PuSH - Publikationsserver des Helmholtz Zentrums München

Zierer, J. ; Kastenmüller, G. ; Suhre, K. ; Gieger, C. ; Codd, V.* ; Tsai, P.C.* ; Bell, J.* ; Peters, A. ; Strauch, K. ; Schulz, H. ; Weidinger, S.* ; Mohney, R.P.* ; Samani, N.J.* ; Spector, T.* ; Mangino, M.* ; Menni, C.*

Metabolomics profiling reveals novel markers for leukocyte telomere length.

Aging 8, 77-94 (2016)
Verlagsversion PMC
Free journal
Creative Commons Lizenzvertrag
Leukocyte telomere length (LTL) is considered one of the most predictive markers of biological aging. The aim of this study was to identify novel pathways regulating LTL using a metabolomics approach. To this end, we tested associations between 280 blood metabolites and LTL in 3511 females from TwinsUK and replicated our results in the KORA cohort. We furthermore tested significant metabolites for associations with several aging-related phenotypes, gene expression markers and epigenetic markers to investigate potential underlying pathways. Five metabolites were associated with LTL: Two lysolipids, 1-stearoylglycerophosphoinositol (P=1.6×10-5) and 1-palmitoylglycerophosphoinositol (P=1.6×10-5), were found to be negatively associated with LTL and positively associated with phospholipase A2 expression levels suggesting an involvement of fatty acid metabolism and particularly membrane composition in biological aging. Moreover, two gamma-glutamyl amino acids, gamma-glutamyltyrosine (P=2.5×10-6) and gamma-glutamylphenylalanine (P=1.7×10-5), were negatively correlated with LTL. Both are products of the glutathione cycle and markers for increased oxidative stress. Metabolites were also correlated with functional measures of aging, i.e. higher blood pressure and HDL cholesterol levels and poorer lung, liver and kidney function. Our results suggest an involvement of altered fatty acid metabolism and increased oxidative stress in human biological aging, reflected by LTL and age-related phenotypes of vital organ systems.
Altmetric
Weitere Metriken?
[➜Einloggen]
Zusatzinfos bearbeiten [➜Einloggen]
Publikationstyp Artikel: Journalartikel
Dokumenttyp Wissenschaftlicher Artikel
Korrespondenzautor
Schlagwörter Biological Aging ; Glutathione ; Metabolomics ; Oxidative Stress ; Telomere Length; Glutathione Metabolism; Alzheimers-disease; Membrane Fluidity; Oxidative-stress; Blood; Cells; Association; Health; Centenarians; Mortality
ISSN (print) / ISBN 1945-4589
e-ISSN 1945-4589
Zeitschrift Aging
Quellenangaben Band: 8, Heft: 1, Seiten: 77-94 Artikelnummer: , Supplement: ,
Verlag Impact Journals LLC
Nichtpatentliteratur Publikationen
Begutachtungsstatus Peer reviewed
Institut(e) Institute of Bioinformatics and Systems Biology (IBIS)
Institute of Epidemiology II (EPI2)
Institute of Genetic Epidemiology (IGE)
Institute of Epidemiology (EPI)