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Published in: BMC Medical Genetics 1/2009

Open Access 01-12-2009 | Research article

Suggestive linkage detected for blood pressure related traits on 2q and 22q in the population on the Samoan islands

Authors: Karolina Åberg, Feng Dai, Satupaitea Viali, John Tuitele, Guangyun Sun, Subba R Indugula, Ranjan Deka, Daniel E Weeks, Stephen T McGarvey

Published in: BMC Medical Genetics | Issue 1/2009

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Abstract

Background

High blood pressure or hypertension is a major risk factor involved in the development of cardiovascular diseases. We conducted genome-wide variance component linkage analyses to search for loci influencing five blood pressure related traits including the quantitative traits systolic blood pressure (SBP), diastolic blood pressure (DBP) and pulse pressure (PP), the dichotomous trait hypertension (HT) and the bivariate quantitative trait SBP-DBP in families residing in American Samoa and Samoa, as well as in the combined sample from the two polities. We adjusted the traits for a number of environmental covariates such as smoking, alcohol consumption, physical activity and material life style.

Results

We found suggestive univariate linkage for SBP on chromosome 2q35-q37 (LOD 2.4) and for PP on chromosome 22q13 (LOD 2.2), two chromosomal regions that recently have been associated with SBP and PP, respectively.

Conclusion

We have detected additional evidence for a recently reported locus associated with SBP on chromosome 2q and a susceptibility locus for PP on chromosome 22q. However, differences observed between the results from our three partly overlapping genetically homogenous study samples from the Samoan islands suggest that additional studies should be performed in order to verify these results.
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Metadata
Title
Suggestive linkage detected for blood pressure related traits on 2q and 22q in the population on the Samoan islands
Authors
Karolina Åberg
Feng Dai
Satupaitea Viali
John Tuitele
Guangyun Sun
Subba R Indugula
Ranjan Deka
Daniel E Weeks
Stephen T McGarvey
Publication date
01-12-2009
Publisher
BioMed Central
Published in
BMC Medical Genetics / Issue 1/2009
Electronic ISSN: 1471-2350
DOI
https://doi.org/10.1186/1471-2350-10-107

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