Evidence map›Paper›PMID 35362642›Full record

ArticleThe European journal of neuroscience2022

A comparison of blood and brain-derived ageing and inflammation-related DNA methylation signatures and their association with microglial burdens.

Anna J Stevenson, Daniel L McCartney, Danni A Gadd, Gemma Shireby, Robert F Hillary, Declan King, Makis Tzioras, Nicola Wrobel, Sarah McCafferty, Lee Murphy and 12 more

Open access · hybridAbstract read
In one paragraph

Article in The European journal of neuroscience, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
1.3field-weighted citation impact, top 21% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 16 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Article
  5. A blood- and brain-based EWAS of smoking.Nature communications · 2025
    Article
  6. Quantification of Epigenetic Aging in Public Health.Annual review of public health · 2025
    Review
  7. Article
  8. Article
  9. Article
  10. Synaptic resilience is associated with maintained cognition during ageing.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2023
    Article
  11. Article
  12. Within subject cross-tissue analyzes of epigenetic clocks in substance use disorder postmortem brain and blood.American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics · 2023
    Article
  13. Article
  14. Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

22 authors at 7 institutions in 1 country.

Anna J StevensonCentre for Genomic and Experimental Medicine, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, UK.ORCID 0000-0002-0435-3562
Daniel L McCartneyCentre for Genomic and Experimental Medicine, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, UK.
Danni A GaddCentre for Genomic and Experimental Medicine, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, UK.
Gemma ShirebyUniversity of Exeter Medical School, University of Exeter, Exeter, UK.
Robert F HillaryCentre for Genomic and Experimental Medicine, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, UK.
Declan KingCentre for Discovery Brain Sciences, University of Edinburgh, Edinburgh, UK.ORCID 0000-0002-2434-9317
Makis TziorasCentre for Discovery Brain Sciences, University of Edinburgh, Edinburgh, UK.
Nicola WrobelEdinburgh Clinical Research Facility, Western General Hospital, Edinburgh, UK.
Sarah McCaffertyEdinburgh Clinical Research Facility, Western General Hospital, Edinburgh, UK.
Lee MurphyEdinburgh Clinical Research Facility, Western General Hospital, Edinburgh, UK.
Barry W McCollCentre for Discovery Brain Sciences, University of Edinburgh, Edinburgh, UK.
Paul RedmondLothian Birth Cohorts, University of Edinburgh, Edinburgh, UK.
Adele M TaylorLothian Birth Cohorts, University of Edinburgh, Edinburgh, UK.
Sarah E HarrisLothian Birth Cohorts, University of Edinburgh, Edinburgh, UK.
Tom C RussLothian Birth Cohorts, University of Edinburgh, Edinburgh, UK.
Andrew M McIntoshDivision of Psychiatry, University of Edinburgh, Royal Edinburgh Hospital, Edinburgh, UK.
Jonathan MillUniversity of Exeter Medical School, University of Exeter, Exeter, UK.
Colin SmithCentre for Clinical Brain Sciences, University of Edinburgh, Edinburgh, UK.
Ian J DearyLothian Birth Cohorts, University of Edinburgh, Edinburgh, UK.
Simon R CoxLothian Birth Cohorts, University of Edinburgh, Edinburgh, UK.ORCID 0000-0003-4036-3642
Riccardo E MarioniCentre for Genomic and Experimental Medicine, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, UK.ORCID 0000-0003-4430-4260
Tara L Spires-JonesCentre for Discovery Brain Sciences, University of Edinburgh, Edinburgh, UK.ORCID 0000-0003-2530-0598
NHS Lothian · GBEdinburgh Cancer Research · GBUK Dementia Research Institute · GBWestern General Hospital · GBUniversity of Exeter · GBRoyal Edinburgh Hospital · GBUniversity of Edinburgh · GB

Funding

Evaluating Longitudinal Changes in the Human Structural Connectome in Relation to Cognitive AgingR01AG054628 · NIA · UNIVERSITY OF TEXAS AT AUSTIN · PI TUCKER-DROB, ELLIOT MAX · 2017 to 2021
$2.7M
Medical Research Council G0700704Medical Research Council MR/K026992/1Medical Research Council MR/M01311/1Medical Research Council MR/M013111/1Medical Research Council MR/R024065/1NIA NIH HHS R01 AG054628Wellcome TrustWellcome Trust 108890/Z/15/ZWellcome Trust 203771/Z/16/Z
6 · The paper itself

Abstract

Inflammation and ageing-related DNA methylation patterns in the blood have been linked to a variety of morbidities, including cognitive decline and neurodegenerative disease. However, it is unclear how these blood-based patterns relate to patterns within the brain and how each associates with central cellular profiles. In this study, we profiled DNA methylation in both the blood and in five post mortem brain regions (BA17, BA20/21, BA24, BA46 and hippocampus) in 14 individuals from the Lothian Birth Cohort 1936. Microglial burdens were additionally quantified in the same brain regions. DNA methylation signatures of five epigenetic ageing biomarkers ('epigenetic clocks'), and two inflammatory biomarkers (methylation proxies for C-reactive protein and interleukin-6) were compared across tissues and regions. Divergent associations between the inflammation and ageing signatures in the blood and brain were identified, depending on region assessed. Four out of the five assessed epigenetic age acceleration measures were found to be highest in the hippocampus (β range = 0.83-1.14, p ≤ 0.02). The inflammation-related DNA methylation signatures showed no clear variation across brain regions. Reactive microglial burdens were found to be highest in the hippocampus (β = 1.32, p = 5 × 10

Indexed as

DNA MethylationNeurodegenerative DiseasesBiomarkersBrainEpigenesis, GeneticHumansInflammationMicrogliaBiomarkersCRPDNA methylationepigenetic clockIL-6inflammationmicroglia

Identifiers

PMID35362642
PMCPMC9525452
OpenAlexW4226016725

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.