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Licensed Unlicensed Requires Authentication Published by De Gruyter October 17, 2015

Galectin-3, osteopontin and successful aging

  • Fabian Sanchis-Gomar EMAIL logo , Alejandro Santos-Lozano , Helios Pareja-Galeano , Nuria Garatachea , Rafael Alis , Carmen Fiuza-Luces , María Morán , Enzo Emanuele and Alejandro Lucia

Abstract

Background:

Individuals who reach exceptional longevity (100+ years of age) free of common chronic age diseases (i.e. ‘dodgers’) arguably represent the paradigm of successful aging in humans. As such, identification of potential biomarkers associated with this phenomenon is of medical interest.

Methods:

We measured serum levels of galectin-3 and osteopontin, both of which have been shown to be linked with major chronic or aging-related disorders in younger populations, in centenarian ‘dodgers’ (n=81; 40 men; 100–104 years) and healthy controls (n=41; 24 men, 70–80 years).

Results:

Both biomarkers showed significantly lower values (p<0.001) in the former (galectin-3: 2.4±1.7 vs. 4.8±2.8 ng/mL; osteopontin: 38.1±27.7 vs. 72.6±33.1 μg/mL). Logistic regression analysis identified the combination of these two biomarkers as a significant predictor variable associated with successful aging regardless of sex (p<0.001). The area under the curve (AUC) classified the ability of galectin-3 and osteopontin to predict the likelihood of successful aging as ‘fair’ (AUC=0.75) and ‘good’ (AUC=0.80), respectively. Particularly, the combination of the two biomarkers showed good discriminatory power for successful aging (AUC=0.86), with sensitivity=83% and specificity=74%.

Conclusions:

Lower levels of both galectin-3 and osteopontin are associated with successful aging, representing potential biomarkers of this condition. Our cross-sectional data must be however approached with caution. Further research is necessary to replicate the present preliminary results in other cohorts and to identify the potential use of galectin-3 and osteopontin as potential targets (or at least predictors) in future personalized anti-aging therapies.


Corresponding author: Fabian Sanchis-Gomar, MD, PhD, Research Institute Hospital 12 de Octubre (‘i+12’), Edificio actividades ambulatorias, 6a planta., Avda. de Córdoba s/n, 28041 Madrid, Spain, Phone: +34 91 779 2784, Fax: +34 91 390 8544, E-mail:
aFabian Sanchis-Gomar and Alejandro Santos-Lozano contributed equally to this article.bEnzo Emanuele and Alejandro Lucia share senior authorship.
  1. Author contributions: All the authors have accepted responsibility for the entire content of this submitted manuscript and approved submission.

  2. Research funding: Research in the field of aging by A. Lucia is funded by Fondo de Investigaciones Sanitarias (FIS, grant #PI15/00558) and Fondos Feder.

  3. Employment or leadership: None declared.

  4. Honorarium: None declared.

  5. Competing interests: The funding organization(s) played no role in the study design; in the collection, analysis, and interpretation of data; in the writing of the report; or in the decision to submit the report for publication.

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Received: 2015-8-25
Accepted: 2015-9-15
Published Online: 2015-10-17
Published in Print: 2016-5-1

©2016 Walter de Gruyter GmbH, Berlin/Boston

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