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Uncovering the Relationship between Selenium Status, Age, Health, and Dietary Habits: Insights from a Large Population Study including Nonagenarian Offspring from the MARK-AGE Project

  • Robertina Giacconi
  • , Francesco Piacenza
  • , Valentina Aversano
  • , Michele Zampieri
  • , Alexander Bürkle
  • , María Moreno Villanueva
  • , Martijn E.T. Dollé
  • , Eugène Jansen
  • , Tilman Grune
  • , Efstathios S. Gonos
  • , Claudio Franceschi
  • , Miriam Capri
  • , Birgit Weinberger
  • , Ewa Sikora
  • , Olivier Toussaint
  • , Florence Debacq-Chainiaux
  • , Wolfgang Stuetz
  • , Pieternella Eline Slagboom
  • , Jürgen Bernhardt
  • , Maria Luisa Fernández-Sánchez
  • Mauro Provinciali, Marco Malavolta

Research output: Contribution to journalArticlepeer-review

Abstract

An inadequate selenium (Se) status can accelerate the aging process, increasing the vulnerability to age-related diseases. The study aimed to investigate plasma Se and Se species in a large population, including 2200 older adults from the general population (RASIG), 514 nonagenarian offspring (GO), and 293 GO Spouses (SGO). Plasma Se levels in women exhibit an inverted U-shaped pattern, increasing with age until the post-menopausal period and then declining. Conversely, men exhibit a linear decline in plasma Se levels with age. Subjects from Finland had the highest plasma Se values, while those from Poland had the lowest ones. Plasma Se was influenced by fish and vitamin consumption, but there were no significant differences between RASIG, GO, and SGO. Plasma Se was positively associated with albumin, HDL, total cholesterol, fibrinogen, and triglycerides and negatively associated with homocysteine. Fractionation analysis showed that Se distribution among plasma selenoproteins is affected by age, glucometabolic and inflammatory factors, and being GO or SGO. These findings show that sex-specific, nutritional, and inflammatory factors play a crucial role in the regulation of Se plasma levels throughout the aging process and that the shared environment of GO and SGO plays a role in their distinctive Se fractionation.

Original languageEnglish
Article number2182
JournalNutrients
Volume15
Issue number9
DOIs
Publication statusPublished - May 2023

Funding

This work was supported by the European Commission (Project Full Name: European Study to Establish Biomarkers of Human Ageing; Project Acronym: MARK-AGE; Project No: 200880) and by the Italian Health Ministry with the Ricerca corrente project: Programmazione triennale IRCCS 2022-2024.

FundersFunder number
European Commission
Seventh Framework Programme200880
Italian Health MinistryIRCCS 2022-2024

    Keywords

    • aging
    • inflammation
    • longevity
    • plasma selenium
    • selenium fractionation

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