bioRxivSystems BiologyPreprint
Multi-modal atlas of lifestyle interventions reveals malleability of ageing-linked molecular features
Chiara Maria Stella HerzogiD, Charlotte D. VavourakisiD, Elisa RedliD, Magdalena HageniD, Gabriel KnolliD, Christina Watschinger, Umesh KumariD, Bente TheeuwesiD, Juliane Gasser, Sophia Zollner-KiechliD, Robert ReihsiD, Heimo MülleriD, Maria Silvia CavinatoiD, Sonja SturmiD, Hermann StuppneriD, Alexander Rupert MoscheniD, Birgit WeinbergeriD, Tobias GreitemeyeriD, Matthias SchmuthiD, Verena Moosbrugger‐MartinziD, Thomas TrafoieriD, Verena Lindner, Anna Wimmer, Peter WidschwendteriD, Hans-Peter Platzer, , Martin WidschwendteriD
Abstract
Extending human healthspan requires understanding how lifestyle interventions impact molecular systems across tissues and time. Here, we present the TirolGESUND Lifestyle Atlas (ClinicalTrials.gov: NCT05678426), a longitudinal, multi-modal resource profiling 156 healthy women (aged 30-60 years) undergoing 6-month intermittent fasting (n=114) or smoking cessation (n=42) interventions. Participants were sampled up to four times across seven tissues and fluids, generating >3,450 biospecimens with harmonised DNA methylation, metabolomics, microbiome, and immune profiling, alongside skin histology, barrier measurements, and rich clinical metadata. We demonstrate the utility of this dataset through: (i) multi-omics-wide association studies linking traits to molecular features; (ii) integrative factor modelling revealing coordinated cross-tissue signatures; (iii) epigenetic-biomarker cross-omic associations, and (iv) CpG-level variance decomposition mapping stable, individual-specific, tissue-restricted, and intervention-responsive methylation patterns. We further show that ageing-linked features are selectively malleable: highly compliant intermittent fasting participants exhibited attenuated or even age-opposing molecular trajectories within six months. The atlas enables unprecedented within-cohort comparisons across omic layers and tissues, supporting discovery of context-dependent biomarkers, cross-system coordination, and intervention responsiveness. Data are available via an interactive portal, with sensitive data under controlled access (https://eutops.github.io/lifestyle-atlas/). This resource provides a foundation for exploring biomarker association and multi-tissue epigenetics, enabling hypothesis generation and benchmarking for systems biology and human healthspan research. Graphical abstract O_FIG O_LINKSMALLFIG WIDTH=186 HEIGHT=200 SRC="FIGDIR/small/673115v2_ufig1.gif" ALT="Figure 1"> View larger version (35K): org.highwire.dtl.DTLVardef@fec2d9org.highwire.dtl.DTLVardef@1aa5d13org.highwire.dtl.DTLVardef@1c4a6f2org.highwire.dtl.DTLVardef@1ac62fb_HPS_FORMAT_FIGEXP M_FIG C_FIG HighlightsO_LIMulti-tissue multi-modal profiling of two clinically-relevant lifestyle interventions in 156 women aged 30-60 C_LIO_LIIntermittent fasting modifies ageing-linked molecular features in an age-opposing direction C_LIO_LICross-tissue epigenetic biomarker mapping links immunity, metabolism, and microbiome C_LIO_LITissue-specific epigenetic plasticity maps reveal candidate meQTLs, C_LIO_LIData sharing and interactive portal enable broad reuse for hypothesis generation and exploration C_LI
- organism: human
- assay: DNA methylation
- assay: metabolomics
- assay: metagenomics
- assay: proteomics
- research focus: database / resource
- approach: statistical model
- Citations
- 3
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