Literature DB >> 27884229

What Have We Learned from the Genetics of Hypertension?

Friedrich C Luft1.   

Abstract

Twin studies show that about half the risk of hypertension development is inherited. Mendelian hypertension has elucidated astounding basic pathways contributing to hypertension over (presumably) dietary salt intake or directly through increased peripheral vascular resistance. The Mendelian mutations exercise large effects on blood pressure. Inversely, studying the entire human genome for sources signaling blood pressure has yielded many signals with small effects. Thus far, few loci have been validated or translated into targets. Both genetic strategies are necessary, and much remains to be done. Copyright Â
© 2016 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Blood pressure; Genetics; Genomewide association studies; Hypertension; Mendelian

Mesh:

Year:  2017        PMID: 27884229     DOI: 10.1016/j.mcna.2016.08.015

Source DB:  PubMed          Journal:  Med Clin North Am        ISSN: 0025-7125            Impact factor:   5.456


  2 in total

1.  Quantitative evaluation of PPAR-γ2 Pro12Ala polymorphism with hypertension.

Authors:  W Yang; J Wang; W Ye; X Li
Journal:  Herz       Date:  2017-09-18       Impact factor: 1.443

Review 2.  Application of Single-Nucleotide Polymorphism-Related Risk Estimates in Identification of Increased Genetic Susceptibility to Cardiovascular Diseases: A Literature Review.

Authors:  Szilvia Fiatal; Róza Ádány
Journal:  Front Public Health       Date:  2018-01-31
  2 in total

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