Evidence map›Paper›PMID 27476161›Full record

ArticleNeuromolecular medicine2017

Integrins AV and B8 Gene Polymorphisms and Risk for Intracerebral Hemorrhage in Greek and Polish Populations.

Efthimios Dardiotis, Vasileios Siokas, Tilemachos Zafeiridis, Konstantinos Paterakis, Georgios Tsivgoulis, Maria Dardioti, Savas Grigoriadis, Constantina Simeonidou, Georgia Deretzi, Elias Zintzaras and 2 more

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In one paragraph

Article in Neuromolecular medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 14% 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

14 citing papers in PubMed, 1 synthesis or guideline pooled it, 26 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Review
  4. Medicina (Kaunas, Lithuania) · 2021
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  7. Journal of clinical medicine · 2021
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  8. CYP1A2 rs762551 polymorphism and risk for amyotrophic lateral sclerosis.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2021
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  9. Article
  10. Review
  11. Does SCFD1 rs10139154 Polymorphism Decrease Alzheimer's Disease Risk?Journal of molecular neuroscience : MN · 2019
    Article
  12. Lack of Association of the rs11655081 ARSG Gene with Blepharospasm.Journal of molecular neuroscience : MN · 2019
    Article
  13. Article
  14. 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

12 authors at 6 institutions in 3 countries.

Efthimios DardiotisLaboratory of Neurogenetics, Department of Neurology, Faculty of Medicine, University of Thessaly, University Hospital of Larissa, Biopolis, Mezourlo Hill, 41100, Larissa, Greece.
Vasileios SiokasLaboratory of Neurogenetics, Department of Neurology, Faculty of Medicine, University of Thessaly, University Hospital of Larissa, Biopolis, Mezourlo Hill, 41100, Larissa, Greece.
Tilemachos ZafeiridisIntensive Care Unit, General Hospital of Larissa, Larissa, Greece.
Konstantinos PaterakisDepartment of Neurosurgery, University of Thessaly, University Hospital of Larissa, Larissa, Greece.
Georgios TsivgoulisSecond Department of Neurology, University of Athens, School of Medicine, "Attikon" University Hospital, Athens, Greece.
Maria DardiotiLaboratory of Neurogenetics, Department of Neurology, Faculty of Medicine, University of Thessaly, University Hospital of Larissa, Biopolis, Mezourlo Hill, 41100, Larissa, Greece.
Savas GrigoriadisSecond Department of Neurosurgery, Hippokration University Hospital, Aristotle University of Thessaloniki, Thessaloníki, Greece.
Constantina SimeonidouDepartment of Physiology, Aristotle University of Thessaloniki, Thessaloníki, Greece.
Georgia DeretziDepartment of Neurology, Papageorgiou General Hospital, Thessaloníki, Greece.
Elias ZintzarasDepartment of Biomathematics, University of Thessaly School of Medicine, Larissa, Greece.
Jeremiasz JagiellaDepartment of Neurology, Medical College Jagiellonian University, Kraków, Poland.
Georgios M HadjigeorgiouLaboratory of Neurogenetics, Department of Neurology, Faculty of Medicine, University of Thessaly, University Hospital of Larissa, Biopolis, Mezourlo Hill, 41100, Larissa, Greece. gmhadji@med.uth.gr.
University of Thessaly · GRUniversity Hospital of Larissa · GRAristotle University of Thessaloniki · GRJagiellonian University · PLNational and Kapodistrian University of Athens · GRPapageorgiou General Hospital · GR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Α limited number of genetic variants have been linked to the development of intracerebral hemorrhage (ICH). Ιntegrin AV and/or B8-deficient mice were found to develop ICH. The present candidate gene association study was designed to investigate possible influence of integrin AV (ITGAV) and integrin B8 (ITGB8) gene region polymorphisms on the risk of ICH. 1015 participants (250 Greek and 193 Polish patients with primary ICH and 250 Greek and 322 Polish controls) were included in the study. Using logistic regression analyses, 11 tag single nucleotide polymorphisms (SNPs) for ITGAV and 11 for ITGB8 gene were tested for associations with ICH risk, lobar ICH risk and non-lobar ICH after adjustment for age, gender, history of hypertension and country of origin. Linear regression models were used to test the effect of tag SNPs on the ICH age of onset. Correction for multiple comparisons was carried out. The rs7565633 tag SNP of the ITGAV gene was independently associated with the risk of lobar ICH in the codominant model of inheritance [odds ratio (95 % confidence interval (CI)) 0.56 (0.36-0.86), p = 0.0013]. Furthermore, heterozygous individuals of the rs10251386 and the rs10239099 of the ITGB8 gene had significantly lower age of ICH onset compared to the wild-type genotypes [regression coefficient (b) -3.884 (95 % CI -6.519, -1.249), p = 0.0039 and b = -4.502 (95 % CI -7.159, -1.845), p = 0.0009, respectively]. The present study provides preliminary indication for an influence of ITGAV gene tag SNP in the development of lobar ICH and of ITGB8 gene variants in the age of ICH onset.

Indexed as

Polymorphism, Single NucleotideAgedAged, 80 and overAge of OnsetCase-Control StudiesCerebral CortexCerebral HemorrhageFemaleGene FrequencyGenetic Predisposition to DiseaseGenotypeGreeceHumansIntegrin alphaVIntegrin beta ChainsMaleIntegrin alphaVintegrin beta8Integrin beta ChainsIntegrinsIntracerebral hemorrhageITGAVITGB8PolymorphismTag SNPs

Identifiers

PMID27476161
OpenAlexW2506066353

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.