Evidence map›Paper›PMID 36617359›Full record

ArticleEuropean journal of applied physiology2023

Defining left ventricular remodeling using lean body mass allometry: a UK Biobank study.

Bruna Gomes, Kristofer Hedman, Tatiana Kuznetsova, Nicholas Cauwenberghs, David Hsu, Yukari Kobayashi, Erik Ingelsson, David Oxborough, Keith George, Michael Salerno and 2 more

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Article in European journal of applied physiology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
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

3 citing papers in PubMed.

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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

12 authors.

Bruna Gomes *Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA, 94304, USA. bgomes@stanford.edu.ORCID http://orcid.org/0000-0002-8977-5966
Kristofer Hedman *Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA, 94304, USA.
Tatiana KuznetsovaResearch Unit Hypertension and Cardiovascular Epidemiology, KU Leuven Department of Cardiovascular Sciences, University of Leuven, Leuven, Belgium.
Nicholas CauwenberghsResearch Unit Hypertension and Cardiovascular Epidemiology, KU Leuven Department of Cardiovascular Sciences, University of Leuven, Leuven, Belgium.
David HsuDivision of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA, 94304, USA.
Yukari KobayashiDivision of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA, 94304, USA.
Erik IngelssonDivision of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA, 94304, USA.
David OxboroughResearch Institute for Sports and Exercise Sciences, Liverpool John Moores University, Liverpool, L3 9UT, UK.
Keith GeorgeResearch Institute for Sports and Exercise Sciences, Liverpool John Moores University, Liverpool, L3 9UT, UK.
Michael SalernoDivision of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA, 94304, USA.
Euan AshleyDivision of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA, 94304, USA.
Francois Haddad *Division of Cardiovascular Medicine, Stanford University School of Medicine, Stanford, CA, 94304, USA. fhaddad@stanford.edu.

Funding

Deutsche Forschungsgemeinschaft 707766 - 809341Deutsche Forschungsgemeinschaft GO 3196/3-1Medical Research Council MC_PC_17228
6 · The paper itself

Abstract

purposeThe geometric patterns of ventricular remodeling are determined using indexed left ventricular mass (LVM), end-diastolic volume (LVEDV) and concentricity, most often measured using the mass-to-volume ratio (MVR). The aims of this study were to validate lean body mass (LBM)-based allometric coefficients for scaling and to determine an index of concentricity that is independent of both volume and LBM.

methodsParticipants from the UK Biobank who underwent both CMR and dual-energy X-ray absorptiometry (DXA) during 2014-2015 were considered (n = 5064). We excluded participants aged ≥ 70 years or those with cardiometabolic risk factors. We determined allometric coefficients for scaling using linear regression of the logarithmically transformed ventricular remodeling parameters. We further defined a multiplicative allometric relationship for LV concentricity (LVC) adjusting for both LVEDV and LBM.

resultsA total of 1638 individuals (1057 female) were included. In subjects with lower body fat percentage (< 25% in males, < 35% in females, n = 644), the LBM allometric coefficients for scaling LVM and LVEDV were 0.85 ± 0.06 and 0.85 ± 0.03 respectively (R

conclusionsWe validated allometric coefficients for LBM-based scaling for CMR indexed parameters relevant for classifying geometric patterns of ventricular remodeling.

Indexed as

Biological Specimen BanksVentricular RemodelingBody Mass IndexFemaleHumansHypertrophy, Left VentricularLinear ModelsMaleUnited KingdomAdiposityAllometryBody compositionLV hypertrophyObesityScalingVentricular remodelingVisceral fat

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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.