Evidence map›Paper›PMID 30834892›Full record

ArticleeLife2019

Genetic and environmental perturbations lead to regulatory decoherence.

Amanda Lea, Meena Subramaniam, Arthur Ko, Terho Lehtimäki, Emma Raitoharju, Mika Kähönen, Ilkka Seppälä, Nina Mononen, Olli T Raitakari, Mika Ala-Korpela and 3 more

Abstract read
In one paragraph

Article in eLife, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 34 papers.

0numbers the graph read from it
0cells of the map it votes in
34citing 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

34 citing papers in PubMed.

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  8. Systems genomics of salinity stress response in rice.bioRxiv : the preprint server for biology · 2024
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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

13 authors.

Amanda Lea *Department of Ecology and Evolution, Princeton University, Princeton, United States.ORCID 0000-0002-8827-2750
Meena Subramaniam *Department of Medicine, Lung Biology Center, University of California, San Francisco, San Francisco, United States.
Arthur KoDepartment of Medicine, David Geffen School of Medicine at UCLA, University of California, Los Angeles, Los Angeles, United States.ORCID 0000-0002-1523-7225
Terho LehtimäkiDepartment of Clinical Chemistry, Fimlab Laboratories, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.
Emma RaitoharjuFinnish Cardiovascular Research Center, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.
Mika KähönenFinnish Cardiovascular Research Center, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.
Ilkka SeppäläFinnish Cardiovascular Research Center, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.
Nina MononenFinnish Cardiovascular Research Center, Faculty of Medicine and Health Technology, Tampere University, Tampere, Finland.
Olli T RaitakariResearch Centre of Applied and Preventive Cardiovascular Medicine, University of Turku, Turku, Finland.
Mika Ala-KorpelaSystems Epidemiology, Baker Heart and Diabetes Institute, Melbourne, Australia.
Päivi PajukantaDepartment of Human Genetics, David Geffen School of Medicine at UCLA, University of California, Los Angeles, Los Angeles, United States.
Noah Zaitlen *Department of Medicine, Lung Biology Center, University of California, San Francisco, San Francisco, United States.
Julien F Ayroles *Department of Ecology and Evolution, Princeton University, Princeton, United States.ORCID 0000-0001-8729-0511

Funding

Systems genomics of metabolic syndrome traitsP01HL028481 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI PAJUKANTA, PAIVI · 1985 to 2019
$50.2M
Methods for Genome-wide Association Studies in Admixed PopulationsR01HG006399 · NHGRI · HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTH · PI PRICE, ALKES L · 2011 to 2024
$6.3M
Genomics of dyslipidemia in MexicansR01HL095056 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI PAJUKANTA, PAIVI · 2009 to 2018
$5.9M
A path to personalized phenotypic prediction: unlocking the context-dependency of allelic effectsR35GM124881 · NIGMS · UNIVERSITY OF CALIFORNIA BERKELEY · PI Julien Ayroles · 2017 to 2026
$3.7M
Improved methods for inference of genotype-specific response to environmental toxinsR01ES029929 · NIEHS · PRINCETON UNIVERSITY · PI AYROLES, JULIEN, CLARK, ANDREW G · 2019 to 2023
$3.6M
P450 METABOLISM OF EPIPODOPHYLLOTOXINS IN CHILDRENR01CA051001 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI RELLING, MARY V. · 1996 to 2006
$2.7M
Richer Models of Asthma Risk: Bridging the Environment-Genetics DivideK25HL121295 · NHLBI · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI ZAITLEN, NOAH A · 2014 to 2018
$784k
Identification of lipid biomarkers via integrative genomic approaches in Hispanic populationsF31HL127921 · NHLBI · UNIVERSITY OF CALIFORNIA LOS ANGELES · PI KO, ARTHUR · 2016 to 2018
$82k
POLYMORPHIC METABOLISM OF ANTINEOPLASTICS IN CHILDRENR29CA051001 · NCI · ST. JUDE CHILDREN'S RESEARCH HOSPITAL · PI RELLING, MARY V. · 1990 to 1994
–
European Research Council 742927Medical Research Council MC_UU_12013/1NHGRI NIH HHS R01 HG006399NHLBI NIH HHS F31 HL127921NHLBI NIH HHS K25 HL121295NHLBI NIH HHS P01 HL028481NHLBI NIH HHS R01 HL095056NIEHS NIH HHS R01 ES029929NIGMS NIH HHS F31HL127921NIGMS NIH HHS GM124881NIGMS NIH HHS R35 GM124881
6 · The paper itself

Abstract

Correlation among traits is a fundamental feature of biological systems that remains difficult to study. To address this problem, we developed a flexible approach that allows us to identify factors associated with inter-individual variation in correlation. We use data from three human cohorts to study the effects of genetic and environmental variation on correlations among mRNA transcripts and among NMR metabolites. We first show that environmental exposures (infection and disease) lead to a systematic loss of correlation, which we define as 'decoherence'. Using longitudinal data, we show that decoherent metabolites are better predictors of whether someone will develop metabolic syndrome than metabolites commonly used as biomarkers of this disease. Finally, we demonstrate that correlation itself is under genetic control by mapping hundreds of 'correlation quantitative trait loci (QTLs)'. Together, this work furthers our understanding of how and why coordinated biological processes break down, and points to a potential role for decoherence in disease. Editorial note: This article has been through an editorial process in which the authors decide how to respond to the issues raised during peer review. The Reviewing Editor's assessment is that all the issues have been addressed (see decision letter).

Indexed as

Environmental ExposureGenetic VariationIndividualityMetabolomeQuantitative Trait LociComputer SimulationGene Expression ProfilingHumansMagnetic Resonance SpectroscopyMetabolic Diseasesco-expressiondecanalizationdecoherencegeneticsgenomicshumanhuman biologymedicinemetabolic syndrome

Identifiers

PMID30834892
PMCPMC6400502

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.