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The multiomics blueprint of the individual with the most extreme lifespan

  • Eloy Santos-Pujol
  • , Aleix Noguera-Castells
  • , Marta Casado-Pelaez
  • , Carlos A. García-Prieto
  • , Claudia Vasallo
  • , Ignacio Campillo-Marcos
  • , Carlos Quero-Dotor
  • , Eva Crespo-García
  • , Alberto Bueno-Costa
  • , Fernando Setién
  • , Gerardo Ferrer
  • , Veronica Davalos
  • , Elisabetta Mereu
  • , Raquel Pluvinet
  • , Carles Arribas
  • , Carolina de la Torre
  • , Francisco Villavicencio
  • , Lauro Sumoy
  • , Isabel Granada
  • , Natalie S. Coles
  • Pamela Acha, Francesc Solé, Mar Mallo, Caterina Mata, Sara Peregrina, Toni Gabaldón, Marc Llirós, Meritxell Pujolassos, Robert Carreras-Torres, Aleix Lluansí, Librado Jesús García-Gil, Xavier Aldeguer, Sara Samino, Pol Torné, Josep Ribalta, Montse Guardiola, Núria Amigó, Oscar Yanes, Paula Martínez, Raúl Sánchez-Vázquez, Maria A. Blasco, Jose Oviedo, Bernardo Lemos, Julia Rius-Bonet, Marta Torrubiano, Marta Massip-Salcedo, Kamal A. Khidir, Thong Huy Cao, Paulene A. Quinn, Donald J.L. Jones, Salvador Macip, Eva Brigos-Barril, Mauricio Moldes, Fabio Barteri, Gerard Muntané, Hafid Laayouni, Arcadi Navarro, Manel Esteller

Research output: Contribution to journalArticlepeer-review

Abstract

Extreme human lifespan, exemplified by supercentenarians, presents a paradox in understanding aging: despite advanced age, they maintain relatively good health. To investigate this duality, we have performed a high-throughput multiomics study of the world’s oldest living person, interrogating her genome, transcriptome, metabolome, proteome, microbiome, and epigenome, comparing the results with larger matched cohorts. The emerging picture highlights different pathways attributed to each process: the record-breaking advanced age is manifested by telomere attrition, abnormal B cell population, and clonal hematopoiesis, whereas absence of typical age-associated diseases is associated with rare European-population genetic variants, low inflammation levels, a rejuvenated bacteriome, and a younger epigenome. These findings provide a fresh look at human aging biology, suggesting biomarkers for healthy aging, and potential strategies to increase life expectancy. The extrapolation of our results to the general population will require larger cohorts and longitudinal prospective studies to design potential anti-aging interventions.

Original languageEnglish (US)
Article number102368
JournalCell Reports Medicine
Volume6
Issue number10
DOIs
StatePublished - Oct 21 2025
Externally publishedYes

Keywords

  • aging
  • epigenetics
  • genetics
  • microbiome
  • supercentenarian

ASJC Scopus subject areas

  • General Medicine
  • General Biochemistry, Genetics and Molecular Biology

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