Evidence map›Paper›PMID 30524135›Full record

ArticleCirculation2018

Assessing the causal role of body mass index on cardiovascular health in young adults: Mendelian randomization and recall-by-genotype analyses.

Kaitlin H Wade, Scott T Chiesa, Alun D Hughes, Nish Chaturvedi, Marietta Charakida, Alicja Rapala, Vivek Muthurangu, Tauseef Khan, Nicholas Finer, Naveed Sattar and 6 more

Open access · hybridAbstract read
In one paragraph

Article in Circulation, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 49 papers.

0numbers the graph read from it
0cells of the map it votes in
49citing papers in PubMed
5.6field-weighted citation impact, top 3% 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

49 citing papers in PubMed, 85 citations in OpenAlex.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors at 2 institutions in 1 country.

Kaitlin H WadeMRC Integrative Epidemiology Unit (IEU) at the University of Bristol, Bristol, UK.
Scott T ChiesaVascular Physiology Unit, Institute of Cardiovascular Science, University College London, 1 St. Martin's Le Grand, London, EC1A 4NP.
Alun D HughesCardiometabolic Phenotyping Group, Institute of Cardiovascular Science, University College London, London, W1T 7HA.
Nish ChaturvediCardiometabolic Phenotyping Group, Institute of Cardiovascular Science, University College London, London, W1T 7HA.
Marietta CharakidaVascular Physiology Unit, Institute of Cardiovascular Science, University College London, 1 St. Martin's Le Grand, London, EC1A 4NP.
Alicja RapalaVascular Physiology Unit, Institute of Cardiovascular Science, University College London, 1 St. Martin's Le Grand, London, EC1A 4NP.
Vivek MuthuranguVascular Physiology Unit, Institute of Cardiovascular Science, University College London, 1 St. Martin's Le Grand, London, EC1A 4NP.
Tauseef KhanVascular Physiology Unit, Institute of Cardiovascular Science, University College London, 1 St. Martin's Le Grand, London, EC1A 4NP.
Nicholas FinerVascular Physiology Unit, Institute of Cardiovascular Science, University College London, 1 St. Martin's Le Grand, London, EC1A 4NP.
Naveed SattarInstitute of Cardiovascular and Medical Sciences, BHF Glasgow Cardiovascular Research Centre, University of Glasgow, Glasgow, G12 8TA.
Laura D HoweMRC Integrative Epidemiology Unit (IEU) at the University of Bristol, Bristol, UK.
Abigail FraserMRC Integrative Epidemiology Unit (IEU) at the University of Bristol, Bristol, UK.
Debbie A LawlorMRC Integrative Epidemiology Unit (IEU) at the University of Bristol, Bristol, UK.
George Davey SmithMRC Integrative Epidemiology Unit (IEU) at the University of Bristol, Bristol, UK.
John E DeanfieldVascular Physiology Unit, Institute of Cardiovascular Science, University College London, 1 St. Martin's Le Grand, London, EC1A 4NP.
Nicholas J TimpsonMRC Integrative Epidemiology Unit (IEU) at the University of Bristol, Bristol, UK.
Medical Research Council · GBMRC Integrative Epidemiology Unit

Funding

British Heart Foundation CS/13/1/30327British Heart Foundation CS/15/6/31468British Heart Foundation PG/06/145/21955British Heart Foundation RG/10/004/28240Medical Research Council G9815508Medical Research Council MC_PC_15018Medical Research Council MC_UU_00011/1Medical Research Council MC_UU_12013/3Medical Research Council MC_UU_12013/5Medical Research Council MR/M009351/1Medical Research Council MR/M020894/1Wellcome Trust 086676Wellcome Trust 096989Wellcome Trust 102215Wellcome Trust 202802
6 · The paper itself

Abstract

Background: Body mass index (BMI) has been suggested to be causally related to cardiovascular health in mid-to-late life, but this has not been explored systematically at younger ages - nor with detailed cardiovascular phenotyping. Recall-by-Genotype (RbG) is an approach that enables the collection of precise phenotypic measures in smaller studies, whilst maintaining statistical power and ability for causal inference. Methods: In this study, we used a combination of conventional multivariable regression analysis, Mendelian randomization (MR) and sub-sample RbG methodologies to estimate the causal effect of BMI on gross-level and detailed cardiovascular health in healthy participants from the Avon Longitudinal Study of Parents and Children at age 17 (N=1420-3108 for different outcomes) and an independent sample from the same cohort (for RbG) study at age 21 (N=386-418). Results: In both MR and RbG analyses, results suggested that higher BMI causes higher blood pressure (BP) and left ventricular mass index (LVMI) in young adults (e.g., difference in LVMI per kg/m Conclusions: Complementary MR and RbG causal methodologies, together with a range of sensitivity analyses, suggest that higher BMI is likely to cause worse cardiovascular health, specifically higher BP and LVMI, even in youth. Higher BMI also resulted in increased CO in the RbG study, which appeared to be solely driven by SV, as neither MR nor RbG analyses suggested a causal effect of BMI on heart rate. These consistent results support efforts to reduce BMI from a young age to prevent later adverse cardiovascular health and illustrate the potential for phenotypic resolution with maintained analytical power using RbG.

Indexed as

Body Mass IndexAdiposityAdolescentCarotid Intima-Media ThicknessFemaleGenome-Wide Association StudyGenotypeHeartHeart RateHumansLife StyleLongitudinal StudiesMaleMendelian Randomization AnalysisPhenotypePolymorphism, Single NucleotideALSPACBody mass indexcardiovascular traitscausalityMendelian randomizationrecall-by-genotype

Identifiers

PMID30524135
PMCPMC6250296
OpenAlexW2953318457

What OpenQuestion holds

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Registered trials

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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.