Imperial College London

ProfessorPaulElliott

Faculty of MedicineSchool of Public Health

Chair in Epidemiology and Public Health Medicine
 
 
 
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Contact

 

+44 (0)20 7594 3328p.elliott Website

 
 
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Assistant

 

Miss Jennifer Wells +44 (0)20 7594 3328

 
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Location

 

154Norfolk PlaceSt Mary's Campus

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Summary

 

Publications

Citation

BibTex format

@article{Malik:2021:10.1161/hypertensionaha.120.16534,
author = {Malik, R and Georgakis, MK and Vujkovic, M and Damrauer, SM and Elliott, P and Karhunen, V and Giontella, A and Fava, C and Hellwege, JN and Shuey, MM and Edwards, TL and Rogne, T and Åsvold, BO and Brumpton, BM and Burgess, S and Dichgans, M and Gill, D},
doi = {10.1161/hypertensionaha.120.16534},
journal = {Hypertension},
pages = {2004--2013},
title = {Relationship Between Blood Pressure and Incident Cardiovascular Disease: Linear and Nonlinear Mendelian Randomization Analyses},
url = {http://dx.doi.org/10.1161/hypertensionaha.120.16534},
volume = {77},
year = {2021}
}

RIS format (EndNote, RefMan)

TY  - JOUR
AB - <jats:p>Observational studies exploring whether there is a nonlinear effect of blood pressure on cardiovascular disease (CVD) risk are hindered by confounding. This limitation can be overcome by leveraging randomly allocated genetic variants in nonlinear Mendelian randomization analyses. Based on their association with blood pressure traits in a genome-wide association study of 299 024 European ancestry individuals, we selected 253 genetic variants to proxy the effect of modifying systolic and diastolic blood pressure. Considering the outcomes of incident coronary artery disease, stroke and the combined outcome of CVD, linear and nonlinear Mendelian randomization analyses were performed on 255 714 European ancestry participants without a history of CVD or antihypertensive medication use. There was no evidence favoring nonlinear relationships of genetically proxied systolic and diastolic blood pressure with the cardiovascular outcomes over linear relationships. For every 10-mm Hg increase in genetically proxied systolic blood pressure, risk of incident CVD increased by 49% (hazard ratio, 1.49 [95% CI, 1.38–1.61]), with similar estimates obtained for coronary artery disease (hazard ratio, 1.50 [95% CI, 1.38–1.63]) and stroke (hazard ratio, 1.44 [95% CI, 1.22–1.70]). Genetically proxied blood pressure had a similar relationship with CVD in men and women. These findings provide evidence to support that even for individuals who do not have elevated blood pressure, public health interventions achieving persistent blood pressure reduction will be of considerable benefit in the primary prevention of CVD.</jats:p>
AU - Malik,R
AU - Georgakis,MK
AU - Vujkovic,M
AU - Damrauer,SM
AU - Elliott,P
AU - Karhunen,V
AU - Giontella,A
AU - Fava,C
AU - Hellwege,JN
AU - Shuey,MM
AU - Edwards,TL
AU - Rogne,T
AU - Åsvold,BO
AU - Brumpton,BM
AU - Burgess,S
AU - Dichgans,M
AU - Gill,D
DO - 10.1161/hypertensionaha.120.16534
EP - 2013
PY - 2021///
SN - 0194-911X
SP - 2004
TI - Relationship Between Blood Pressure and Incident Cardiovascular Disease: Linear and Nonlinear Mendelian Randomization Analyses
T2 - Hypertension
UR - http://dx.doi.org/10.1161/hypertensionaha.120.16534
VL - 77
ER -