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Associations of mortality with own blood pressure using son's blood pressure as an instrumental variable

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Associations of mortality with own blood pressure using son's blood pressure as an instrumental variable. / Carslake, David; Fraser, Abigail; May, Margaret et al.
In: Scientific Reports, Vol. 9, 8986, 20.06.2019.

Research output: Contribution to Journal/MagazineJournal articlepeer-review

Harvard

Carslake, D, Fraser, A, May, M, Palmer, T, Silventoinen, K, Tynelius, P, Lawlor, D & Smith, GD 2019, 'Associations of mortality with own blood pressure using son's blood pressure as an instrumental variable', Scientific Reports, vol. 9, 8986. https://doi.org/10.1038/s41598-019-45391-w

APA

Carslake, D., Fraser, A., May, M., Palmer, T., Silventoinen, K., Tynelius, P., Lawlor, D., & Smith, G. D. (2019). Associations of mortality with own blood pressure using son's blood pressure as an instrumental variable. Scientific Reports, 9, Article 8986. https://doi.org/10.1038/s41598-019-45391-w

Vancouver

Carslake D, Fraser A, May M, Palmer T, Silventoinen K, Tynelius P et al. Associations of mortality with own blood pressure using son's blood pressure as an instrumental variable. Scientific Reports. 2019 Jun 20;9:8986. doi: 10.1038/s41598-019-45391-w

Author

Carslake, David ; Fraser, Abigail ; May, Margaret et al. / Associations of mortality with own blood pressure using son's blood pressure as an instrumental variable. In: Scientific Reports. 2019 ; Vol. 9.

Bibtex

@article{73a17c5ccc1a4c5d8ba94432f27c7730,
title = "Associations of mortality with own blood pressure using son's blood pressure as an instrumental variable",
abstract = "High systolic blood pressure (SBP) causes cardiovascular disease (CVD) and is associated with mortality from other causes, but conventional multivariably-adjusted results may be confounded. Here we used a son{\textquoteright}s SBP (>1 million Swedish men) as an instrumental variable for parental SBP and examined associations with parents{\textquoteright} cause-specific mortality, avoiding reverse causation. The hazard ratio for CVD mortality per SD (10.80 mmHg) of SBP was 1.49 (95% CI: 1.43, 1.56); SBP was positively associated with coronary heart disease and stroke. SBP was also associated positively with all-cause, diabetes and kidney cancer mortality, and negatively with external causes. Negative associations with respiratory-related mortality were probably confounded by smoking. Hazard ratios for other causes were imprecise or null. Diastolic blood pressure gave similar results to SBP. CVD hazard ratios were intermediate between those from conventional multivariable studies and Mendelian randomization and stronger than those from clinical trials, approximately consistent with an effect of exposure duration on effect sizes. Plots of parental mortality against offspring SBP were approximately linear, supporting calls for lower SBP targets. Results suggest that conventional multivariable analyses of mortality and SBP are not substantially confounded by reverse causation and confirm positive effects of SBP on all-cause, CVD and diabetes mortality.",
author = "David Carslake and Abigail Fraser and Margaret May and Tom Palmer and Karri Silventoinen and Per Tynelius and Debbie Lawlor and Smith, {George Davey}",
year = "2019",
month = jun,
day = "20",
doi = "10.1038/s41598-019-45391-w",
language = "English",
volume = "9",
journal = "Scientific Reports",
issn = "2045-2322",
publisher = "Nature Publishing Group",

}

RIS

TY - JOUR

T1 - Associations of mortality with own blood pressure using son's blood pressure as an instrumental variable

AU - Carslake, David

AU - Fraser, Abigail

AU - May, Margaret

AU - Palmer, Tom

AU - Silventoinen, Karri

AU - Tynelius, Per

AU - Lawlor, Debbie

AU - Smith, George Davey

PY - 2019/6/20

Y1 - 2019/6/20

N2 - High systolic blood pressure (SBP) causes cardiovascular disease (CVD) and is associated with mortality from other causes, but conventional multivariably-adjusted results may be confounded. Here we used a son’s SBP (>1 million Swedish men) as an instrumental variable for parental SBP and examined associations with parents’ cause-specific mortality, avoiding reverse causation. The hazard ratio for CVD mortality per SD (10.80 mmHg) of SBP was 1.49 (95% CI: 1.43, 1.56); SBP was positively associated with coronary heart disease and stroke. SBP was also associated positively with all-cause, diabetes and kidney cancer mortality, and negatively with external causes. Negative associations with respiratory-related mortality were probably confounded by smoking. Hazard ratios for other causes were imprecise or null. Diastolic blood pressure gave similar results to SBP. CVD hazard ratios were intermediate between those from conventional multivariable studies and Mendelian randomization and stronger than those from clinical trials, approximately consistent with an effect of exposure duration on effect sizes. Plots of parental mortality against offspring SBP were approximately linear, supporting calls for lower SBP targets. Results suggest that conventional multivariable analyses of mortality and SBP are not substantially confounded by reverse causation and confirm positive effects of SBP on all-cause, CVD and diabetes mortality.

AB - High systolic blood pressure (SBP) causes cardiovascular disease (CVD) and is associated with mortality from other causes, but conventional multivariably-adjusted results may be confounded. Here we used a son’s SBP (>1 million Swedish men) as an instrumental variable for parental SBP and examined associations with parents’ cause-specific mortality, avoiding reverse causation. The hazard ratio for CVD mortality per SD (10.80 mmHg) of SBP was 1.49 (95% CI: 1.43, 1.56); SBP was positively associated with coronary heart disease and stroke. SBP was also associated positively with all-cause, diabetes and kidney cancer mortality, and negatively with external causes. Negative associations with respiratory-related mortality were probably confounded by smoking. Hazard ratios for other causes were imprecise or null. Diastolic blood pressure gave similar results to SBP. CVD hazard ratios were intermediate between those from conventional multivariable studies and Mendelian randomization and stronger than those from clinical trials, approximately consistent with an effect of exposure duration on effect sizes. Plots of parental mortality against offspring SBP were approximately linear, supporting calls for lower SBP targets. Results suggest that conventional multivariable analyses of mortality and SBP are not substantially confounded by reverse causation and confirm positive effects of SBP on all-cause, CVD and diabetes mortality.

U2 - 10.1038/s41598-019-45391-w

DO - 10.1038/s41598-019-45391-w

M3 - Journal article

VL - 9

JO - Scientific Reports

JF - Scientific Reports

SN - 2045-2322

M1 - 8986

ER -