Evidence map›Paper›PMID 31223240›Full record

ArticleNoro psikiyatri arsivi2019

Mannose-Binding Lectin 2 Gene Polymorphism in PANDAS Patients.

Gonca Gül Çelik, Didem Arslan Taş, Ayşegül Yolga Tahiroglu, Eren Erken, Gülşah Seydaoğlu, Perihan Çam Ray, Ayşe Avci

Open access · greenAbstract read
In one paragraph

Article in Noro psikiyatri arsivi, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
0.8field-weighted citation impact, top 24% 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

3 citing papers in PubMed, 3 citations in OpenAlex.

  1. Article
  2. Review
  3. Alterations in the Nervous System and Gut Microbiota afterInternational journal of molecular sciences · 2020
    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

7 authors at 1 institution in 1 country.

Gonca Gül ÇelikDepartment of Child Psychiatry, Çukurova University School of Medicine, Adana, Turkey.
Didem Arslan TaşDepartment of Internal Medicine, Rheumatology-Immunology, Çukurova University School of Medicine, Adana, Turkey.
Ayşegül Yolga TahirogluDepartment of Child Psychiatry, Çukurova University School of Medicine, Adana, Turkey.
Eren ErkenDepartment of Internal Medicine, Rheumatology-Immunology, Çukurova University School of Medicine, Adana, Turkey.
Gülşah SeydaoğluDepartment of Biostatistics, Çukurova University School of Medicine, Adana, Turkey.
Perihan Çam RayDepartment of Child Psychiatry, Çukurova University School of Medicine, Adana, Turkey.
Ayşe AvciDepartment of Child Psychiatry, Çukurova University School of Medicine, Adana, Turkey.
Cukurova University · TR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionPediatric autoimmune neuropsychiatric disorders associated with streptococcal infections (PANDAS), a subgroup of obsessive-compulsive disorder (OCD), has received much attention even though the specific underlying mechanisms remain unknown. Mannose-binding lectin (MBL) is a key factor in the innate immune response. The aim of this study was to investigate the role of MBL2 gene polymorphisms in pediatric OCD patients diagnosed as PANDAS, PANDAS-Variant and non-PANDAS.

methodsThe study included 102 pediatric OCD patients (59 [57.8% ] PANDAS, 20 [19.6% ] non-PANDAS, and 23 [22.5% ] PANDAS-Variant) and 60 healthy controls. Polymorphisms at codon 52, 54 and 57 of the MBL2 gene were investigated.

resultsCodon 54 polymorphism and any variant of MBL2 gene were significantly more frequent in the OCD group than in the control group (OR=2.97, 95% CI: 1.26-6.97; and OR=2.66, 95% CI: 1.32-5.38, respectively). According to regression analysis, the presence of any variant of MBL2 gene was found in 14.50-fold increased frequency in the PANDAS subgroup compared with the non-PANDAS subgroup (95% CI: 2.49-84.19).

conclusionsOur findings support an association between MBL2 genotypes and pediatric OCD, particularly PANDAS-OCD.

Indexed as

Mannose-binding-lectin2 geneobsessive-compulsive disorderpediatric autoimmune neuropsychiatric disorders associated with streptococcal infections

Identifiers

PMID31223240
PMCPMC6563857
OpenAlexW2795786790

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.