Literature DB >> 30689460

The roles of vascular endothelial growth factor gene polymorphisms in congenital heart diseases: a meta-analysis.

Weiping Wang1, Aiping Xu1, Hong Xu1.   

Abstract

We performed this study to better elucidate the correlations between vascular endothelial growth factor (VEGF) gene polymorphisms and congenital heart diseases (CHD). Eligible articles were searched in PubMed, Medline, Embase and CNKI. Eighteen studies were finally included in our meta-analysis. A significant association with the risk of CHD was detected for the rs1570360 polymorphism in additive comparison in overall analyses. Further subgroup analyses according to ethnicity of study participants and type of disease demonstrated that the rs833061 polymorphism was significantly correlated with the risk of CHD in Asians under additive genetic model, and the rs3025039 polymorphism was significantly correlated with the risk of Tetralogy of Fallot (TOF) in dominant, recessive and allele models. In conclusion, our findings indicated that rs1570360 and rs833061 polymorphisms may affect the risk of CHD. In addition, the rs3025039 polymorphism may serve as a genetic biomarker of TOF.

Entities:  

Keywords:  Vascular endothelial growth factor; congenital heart diseases; gene polymorphisms

Mesh:

Substances:

Year:  2019        PMID: 30689460     DOI: 10.1080/08977194.2018.1513505

Source DB:  PubMed          Journal:  Growth Factors        ISSN: 0897-7194            Impact factor:   2.511


  3 in total

Review 1.  The physiological and pathological functions of VEGFR3 in cardiac and lymphatic development and related diseases.

Authors:  Richard M Monaghan; Donna J Page; Pia Ostergaard; Bernard D Keavney
Journal:  Cardiovasc Res       Date:  2021-07-07       Impact factor: 10.787

2.  KDR (VEGFR2) Genetic Variants and Serum Levels in Patients with Rheumatoid Arthritis.

Authors:  Agnieszka Paradowska-Gorycka; Barbara Stypinska; Andrzej Pawlik; Damian Malinowski; Katarzyna Romanowska-Prochnicka; Malgorzata Manczak; Marzena Olesinska
Journal:  Biomolecules       Date:  2019-08-09

3.  Susceptibility to Heart Defects in Down Syndrome Is Associated with Single Nucleotide Polymorphisms in HAS 21 Interferon Receptor Cluster and VEGFA Genes.

Authors:  Carmela Rita Balistreri; Claudia Leonarda Ammoscato; Letizia Scola; Tiziana Fragapane; Rosa Maria Giarratana; Domenico Lio; Maria Piccione
Journal:  Genes (Basel)       Date:  2020-11-28       Impact factor: 4.096

  3 in total

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