Evidence map›Paper›PMID 26846287›Full record

ArticleJournal of clinical immunology2016

The Challenge of Immunoglobulin-G Subclass Deficiency and Specific Polysaccharide Antibody Deficiency--a Dutch Pediatric Cohort Study.

Ellen J H Schatorjé, Everieke de Jong, Roeland W N M van Hout, Yumely García Vivas, Esther de Vries

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Article in Journal of clinical immunology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.6field-weighted citation impact, top 18% 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

11 citing papers in PubMed, 26 citations in OpenAlex.

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  7. B Cell Disorders in Children: Part II.Current allergy and asthma reports · 2020
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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

5 authors at 3 institutions in 1 country.

Ellen J H SchatorjéDepartment of Pediatrics, Jeroen Bosch Hospital, 's-Hertogenbosch, The Netherlands.
Everieke de JongDepartment of Pediatrics, Jeroen Bosch Hospital, 's-Hertogenbosch, The Netherlands.
Roeland W N M van HoutDepartment of Linguistics, Radboud University, Nijmegen, The Netherlands.
Yumely García VivasDepartment of Pediatrics, Jeroen Bosch Hospital, 's-Hertogenbosch, The Netherlands.
Esther de VriesDepartment of Pediatrics, Jeroen Bosch Hospital, 's-Hertogenbosch, The Netherlands. esid@estherdevries.nl.
Jeroen Bosch Ziekenhuis · NLRadboud University Nijmegen · NLTilburg University · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeImmunoglobulin(Ig)G-subclass deficiency and specific polysaccharide antibody deficiency (SPAD) are among the most frequent causes of recurrent respiratory infections in children. Little is known about their prevalence, clinical presentation and prognosis. No study has been published in a Western-European nor in a mainly non-tertiary cohort until now. Therefore, we performed this observational cohort study in children recruited from secondary and tertiary pediatric practices all over The Netherlands.

methodsDutch pediatricians were monthly asked to report patients with IgG-subclass deficiency and/or SPAD. Demographic, clinical and laboratory characteristics were collected. Separate informed consent was asked from parents and children (≥ 12 years of age) for annual update of the medical status.

results49 children with confirmed IgG-subclass deficiency and/or SPAD were included. The majority of children (69%) was reported by four (out of 12) secondary hospitals with a pediatric immunologist in the staff. 45 children had ≥ 1 low IgG-subclass level and 11 had SPAD. IgG2 deficiency was the most prevalent IgG-subclass deficiency (37/49;76%). 10% of these children already showed bronchiectasis. Two-thirds were male (33/49;67%, p = 0.015). From 10 years of age, only boys were left and only boys showed progressive immunodeficiency during follow-up (11/24; 46%).

conclusionsThis is the first Western-European mainly non-tertiary cohort of children with IgG-subclass deficiency and/or SPAD. The disease course is not always benign, especially in boys. Most children were reported and managed in secondary hospitals with a pediatric immunologist in the staff. To identify more patients, the awareness of these diseases among general pediatricians should increase.

Indexed as

AdolescentChildChild, PreschoolCohort StudiesFemaleHumansIgG DeficiencyImmunoglobulin GImmunoglobulin IsotypesMaleNetherlandsPhenotypePolysaccharidesPolysaccharides, BacterialImmunoglobulin GImmunoglobulin IsotypesPolysaccharidesPolysaccharides, Bacterialantibody deficiencychildIgG subclass deficiencyPrimary immunodeficiencyspecific polysaccharide antibody deficiency

Identifiers

PMID26846287
OpenAlexW2253418903

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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.