Evidence map›Paper›PMID 36817395›Full record

ArticleCentral-European journal of immunology2022

Evaluation of immunological abnormalities in patients with rare syndromes.

Yahya Gul, Hasan Kapaklı, Selma Erol Aytekin, Şukru Nail Guner, Sevgi Keles, Ayşe Gül Zamani, Mahmut Selman Yıldırım, Ïsmail Reisli

Open access · goldAbstract read
In one paragraph

Article in Central-European journal of immunology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed, 1 pooled it
0.8field-weighted citation impact, top 26% 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

2 citing papers in PubMed, 1 synthesis or guideline pooled it, 5 citations in OpenAlex.

  1. Pooled it
  2. Article
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

8 authors at 1 institution in 1 country.

Yahya GulNecmettin Erbakan University, Meram Medical School, Division of Pediatric Allergy and Immunology, Konya, Turkey.
Hasan KapaklıBallkesir City Hospital, Pediatric Allergy and Immunology Clinic, Ballkesir, Turkey.
Selma Erol AytekinNecmettin Erbakan University, Meram Medical School, Division of Pediatric Allergy and Immunology, Konya, Turkey.
Şukru Nail GunerNecmettin Erbakan University, Meram Medical School, Division of Pediatric Allergy and Immunology, Konya, Turkey.
Sevgi KelesNecmettin Erbakan University, Meram Medical School, Division of Pediatric Allergy and Immunology, Konya, Turkey.
Ayşe Gül ZamaniNecmettin Erbakan University, Meram Medical School, Department of Medical Genetics, Konya, Turkey.
Mahmut Selman YıldırımNecmettin Erbakan University, Meram Medical School, Department of Medical Genetics, Konya, Turkey.
Ïsmail ReisliNecmettin Erbakan University, Meram Medical School, Division of Pediatric Allergy and Immunology, Konya, Turkey.
Necmettin Erbakan University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Recurrent infections are important problems in syndromic patients. This study aimed to evaluate immunological abnormalities in patients who presented with recurrent infections and were diagnosed with rare syndromes. Material and methods: This retrospective analysis included 14 patients with complaints of recurrent infections, all of whom were diagnosed with a rare syndrome. Results: The study group consisted of patients with Aicardi syndrome, Brugada syndrome, Phelan- McDermid syndrome, trichothiodystrophy, LEOPARD syndrome, Prader-Willi syndrome, Seckel syndrome, trisomy 18 (Edwards' syndrome), Wiedemann-Steiner syndrome, West syndrome, Williams syndrome, 47,XYY syndrome, 16p13 deletion syndrome, and 13q1.3 deletion syndrome. Seven patients (50%) were girls and seven (50%) were boys (mean age, 56.7 ±32.9 months; median [range] age: 45.5 [27-153] months). There were high rates of consanguinity (50%), cesarean section delivery (71%), and hospitalization in the intensive care unit (78.5%). No patients had a family history of immunodeficiency. On admission, all patients exhibited humoral and/or cellular immune system abnormalities. During the follow-up period, all T-cell abnormalities were improved after immunoglobulin replacement therapy (IGRT), while B-cell abnormalities persisted. These findings suggested that the patients predominantly had antibody deficiencies associated with mild T-cell abnormalities because of recurrent infections. The rates of infections and hospitalizations were significantly reduced after IGRT (p < 0.001); the rate of intensive care unit admission also significantly decreased (from 78.5% to 21.4%). Two of the three oxygen-dependent patients exhibited improvement therein. IGRT was discontinued in two patients with significant clinical improvement during follow-up. Conclusions: An immunological evaluation should be considered in pediatric patients with rare syndromes and recurrent infections. IGRT may help to improve the prognoses of these patients.

Indexed as

immunodeficiencyimmunoglobulin replacement therapyrare syndromerecurrent infection

Identifiers

PMID36817395
PMCPMC9901257
OpenAlexW4320157014

What OpenQuestion holds

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LicenceCC BY-NC-SA
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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.