Evidence map›Paper›PMID 35684951›Full record

ArticleAnnals of clinical and translational neurology2022

Dissecting the limited genetic overlap of Parkinson's and Alzheimer's disease.

Maren Stolp Andersen, Manuela Tan, Inge R Holtman, John Hardy, International Parkinson's Disease Genomics Consortium, Lasse Pihlstrøm

Open access · goldAbstract read
In one paragraph

Article in Annals of clinical and translational neurology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed, 1 pooled it
3.2field-weighted citation impact, top 8% 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

10 citing papers in PubMed, 1 synthesis or guideline pooled it, 17 citations in OpenAlex.

  1. Pooled it
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  10. Dissecting the limited genetic overlap of Parkinson's and Alzheimer's disease.Annals of clinical and translational neurology · 2022
    Article
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

6 authors at 3 institutions in 5 countries.

Maren Stolp AndersenDepartment of Neurology, Oslo University Hospital, Oslo, Norway.
Manuela TanDepartment of Neurology, Oslo University Hospital, Oslo, Norway.
Inge R HoltmanSection Molecular Neurobiology, Department of Biomedical Sciences of Cells & Systems, University of Groningen, University Medical Center Groningen, Groningen, The Netherlands.
John HardyDepartment of Neurodegenerative Disease, Queen Square Institute of Neurology, University College London, London, UK.
International Parkinson's Disease Genomics Consortium
Lasse PihlstrømDepartment of Neurology, Oslo University Hospital, Oslo, Norway.ORCID 0000-0002-7635-8645
Oslo University Hospital · NOHong Kong University of Science and Technology · HKUniversity Medical Center Groningen · NL

Funding

Department of HealthMedical Research Council G0701075Medical Research Council G0901254Medical Research Council MR/N026004/1Wellcome TrustWellcome Trust 202903/Z/16/Z
6 · The paper itself

Abstract

Parkinson's disease and Alzheimer's disease show overlapping features both clinically and neuropathologically and elucidating shared mechanisms could have important implications for therapeutic strategies. Evidence for genetic overlap is limited, although enrichment of heritability in genomic regions relevant to microglia has been demonstrated in both disorders. Using summary statistics from genome-wide association studies, we assessed genetic covariance stratified by cell types and local genetic correlation between Parkinson's and Alzheimer's disease. Significant covariance was observed for neurons only (p = 0.00046), and local genetic correlation was significant only in the human leukocyte antigen region (p = 1.0e-05). Our findings support a minor genetic overlap between these two disorders.

Indexed as

Alzheimer DiseaseParkinson DiseaseGenome-Wide Association StudyHumansMicrogliaNeurons

Identifiers

PMID35684951
PMCPMC9380131
OpenAlexW4281690897

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.