Genome-wide association study identifies six new loci influencing pulse pressure and mean arterial pressure
Paul Elliott, Martin Tobin, Cornelia van Duijn and colleagues report a genome-wide association study for pulse pressure and mean arterial pressure, identifying six new loci influencing these two traits. Numerous genetic loci have been associated with systolic blood pressure (SBP) and diastolic blood...
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Published in | Nature genetics Vol. 43; no. 10; pp. 1005 - 1011 |
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Main Authors | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
New York
Nature Publishing Group US
01.10.2011
Nature Publishing Group |
Subjects | |
Online Access | Get full text |
ISSN | 1061-4036 1546-1718 1546-1718 |
DOI | 10.1038/ng.922 |
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Summary: | Paul Elliott, Martin Tobin, Cornelia van Duijn and colleagues report a genome-wide association study for pulse pressure and mean arterial pressure, identifying six new loci influencing these two traits.
Numerous genetic loci have been associated with systolic blood pressure (SBP) and diastolic blood pressure (DBP) in Europeans
1
,
2
,
3
. We now report genome-wide association studies of pulse pressure (PP) and mean arterial pressure (MAP). In discovery (
N
= 74,064) and follow-up studies (
N
= 48,607), we identified at genome-wide significance (
P
= 2.7 × 10
−8
to
P
= 2.3 × 10
−13
) four new PP loci (at 4q12 near
CHIC2
, 7q22.3 near
PIK3CG
, 8q24.12 in
NOV
and 11q24.3 near
ADAMTS8
), two new MAP loci (3p21.31 in
MAP4
and 10q25.3 near
ADRB1
) and one locus associated with both of these traits (2q24.3 near
FIGN
) that has also recently been associated with SBP in east Asians. For three of the new PP loci, the estimated effect for SBP was opposite of that for DBP, in contrast to the majority of common SBP- and DBP-associated variants, which show concordant effects on both traits. These findings suggest new genetic pathways underlying blood pressure variation, some of which may differentially influence SBP and DBP. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 14 ObjectType-Article-1 ObjectType-Feature-2 content type line 23 PMCID: PMC3445021 These authors contributed equally. A list of consortium members is supplied in the Supplementary Note. |
ISSN: | 1061-4036 1546-1718 1546-1718 |
DOI: | 10.1038/ng.922 |