Evidence map›Paper›PMID 29978731›Full record

ArticleInternational journal of immunopathology and pharmacology

Familial inheritance and screening of first-degree relatives in common variable immunodeficiency and immunoglobulin A deficiency patients.

Neslihan Edeer Karaca, Ezgi Ulusoy Severcan, Burcu Guven Bilgin, Elif Azarsiz, Sanem Akarcan, Nursen Cigerci Gunaydın, Nesrin Gulez, Ferah Genel, Guzide Aksu, Necil Kutukculer

Open access · goldAbstract read
In one paragraph

Article in International journal of immunopathology and pharmacology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 9 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
9citing papers in PubMed, 2 pooled it
0.8field-weighted citation impact, top 30% 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

9 citing papers in PubMed, 2 syntheses or guidelines pooled it, 18 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
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  7. Review
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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

10 authors at 2 institutions in 1 country.

Neslihan Edeer Karaca1 Department of Pediatric Immunology, Faculty of Medicine, Ege University, Izmir, Turkey.
Ezgi Ulusoy Severcan1 Department of Pediatric Immunology, Faculty of Medicine, Ege University, Izmir, Turkey.
Burcu Guven Bilgin1 Department of Pediatric Immunology, Faculty of Medicine, Ege University, Izmir, Turkey.
Elif Azarsiz1 Department of Pediatric Immunology, Faculty of Medicine, Ege University, Izmir, Turkey.
Sanem Akarcan1 Department of Pediatric Immunology, Faculty of Medicine, Ege University, Izmir, Turkey.
Nursen Cigerci Gunaydın1 Department of Pediatric Immunology, Faculty of Medicine, Ege University, Izmir, Turkey.
Nesrin Gulez2 Dr Behcet Uz Children Training and Research Hospital, Department of Immunology, Izmir, Turkey.
Ferah Genel2 Dr Behcet Uz Children Training and Research Hospital, Department of Immunology, Izmir, Turkey.
Guzide Aksu1 Department of Pediatric Immunology, Faculty of Medicine, Ege University, Izmir, Turkey.
Necil Kutukculer1 Department of Pediatric Immunology, Faculty of Medicine, Ege University, Izmir, Turkey.
Ege University · TRDr. Behçet Uz Çocuk Hastalıkları Hastanesi · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Common variable immunodeficiency (CVID) and immunoglobulin A deficiency (IgAD) are the most prevalent primary immunodeficiency disorders. High rates of familial inheritance have been described in CVID and IgAD, but it is unknown in different ethnic populations. We aimed to determine the prevalence of familial cases and whether they showed more severe clinical characteristics than sporadic ones in Turkish patients. A total of 40 CVID and 70 IgAD patients and their 251 first-degree relatives (FDRs) were evaluated. Demographic, clinical, and laboratory data were reviewed. A familial case was defined as a patient with at least one affected FDR (A-FDR). The rate of parental consanguinity was 19.1%. There were 37 familial cases (37/110) (33.6%) with at least one A-FDR. There were 48 A-FDRs who had immunoglobulins lower than age-related normals (48/251) (19.1%). Pulmonary infections were significantly higher in familial cases. To our knowledge, this study includes the highest number of CVID/IgAD patients and their FDRs in literature. Familial cases are at least 30% of the IgAD and CVID patients, and they have more frequent lower respiratory tract infections than sporadic ones, so these patients have to be evaluated depending on their being familial or sporadic for better management. The risk of carrying any immunologic alterations in relatives of patients with IgAD and CVID is approximately 20%. Although most A-FDRs are asymptomatic, considering the risk of progression to CVID by age, we highly recommend routine screening for FDRs.

Indexed as

ConsanguinityAdultCommon Variable ImmunodeficiencyFemaleHeredityHumansIgA DeficiencyImmunoglobulin AMaleMiddle AgedPedigreeTurkeyImmunoglobulin ACVIDfamilialIgA deficiencyscreening

Identifiers

PMID29978731
PMCPMC6073834
OpenAlexW2833987878

What OpenQuestion holds

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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.