Evidence map›Paper›PMID 34233669›Full record

ArticleRespiratory research2021

Genetic evidence for a causative effect of airflow obstruction on left ventricular filling: a Mendelian randomisation study.

Lars Harbaum, Jan K Hennigs, Marcel Simon, Tim Oqueka, Henrik Watz, Hans Klose

Open access · goldAbstract read
In one paragraph

Article in Respiratory research, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. 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 33% 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

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

6 authors at 2 institutions in 1 country.

Lars HarbaumAbteilung für Pneumologie, Centrum für Pulmonal Arterielle Hypertonie Hamburg (CPAHH), Universitätsklinikum Hamburg-Eppendorf, Hamburg, Germany. l.harbaum@uke.de.ORCID http://orcid.org/0000-0002-9422-6195
Jan K HennigsAbteilung für Pneumologie, Centrum für Pulmonal Arterielle Hypertonie Hamburg (CPAHH), Universitätsklinikum Hamburg-Eppendorf, Hamburg, Germany.
Marcel SimonAbteilung für Pneumologie, Centrum für Pulmonal Arterielle Hypertonie Hamburg (CPAHH), Universitätsklinikum Hamburg-Eppendorf, Hamburg, Germany.
Tim OquekaAbteilung für Pneumologie, Centrum für Pulmonal Arterielle Hypertonie Hamburg (CPAHH), Universitätsklinikum Hamburg-Eppendorf, Hamburg, Germany.
Henrik WatzPneumologische Forschungsinstitut an der LungenClinic Grosshansdorf, Airway Research Center North (ARCN), German Center for Lung Research (DZL), Grosshansdorf, Germany.
Hans KloseAbteilung für Pneumologie, Centrum für Pulmonal Arterielle Hypertonie Hamburg (CPAHH), Universitätsklinikum Hamburg-Eppendorf, Hamburg, Germany.
Universität Hamburg · DEGerman Center for Lung Research · DE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundObservational studies on the general population have suggested that airflow obstruction associates with left ventricular (LV) filling. To limit the influence of environmental risk factors/exposures, we used a Mendelian randomisation (MR) approach based on common genetic variations and tested whether a causative relation between airflow obstruction and LV filling can be detected.

methodsWe used summary statistics from large genome-wide association studies (GWAS) on the ratio of forced expiratory volume in 1 s to forced vital capacity (FEV1/FVC) measured by spirometry and the LV end-diastolic volume (LVEDV) as assessed by cardiac magnetic resonance imaging. The primary MR was based on an inverse variance weighted regression. Various complementary MR methods and subsets of the instrument variables were used to assess the plausibility of the findings.

resultsWe obtained consistent evidence in our primary MR analysis and subsequent sensitivity analyses that reducing airflow obstruction leads to increased inflow to the LV (odds ratio [OR] from inverse variance weighted regression 1.05, 95% confidence interval [CI] 1.01-1.09, P = 0.0172). Sensitivity analyses indicated a certain extent of negative horizontal pleiotropy and the estimate from biased-corrected MR-Egger was adjusted upward (OR 1.2, 95% CI 1.09-1.31, P < 0.001). Prioritisation of single genetic variants revealed rs995758, rs2070600 and rs7733410 as major contributors to the MR result.

conclusionOur findings indicate a causal relationship between airflow obstruction and LV filling in the general population providing genetic context to observational associations. The results suggest that targeting (even subclinical) airflow obstruction can lead to direct cardiac improvements, demonstrated by an increase in LVEDV. Functional annotation of single genetic variants contributing most to the causal effect estimate could help to prioritise biological underpinnings.

Indexed as

Cohort StudiesForced Expiratory VolumeGenome-Wide Association StudyHumansMendelian Randomization AnalysisPolymorphism, Single NucleotidePulmonary Disease, Chronic ObstructiveVentricular Function, LeftVital Capacity

Identifiers

PMID34233669
PMCPMC8261939
OpenAlexW3181812138

What OpenQuestion holds

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LicenceCC BY
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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.