Evidence map›Paper›PMID 41801886›Full record

ArticlePLoS genetics2026

Polygenic risk scores and Parkinson's disease in South Africa advancing ancestry informed disease prediction.

Kathryn Step, Carene Anne Alene Ndong Sima, Spencer Grant, Jonggeol Jeffrey Kim, Emily Waldo, Soraya Bardien, Ignacio F Mata, Global Parkinson’s Genetics Program (GP2)

Abstract read
In one paragraph

Article in PLoS genetics, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0cells of the map it votes in
0citing papers in PubMed
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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

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

8 authors.

Kathryn StepDivision of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa.ORCID https://orcid.org/0000-0002-4054-7030
Carene Anne Alene Ndong SimaDivision of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa.ORCID https://orcid.org/0000-0002-8226-6288
Spencer GrantCenter for Alzheimer's and Related Dementias, National Institute on Aging and National Institute of Neurological Disorders and Stroke, National Institutes of Health, Bethesda, Maryland, United States of America.ORCID https://orcid.org/0000-0002-7278-0347
Jonggeol Jeffrey KimDepartment of Molecular and Human Genetics, Baylor College of Medicine, Houston, Texas, United States of America.ORCID https://orcid.org/0000-0003-0738-0512
Emily WaldoGenomic Medicine, Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, Ohio, United States of America.ORCID https://orcid.org/0009-0009-1485-3710
Soraya BardienDivision of Molecular Biology and Human Genetics, Faculty of Medicine and Health Sciences, Stellenbosch University, Cape Town, South Africa.ORCID https://orcid.org/0000-0002-3508-3438
Ignacio F MataGenomic Medicine, Lerner Research Institute, Cleveland Clinic Foundation, Cleveland, Ohio, United States of America.ORCID https://orcid.org/0000-0003-1198-0633
Global Parkinson’s Genetics Program (GP2)

Funding

Additional Sequencing for the Alzheimer Disease Sequencing Project (ADSP) the Follow-Up Study (FUS), The Global Population InitiativeU01AG076482 · NIA · UNIVERSITY OF MIAMI SCHOOL OF MEDICINE · PI Clifton L Dalgard, ANTHONY JOHN GRISWOLD · 2022 to 2026
$26.9M
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
The Interplay between Genetics and Aerobic Exercise to Slow Parkinson's disease (GEARS) TrialR01NS132437 · NINDS · CLEVELAND CLINIC LERNER COM-CWRU · PI JAY L. ALBERTS · 2024 to 2026
$1.8M
BLRD VA I01 BX005978NIA NIH HHS U01 AG076482NINDS NIH HHS R01 NS112499NINDS NIH HHS R01 NS132437
6 · The paper itself

Abstract

Parkinson's disease (PD) is a complex neurodegenerative disorder with environmental and genetic influences. Using genotyping array data of 661 South African PD cases and 737 controls, we conduct a polygenic risk score (PRS) analysis using PRSice-2. Summary statistics from two PD association studies have been used as base datasets. We split the target dataset into training (70%; n = 979) and validation (30%; n = 419) cohorts. We test various clumping window sizes, linkage disequilibrium thresholds, and p-value thresholds to determine the optimal combination for risk prediction. Additionally, we investigate the variance explained by different combinations of covariates. Overall, we observe modest predictive performance (AUC: 0.5847-0.6183). Age at recruitment emerges as the strongest individual predictor, while sex contributes the least. These findings provide the first evaluation of PRS performance for PD in a highly admixed South African cohort, underscoring the importance of including underrepresented populations in genetic risk prediction. By systematically assessing predictive performance across two base datasets, we highlight how ancestry composition and study design affect risk estimation in diverse populations. This work lays a foundation for refining genomic prediction in admixed populations and contributes to ongoing efforts to ensure that advances in precision medicine are globally relevant.

Indexed as

Genetic Predisposition to DiseaseMultifactorial InheritanceParkinson DiseaseAgedFemaleGenetic Risk ScoreGenome-Wide Association StudyHumansLinkage DisequilibriumMaleMiddle AgedPolymorphism, Single NucleotideSouth Africa

Identifiers

PMID41801886
PMCPMC12987585

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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.