Literature DB >> 9039094

Genetically complex cardiovascular traits. Origins, problems, and potential solutions.

N J Schork1.   

Abstract

Modern molecular genetic analysis tools are making it possible for researchers to investigate, and in many cases actually disclose, mutations and other genetic factors that contribute to disease susceptibility. However, the ease with which these factors can be identified is dictated by not only the number of factors underlying or influencing the trait, but also by the manner in which these factors interact. Traits that are influenced by multiple genetic and nongenetic factors are termed "complex" genetic traits and are receiving a great deal of attention in the current medical literature. Hypertension and blood pressure regulation are considered paradigmatic complex traits. In this paper, the origin, nature, and dilemmas associated with the analysis of complex traits are considered. Basic biochemical and physiological determinants of blood pressure are described in an effort to show how genetic complexity could arise within an individual, and fundamental concepts in population genetics and evolutionary theory are discussed to expose the reasons certain forms of genetic complexity can emerge and be sustained in the population at large. Methods for approaching the genetic dissection of complex traits and diseases are also enumerated, with simple descriptions of the scientific motivation offered for each. Problems plaguing these approaches are also discussed. Finally, areas for future research are outlined with the hope of sparking further debate on the subject.

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Mesh:

Year:  1997        PMID: 9039094     DOI: 10.1161/01.hyp.29.1.145

Source DB:  PubMed          Journal:  Hypertension        ISSN: 0194-911X            Impact factor:   10.190


  7 in total

1.  Mining SNPs from EST databases.

Authors:  L Picoult-Newberg; T E Ideker; M G Pohl; S L Taylor; M A Donaldson; D A Nickerson; M Boyce-Jacino
Journal:  Genome Res       Date:  1999-02       Impact factor: 9.043

2.  Non-recombining chromosome Y haplogroups and centromeric HindIII RFLP in relation to blood pressure in 2,743 middle-aged Caucasian men from the UK.

Authors:  Santiago Rodríguez; Xiao-He Chen; George J Miller; Ian N M Day
Journal:  Hum Genet       Date:  2005-01-27       Impact factor: 4.132

3.  Association between paraoxonase-1 gene polymorphisms and risk of metabolic syndrome.

Authors:  Dor Mohammad Kordi-Tamandani; Mohammad Hashemi; Nooshin Sharifi; Mahmoud Ali Kaykhaei; Adam Torkamanzehi
Journal:  Mol Biol Rep       Date:  2011-05-15       Impact factor: 2.316

Review 4.  The genomics of cardiovascular disorders: therapeutic implications.

Authors:  P Ferrari; G Bianchi
Journal:  Drugs       Date:  2000-05       Impact factor: 9.546

5.  Lack of association of methylenetetrahydrofolate reductase 677C>T mutation with coronary artery disease in a Pakistani population.

Authors:  M Perwaiz Iqbal; Tasneem Fatima; Siddiqa Parveen; Farzana A Yousuf; Majid Shafiq; Naseema Mehboobali; Abrar H Khan; Iqbal Azam; Philippe M Frossard
Journal:  J Mol Genet Med       Date:  2005-07-28

6.  Single nucleotide polymorphisms of the angiotensin-converting enzyme (ACE) gene are associated with essential hypertension and increased ACE enzyme levels in Mexican individuals.

Authors:  Nancy Martínez-Rodríguez; Carlos Posadas-Romero; Teresa Villarreal-Molina; Maite Vallejo; Leonardo Del-Valle-Mondragón; Julian Ramírez-Bello; Adan Valladares; Miguel Cruz-López; Gilberto Vargas-Alarcón
Journal:  PLoS One       Date:  2013-05-31       Impact factor: 3.240

7.  Epistatic Networks Jointly Influence Phenotypes Related to Metabolic Disease and Gene Expression in Diversity Outbred Mice.

Authors:  Anna L Tyler; Bo Ji; Daniel M Gatti; Steven C Munger; Gary A Churchill; Karen L Svenson; Gregory W Carter
Journal:  Genetics       Date:  2017-06       Impact factor: 4.562

  7 in total

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