Piacenza Francesco, Giacconi Robertina, Costarelli Laura, Basso Andrea, Bürkle Alexander, Moreno-Villanueva María, Dollé Martijn E T, Jansen Eugène, Grune Tilman, Weber Daniela, Stuetz Wolfgang, Gonos Efstathios S, Schön Christiane, Bernhardt Jürgen, Grubeck-Loebenstein Beatrix, Sikora Ewa, Toussaint Olivier, Debacq-Chainiaux Florence, Franceschi Claudio, Capri Miriam, Hervonen Antti, Hurme Mikko, Slagboom Eline, Breusing Nicolle, Mocchegiani Eugenio, Malavolta Marco
Translational Research Center of Nutrition and Ageing, IRCCS INRCA, Ancona, Italy.
Department of Biology, University of Konstanz, Germany.
J Gerontol A Biol Sci Med Sci. 2021 Nov 15;76(12):2097-2106. doi: 10.1093/gerona/glab134.
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.
对铜(Cu)和锌(Zn)及其主要血清载体白蛋白(Alb)和铜蓝蛋白(Cp)进行分析,可为了解人体维持金属稳态的能力提供信息。然而,此前从未在大规模研究中探究过它们与衰老、性别、体重指数以及营养和炎症标志物之间的关系。在此,我们报告欧洲大规模横断面研究MARK-AGE的结果,该研究测定了2424名年龄分层参与者(35至75岁)的铜、锌、白蛋白、铜蓝蛋白以及营养和炎症参数,这些参与者包括普通人群(RASIG)、百岁老人后代(GO),后者是一个经过充分研究的长寿遗传模型,以及GO的配偶(SGO)。在RASIG中,女性的铜锌比和铜蓝蛋白与白蛋白之比高于男性。这两个比值均随衰老而升高,因为铜和铜蓝蛋白增加,而白蛋白和锌减少。研究发现铜、锌、白蛋白和铜蓝蛋白与多种炎症及营养生物标志物相关。与RASIG相比,GO的锌水平和锌与白蛋白之比更高,但我们未观察到与SGO有显著差异,这可能是由于SGO样本量较小且环境相同所致。我们的结果表明,衰老、性别、体重指数和GO状态具有不同水平的铜、锌及其血清载体蛋白特征。这些数据及其与炎症生物标志物的关系支持了金属稳态丧失是炎症衰老特征之一的概念。