out of the 15 patients. Pathologically, muscle fibers of different sizes, atrophic muscle fibers and compensatory hypertrophic fibers could be found, and occasionally degenerated and necrotic muscle fibers were observed. Different degrees of nemaline bodies aggregation could be seen in all 9 patients. The distribution of type I and type II muscle fibers were significantly abnormal in patients with nemaline myopathy caused by NEB gene, however, it was basically normal in patients with nemaline myopathy caused by TPM3 gene and ACTA1 gene. Electron microscopic analysis of 6 patients showed that nemaline bodies aggregated between myofibrils were found in 5(83.33%) cases, and most of them were located near the Z band, but no intranuclear rods were found. The gene analysis of 15 NM patients showed that three NM-related genes were harbored, including 11 (73.33%) patients with NEB, 3 (20.00%) patients with TPM3, and 1 (6.67%) patient with ACTA1, respectively. A total of 12 mutation sites were identified and included 10 (83.33%) mutations in exon and 2(16.67%) mutations in intron. CONCLUSIONS: The clinical phenotype of nemaline myopathy is highly heterogeneous. Muscle pathology shows that nemaline bodies aggregation is an important feature for the diagnosis of NM. NEB is the most frequent causative gene in this cohort. The splicing mutation, c.21522 + 3A > G may be the hotspot mutation of the NEB gene in Chinese NM patients.
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Haidong et al. (2023) conducted an observational in Nemaline myopathy (n=15). Genetic mutations (NEB, TPM3, ACTA1) was evaluated on Genetic mutations and clinico-pathological features. NEB was the most frequent causative gene (73.33%) in a cohort of 15 Chinese patients with nemaline myopathy, with the splicing mutation c.21522+3A>G identified as a potential hotspot.
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