Common diseases alter the physiological age-related blood microRNA profile

Author:

Fehlmann TobiasORCID,Lehallier BenoitORCID,Schaum Nicholas,Hahn Oliver,Kahraman MustafaORCID,Li Yongping,Grammes Nadja,Geffers LarsORCID,Backes ChristinaORCID,Balling RudiORCID,Kern Fabian,Krüger Rejko,Lammert FrankORCID,Ludwig Nicole,Meder Benjamin,Fromm BastianORCID,Maetzler Walter,Berg Daniela,Brockmann Kathrin,Deuschle Christian,von Thaler Anna-KatharinaORCID,Eschweiler Gerhard W.,Milman Sofiya,Barziliai Nir,Reichert MatthiasORCID,Wyss-Coray TonyORCID,Meese Eckart,Keller AndreasORCID

Abstract

AbstractAging is a key risk factor for chronic diseases of the elderly. MicroRNAs regulate post-transcriptional gene silencing through base-pair binding on their target mRNAs. We identified nonlinear changes in age-related microRNAs by analyzing whole blood from 1334 healthy individuals. We observed a larger influence of the age as compared to the sex and provide evidence for a shift to the 5’ mature form of miRNAs in healthy aging. The addition of 3059 diseased patients uncovered pan-disease and disease-specific alterations in aging profiles. Disease biomarker sets for all diseases were different between young and old patients. Computational deconvolution of whole-blood miRNAs into blood cell types suggests that cell intrinsic gene expression changes may impart greater significance than cell abundance changes to the whole blood miRNA profile. Altogether, these data provide a foundation for understanding the relationship between healthy aging and disease, and for the development of age-specific disease biomarkers.

Funder

Michael J. Fox Foundation for Parkinson’s Research

Fonds National de la Recherche Luxembourg

Deutsche Krebshilfe

Parts of the measurements have been funded by Hummingbird Diagnostics GmbH.

Publisher

Springer Science and Business Media LLC

Subject

General Physics and Astronomy,General Biochemistry, Genetics and Molecular Biology,General Chemistry

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