Key result
Myopathological analysis of 18 Dutch patients with NEM6 revealed rods in 85% of biopsies by light microscopy and cores in 79%, supporting its classification as a rod-core myopathy.
Why the study?
Nemaline myopathy type 6 (NEM6), a KBTBD13-related congenital myopathy, is caused by mutated KBTBD13 protein provoking impaired muscle-relaxation kinetics, prompting description of muscle morphology and its correlation with clinical phenotype and pathophysiological mechanisms.
Observational (n=18)
KBTBD13-related congenital myopathy (NEM6) is characterized by prominent cores, rods, nuclear clumps, and granulofilamentous protein material, suggesting it should be classified as a rod-core myopathy.
Nemaline myopathy type 6 (NEM6), KBTBD13-related congenital myopathy is caused by mutated KBTBD13 protein that interacts improperly with thin filaments/actin, provoking impaired muscle-relaxation kinetics. We describe muscle morphology in 18 Dutch NEM6 patients and correlate it with clinical phenotype and pathophysiological mechanisms. Rods were found in in 85% of biopsies by light microscopy, and 89% by electron microscopy. A peculiar ring disposition of rods resulting in ring-rods fiber was observed. Cores were found in 79% of NEM6 biopsies by light microscopy, and 83% by electron microscopy. Electron microscopy also disclosed granulofilamentous protein material in 9 biopsies. Fiber type 1 predominance and prominent nuclear internalization were found. Rods were immunoreactive for α-actinin and myotilin. Areas surrounding the rods showed titin overexpression suggesting derangement of the surrounding sarcomeres. NEM6 myopathology hallmarks are prominent cores, rods including ring-rods fibers, nuclear clumps, and granulofilamentous protein material. This material might represent the histopathologic epiphenomenon of altered interaction between mutated KBTBD13 protein and thin filaments. We claim to classify KBTBD13-related congenital myopathy as rod-core myopathy.
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Bouman et al. (2021) conducted an observational in Nemaline myopathy type 6 (NEM6), KBTBD13-related congenital myopathy (n=18). KBTBD13 mutation was evaluated on Muscle morphology characteristics. Myopathological analysis of 18 Dutch patients with NEM6 revealed rods in 85% of biopsies by light microscopy and cores in 79%, supporting its classification as a rod-core myopathy.
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