Evidence map›Paper›PMID 33184277›Full record

ArticleNature communications2020

Collider bias undermines our understanding of COVID-19 disease risk and severity.

Gareth J Griffith, Tim T Morris, Matthew J Tudball, Annie Herbert, Giulia Mancano, Lindsey Pike, Gemma C Sharp, Jonathan Sterne, Tom M Palmer, George Davey Smith and 4 more

2 registry-linked trialsAbstract read
In one paragraph

Article in Nature communications, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 504 papers, 6 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
504citing papers in PubMed, 6 pooled it
–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.

NCT04689711 completednot on this map

Generalizable Prognostic Models for Patient-Centered Decisions in COVID-19

TypeobservationalSponsorTufts Medical CenterRan2020 to 2021Enrolled21ConditionsCovid19
NCT04915781 completednot on this map

Tobacco Use and Incidence of SARS-CoV-2 Infection in the Finnish General Population

TypeobservationalSponsorFinnish Institute for Health and WelfareRan2017 to 2021Enrolled60,872ConditionsSARS-CoV-2 Infection, Covid19ArmsNot applicable, this is an observational study
3 · Its place in the literature

Who cites it

504 citing papers in PubMed, 6 syntheses or guidelines pooled it.

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444 more citing papers are in PubMed but not listed here.

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

14 authors.

Gareth J GriffithMedical Research Council Integrative Epidemiology Unit, University of Bristol, Bristol, BS8 2BN, UK.ORCID 0000-0003-0481-3175
Tim T MorrisMedical Research Council Integrative Epidemiology Unit, University of Bristol, Bristol, BS8 2BN, UK.ORCID 0000-0001-8178-6815
Matthew J TudballMedical Research Council Integrative Epidemiology Unit, University of Bristol, Bristol, BS8 2BN, UK.ORCID 0000-0002-7897-6180
Annie HerbertMedical Research Council Integrative Epidemiology Unit, University of Bristol, Bristol, BS8 2BN, UK.
Giulia MancanoMedical Research Council Integrative Epidemiology Unit, University of Bristol, Bristol, BS8 2BN, UK.
Lindsey PikeMedical Research Council Integrative Epidemiology Unit, University of Bristol, Bristol, BS8 2BN, UK.
Gemma C SharpMedical Research Council Integrative Epidemiology Unit, University of Bristol, Bristol, BS8 2BN, UK.ORCID 0000-0003-2906-4035
Jonathan SternePopulation Health Sciences, Bristol Medical School, University of Bristol, Oakfield House, Oakfield Grove, Bristol, BS8 2BN, UK.
Tom M PalmerMedical Research Council Integrative Epidemiology Unit, University of Bristol, Bristol, BS8 2BN, UK.ORCID 0000-0003-4655-4511
George Davey SmithMedical Research Council Integrative Epidemiology Unit, University of Bristol, Bristol, BS8 2BN, UK.ORCID 0000-0002-1407-8314
Kate TillingMedical Research Council Integrative Epidemiology Unit, University of Bristol, Bristol, BS8 2BN, UK.ORCID 0000-0002-1010-8926
Luisa ZuccoloMedical Research Council Integrative Epidemiology Unit, University of Bristol, Bristol, BS8 2BN, UK.
Neil M DaviesMedical Research Council Integrative Epidemiology Unit, University of Bristol, Bristol, BS8 2BN, UK.ORCID 0000-0002-2460-0508
Gibran HemaniMedical Research Council Integrative Epidemiology Unit, University of Bristol, Bristol, BS8 2BN, UK. g.hemani@bristol.ac.uk.ORCID 0000-0003-0920-1055

Funding

Medical Research Council MC_PC_17228Medical Research Council MC_QA137853Medical Research Council MC_UU_00011/1Medical Research Council MC_UU_00011/3Medical Research Council MR/S002634/1Wellcome Trust 208806/Z/17/ZWellcome Trust 220067/Z/20/Z
6 · The paper itself

Abstract

Numerous observational studies have attempted to identify risk factors for infection with SARS-CoV-2 and COVID-19 disease outcomes. Studies have used datasets sampled from patients admitted to hospital, people tested for active infection, or people who volunteered to participate. Here, we highlight the challenge of interpreting observational evidence from such non-representative samples. Collider bias can induce associations between two or more variables which affect the likelihood of an individual being sampled, distorting associations between these variables in the sample. Analysing UK Biobank data, compared to the wider cohort the participants tested for COVID-19 were highly selected for a range of genetic, behavioural, cardiovascular, demographic, and anthropometric traits. We discuss the mechanisms inducing these problems, and approaches that could help mitigate them. While collider bias should be explored in existing studies, the optimal way to mitigate the problem is to use appropriate sampling strategies at the study design stage.

Indexed as

BetacoronavirusBiasCoronavirus InfectionsCOVID-19HumansObservational Studies as TopicPandemicsPneumonia, ViralRisk FactorsSARS-CoV-2Treatment Outcome

Identifiers

PMID33184277
PMCPMC7665028

What OpenQuestion holds

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Registered trials

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.