Evidence map›Paper›PMID 38676773›Full record

Observational studyJournal of clinical immunology2024

Immunological Aspects of Kabuki Syndrome: A Retrospective Multicenter Study of the Italian Primary Immunodeficiency Network (IPINet).

Linda Rossini, Silvia Ricci, Davide Montin, Chiara Azzari, Eleonora Gambineri, Marco Tellini, Francesca Conti, Andrea Pession, Francesco Saettini, Samuele Naviglio and 17 more

Abstract readMulticenter StudyObservational Study
PubMed Publisher
In one paragraph

Observational study in Journal of clinical immunology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.7field-weighted citation impact, top 17% 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

10 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
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  3. Review
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  7. Article
  8. Observational
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  10. 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

27 authors at 13 institutions in 1 country.

Linda RossiniPediatric Hematology, Oncology and Stem Cell Transplant Division, Padua University Hospital, Via Giustiniani 3, Padua, 35128, Italy.
Silvia RicciImmunology, Pediatric Unit, IRCCS Meyer Children's Hospital, viale G.Pieraccini 24, Florence, 50139, Italy.
Davide MontinImmunology and Rheumatology Unit, Regina Margherita Children Hospital, Turin, Italy.
Chiara AzzariImmunology, Pediatric Unit, IRCCS Meyer Children's Hospital, viale G.Pieraccini 24, Florence, 50139, Italy.
Eleonora GambineriCentre of Excellence, Department of Pediatric Hematology-Oncology, IRCCS Meyer Children's Hospital, Florence, Italy.
Marco TelliniCentre of Excellence, Department of Pediatric Hematology-Oncology, IRCCS Meyer Children's Hospital, Florence, Italy.
Francesca ContiPediatric Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, 40138, Italy.
Andrea PessionPediatric Unit, IRCCS Azienda Ospedaliero-Universitaria di Bologna, Bologna, 40138, Italy.
Francesco SaettiniTettamanti Research Center, University of Milano-Bicocca, University of Milano Bicocca, Monza, Italy.
Samuele NaviglioInstitute for Maternal and Child Health IRCCS "Burlo Garofolo", Trieste, Italy.
Erica ValencicInstitute for Maternal and Child Health IRCCS "Burlo Garofolo", Trieste, Italy.
Andrea MagnolatoInstitute for Maternal and Child Health IRCCS "Burlo Garofolo", Trieste, Italy.
Lucia BaselliDepartment of Pediatrics, Fondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico, Milan, Italy.
Sara AzzoliniUOC Pediatria, San Bortolo Hospital, Vicenza, Italy.
Rita ConsoliniSection of Clinical and Laboratory Immunology, Division of Pediatrics, Department of Clinical and Experimental Medicine, University of Pisa, Pisa, Italy.
Lucia LeonardiMaternal, Infantile and Urological Sciences Department, Sapienza University of Rome, Rome, Italy.
Irene D'AlbaPaediatric Haematology-Oncology, Maternal Infant Hospital "G. Salesi", Ancona, Italy.
Elisa CarraroPediatric Hematology, Oncology and Stem Cell Transplant Division, Padua University Hospital, Via Giustiniani 3, Padua, 35128, Italy.
Roberta RomanoDepartment of Translational Medical Sciences, Section of Pediatrics, Federico II University, Naples, Italy.
Daniela MelisDepartment of Medicine, Surgery and Dentistry, University of Salerno, Via Salvador Allende Baronissi, Campania, 84081, Italy.
Stefano StagiDepartment of Health Sciences, University of Florence, Florence, Italy.
Emilia CirilloDepartment of Translational Medical Sciences, Section of Pediatrics, Federico II University, Naples, Italy.
Giuliana GiardinoDepartment of Translational Medical Sciences, Section of Pediatrics, Federico II University, Naples, Italy.
Alessandra BiffiPediatric Hematology, Oncology and Stem Cell Transplant Division, Padua University Hospital, Via Giustiniani 3, Padua, 35128, Italy.
Claudio PignataDepartment of Translational Medical Sciences, Section of Pediatrics, Federico II University, Naples, Italy.
Maria Caterina PuttiPediatric Hematology, Oncology and Stem Cell Transplant Division, Padua University Hospital, Via Giustiniani 3, Padua, 35128, Italy.
Antonio MarzolloPediatric Hematology, Oncology and Stem Cell Transplant Division, Padua University Hospital, Via Giustiniani 3, Padua, 35128, Italy. antonio.marzollo@aopd.veneto.it.ORCID 0000-0003-2177-8500
Meyer Children's Hospital · ITUniversity of Padua · ITFederico II University Hospital · ITIRCCS Materno Infantile Burlo Garofolo · ITAzienda USL di Bologna · ITFondazione IRCCS Ca' Granda Ospedale Maggiore Policlinico · ITOspedale Regina Margherita · ITOspedale San Bortolo · ITOspedali Riuniti di Ancona · ITSapienza University of Rome · ITUniversity of Milano-Bicocca · ITUniversity of Pisa · ITUniversity of Salerno · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Kabuki Syndrome (KS) is a multisystemic genetic disorder. A portion of patients has immunological manifestations characterized by increased susceptibility to infections and autoimmunity. Aiming to describe the clinical and laboratory immunological aspects of KS, we conducted a retrospective multicenter observational study on patients with KS treated in centers affiliated to the Italian Primary Immunodeficiency Network.Thirty-nine patients were enrolled, with a median age at evaluation of 10 years (range: 3 m-21y). All individuals had organ malformations of variable severity. Congenital heart defect (CHD) was present in 19/39 patients (49%) and required surgical correction in 9/39 (23%), with associated thymectomy in 7/39 (18%). Autoimmune cytopenia occurred in 6/39 patients (15%) and was significantly correlated with thymectomy (p < 0.002), but not CHD. Individuals with cytopenia treated with mycophenolate as long-term immunomodulatory treatment (n = 4) showed complete response. Increased susceptibility to infections was observed in 22/32 patients (69%). IgG, IgA, and IgM were low in 13/29 (45%), 13/30 (43%) and 4/29 (14%) patients, respectively. Immunoglobulin substitution was required in three patients. Lymphocyte subsets were normal in all patients except for reduced naïve T-cells in 3/15 patients (20%) and reduced memory switched B-cells in 3/17 patients (18%). Elevated CD3 + TCRαβ + CD4-CD8-T-cells were present in 5/17 individuals (23%) and were correlated with hematological and overall autoimmunity (p < 0.05).In conclusion, immunological manifestations of KS in our cohort include susceptibility to infections, antibody deficiency, and autoimmunity. Autoimmune cytopenia is correlated with thymectomy and elevated CD3 + TCRαβ + CD4-CD8-T-cells, and benefits from treatment with mycophenolate.

Indexed as

Abnormalities, MultipleFaceHematologic DiseasesVestibular DiseasesAdolescentAdultAutoimmunityChildChild, PreschoolFemaleHumansInfantItalyMaleRetrospective StudiesYoung AdultAutoimmunityEpigeneticInborn errors of immunityKabuki syndromePrimary immunoregulatory disorderRecurrent infectionsThymectomy

Identifiers

PMID38676773
OpenAlexW4395702321

What OpenQuestion holds

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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.