Evidence map›Paper›PMID 24449362›Full record

ArticleMolecular biology reports2014

ABO blood group polymorphisms and risk for ischemic stroke and peripheral arterial disease.

Adriano de Paula Sabino, Daniel Dias Ribeiro, Caroline Pereira Domingheti, Danyelle Romana Alves Rios, Luci Maria SantAna Dusse, Maria das Graças Carvalho, Ana Paula Fernandes

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Article in Molecular biology reports, 2014. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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.

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3 · Its place in the literature

Who cites it

12 citing papers in PubMed.

  1. Article
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  8. Allelic distribution ofAging medicine (Milton (N.S.W)) · 2020
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4 · The record

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5 · Who and what money

Authors and funding

7 authors.

Adriano de Paula SabinoFaculty of Pharmacy, Federal University of Minas Gerais, Av. Antônio Carlos 6627, Pampulha, Belo Horizonte, MG, Brazil, adriansabin@yahoo.com.
Daniel Dias Ribeiro
Caroline Pereira Domingheti
Danyelle Romana Alves Rios
Luci Maria SantAna Dusse
Maria das Graças Carvalho
Ana Paula Fernandes

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Recent studies have demonstrated association between ABO blood system and thrombosis, indicating that individuals belonging to non-O blood groups (A, B or AB) present an increased risk of venous thrombosis, heart disease, and ischemic stroke (IS) as compared to O blood group carriers. In this study, we investigated the frequency of ABO blood group polymorphisms and its association with IS and peripheral arterial disease. Significant differences were observed for O1 (OR 0.57, 95% CI 0.35-0.95, p < 0.05) and O2 (OR 3.47, 95% CI 1.15-10.28, p < 0.05) alleles among IS patients while significant differences were observed for B phenotype (26.3 vs 9.5%, OR 3.42, 95% CI 1.32-8.76, p = 0.01, patients vs controls, respectively) and alleles A1 (OR 0.31, 95% CI 0.11-0.84, p < 0.05), O2 (OR 4.61, 95% CI 1.59-13.23, p < 0.01) and B (OR 3.42, 95% CI 1.62-7.13, p < 0.001) alleles for PAD patients. O1 allele was an independent variable (OR 0.27, 95% CI 0.12-0.57, p < 0.001) for IS patients. These data suggest the relationship of non-O blood groups in pathogenesis of thrombosis events and a possible protective effect of O blood group.

Indexed as

Polymorphism, GeneticABO Blood-Group SystemAdultAllelesFemaleGenetic Association StudiesGenetic Predisposition to DiseaseHumansMaleMiddle AgedPeripheral Arterial DiseaseRisk FactorsStrokeABO Blood-Group System

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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.