Evidence map›Paper›PMID 35055435›Full record

ArticleJournal of personalized medicine2022

"Spazio Huntington": Tracing the Early Motor, Cognitive and Behavioral Profiles of Kids with Proven Pediatric Huntington Disease and Expanded Mutations > 80 CAG Repeats.

Federica Graziola, Sabrina Maffi, Melissa Grasso, Giacomo Garone, Simone Migliore, Eugenia Scaricamazza, Consuelo Ceccarelli, Melissa Casella, Ludovica Busi, Barbara D'Alessio and 5 more

Open access · goldAbstract read
In one paragraph

Article in Journal of personalized medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.4field-weighted citation impact, top 49% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Clinical Review of Juvenile Huntington's Disease.Journal of Huntington's disease · 2024
    Review
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

15 authors at 3 institutions in 1 country.

Federica GraziolaNeurology Unit, Department of Neurosciences, IRCCS Bambino Gesù Children Hospital, 00146 Rome, Italy.ORCID 0000-0003-1554-9517
Sabrina MaffiHuntington and Rare Diseases Unit, Fondazione IRCCS Casa Sollievo della Sofferenza Hospital, Viale Cappuccini, 71013 San Giovanni Rotondo, Italy.
Melissa GrassoNeurology Unit, Department of Neurosciences, IRCCS Bambino Gesù Children Hospital, 00146 Rome, Italy.
Giacomo GaroneNeurology Unit, Department of Neurosciences, IRCCS Bambino Gesù Children Hospital, 00146 Rome, Italy.ORCID 0000-0002-3029-8536
Simone MiglioreHuntington and Rare Diseases Unit, Fondazione IRCCS Casa Sollievo della Sofferenza Hospital, Viale Cappuccini, 71013 San Giovanni Rotondo, Italy.ORCID 0000-0002-2665-231X
Eugenia ScaricamazzaHuntington and Rare Diseases Unit, Fondazione IRCCS Casa Sollievo della Sofferenza Hospital, Viale Cappuccini, 71013 San Giovanni Rotondo, Italy.ORCID 0000-0002-2767-7295
Consuelo CeccarelliItalian League for Research on Huntington Foundation, Via Varese 31, 00185 Rome, Italy.
Melissa CasellaItalian League for Research on Huntington Foundation, Via Varese 31, 00185 Rome, Italy.
Ludovica BusiItalian League for Research on Huntington Foundation, Via Varese 31, 00185 Rome, Italy.
Barbara D'AlessioItalian League for Research on Huntington Foundation, Via Varese 31, 00185 Rome, Italy.
Alessandro De LucaMedical Genetics Division, Fondazione IRCCS Casa Sollievo della Sofferenza Hospital, Viale Cappuccini, 71013 San Giovanni Rotondo, Italy.ORCID 0000-0002-4408-8062
Giovanna Stefania ColafatiNeuroradiology Unit, Imaging Department, IRCCS Bambino Gesù Children Hospital, 00146 Rome, Italy.ORCID 0000-0002-1142-4904
Umberto SabatiniNeuroradiology Unit, Department of Medical and Surgical Sciences, Magna Graecia University, Viale Europa, 88100 Catanzaro, Italy.ORCID 0000-0001-5321-8626
Alessandro CapuanoNeurology Unit, Department of Neurosciences, IRCCS Bambino Gesù Children Hospital, 00146 Rome, Italy.ORCID 0000-0002-7729-7952
Ferdinando SquitieriHuntington and Rare Diseases Unit, Fondazione IRCCS Casa Sollievo della Sofferenza Hospital, Viale Cappuccini, 71013 San Giovanni Rotondo, Italy.ORCID 0000-0002-7397-1727
Bambino Gesù Children's Hospital · ITCasa Sollievo della Sofferenza · ITMagna Graecia University · IT

Funding

Italian Ministry of Health RF-2016-02364123LIRH Foundation RC2101MH09
6 · The paper itself

Abstract

The "Spazio Huntington-A Place for Children" program was launched in 2019. The aim was to contact at risk kids within Huntington disease (HD) families, to provide counseling to their parents and to start a prospective follow-up of kids suspicious to manifest pediatric HD (PHD). We met 25 at risk kids in two years, four of whom with PHD and highly expanded (HE) mutations beyond 80 CAG repeats. We rated motor, neuropsychological and behavioral changes in all PHD kids by the Unified HD Rating Scale (UHDRS)-total motor score (TMS) and additional measures of (1) cognitive level (Leiter International Performance Scale), (2) adaptive functioning (Adaptive Behavior Assessment Systems), (3) receptive language (Peabody Picture Vocabulary Test) and (4) behavioral abnormalities (Child Behavior Check List and Children's Yale-Brown Obsessive Compulsive Scale). All PHD kids showed a severe progression of neurological and psychiatric manifestations including motor, cognitive and behavioral changes. The magnetic resonance imaging contributed to confirm the suspicious clinical observation by highlighting very initial striatum abnormalities in PHD. Spazio Huntington is a program to prospectively study PHD, the most atypical face of HD, and may represent the basis to recruit PHD patients in future clinical trials.

Indexed as

atypical Huntington diseasehigh CAG expansionsobservational studiespediatric Huntington diseaseprospective studies

Identifiers

PMID35055435
PMCPMC8778418
OpenAlexW4205670756

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

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.