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Development of a standard of care for patients with valosin-containing protein associated multisystem proteinopathy
Valosin-containing protein (VCP) associated multisystem proteinopathy (MSP) is a rare inherited disorder that may result in multisystem involvement of varying phenotypes including inclusion body myopathy, Paget’s disease of bone (PDB), frontotemporal dementia (FTD), parkinsonism, and amyotrophic lat...
Autores principales: | , , , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8800193/ https://www.ncbi.nlm.nih.gov/pubmed/35093159 http://dx.doi.org/10.1186/s13023-022-02172-5 |
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author | Korb, Manisha Peck, Allison Alfano, Lindsay N. Berger, Kenneth I. James, Meredith K. Ghoshal, Nupur Healzer, Elise Henchcliffe, Claire Khan, Shaida Mammen, Pradeep P. A. Patel, Sujata Pfeffer, Gerald Ralston, Stuart H. Roy, Bhaskar Seeley, William W. Swenson, Andrea Mozaffar, Tahseen Weihl, Conrad Kimonis, Virginia |
author_facet | Korb, Manisha Peck, Allison Alfano, Lindsay N. Berger, Kenneth I. James, Meredith K. Ghoshal, Nupur Healzer, Elise Henchcliffe, Claire Khan, Shaida Mammen, Pradeep P. A. Patel, Sujata Pfeffer, Gerald Ralston, Stuart H. Roy, Bhaskar Seeley, William W. Swenson, Andrea Mozaffar, Tahseen Weihl, Conrad Kimonis, Virginia |
author_sort | Korb, Manisha |
collection | PubMed |
description | Valosin-containing protein (VCP) associated multisystem proteinopathy (MSP) is a rare inherited disorder that may result in multisystem involvement of varying phenotypes including inclusion body myopathy, Paget’s disease of bone (PDB), frontotemporal dementia (FTD), parkinsonism, and amyotrophic lateral sclerosis (ALS), among others. An international multidisciplinary consortium of 40+ experts in neuromuscular disease, dementia, movement disorders, psychology, cardiology, pulmonology, physical therapy, occupational therapy, speech and language pathology, nutrition, genetics, integrative medicine, and endocrinology were convened by the patient advocacy organization, Cure VCP Disease, in December 2020 to develop a standard of care for this heterogeneous and under-diagnosed disease. To achieve this goal, working groups collaborated to generate expert consensus recommendations in 10 key areas: genetic diagnosis, myopathy, FTD, PDB, ALS, Charcot Marie Tooth disease (CMT), parkinsonism, cardiomyopathy, pulmonology, supportive therapies, nutrition and supplements, and mental health. In April 2021, facilitated discussion of each working group’s conclusions with consensus building techniques enabled final agreement on the proposed standard of care for VCP patients. Timely referral to a specialty neuromuscular center is recommended to aid in efficient diagnosis of VCP MSP via single-gene testing in the case of a known familial VCP variant, or multi-gene panel sequencing in undifferentiated cases. Additionally, regular and ongoing multidisciplinary team follow up is essential for proactive screening and management of secondary complications. The goal of our consortium is to raise awareness of VCP MSP, expedite the time to accurate diagnosis, define gaps and inequities in patient care, initiate appropriate pharmacotherapies and supportive therapies for optimal management, and elevate the recommended best practices guidelines for multidisciplinary care internationally. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13023-022-02172-5. |
format | Online Article Text |
id | pubmed-8800193 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-88001932022-02-02 Development of a standard of care for patients with valosin-containing protein associated multisystem proteinopathy Korb, Manisha Peck, Allison Alfano, Lindsay N. Berger, Kenneth I. James, Meredith K. Ghoshal, Nupur Healzer, Elise Henchcliffe, Claire Khan, Shaida Mammen, Pradeep P. A. Patel, Sujata Pfeffer, Gerald Ralston, Stuart H. Roy, Bhaskar Seeley, William W. Swenson, Andrea Mozaffar, Tahseen Weihl, Conrad Kimonis, Virginia Orphanet J Rare Dis Review Valosin-containing protein (VCP) associated multisystem proteinopathy (MSP) is a rare inherited disorder that may result in multisystem involvement of varying phenotypes including inclusion body myopathy, Paget’s disease of bone (PDB), frontotemporal dementia (FTD), parkinsonism, and amyotrophic lateral sclerosis (ALS), among others. An international multidisciplinary consortium of 40+ experts in neuromuscular disease, dementia, movement disorders, psychology, cardiology, pulmonology, physical therapy, occupational therapy, speech and language pathology, nutrition, genetics, integrative medicine, and endocrinology were convened by the patient advocacy organization, Cure VCP Disease, in December 2020 to develop a standard of care for this heterogeneous and under-diagnosed disease. To achieve this goal, working groups collaborated to generate expert consensus recommendations in 10 key areas: genetic diagnosis, myopathy, FTD, PDB, ALS, Charcot Marie Tooth disease (CMT), parkinsonism, cardiomyopathy, pulmonology, supportive therapies, nutrition and supplements, and mental health. In April 2021, facilitated discussion of each working group’s conclusions with consensus building techniques enabled final agreement on the proposed standard of care for VCP patients. Timely referral to a specialty neuromuscular center is recommended to aid in efficient diagnosis of VCP MSP via single-gene testing in the case of a known familial VCP variant, or multi-gene panel sequencing in undifferentiated cases. Additionally, regular and ongoing multidisciplinary team follow up is essential for proactive screening and management of secondary complications. The goal of our consortium is to raise awareness of VCP MSP, expedite the time to accurate diagnosis, define gaps and inequities in patient care, initiate appropriate pharmacotherapies and supportive therapies for optimal management, and elevate the recommended best practices guidelines for multidisciplinary care internationally. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s13023-022-02172-5. BioMed Central 2022-01-29 /pmc/articles/PMC8800193/ /pubmed/35093159 http://dx.doi.org/10.1186/s13023-022-02172-5 Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Review Korb, Manisha Peck, Allison Alfano, Lindsay N. Berger, Kenneth I. James, Meredith K. Ghoshal, Nupur Healzer, Elise Henchcliffe, Claire Khan, Shaida Mammen, Pradeep P. A. Patel, Sujata Pfeffer, Gerald Ralston, Stuart H. Roy, Bhaskar Seeley, William W. Swenson, Andrea Mozaffar, Tahseen Weihl, Conrad Kimonis, Virginia Development of a standard of care for patients with valosin-containing protein associated multisystem proteinopathy |
title | Development of a standard of care for patients with valosin-containing protein associated multisystem proteinopathy |
title_full | Development of a standard of care for patients with valosin-containing protein associated multisystem proteinopathy |
title_fullStr | Development of a standard of care for patients with valosin-containing protein associated multisystem proteinopathy |
title_full_unstemmed | Development of a standard of care for patients with valosin-containing protein associated multisystem proteinopathy |
title_short | Development of a standard of care for patients with valosin-containing protein associated multisystem proteinopathy |
title_sort | development of a standard of care for patients with valosin-containing protein associated multisystem proteinopathy |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8800193/ https://www.ncbi.nlm.nih.gov/pubmed/35093159 http://dx.doi.org/10.1186/s13023-022-02172-5 |
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