Thromb Haemost 2007; 97(03): 458-463
DOI: 10.1160/TH06-11-0676
Cardiovascular Biology and Cell Signalling
Schattauer GmbH

Factor XIII Val34Leu variant protects against coronary artery disease

A meta-analysis
Zoltán Vokó
1   Department of Preventive Medicine, Faculty of Public Health, Medical & Health Science Centre University of Debrecen, Debrecen, Hungary
4   Public Health Research Group of the Hungarian Academy of Sciences, at the Medical & Health Science Centre, University of Debrecen, Debrecen, Hungary
,
Zsuzsanna Bereczky
2   Clinical Research Center, Medical & Health Science Centre, University of Debrecen, Debrecen, Hungary
,
Éva Katona
2   Clinical Research Center, Medical & Health Science Centre, University of Debrecen, Debrecen, Hungary
,
Róza Ádány
1   Department of Preventive Medicine, Faculty of Public Health, Medical & Health Science Centre University of Debrecen, Debrecen, Hungary
4   Public Health Research Group of the Hungarian Academy of Sciences, at the Medical & Health Science Centre, University of Debrecen, Debrecen, Hungary
,
László Muszbek
2   Clinical Research Center, Medical & Health Science Centre, University of Debrecen, Debrecen, Hungary
3   Thrombosis and Hemostasis Research Group of the Hungarian Academy of Sciences, at the Medical & Health Science Centre, University of Debrecen, Debrecen, Hungary
› Author Affiliations
Financial support: The study was supported by grants from the National Research and Development Program (NKFP-1B/0013/2002, NKFP-1/0003/2005), from the Hungarian National Research Fund (OTKAT043086, OTKAT048964), from the Hungarian Academy of Sciences (MTA 11003, 2006TKI227), and from the Hungarian Ministry of Health and Social Affairs (ETT 406/2006).
Further Information

Publication History

Received 30 November 2006

Accepted after revision 19 January 2007

Publication Date:
28 November 2017 (online)

Summary

Several studies suggested that Val34Leu variant of factor XIII (FXIII) might have a protective effect against coronary artery disease (CAD), but studies not supporting these findings have also been published. The authors performed a meta-analysis of 16 studies on 5,346 cases and 7,053 controls that investigated the association between Val34Leu polymorphism and CAD defined as history of myocardial infarction or significant stenosis on a coronary artery assessed by coronary angiography. Because of the heterogeneity of the study-specific results, the pooled effect estimates were calculated by a random-effects empirical Bayes model. The combined odds ratios for CAD were 0.82 (95% confidence interval [95% Cl] 0.73, 0.94) for the heterozygotes of the FXIIIVal34Leu variant, 0.89 (95% CI 0.69, 1.13) for the homozygotes, and 0.81 (95% CI 0.70, 0.92) for the heterozygotes and homozygotes combined. The results were essentially the same when only myocardial infarction was considered as outcome. The beneficial effect of the polymorphism might be smaller than the effect estimates obtained in this metaanalysis, because the analysis raised the possibility of publication bias. Data published in the literature suggest that gene-gene and gene-environmental interactions might significantly influence the protective effect of FXIII-AVal34Leu polymorphism.

 
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