Evidence map›Paper›PMID 41826374›Full record

Articlenpj aging2026

DeepStrataAge: an interpretable deep-learning clock that reveals stage- and sex-divergent DNA methylation aging dynamics.

Aaron Lin, Ilinca Giosan, Andrea Aparicio, Tao Guo, Max Melnikas, Laura Balagué-Dobón, Natàlia Carreras-Gallo, Sayf Al-Deen Hassouneh, Kirsten Seale, Alex Kowalewski and 5 more

Abstract read
In one paragraph

Article in npj aging, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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.

Aaron Lin *TruDiagnostic, 881 Corporate Drive, Lexington, KY, USA.
Ilinca Giosan *TruDiagnostic, 881 Corporate Drive, Lexington, KY, USA.
Andrea AparicioChanning Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.
Tao GuoChanning Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.
Max MelnikasChanning Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.
Laura Balagué-DobónTruDiagnostic, 881 Corporate Drive, Lexington, KY, USA.
Natàlia Carreras-GalloTruDiagnostic, 881 Corporate Drive, Lexington, KY, USA.
Sayf Al-Deen HassounehTruDiagnostic, 881 Corporate Drive, Lexington, KY, USA.
Kirsten SealeTruDiagnostic, 881 Corporate Drive, Lexington, KY, USA.
Alex KowalewskiTruDiagnostic, 881 Corporate Drive, Lexington, KY, USA.
Brent HarrisonUniversity of Kentucky, College of Engineering, Department of Computer Science, Lexington, KY, USA.
Ryan SmithTruDiagnostic, 881 Corporate Drive, Lexington, KY, USA.
Lucas Paulo de Lima CamilloShift Bioscience, Toronto, ON, USA.
Jessica Lasky-SuChanning Division of Network Medicine, Department of Medicine, Brigham and Women's Hospital and Harvard Medical School, Boston, MA, USA.
Varun B DwarakaTruDiagnostic, 881 Corporate Drive, Lexington, KY, USA. varun.dwaraka@trudiagnostic.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Aging is the strongest risk factor for chronic diseases such as cardiovascular disease, Alzheimer's, and cancer. DNA methylation (DNAm) clocks offer a promising measure of biological age, but most rely on linear models that miss non-linear dynamics and CpG interactions. To address this, we developed a deep neural network (DNN)-based DNAm clock trained on 29,167 samples profiled on Illumina EPIC v1.0 and v2.0 arrays. Using 12,234 CpGs selected through sex- and age-stratified correlations, our model achieved high accuracy (1.89 years) and outperformed published deep learning and elastic net based epigenetic clocks in a separate validation cohort. Using Shapley Additive Explanations (SHAP), we further uncovered phase-structured, wave-like dynamics in age-influential CpGs: an early-life module, a midlife transition, and late-life remodeling, with distinct timings by sex. These epigenetic waves cohere with non-linear, multi-omic "aging waves" reported in proteomics and longitudinal omics. SHAP further enabled interpretable CpG attribution, revealing structured, sex-specific aging phases: early-life male clocks involved developmental pathways, while female clocks emphasized cytoskeletal regulation; late-life divergence included immune activation in males and transcriptional remodeling in females. Our framework thus unites accuracy with mechanistic interpretability, revealing sex-specific windows when molecular aging reconfigures most rapidly.

Identifiers

PMID41826374
PMCPMC13128896

What Socratic 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 Socratic graph.