Evidence map›Paper›PMID 32729323›Full record

ArticleClinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis

Toll-Like Receptor 9 (TLR9) Gene C/T (rs352140) Polymorphisms in Adult Primary Immune Thrombocytopenia.

Alaa Efat Hassan, Sabry Shoeib, Esaam Abdelmohsen, Aida Nazir, Ashraf Dawood, Heba Gamal, Mohamed Abdelhafez

Open access · goldAbstract read
In one paragraph

Article in Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
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

7 citing papers in PubMed, 13 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Biology · 2023
    Article
  5. Review
  6. Innate immunity - the hallmark ofWorld journal of clinical cases · 2021
    Article
  7. Endothelial Activation and Immune Thrombocytopenia: An Engagement Waiting for Consolidation.Clinical and applied thrombosis/hemostasis : official journal of the International Academy of Clinical and Applied Thrombosis/Hemostasis
    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

7 authors at 3 institutions in 1 country.

Alaa Efat HassanHematology Unit, Internal Medicine Department, Faculty of Medicine, Menoufia University, Menoufia, Egypt.ORCID https://orcid.org/0000-0001-8148-3443
Sabry ShoeibHematology Unit, Internal Medicine Department, Faculty of Medicine, Menoufia University, Menoufia, Egypt.
Esaam AbdelmohsenHematology Hospital, Almaady Military Compound, Cairo, Egypt.
Aida NazirHematology Unit, Internal Medicine Department, Faculty of Medicine, Alexandria University, Alexandria, Egypt.
Ashraf DawoodMedical Biochemistry Department, Faculty of Medicine, Menoufia University, Menoufia, Egypt.
Heba GamalHematology Unit, Internal Medicine Department, Faculty of Medicine, Menoufia University, Menoufia, Egypt.
Mohamed AbdelhafezHematology Unit, Internal Medicine Department, Faculty of Medicine, Menoufia University, Menoufia, Egypt.
Menoufia University · EGAlexandria University · EGMilitary Medical Academy · EG

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Immune thrombocytopenia (ITP) is an autoimmune disease characterized by low platelet count and increased bleeding risk. The initial event(s) leading to antiplatelet autoimmunity remains unclear. Toll-like receptors (TLRs) are the most well-characterized pattern recognition receptors and are a transmembrane protein coded by the Toll genes family. In addition to their protective role in immunity, it is also becoming clear that TLRs exhibit homeostatic roles. Toll-like receptors play potential roles in the development of disease and its maintenance. The objective of this study is to evaluate the distribution of TLR9 gene C/T (rs352140) polymorphisms and its possible association with clinicopathological finding in Egyptian adult primary ITP. This study was carried out at Internal Medicine Department, Menoufia University Hospital, Egypt, from August 2018 to January 2020. Eighty adults (≥ 18 years) were enrolled in the study; 40 patients with primary ITP and 40 healthy individuals as controls. Identification of the TLR9 C/T (rs352140) polymorphic variant was performed by polymerase chain reaction-restriction fragment length polymorphism. In our study, we excluded any other causes of secondary ITP. Distribution of the TLR9 C/T genotypes did not exhibit significant deviation between patients and controls. There was no significant difference between studied groups as regards allele (C and T) frequency. There was no significant difference regarding TLR9 gene C/T (rs352140) polymorphisms between Egyptian adult with primary ITP and controls. TLR9 gene C/T (rs352140) polymorphisms have no relation to any of the clinicohematological variables in primary ITP in Egyptians.

Indexed as

AdultCross-Sectional StudiesFemaleGenetic Predisposition to DiseaseGenotypeHumansMalePolymorphism, Single NucleotidePurpura, Thrombocytopenic, IdiopathicToll-Like Receptor 9TLR9 protein, humanToll-Like Receptor 9immune thrombocytopeniapolymorphismToll-like receptors

Identifiers

PMID32729323
PMCPMC7394025
OpenAlexW3045900684

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.