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Ganesh, S.K.* ; Chasman, D.I.* ; Larson, M.G.* ; Guo, X.* ; Verwoert, G.* ; Bis, J.C.* ; Gu, X.* ; Smith, A.V.* ; Yang, M.L.* ; Zhang, Y.* ; Ehret, G.* ; Rose, L.M.* ; Hwang, S.J.* ; Papanicolau, G.J.* ; Sijbrands, E.J.* ; Rice, K.* ; Eiriksdottir, G.* ; Pihur, V.* ; Ridker, P.M.* ; Vasan, R.S.* ; Newton-Cheh, C.* ; Global BPgen Consortium (Chakravarti, A. ; Döring, A. ; Gieger, C. ; Illig, T. ; Meitinger, T. ; Pfeufer, A. ; Wichmann, H.-E.) ; Raffel, L.J.* ; Amin, N.* ; Rotter, J.I.* ; Liu, K.* ; Launer, L.J.* ; Xu, M.* ; Caulfield, M.* ; Morrison, A.C.* ; Johnson, A.D.* ; Vaidya, D.* ; Dehghan, A.* ; Li, G.* ; Bouchard, C.* ; Harris, T.B.* ; Zhang, H.* ; Boerwinkle, E.* ; Siscovick, D.S.* ; Gao, W.* ; Uitterlinden, A.G.* ; Rivadeneira, F.* ; Hofman, A.* ; Willer, C.J.* ; Franco, O.H.* ; Huo, Y.* ; Witteman, J.C.* ; Munroe, P.B.* ; Gudnason, V.* ; Palmas, W.* ; van Duijn, C.M.* ; Fornage, M.* ; Levy, D.* ; Psaty, B.M.*

Effects of long-term averaging of quantitative blood pressure traits on the detection of genetic associations.

Am. J. Hum. Genet. 95, 49-65 (2014)
Verlagsversion DOI
Free by publisher
Open Access Green möglich sobald Postprint bei der ZB eingereicht worden ist.
Blood pressure (BP) is a heritable, quantitative trait with intraindividual variability and susceptibility to measurement error. Genetic studies of BP generally use single-visit measurements and thus cannot remove variability occurring over months or years. We leveraged the idea that averaging BP measured across time would improve phenotypic accuracy and thereby increase statistical power to detect genetic associations. We studied systolic BP (SBP), diastolic BP (DBP), mean arterial pressure (MAP), and pulse pressure (PP) averaged over multiple years in 46,629 individuals of European ancestry. We identified 39 trait-variant associations across 19 independent loci (p < 5 × 10(-8)); five associations (in four loci) uniquely identified by our LTA analyses included those of SBP and MAP at 2p23 (rs1275988, near KCNK3), DBP at 2q11.2 (rs7599598, in FER1L5), and PP at 6p21 (rs10948071, near CRIP3) and 7p13 (rs2949837, near IGFBP3). Replication analyses conducted in cohorts with single-visit BP data showed positive replication of associations and a nominal association (p < 0.05). We estimated a 20% gain in statistical power with long-term average (LTA) as compared to single-visit BP association studies. Using LTA analysis, we identified genetic loci influencing BP. LTA might be one way of increasing the power of genetic associations for continuous traits in extant samples for other phenotypes that are measured serially over time.
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Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Schlagwörter Genome-wide Association; Human Prefrontal Cortex; Growth-factor-i; Cardiovascular-disease; Measurement Error; Candidate Genes; Whole-blood; Human Brain; Expression; Loci
ISSN (print) / ISBN 0002-9297
e-ISSN 1537-6605
Quellenangaben Band: 95, Heft: 1, Seiten: 49-65 Artikelnummer: , Supplement: ,
Verlag Elsevier
Verlagsort New York, NY
Begutachtungsstatus Peer reviewed