Evidence map›Paper›PMID 36941332›Full record

ArticleNature medicine2023

Multiomic signatures of body mass index identify heterogeneous health phenotypes and responses to a lifestyle intervention.

Kengo Watanabe, Tomasz Wilmanski, Christian Diener, John C Earls, Anat Zimmer, Briana Lincoln, Jennifer J Hadlock, Jennifer C Lovejoy, Sean M Gibbons, Andrew T Magis and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Nature medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 87 papers.

0numbers the graph read from it
0cells of the map it votes in
87citing papers in PubMed
23.7field-weighted citation impact, top 1% 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

87 citing papers in PubMed, 133 citations in OpenAlex.

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  18. Premature aging in serious mental illness.Neuropsychopharmacology : official publication of the American College of Neuropsychopharmacology · 2026
    Review
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  20. Article

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

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors at 2 institutions in 1 country.

Kengo WatanabeInstitute for Systems Biology, Seattle, WA, USA.ORCID http://orcid.org/0000-0002-0348-1634
Tomasz WilmanskiInstitute for Systems Biology, Seattle, WA, USA.
Christian DienerInstitute for Systems Biology, Seattle, WA, USA.
John C EarlsInstitute for Systems Biology, Seattle, WA, USA.
Anat ZimmerInstitute for Systems Biology, Seattle, WA, USA.
Briana LincolnInstitute for Systems Biology, Seattle, WA, USA.
Jennifer J HadlockInstitute for Systems Biology, Seattle, WA, USA.ORCID http://orcid.org/0000-0001-6103-7606
Jennifer C LovejoyInstitute for Systems Biology, Seattle, WA, USA.
Sean M GibbonsInstitute for Systems Biology, Seattle, WA, USA.ORCID http://orcid.org/0000-0002-8724-7916
Andrew T MagisInstitute for Systems Biology, Seattle, WA, USA.
Leroy HoodInstitute for Systems Biology, Seattle, WA, USA.
Nathan D PriceInstitute for Systems Biology, Seattle, WA, USA.ORCID http://orcid.org/0000-0002-4157-0267
Noa RappaportInstitute for Systems Biology, Seattle, WA, USA. noa.rappaport@isbscience.org.ORCID http://orcid.org/0000-0001-8643-2055
Institute for Systems Biology · USUniversity of Washington · US

Funding

Systems BiologyU19AG023122 · NIA · TRANSLATIONAL GENOMICS RESEARCH INST · PI Thomas Girke, NICHOLAS Joseph SCHORK · 2004 to 2026
$102.6M
Metabolomic Signatures for Disease Sub-classification and Target Prioritization in AMP-ADU01AG061359 · NIA · DUKE UNIVERSITY · PI KADDURAH-DAOUK, RIMA F, KASTENMULLER, GABI · 2018 to 2022
$10.0M
Integrative Omics to enhance therapeutics development for healthy agingUH3AG064706 · NIA · TRANSLATIONAL GENOMICS RESEARCH INST · PI MILLER, RICHARD A, SCHORK, NICHOLAS JOSEPH · 2021 to 2024
$3.3M
Medical Research CouncilNIA NIH HHS U01 AG061359NIA NIH HHS U19 AG023122NIA NIH HHS UH3 AG064706Versus ArthritisWellcome Trust
6 · The paper itself

Abstract

Multiomic profiling can reveal population heterogeneity for both health and disease states. Obesity drives a myriad of metabolic perturbations and is a risk factor for multiple chronic diseases. Here we report an atlas of cross-sectional and longitudinal changes in 1,111 blood analytes associated with variation in body mass index (BMI), as well as multiomic associations with host polygenic risk scores and gut microbiome composition, from a cohort of 1,277 individuals enrolled in a wellness program (Arivale). Machine learning model predictions of BMI from blood multiomics captured heterogeneous phenotypic states of host metabolism and gut microbiome composition better than BMI, which was also validated in an external cohort (TwinsUK). Moreover, longitudinal analyses identified variable BMI trajectories for different omics measures in response to a healthy lifestyle intervention; metabolomics-inferred BMI decreased to a greater extent than actual BMI, whereas proteomics-inferred BMI exhibited greater resistance to change. Our analyses further identified blood analyte-analyte associations that were modified by metabolomics-inferred BMI and partially reversed in individuals with metabolic obesity during the intervention. Taken together, our findings provide a blood atlas of the molecular perturbations associated with changes in obesity status, serving as a resource to quantify metabolic health for predictive and preventive medicine.

Indexed as

MultiomicsObesityBody Mass IndexCross-Sectional StudiesHumansPhenotype

Identifiers

PMID36941332
PMCPMC10115644
OpenAlexW4328048668

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.