MétaCan
Menu
Back to cohort
Record W4288074845 · doi:10.1136/jnnp-2022-328921

Genotype–phenotype correlations in valosin-containing protein disease: a retrospective muticentre study

2022· article· en· W4288074845 on OpenAlexafffund
Marianela Schiava, Chiseko Ikenaga, Rocío N. Villar‐Quiles, Marta Caballero‐Ávila, Ana Töpf, Ichizo Nishino, Virginia Kimonis, Bjarne Udd, Benedikt Schoser, Edmar Zanoteli, Paulo Victor Sgobbi de Souza, Giorgio Tasca, Thomas Lloyd, Adolfo Lopez-de Munain, Carmen Paradas, Elena Pegoraro, Aleksandra Nadaj-Pakleza, Jan De Bleecker, Umesh A. Badrising, Alicia Alonso‐Jiménez, Anna Kostera‐Pruszczyk, Francesc X. Miralles, Jin‐Hong Shin, Jorge A. Bevilacqua, Montse Olivé, Matthias Vorgerd, Rudi Kley, Stefen Brady, Timothy L. Williams, Cristina Domínguez‐González, George K. Papadimas, Jodi Warman‐Chardon, Kristl G. Claeys, Marianne de Visser, Nuria Muelas, Pascal Laforêt, Edoardo Malfatti, Lindsay N. Alfano, Sruthi Nair, Georgios Manousakis, Hani Kushlaf, Matthew Harms, Christopher Nance, Alba Ramos‐Fransí, Carmelo Rodolico, Channa Hewamadduma, Hakan Çetin, Jorge García‐García, Endre Pál, Maria Elena Farrugia, Phillipa J. Lamont, Colin Quinn, Velina Nedkova-Hristova, Stojan Peric, Sushan Luo, Anders Oldfors, Kate Taylor, Stuart H. Ralston, Tanya Stojkovic, Conrad C. Weihl, Jordi Díaz‐Manera

Bibliographic record

VenueJournal of Neurology Neurosurgery & Psychiatry · 2022
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicEndoplasmic Reticulum Stress and Disease
Canadian institutionsOttawa Hospital
FundersNational Institute of Arthritis and Musculoskeletal and Skin DiseasesNational Institute of Neurological Disorders and StrokeNational Institute on AgingRoy J. and Lucille A. Carver College of Medicine, University of IowaSorbonne UniversitéCentro de Investigación Biomédica en Red sobre Enfermedades NeurodegenerativasTaysNational Center of Neurology and PsychiatryInstituto de Salud Carlos IIIOhio State UniversityGöteborgs UniversitetNational and Kapodistrian University of AthensMedizinische Universität WienFaculdade de Medicina da Universidade de São PauloInstitute of GeneticsUniversity of CincinnatiUniversidade de São PauloWarszawski Uniwersytet MedycznyKU LeuvenJohns Hopkins UniversityUniversità degli Studi di PadovaResearch Institute, Nationwide Children's HospitalFudan UniversityUniversitair Ziekenhuis GentUniversität WienNationwide Children's HospitalPusan National UniversityUniversiteit LeidenHuashan HospitalUniwersytet WarszawskiUniversiteit GentUniversity of PennsylvaniaUniversité de Versailles Saint-Quentin-en-YvelinesUniversità degli Studi di MessinaNewcastle UniversityAssistance publique-Hôpitaux de ParisPécsi TudományegyetemUniversity of MinnesotaUniversidad de ChileInstitut National de la Santé et de la Recherche MédicaleUniversity of Oxford
KeywordsMedicineFrontotemporal dementiaWeaknessDysautonomiaRetrospective cohort studyGenotypeDiseaseInternal medicineAge of onsetMuscle biopsyMuscle weaknessPediatricsDementiaSurgeryGeneticsGeneBiologyBiopsy

Abstract

fetched live from OpenAlex

Background Valosin-containing protein (VCP) disease, caused by mutations in the VCP gene, results in myopathy, Paget’s disease of bone (PBD) and frontotemporal dementia (FTD). Natural history and genotype–phenotype correlation data are limited. This study characterises patients with mutations in VCP gene and investigates genotype–phenotype correlations. Methods Descriptive retrospective international study collecting clinical and genetic data of patients with mutations in the VCP gene. Results Two hundred and fifty-five patients (70.0% males) were included in the study. Mean age was 56.8±9.6 years and mean age of onset 45.6±9.3 years. Mean diagnostic delay was 7.7±6 years. Symmetric lower limb weakness was reported in 50% at onset progressing to generalised muscle weakness. Other common symptoms were ventilatory insufficiency 40.3%, PDB 28.2%, dysautonomia 21.4% and FTD 14.3%. Fifty-seven genetic variants were identified, 18 of these no previously reported. c.464G>A (p.Arg155His) was the most frequent variant, identified in the 28%. Full time wheelchair users accounted for 19.1% with a median time from disease onset to been wheelchair user of 8.5 years. Variant c.463C>T (p.Arg155Cys) showed an earlier onset (37.8±7.6 year) and a higher frequency of axial and upper limb weakness, scapular winging and cognitive impairment. Forced vital capacity (FVC) below 50% was as risk factor for being full-time wheelchair user, while FVC <70% and being a full-time wheelchair user were associated with death. Conclusion This study expands the knowledge on the phenotypic presentation, natural history, genotype–phenotype correlations and risk factors for disease progression of VCP disease and is useful to improve the care provided to patient with this complex disease.

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.001
metaresearch head score (Gemma)0.002
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.002
Threshold uncertainty score0.006

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0010.002
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0010.000
Bibliometrics0.0010.001
Science and technology studies0.0010.000
Scholarly communication0.0010.001
Open science0.0000.000
Research integrity0.0010.000
Insufficient payload (model declined to judge)0.0020.001

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.007
GPT teacher head0.235
Teacher spread0.229 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations41
Published2022
Admission routes2
Has abstractyes

Explore more

Same venueJournal of Neurology Neurosurgery & PsychiatrySame topicEndoplasmic Reticulum Stress and DiseaseFrench-language works237,207