| Literature DB >> 33145792 |
Manisha K Korb1, Virginia E Kimonis2, Tahseen Mozaffar1,3,4.
Abstract
Multisystem proteinopathy (MSP) is a pleiotropic group of inherited disorders that cause neurodegeneration, myopathy, and bone disease, and share common pathophysiology. Originally referred to as inclusion body myopathy associated with Paget disease of bone and frontotemporal dementia (IBMPFD), attributed to mutations in the gene encoding valosin-containing protein (VCP), it has more recently been discovered that there are several other genes responsible for similar clinical and pathological phenotypes with muscle, brain, nerve, and bone involvement, in various combinations. These include heterogeneous nuclear ribonucleoprotein A2B1 and A1 (hnRNPA2B1, hnRNPA1), sequestosome 1 (SQSTM1), matrin 3 (MATR3), T-cell restricted intracellular antigen 1 (TIA1), and optineurin (OPTN), all of which share disruption of RNA stress granule function and autophagic degradation. This review will discuss each of the genes implicated in MSP, exploring the molecular pathogenesis, clinical features, current standards of care, and future directions for this diverse yet mechanistically linked spectrum of disorders.Entities:
Keywords: Paget disease of bone; VCP; amyotrophic lateral sclerosis; inclusion body myopathy; multiple system proteinopathy
Year: 2020 PMID: 33145792 DOI: 10.1002/mus.27097
Source DB: PubMed Journal: Muscle Nerve ISSN: 0148-639X Impact factor: 3.217