Source:http://linkedlifedata.com/resource/pubmed/id/17492314
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
2007-7-4
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pubmed:abstractText |
Evidence shows that an elevated pulse pressure (PP) may lead to an increased risk of cardiovascular morbidity and mortality. There is also evidence that PP is a sexually dimorphic trait, and that genetic factors influence inter-individual variation in PP. The aim of this project was to assess the genotype-by-sex interaction on PP in a sample of mostly hypertensive African American and White participants using candidate genes involved in the renin-angiotensin-aldosterone system. Subjects were participants in the HyperGEN Study, including men (43%) and women (57%) over the age of 55 years (mean age = 65). Candidate gene polymorphisms used were ACE insertion/deletion (1,789 subjects genotyped) and AGT-M235T (1,800 subjects genotyped). We employed linear regression methods to assess the genotype-by-sex interaction. For ACE, genotype-by-sex interaction on PP was detected (P = 0.04): the "D/D" genotype predicted a 2.2 mmHg higher pulse pressure among women, but a 1.2 mmHg lower PP among men, compared to those with an "I" allele, after adjusting for age, weight, height, ethnicity, and antihypertension medication use. A similar interaction was found for systolic blood pressure. The genotype-by-sex interaction was consistent across ethnicity. The interaction was evident among those on antihypertensive medications (P = 0.05), but not among those not taking such medications (P = 0.55). In our analysis of AGT, no evidence of a genotype-by-sex interaction affecting PP, SBP, or DBP was detected. This evidence for a genotype-by-sex interaction helps our understanding of the complex genetic underpinnings of blood pressure phenotypes.
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pubmed:grant |
http://linkedlifedata.com/resource/pubmed/grant/HL 54472,
http://linkedlifedata.com/resource/pubmed/grant/HL007972,
http://linkedlifedata.com/resource/pubmed/grant/HL54471,
http://linkedlifedata.com/resource/pubmed/grant/HL54473,
http://linkedlifedata.com/resource/pubmed/grant/HL54495,
http://linkedlifedata.com/resource/pubmed/grant/HL54496,
http://linkedlifedata.com/resource/pubmed/grant/HL54497,
http://linkedlifedata.com/resource/pubmed/grant/HL54509,
http://linkedlifedata.com/resource/pubmed/grant/HL54515,
http://linkedlifedata.com/resource/pubmed/grant/HL55673,
http://linkedlifedata.com/resource/pubmed/grant/M10RR0047-34
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical | |
pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
1432-1203
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
122
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
33-40
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pubmed:dateRevised |
2008-6-27
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pubmed:meshHeading |
pubmed-meshheading:17492314-Aged,
pubmed-meshheading:17492314-Aged, 80 and over,
pubmed-meshheading:17492314-Angiotensinogen,
pubmed-meshheading:17492314-Antihypertensive Agents,
pubmed-meshheading:17492314-Blood Pressure,
pubmed-meshheading:17492314-Epidemiologic Studies,
pubmed-meshheading:17492314-Female,
pubmed-meshheading:17492314-Gene Frequency,
pubmed-meshheading:17492314-Genotype,
pubmed-meshheading:17492314-Humans,
pubmed-meshheading:17492314-Hypertension,
pubmed-meshheading:17492314-INDEL Mutation,
pubmed-meshheading:17492314-Male,
pubmed-meshheading:17492314-Middle Aged,
pubmed-meshheading:17492314-Peptidyl-Dipeptidase A,
pubmed-meshheading:17492314-Polymorphism, Single Nucleotide,
pubmed-meshheading:17492314-Sex Characteristics
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pubmed:year |
2007
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pubmed:articleTitle |
Sex-specific effects of ACE I/D and AGT-M235T on pulse pressure: the HyperGEN Study.
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pubmed:affiliation |
Department of Laboratory Medicine and Pathology, University of Minnesota, Minneapolis, MN, USA.
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pubmed:publicationType |
Journal Article,
Research Support, N.I.H., Extramural
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