Muscular MRI-based algorithm to differentiate inherited myopathies presenting with spinal rigidity

Archive ouverte

Tordjman, M | Dabaj, I | Laforet, P | Felter, A | Ferreiro, A | Biyoukar, M | Law-Ye, B | Zanoteli, E | Castiglioni, C | Rendu, J | Beroud, C | Chamouni, A | Richard, P | Mompoint, D | Quijano-Roy, S | Carlier, Ry

Edité par CCSD ; Springer Verlag -

International audience. Objectives Inherited myopathies are major causes of muscle atrophy and are often characterized by rigid spine syndrome, a clinical feature designating patients with early spinal contractures. We aim to present a decision algorithm based on muscular whole body magnetic resonance imaging (mWB-MRI) as a unique tool to orientate the diagnosis of each inherited myopathy long before the genetically confirmed diagnosis.MethodsThis multicentre retrospective study enrolled 79 patients from referral centres in France, Brazil and Chile. The patients underwent 1.5-T or 3-T mWB-MRI. The protocol comprised STIR and T1 sequences in axial and coronal planes, from head to toe. All images were analyzed manually by multiple raters. Fatty muscle replacement was evaluated on mWB-MRI using both the Mercuri scale and statistical comparison based on the percentage of affected muscle.ResultsBetween February 2005 and December 2015, 76 patients with genetically confirmed inherited myopathy were included. They were affected by Pompe disease or harbored mutations in RYR1, Collagen VI, LMNA, SEPN1, LAMA2 and MYH7 genes. Each myopathy had a specific pattern of affected muscles recognizable on mWB-MRI. This allowed us to create a novel decision algorithm for patients with rigid spine syndrome by segregating these signs. This algorithm was validated by five external evaluators on a cohort of seven patients with a diagnostic accuracy of 94.3% compared with the genetic diagnosis.ConclusionWe provide a novel decision algorithm based on muscle fat replacement graded on mWB-MRI that allows diagnosis and differentiation of inherited myopathies presenting with spinal rigidity.Key Points center dot Inherited myopathies are rare, diagnosis is challenging and genetic tests require specialized centres and often take years.center dot Inherited myopathies are often characterized by spinal rigidity.center dot Whole body magnetic resonance imaging is a unique tool to orientate the diagnosis of each inherited myopathy presenting with spinal rigidity.center dot Each inherited myopathy in this study has a specific pattern of affected muscles that orientate diagnosis.center dot A novel MRI-based algorithm, usable by every radiologist, can help the early diagnosis of these myopathies.

Consulter en ligne

Suggestions

Du même auteur

Diaphragmatic dysfunction in SEPN1-related myopathy

Archive ouverte | Caggiano, S | CCSD

International audience. SEPN1-related myopathy (SEPN1-RM) is characterized by predominant axial muscle weakness, early scoliosis, rigid spine and severe respiratory insufficiency. The aim of the study was to charact...

The DM-scope registry: a rare disease innovative framework bridging the gap between research and medical care

Archive ouverte | de Antonio, M | CCSD

International audience. Background: The relevance of registries as a key component for developing clinical research for rare diseases (RD) and improving patient care has been acknowledged by most stakeholders. As re...

LES CORTICOIDES ORAUX, UNE OPTION THERAPEUTIQUE DANS LES LAMINOPATHIES CONGENITALES ?

Archive ouverte | Gomez-Garcia de la Banda, M | CCSD

International audience

Chargement des enrichissements...