Literature DB >> 22971142

Common genetic variants of the BMP4, BMPR1A, BMPR1B, and ACVR1 genes, left ventricular mass, and other parameters of the heart in newborns.

Iwona Gorący1, Krzysztof Safranow, Grażyna Dawid, Karolina Skonieczna-Żydecka, Mariusz Kaczmarczyk, Jarosław Gorący, Beata Loniewska, Andrzej Ciechanowicz.   

Abstract

The members of the family of bone morphogenetic proteins (BMPs) are important regulators in cardiac development. The present study was designed to evaluate the effect of common genetic variants of BMP-4 and its receptors BMPR1A, BMPR1B, and ACVR1 on left ventricular mass (LVM) and other parameters of the heart and blood pressure in newborns. The study included 210 healthy newborns. Two-dimensional M-mode echocardiography was used to assess LVM between days 3 and 4 after birth. Polymorphisms were determined by the polymerase chain reaction-restriction fragment length polymorphism technique. We found lack of associations between LVM, values of blood pressure, and the BMP4, BMPR1A, BMPR1B, and ACVR1 genotypes. A significant association was observed between the 455C allele of BMP4 and increased left ventricular internal diameter systolic (p=0.004) and between 1650T allele of BMPR1B and lower left atrium diameter (p=0.038). Presence of the 455C allele of BMP4 and the 8474T allele of ACVR1 gene was significantly associated with decreased left ventricular ejection fraction (LVEF) (p=0.0004 and p=0.046, respectively). The 455C allele of BMP4 and the 8474T allele of ACVR1 may play a role as significant predictors for decreased LVEF in newborns.

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Year:  2012        PMID: 22971142     DOI: 10.1089/gtmb.2012.0164

Source DB:  PubMed          Journal:  Genet Test Mol Biomarkers        ISSN: 1945-0257


  6 in total

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Authors:  Rebecca M Lewis; Jesse J Keller; Liangcai Wan; Jennifer S Stone
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3.  The association between BMP4 gene polymorphism and its serum level with the incidence of LVH in hypertensive patients.

Authors:  G L Gu; Q Y Yang; R L Zeng; X L Xu
Journal:  J Transl Med       Date:  2015-01-16       Impact factor: 5.531

4.  Recessive ciliopathy mutations in primary endocardial fibroelastosis: a rare neonatal cardiomyopathy in a case of Alstrom syndrome.

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Journal:  J Mol Med (Berl)       Date:  2021-08-13       Impact factor: 5.606

5.  High-Density Genotypes of Inbred Mouse Strains: Improved Power and Precision of Association Mapping.

Authors:  Christoph D Rau; Brian Parks; Yibin Wang; Eleazar Eskin; Petr Simecek; Gary A Churchill; Aldons J Lusis
Journal:  G3 (Bethesda)       Date:  2015-07-28       Impact factor: 3.154

6.  Association of genetic variation in calmodulin and left ventricular mass in full-term newborns.

Authors:  Iwona Gorący; Jarosław Gorący; Karolina Skonieczna-Żydecka; Mariusz Kaczmarczyk; Grażyna Dawid; Andrzej Ciechanowicz
Journal:  Int J Genomics       Date:  2013-11-05       Impact factor: 2.326

  6 in total

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