Evidence map›Paper›PMID 40974298›Full record

ArticleHuman brain mapping2025

Integration of Genetic Information to Improve Brain Age Gap Estimation Models in the UK Biobank.

Aashka Mohite, Karen Ardila, Pattarawut Charatpangoon, Emily Munro, Qingrun Zhang, Quan Long, Charlotte Curtis, M Ethan MacDonald

Abstract read
In one paragraph

Article in Human brain mapping, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. 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

8 authors.

Aashka MohiteDepartment of Electrical & Software Engineering, University of Calgary, Calgary, Canada.ORCID 0000-0003-2856-2518
Karen ArdilaHotchkiss Brain Institute, University of Calgary, Calgary, Canada.ORCID 0000-0001-6676-4992
Pattarawut CharatpangoonAlberta Children's Hospital Research Institute, University of Calgary, Calgary, Canada.
Emily MunroHotchkiss Brain Institute, University of Calgary, Calgary, Canada.
Qingrun ZhangAlberta Children's Hospital Research Institute, University of Calgary, Calgary, Canada.
Quan LongHotchkiss Brain Institute, University of Calgary, Calgary, Canada.
Charlotte CurtisDepartment of Electrical & Software Engineering, University of Calgary, Calgary, Canada.
M Ethan MacDonaldDepartment of Electrical & Software Engineering, University of Calgary, Calgary, Canada.ORCID 0000-0001-5421-3536

Funding

Alberta Graduate Excellence ScholarshipAlberta Innovates Graduate Student ScholarshipBrain CREATE Graduate ScholarshipEarly Career Researcher Supplement DGECR-00124Natural Sciences and Engineering Research Council Discovery RGPIN-03552University of Calgary
6 · The paper itself

Abstract

Neurodegeneration occurs when the body's central nervous system becomes impaired as a person ages, which can happen at an accelerated pace. Neurodegeneration impairs quality of life, affecting essential functions, including memory and the ability to self-care. Genetics play an important role in neurodegeneration and longevity. Brain age gap estimation (BrainAGE) is a biomarker that quantifies the difference between a machine learning model-predicted biological age of the brain and the true chronological age for healthy subjects; however, a large portion of the variance remains unaccounted for in these models, attributed to individual differences. This study focuses on predicting the BrainAGE more accurately, aided by genetic information associated with neurodegeneration. To achieve this, a BrainAGE model was developed based on MRI measures, and then the associated genes were determined with a Genome-Wide Association Study. Subsequently, genetic information was incorporated into the models. The incorporation of genetic information yielded improvements in the model performances by 7% to 12%, showing that the incorporation of genetic information can notably reduce unexplained variance. This work helps to define new ways of determining persons susceptible to neurological aging decline and reveals genes for targeted precision medicine therapies.

Indexed as

AgingBrainMachine LearningAdultAgedAged, 80 and overBiological Specimen BanksFemaleGenome-Wide Association StudyHumansMagnetic Resonance ImagingMaleMiddle AgedUK BiobankUnited Kingdombrain age gap estimationgenome‐wide association studymachine learningmagnetic resonance imagingneurodegenerationneurogenetics

Identifiers

PMID40974298
PMCPMC12449772

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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 Socratic graph.