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Brain microRNAs associated with late-life depressive symptoms are also associated with cognitive trajectory and dementia
- Source :
- npj Genomic Medicine, Vol 5, Iss 1, Pp 1-8 (2020), NPJ Genomic Medicine
- Publication Year :
- 2020
- Publisher :
- Springer Science and Business Media LLC, 2020.
-
Abstract
- Late-life depression is associated with an increased risk for dementia but we have limited knowledge of the molecular mechanisms underlying this association. Here we investigated whether brain microRNAs, important posttranscriptional regulators of gene expression, contribute to this association. Late-life depressive symptoms were assessed annually in 300 participants of the Religious Orders Study and Rush Memory and Aging Project for a mean of 7 years. Participants underwent annual cognitive testing, clinical assessment of cognitive status, and uniform neuropathologic examination after death. microRNAs were profiled from the prefrontal cortex using NanoString platform in the discovery cohort and small RNA sequencing in the replication cohort. A global microRNA association study of late-life depressive symptoms was performed using linear mixed model adjusting for the potential confounding factors. Four brain microRNAs were associated with late-life depressive symptoms at adjusted p
- Subjects :
- 0301 basic medicine
Oncology
medicine.medical_specialty
lcsh:QH426-470
lcsh:Medicine
Article
03 medical and health sciences
0302 clinical medicine
Internal medicine
Genetics
medicine
Dementia
Prefrontal cortex
Molecular Biology
Genetics (clinical)
Depression (differential diagnoses)
Memory and aging
Molecular medicine
Depression
business.industry
lcsh:R
Confounding
Cognition
medicine.disease
3. Good health
Cognitive test
lcsh:Genetics
030104 developmental biology
Cohort
business
030217 neurology & neurosurgery
Subjects
Details
- ISSN :
- 20567944
- Volume :
- 5
- Database :
- OpenAIRE
- Journal :
- npj Genomic Medicine
- Accession number :
- edsair.doi.dedup.....caa9e841d9344c1f14067090cf9c2254
- Full Text :
- https://doi.org/10.1038/s41525-019-0113-8