Evidence map›Paper›PMID 34301914›Full record

ArticleTranslational psychiatry2021

Heterogeneous effects of genetic risk for Alzheimer's disease on the phenome.

Hei Man Wu, Alison M Goate, Paul F O'Reilly

Open access · goldAbstract read
In one paragraph

Article in Translational psychiatry, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 34% 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

8 citing papers in PubMed, 1 synthesis or guideline pooled it, 6 citations in OpenAlex.

  1. Pooled it
  2. Review
  3. Review
  4. Article
  5. Advancements in APOE and dementia research: Highlights from the 2023 AAIC Advancements: APOE conference.Alzheimer's & dementia : the journal of the Alzheimer's Association · 2024
    Review
  6. Review
  7. Apolipoprotein E in lipid metabolism and neurodegenerative disease.Trends in endocrinology and metabolism: TEM · 2023
    Review
  8. Myelin in Alzheimer's disease: culprit or bystander?Acta neuropathologica communications · 2023
    Review
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

3 authors at 1 institution in 1 country.

Hei Man WuDepartment of Genetics and Genomic Sciences, Icahn School of Medicine, Mount Sinai, New York, NY, USA. heiman.wu@mssm.edu.ORCID 0000-0003-1559-7586
Alison M GoateDepartment of Genetics and Genomic Sciences, Icahn School of Medicine, Mount Sinai, New York, NY, USA.ORCID 0000-0002-0576-2472
Paul F O'ReillyDepartment of Genetics and Genomic Sciences, Icahn School of Medicine, Mount Sinai, New York, NY, USA. paul.oreilly@mssm.edu.ORCID 0000-0001-7515-0845
Icahn School of Medicine at Mount Sinai · US

Funding

Genomic approach to identification of microglial networks involved in Alzheimer’s disease riskU01AG058635 · NIA · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI GOATE, ALISON M · 2018 to 2022
$4.8M
Identification and characterization of AD risk networks using multi-dimensional "omics" dataU01AG052411 · NIA · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI CRUCHAGA, CARLOS, GOATE, ALISON M · 2016 to 2020
$4.5M
Next-generation, pathway-specific, polygenic risk scoresR01MH122866 · NIMH · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI O'REILLY, PAUL FRANCIS · 2020 to 2024
$3.1M
Big Omics Data Engine 2 SupercomputerS10OD026880 · OD · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI KOVATCH, PATRICIA · 2019 to 2019
$2.0M
Medical Research Council MC_PC_17228Medical Research Council MC_QA137853NIA NIH HHS U01 AG052411NIA NIH HHS U01 AG058635NIH HHS S10 OD026880NIMH NIH HHS R01 MH122866RCUK | Medical Research Council (MRC) MR/N015746/1U.S. Department of Health & Human Services | NIH | National Institute of Mental Health (NIMH) R01MH122866
6 · The paper itself

Abstract

Here we report how four major forms of Alzheimer's disease (AD) genetic risk-APOE-ε4, APOE-ε2, polygenic risk and familial risk-are associated with 273 traits in ~500,000 individuals in the UK Biobank. The traits cover blood biochemistry and cell traits, metabolic and general health, psychosocial health, and cognitive function. The difference in the profile of traits associated with the different forms of AD risk is striking and may contribute to heterogenous presentation of the disease. However, we also identify traits significantly associated with multiple forms of AD genetic risk, as well as traits showing significant changes across ages in those at high risk of AD, which may point to their potential roles in AD etiology. Finally, we highlight how survivor effects, in particular those relating to shared risks of cardiovascular disease and AD, can generate associations that may mislead interpretation in epidemiological AD studies. The UK Biobank provides a unique opportunity to powerfully compare the effects of different forms of AD genetic risk on the phenome in the same cohort.

Indexed as

Alzheimer DiseaseApolipoproteins EGenotypeHumansMultifactorial InheritancePhenotypeRisk FactorsApolipoproteins E

Identifiers

PMID34301914
PMCPMC8302633
OpenAlexW3184056734

What OpenQuestion holds

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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.