TY - JOUR
T1 - Age, Sex, and BMI Influence on Copper, Zinc, and Their Major Serum Carrier Proteins in a Large European Population including Nonagenarian Offspring from MARK-AGE Study
AU - Piacenza, Francesco
AU - Giacconi, Robertina
AU - Costarelli, Laura
AU - Basso, Andrea
AU - Bürkle, Alexander
AU - Moreno-Villanueva, María
AU - Dollé, Martijn E.T.
AU - Jansen, Eugène
AU - Grune, Tilman
AU - Weber, Daniela
AU - Stuetz, Wolfgang
AU - Gonos, Efstathios S.
AU - Schön, Christiane
AU - Bernhardt, Jürgen
AU - Grubeck-Loebenstein, Beatrix
AU - Sikora, Ewa
AU - Toussaint, Olivier
AU - Debacq-Chainiaux, Florence
AU - Franceschi, Claudio
AU - Capri, Miriam
AU - Hervonen, Antti
AU - Hurme, Mikko
AU - Slagboom, Eline
AU - Breusing, Nicolle
AU - Mocchegiani, Eugenio
AU - Malavolta, Marco
N1 - Publisher Copyright:
© 2021 The Author(s) 2021.
PY - 2021/12/1
Y1 - 2021/12/1
N2 - The analysis of copper (Cu) and zinc (Zn) along with their major serum carriers, albumin (Alb) and ceruloplasmin (Cp), could provide information on the capacity of humans to maintain homeostasis of metals (metallostasis). However, their relationship with aging, sex, body mass index, as well as with nutritional and inflammatory markers was never investigated in a large-scale study. Here, we report results from the European large-scale cross-sectional study MARK-AGE in which Cu, Zn, Alb, Cp, as well as nutritional and inflammatory parameters were determined in 2424 age-stratified participants (35-75 years), including the general population (RASIG), nonagenarian offspring (GO), a well-studied genetic model of longevity, and spouses of GO (SGO). In RASIG, Cu to Zn ratio and Cp to Alb ratio were higher in women than in men. Both ratios increased with aging because Cu and Cp increased and Alb and Zn decreased. Cu, Zn, Alb, and Cp were found associated with several inflammatory as well as nutritional biomarkers. GO showed higher Zn levels and higher Zn to Alb ratio compared to RASIG, but we did not observe significant differences with SGO, likely as a consequence of the low sample size of SGO and the shared environment. Our results show that aging, sex, body mass index, and GO status are characterized by different levels of Cu, Zn, and their serum carrier proteins. These data and their relationship with inflammatory biomarkers support the concept that loss of metallostasis is a characteristic of inflammaging.
AB - The analysis of copper (Cu) and zinc (Zn) along with their major serum carriers, albumin (Alb) and ceruloplasmin (Cp), could provide information on the capacity of humans to maintain homeostasis of metals (metallostasis). However, their relationship with aging, sex, body mass index, as well as with nutritional and inflammatory markers was never investigated in a large-scale study. Here, we report results from the European large-scale cross-sectional study MARK-AGE in which Cu, Zn, Alb, Cp, as well as nutritional and inflammatory parameters were determined in 2424 age-stratified participants (35-75 years), including the general population (RASIG), nonagenarian offspring (GO), a well-studied genetic model of longevity, and spouses of GO (SGO). In RASIG, Cu to Zn ratio and Cp to Alb ratio were higher in women than in men. Both ratios increased with aging because Cu and Cp increased and Alb and Zn decreased. Cu, Zn, Alb, and Cp were found associated with several inflammatory as well as nutritional biomarkers. GO showed higher Zn levels and higher Zn to Alb ratio compared to RASIG, but we did not observe significant differences with SGO, likely as a consequence of the low sample size of SGO and the shared environment. Our results show that aging, sex, body mass index, and GO status are characterized by different levels of Cu, Zn, and their serum carrier proteins. These data and their relationship with inflammatory biomarkers support the concept that loss of metallostasis is a characteristic of inflammaging.
KW - Albumin
KW - Ceruloplasmin
KW - Chronic inflammatory status
KW - Homeostasis
KW - Metallostasis
UR - http://www.scopus.com/inward/record.url?scp=85112178694&partnerID=8YFLogxK
U2 - 10.1093/gerona/glab134
DO - 10.1093/gerona/glab134
M3 - Article
C2 - 33983441
AN - SCOPUS:85112178694
SN - 1079-5006
VL - 76
SP - 2097
EP - 2106
JO - The journals of gerontology. Series A, Biological sciences and medical sciences
JF - The journals of gerontology. Series A, Biological sciences and medical sciences
IS - 12
ER -