Evidence map›Paper›PMID 31222129›Full record

ArticleScientific reports2019

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

David Carslake, Abigail Fraser, Margaret T May, Tom Palmer, Karri Silventoinen, Per Tynelius, Debbie A Lawlor, George Davey Smith

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 37% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors at 4 institutions in 3 countries.

David CarslakeMRC Integrative Epidemiology Unit at the University of Bristol, Bristol, UK. David.Carslake@bristol.ac.uk.
Abigail FraserMRC Integrative Epidemiology Unit at the University of Bristol, Bristol, UK.
Margaret T MayPopulation Health Sciences, Bristol Medical School, Bristol, UK.
Tom PalmerDepartment of Mathematics and Statistics, University of Lancaster, Lancaster, UK.ORCID http://orcid.org/0000-0003-4655-4511
Karri SilventoinenPopulation Research Unit, Department of Social Research, University of Helsinki, Helsinki, Finland.
Per TyneliusDepartment of Public Health Sciences, Karolinska Institute, Stockholm, Sweden.
Debbie A LawlorMRC Integrative Epidemiology Unit at the University of Bristol, Bristol, UK.
George Davey SmithMRC Integrative Epidemiology Unit at the University of Bristol, Bristol, UK.
At Bristol · GBKarolinska Institutet · SELancaster University · GBUniversity of Helsinki · FI

Funding

Medical Research Council MC_UU_00011/1Medical Research Council MC_UU_00011/6Medical Research Council MC_UU_12013/1Medical Research Council MC_UU_12013/5Medical Research Council MC_UU_12013/9Medical Research Council MR/M009351/1
6 · The paper itself

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'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.

Indexed as

Blood PressureBlood Pressure DeterminationNuclear FamilyCardiovascular DiseasesCause of DeathFemaleHumansHypertensionMaleMortalityMultivariate AnalysisPrognosisProportional Hazards ModelsRegistriesSweden

Identifiers

PMID31222129
PMCPMC6586810
OpenAlexW2950941859

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.