Evidence map›Paper›PMID 37039013›Full record

ArticleCirculation. Genomic and precision medicine2023

Accelerated Epigenetic Aging Is Associated With Multiple Cardiometabolic, Hematologic, and Renal Abnormalities: A Project Baseline Health Substudy.

Best Uchehara, Lydia Coulter Kwee, Jessica Regan, Ranee Chatterjee, Julie Eckstrand, Sue Swope, Gary Gold, Terry Schaack, Pamela Douglas, Prithu Mettu and 7 more

Registry-linked trialAbstract read
In one paragraph

Article in Circulation. Genomic and precision medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT03154346 (Project Baseline Health Study), which is not on this map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing 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.

NCT03154346 active not recruitingnot on this map

Project Baseline Health Study

Typeobservational_patient_registrySponsorBaseline Study LLCRan2017 to 2024Enrolled10,000ConditionsAll
3 · Its place in the literature

Who cites it

14 citing papers in PubMed.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Article
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  9. Article
  10. Review
  11. Article
  12. Article
  13. Article
  14. Biological Age in Congenital Heart Disease-Exploring the Ticking Clock.Journal of cardiovascular development and disease · 2023
    Review
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

17 authors.

Best UcheharaDuke University Medical Center (B.U.), Duke University.ORCID 0000-0002-0027-6483
Lydia Coulter KweeDuke Molecular Physiology Institute (L.C.K., S.H.S.), Duke University.ORCID 0000-0002-6997-8571
Jessica ReganDivision of General Internal Medicine, Department of Medicine (J.R., R.C.), Duke University School of Medicine, Durham, NC.ORCID 0000-0002-3541-8146
Ranee ChatterjeeDivision of General Internal Medicine, Department of Medicine (J.R., R.C.), Duke University School of Medicine, Durham, NC.
Julie EckstrandDuke Clinical and Translational Science Institute (J.E.), Duke University School of Medicine, Durham, NC.ORCID 0000-0003-2407-9393
Sue SwopeStanford Center for Clinical Research, Department of Medicine, Stanford University School of Medicine (S. Swope, G.G., F.H., K.W.M.).ORCID 0000-0002-6941-9753
Gary GoldStanford Center for Clinical Research, Department of Medicine, Stanford University School of Medicine (S. Swope, G.G., F.H., K.W.M.).ORCID 0000-0002-3207-822X
Terry SchaackCalifornia Health & Longevity Institute, Westlake Village (T.S.).
Pamela DouglasDivision of Cardiology, Department of Medicine (P.D., N.P.), Duke University School of Medicine, Durham, NC.ORCID 0000-0001-9876-4049
Prithu MettuDivision of Retinal Ophthalmology, Department of Ophthalmology (P.M.), Duke University School of Medicine, Durham, NC.ORCID 0000-0002-1797-9003
Francois HaddadStanford Center for Clinical Research, Department of Medicine, Stanford University School of Medicine (S. Swope, G.G., F.H., K.W.M.).
Scarlet ShoreVerily Life Sciences, San Francisco, CA (S. Shore).
Adrian HernandezDuke Clinical Research Institute (A.H.), Duke University School of Medicine, Durham, NC.ORCID 0000-0003-3387-9616
Kenneth W MahaffeyStanford Center for Clinical Research, Department of Medicine, Stanford University School of Medicine (S. Swope, G.G., F.H., K.W.M.).ORCID 0000-0002-3791-2148
Neha PagidipatiDivision of Cardiology, Department of Medicine (P.D., N.P.), Duke University School of Medicine, Durham, NC.ORCID 0000-0002-5004-8868
Svati H ShahDuke Molecular Physiology Institute (L.C.K., S.H.S.), Duke University.ORCID 0000-0002-3495-2830
Project Baseline Health Study Group

Funding

Clinical and Molecular Epidemiology of High Risk Coronary PlaqueR01HL146145 · NHLBI · DUKE UNIVERSITY · PI DOUGLAS, PAMELA SUSAN, FOLDYNA, BOREK · 2019 to 2022
$4.8M
Stimulating Access to Research in Residency (StARR) - NHLBIR38HL143612 · NHLBI · DUKE UNIVERSITY · PI Mai ElMallah, David H. Harpole · 2018 to 2026
$2.6M
NHLBI NIH HHS R01 HL146145NHLBI NIH HHS R38 HL143612
6 · The paper itself

Abstract

backgroundEpigenetic clocks estimate chronologic age using methylation levels at specific loci. We tested the hypothesis that accelerated epigenetic aging is associated with abnormal values in a range of clinical, imaging, and laboratory characteristics.

methodsThe Project Baseline Health Study recruited 2502 participants, including 1661 with epigenetic age estimates from the Horvath pan-tissue clock. We classified individuals with extreme values as having epigenetic age acceleration (EAA) or epigenetic age deceleration. A subset of participants with longitudinal methylation profiling was categorized as accelerated versus nonaccelerated. Using principal components analysis, we created phenoclusters using 122 phenotypic variables and compared individuals with EAA versus epigenetic age deceleration, and at one year of follow-up, using logistic regression models adjusted for sex (false discovery rate [

resultsThe EAA (n=188) and epigenetic age deceleration (n=195) groups were identified as having EAA estimates ≥5 years or ≤-5 years, respectively. In primary analyses, individuals with EAA had higher values for phenoclusters summarizing lung function and lipids, and lower values for a phenocluster representing physical function. In secondary analyses of individual variables, neutrophils, body mass index, and waist circumference were significantly higher in individuals with EAA (

conclusionsWe report multiple cardiometabolic, hematologic, and physical function features characterizing individuals with EAA. These highlight factors that may mediate the adverse effects of aging and identify potential targets for study of mitigation of these effects. REGISTRATION: URL: https://www. CLINICALTRIALS: gov; Unique identifier: NCT03154346.

Indexed as

Cardiovascular DiseasesEpigenesis, GeneticAgingChild, PreschoolDNA MethylationEpigenomicsHumansagingbody mass indexdecelerationlipidsmethylation

Identifiers

PMID37039013
PMCPMC10330131

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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.