Evidence map›Paper›PMID 32999390›Full record

ArticleCommunications biology2020

Genetic basis of falling risk susceptibility in the UK Biobank Study.

Katerina Trajanoska, Lotta J Seppala, Carolina Medina-Gomez, Yi-Hsiang Hsu, Sirui Zhou, Natasja M van Schoor, Lisette C P G M de Groot, David Karasik, J Brent Richards, Douglas P Kiel and 5 more

Abstract read
In one paragraph

Article in Communications biology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 30 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
30citing papers in PubMed, 1 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.

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

30 citing papers in PubMed, 1 synthesis or guideline pooled it.

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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

15 authors.

Katerina TrajanoskaDepartment of Internal Medicine, Erasmus MC University Medical Center, Rotterdam, The Netherlands.ORCID http://orcid.org/0000-0002-3792-4296
Lotta J SeppalaDepartment of Internal Medicine, Section of Geriatric Medicine, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
Carolina Medina-GomezDepartment of Internal Medicine, Erasmus MC University Medical Center, Rotterdam, The Netherlands.ORCID http://orcid.org/0000-0001-7999-5538
Yi-Hsiang HsuHinda and Arthur Marcus Institute for Aging Research, Hebrew SeniorLife, Boston, MA, USA.
Sirui ZhouLady Davis Institute, Jewish General Hospital, McGill University, Montréal, Québec, Canada.
Natasja M van SchoorDepartment of Epidemiology and Biostatistics, Amsterdam Public Health Research Institute, VU University Medical Center, Amsterdam, The Netherlands.
Lisette C P G M de GrootWageningen University, Division of Human Nutrition, PO-box 17, 6700 AA, Wageningen, The Netherlands.ORCID http://orcid.org/0000-0003-2778-2789
David KarasikHinda and Arthur Marcus Institute for Aging Research, Hebrew SeniorLife, Boston, MA, USA.ORCID http://orcid.org/0000-0002-8826-0530
J Brent RichardsLady Davis Institute, Jewish General Hospital, McGill University, Montréal, Québec, Canada.ORCID http://orcid.org/0000-0002-3746-9086
Douglas P KielHinda and Arthur Marcus Institute for Aging Research, Hebrew SeniorLife, Boston, MA, USA.ORCID http://orcid.org/0000-0001-8474-0310
Andre G UitterlindenDepartment of Internal Medicine, Erasmus MC University Medical Center, Rotterdam, The Netherlands.ORCID http://orcid.org/0000-0002-7276-3387
John R B PerryDepartment of Internal Medicine, Erasmus MC University Medical Center, Rotterdam, The Netherlands.
Nathalie van der VeldeDepartment of Internal Medicine, Section of Geriatric Medicine, Academic Medical Center, University of Amsterdam, Amsterdam, The Netherlands.
Felix R Day *Department of Internal Medicine, Erasmus MC University Medical Center, Rotterdam, The Netherlands.ORCID http://orcid.org/0000-0003-3789-7651
Fernando Rivadeneira *Department of Internal Medicine, Erasmus MC University Medical Center, Rotterdam, The Netherlands. f.rivadeneira@erasmusmc.nl.ORCID http://orcid.org/0000-0001-9435-9441

Funding

Identifying Osteoporosis Genes by Whole Genome Sequencing and Functional Validation in Zebra FishR01AR072199 · NIAMS · HEBREW REHABILITATION CENTER FOR AGED · PI HSU, YI-HSIANG · 2017 to 2022
$3.2M
Medical Research Council MC_PC_17228Medical Research Council MC_QA137853Medical Research Council MC_UU_00006/2Medical Research Council MC_UU_12015/2NIAMS NIH HHS R01 AR072199
6 · The paper itself

Abstract

Both extrinsic and intrinsic factors predispose older people to fall. We performed a genome-wide association analysis to investigate how much of an individual's fall susceptibility can be attributed to genetics in 89,076 cases and 362,103 controls from the UK Biobank Study. The analysis revealed a small, but significant SNP-based heritability (2.7%) and identified three novel fall-associated loci (P

Indexed as

Accidental FallsAdultAgedBiological Specimen BanksCase-Control StudiesFemaleGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansLinkage DisequilibriumMaleMendelian Randomization AnalysisMiddle AgedMultifactorial InheritancePolymorphism, Single NucleotideQuantitative Trait Loci

Identifiers

PMID32999390
PMCPMC7527955

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.