Evidence map›Paper›PMID 35093159›Full record

ReviewOrphanet journal of rare diseases2022

Development of a standard of care for patients with valosin-containing protein associated multisystem proteinopathy.

Manisha Korb, Allison Peck, Lindsay N Alfano, Kenneth I Berger, Meredith K James, Nupur Ghoshal, Elise Healzer, Claire Henchcliffe, Shaida Khan, Pradeep P A Mammen and 10 more

Open access · goldAbstract readReview
In one paragraph

Review in Orphanet journal of rare diseases, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed
3.9field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

22 citing papers in PubMed, 35 citations in OpenAlex.

  1. Review
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  7. Article
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  9. Review
  10. Nationwide survey of patients with multisystem proteinopathy in Japan.Annals of clinical and translational neurology · 2024
    Article
  11. Article
  12. Article
  13. Article
  14. Review
  15. Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors at 11 institutions in 3 countries.

Manisha KorbDepartment of Neurology, University of California - Irvine School of Medicine, Orange, CA, USA. mkak@uci.edu.ORCID 0000-0002-4626-4007
Allison PeckCure VCP Disease, Americus, GA, USA.
Lindsay N AlfanoThe Abigail Wexner Research Institute at Nationwide Children's Hospital, Columbus, OH, USA.
Kenneth I BergerDepartment of Medicine (Pulmonary), NYU Grossman School of Medicine, New York, NY, USA.
Meredith K JamesThe John Walton Muscular Dystrophy Research Centre, Newcastle University and Newcastle Hospitals NHS Foundation Trust, Newcastle Upon Tyne, UK.
Nupur GhoshalDepartment of Neurology and Psychiatry, Washington University in St. Louis, St. Louis, MO, USA.
Elise HealzerThriving Hope Consulting, Vinton, IA, USA.
Claire HenchcliffeDepartment of Neurology, University of California - Irvine School of Medicine, Orange, CA, USA.
Shaida KhanDepartment of Neurology & Neurotherapeutics, University of Texas Southwestern Medical Center, Dallas, TX, USA.
Pradeep P A MammenDepartment of Medicine (Cardiology), University of Texas Southwestern Medical Center, Dallas, TX, USA.
Sujata PatelWellness with Sujata, Wadsworth, OH, USA.
Gerald PfefferHotchkiss Brain Institute, University of Calgary Cumming School of Medicine, Calgary, AB, Canada.
Stuart H RalstonInstitute of Genetics and Cancer at the University of Edinburgh, Edinburgh, SCT, UK.
Bhaskar RoyDepartment of Neurology, Yale School of Medicine, New Haven, CT, USA.
William W SeeleyWeill Institute for Neurosciences, University of California San Francisco, San Francisco, CA, USA.
Andrea SwensonDepartment of Neurology, University of Iowa Hospitals and Clinics, Iowa City, IA, USA.
Tahseen MozaffarDepartment of Neurology, University of California - Irvine School of Medicine, Orange, CA, USA.
Conrad WeihlDepartment of Neurology, Washington University in St. Louis, St. Louis, MO, USA.
Virginia KimonisDepartment of Pediatrics, University of California - Irvine School of Medicine, Orange, CA, USA.
VCP Standards of Care Working Group
University of California, Irvine · USUniversity of Iowa Hospitals and Clinics · USNewcastle upon Tyne Hospitals NHS Foundation Trust · GBThe University of Texas Southwestern Medical Center · USWashington University in St. Louis · USEdinburgh Cancer Research · GBNationwide Children's Hospital · USNew York University · USUniversity of Calgary · CAUniversity of California, San Francisco · USYale University · US

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
University of California Health Participation in the National COVID Cohort Collaborative (N3C)UL1TR001414 · NCATS · UNIVERSITY OF CALIFORNIA-IRVINE · PI COOPER, DAN M, VILAIN, ERIC J. · 2015 to 2023
$35.1M
VCP in myopathy and dementiaR01AG031867 · NIA · WASHINGTON UNIVERSITY · PI CONRAD C WEIHL · 2009 to 2026
$9.1M
Training CoreP50HD087351 · NICHD · UT SOUTHWESTERN MEDICAL CENTER · PI MAMMEN, PRADEEP P.A. · 2020 to 2024
$8.0M
Clinical and Translational Studies in Muscle DiseaseK24AR073317 · NIAMS · WASHINGTON UNIVERSITY · PI CONRAD C WEIHL · 2018 to 2026
$1.6M
Medical Research Council G0600974Medical Research Council MR/L501529/1Medical Research Council MR/R024804/1Motor Neurone Disease Association ALCHALABI-DOBSON/APR14/829-791Motor Neurone Disease Association ALCHALABI-TALBOT/APR14/926-794NCATS NIH HHS UL1 TR001414NCATS NIH HHS UL1 TR001863NIAMS NIH HHS K24 AR073317NIA NIH HHS R01 AG031867NICHD NIH HHS P50 HD087351NIH HHS P50HD087351NIH HHS R01AR074457
6 · The paper itself

Abstract

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.

Indexed as

Amyotrophic Lateral SclerosisMyositis, Inclusion BodyOsteitis DeformansCell Cycle ProteinsHumansMutationStandard of CareValosin Containing ProteinCell Cycle ProteinsValosin Containing Protein

Identifiers

PMID35093159
PMCPMC8800193
OpenAlexW4210737894

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.