Evidence map›Paper›PMID 40181078›Full record

ArticleScientific reports2025

Polygenic score analysis identifies distinct genetic risk profiles in Alzheimer's disease comorbidities.

Carlos F Hernández, Camilo Villaman, Costin Leu, Dennis Lal, Ignacio Mata, Andrés D Klein, Eduardo Pérez-Palma

Abstract read
In one paragraph

Article in Scientific reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
–field-weighted citation impact
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

5 citing papers in PubMed.

  1. Trial
  2. Article
  3. Genetic Burden andJournal of personalized medicine · 2026
    Article
  4. Review
  5. 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

7 authors.

Carlos F HernándezUniversidad del Desarrollo, Centro de Genética y Genómica, Facultad de Medicina Clínica Alemana, 7610658, Santiago, Chile.
Camilo VillamanUniversidad del Desarrollo, Centro de Genética y Genómica, Facultad de Medicina Clínica Alemana, 7610658, Santiago, Chile.
Costin LeuCenter for Neurogenetics, The University of Texas Health Science Center at Houston, Houston, TX, 77030, USA.
Dennis LalCenter for Neurogenetics, The University of Texas Health Science Center at Houston, Houston, TX, 77030, USA.
Ignacio MataGenomic Medicine Institute, Lerner Research Institute, Cleveland Clinic, Cleveland, OH, USA.
Andrés D KleinUniversidad del Desarrollo, Centro de Genética y Genómica, Facultad de Medicina Clínica Alemana, 7610658, Santiago, Chile.
Eduardo Pérez-PalmaUniversidad del Desarrollo, Centro de Genética y Genómica, Facultad de Medicina Clínica Alemana, 7610658, Santiago, Chile. eduardoperez@udd.cl.

Funding

Modeling the impact of Women's Specific Health Factors in PD outcomes in LatinasR01NS112499 · NINDS · CLEVELAND CLINIC LERNER COM-CWRU · PI FERNANDEZ MATA, IGNACIO · 2020 to 2024
$3.3M
Agencia Nacional de Investigación y Desarrollo Beca Doctorado Nacional 2020 Folio 21201541Agencia Nacional de Investigación y Desarrollo FONDECYT 1221464NIH HHS 1R01NS112499NINDS NIH HHS R01 NS112499
6 · The paper itself

Abstract

Alzheimer's disease (AD) is usually accompanied by comorbidities such as type 2 diabetes (T2D), epilepsy, major depressive disorder (MDD), and migraine headaches (MH) that can significantly affect patient management and progression. As AD, these comorbidities have their own cumulative common genetic risk component that can be explored in a single individual through polygenic scores. Utilizing data from the UK Biobank, we investigated the correlation between polygenic scores (PGS) for these comorbidities and their actual presentation in AD patients. We show that individuals with higher PGS values showed an elevated risk of developing T2D (OR 2.1, p = 1.07 × 10

Indexed as

Alzheimer DiseaseDiabetes Mellitus, Type 2EpilepsyGenetic Predisposition to DiseaseMultifactorial InheritanceAgedComorbidityFemaleHumansMajor Depressive DisorderMaleMiddle AgedMigraine DisordersPolymorphism, Single NucleotideRisk FactorsUnited KingdomCommon variantsComorbiditiesPGSPRS

Identifiers

PMID40181078
PMCPMC11968852

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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.