Evidence map›Paper›PMID 28097204›Full record

ArticleAnnals of clinical and translational neurology2016

Genomics implicates adaptive and innate immunity in Alzheimer's and Parkinson's diseases.

Sarah A Gagliano, Jennie G Pouget, John Hardy, Jo Knight, Michael R Barnes, Mina Ryten, Michael E Weale

Open access · goldAbstract read
In one paragraph

Article in Annals of clinical and translational neurology, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 65 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
65citing papers in PubMed, 2 pooled it
7.1field-weighted citation impact, top 3% 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

65 citing papers in PubMed, 2 syntheses or guidelines pooled it, 92 citations in OpenAlex.

  1. Pooled it
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  6. Tuft Cells in the Gut Limit Cognitive Disorders by Regulating Gut Homeostasis.Cellular and molecular gastroenterology and hepatology · 2026
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  11. bioRxiv : the preprint server for biology · 2024
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5 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

7 authors at 4 institutions in 2 countries.

Sarah A GaglianoDepartment of Medical & Molecular Genetics Guy's Hospital King's College London 8th Floor Tower Wing London SE1 9RT United Kingdom; Campbell Family Mental Health Research Institute Centre for Addiction and Mental Health 250 College Street Toronto Ontario M5T 1R8 Canada; Institute of Medical Science University of Toronto 1 King's College Circle Room 2374 Toronto Ontario M5S 1A8 Canada.ORCID 0000-0003-1306-1868
Jennie G PougetCampbell Family Mental Health Research Institute Centre for Addiction and Mental Health 250 College Street Toronto Ontario M5T 1R8 Canada; Institute of Medical Science University of Toronto 1 King's College Circle Room 2374 Toronto Ontario M5S 1A8 Canada; Department of Psychiatry University of Toronto 250 College Street 8th Floor Toronto Ontario M5T 1R8 Canada.
John HardyInstitute of Neurology University College London Queen Square London WC1N 3BG United Kingdom.
Jo KnightCampbell Family Mental Health Research Institute Centre for Addiction and Mental Health 250 College Street Toronto Ontario M5T 1R8 Canada; Institute of Medical Science University of Toronto 1 King's College Circle Room 2374 Toronto Ontario M5S 1A8 Canada; Department of Psychiatry University of Toronto 250 College Street 8th Floor Toronto Ontario M5T 1R8 Canada; Data Science Institute and Faculty of Health and Medicine Furness College Lancaster University Lancaster LA1 4YG United Kingdom.
Michael R BarnesWilliam Harvey Research Institute Barts and The London School of Medicine and Dentistry Queen Mary University of London Charterhouse Square London EC1M 6BQ United Kingdom.
Mina RytenInstitute of Neurology University College London Queen Square London WC1N 3BG United Kingdom.
Michael E WealeDepartment of Medical & Molecular Genetics Guy's Hospital King's College London 8th Floor Tower Wing London SE1 9RT United Kingdom.
Centre for Addiction and Mental Health · CAGuy's Hospital · GBNational Hospital for Neurology and Neurosurgery · GBQueen Mary University of London · GB

Funding

National Centralized Repository for Alzheimer's Disease and Related Dementias (NCRAD)U24AG021886 · NIA · INDIANA UNIV-PURDUE UNIV AT INDIANAPOLIS · PI TATIANA M. FOROUD · 2002 to 2026
$119.8M
NATIONAL ALZHEIMERS COORDINATING CENTER (NACC)U01AG016976 · NIA · UNIVERSITY OF WASHINGTON · PI KUKULL, WALTER ANTHONY · 1999 to 2020
$72.8M
Alzheimer's Disease Genetics ConsortiumU01AG032984 · NIA · UNIVERSITY OF PENNSYLVANIA · PI SCHELLENBERG, GERARD DAVID · 2009 to 2024
$60.4M
CHARGE Consortium: Omics Discovery for CVD and Aging PhenotypesR01HL105756 · NHLBI · UNIVERSITY OF WASHINGTON · PI Bruce M Psaty, NICHOLAS L SMITH · 2011 to 2026
$9.5M
Collaborative GWAS of Dementia, AD and related MRI and Cognitive EndophenotypesR01AG033193 · NIA · BOSTON UNIVERSITY MEDICAL CAMPUS · PI SESHADRI, SUDHA · 2009 to 2016
$4.4M
Medical Research Council G0802462Medical Research Council MR/K01417X/1Medical Research Council MR/N008324/1NHLBI NIH HHS R01 HL105756NIA NIH HHS R01 AG033193NIA NIH HHS U01 AG016976NIA NIH HHS U01 AG032984NIA NIH HHS U24 AG021886Wellcome Trust
6 · The paper itself

Abstract

objectivesWe assessed the current genetic evidence for the involvement of various cell types and tissue types in the etiology of neurodegenerative diseases, especially in relation to the neuroinflammatory hypothesis of neurodegenerative diseases.

methodsWe obtained large-scale genome-wide association study (GWAS) summary statistics from Parkinson's disease (PD), Alzheimer's disease (AD), and amyotrophic lateral sclerosis (ALS). We used multiple sclerosis (MS), an autoimmune disease of the central nervous system, as a positive control. We applied stratified LD score regression to determine if functional marks for cell type and tissue activity, and gene-set lists were enriched for genetic heritability. We compared our results to those from two gene-set enrichment methods (Ingenuity Pathway Analysis and enrichr).

resultsThere were no significant heritability enrichments for annotations marking genes active within brain regions, but there were significant heritability enrichments for annotations marking genes active within cell types that form part of both the innate and adaptive immune systems. We found this for MS (as expected) and also for AD and PD. The strongest signals were from the adaptive immune system (e.g., T cells) for PD, and from both the adaptive (e.g., T cells) and innate (e.g., CD14: a marker for monocytes, and CD15: a marker for neutrophils) immune systems for AD. Annotations from the liver were also significant for AD. Pathway analysis provided complementary results.

interpretationFor AD and PD, we found significant enrichment of heritability in annotations marking gene activity in immune cells.

Identifiers

PMID28097204
PMCPMC5224821
OpenAlexW2531792466

What OpenQuestion holds

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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.