Evidence map›Paper›PMID 40767503›Full record

SynthesisGenetic epidemiology2025

Correcting for Genomic Inflation Leads to Loss of Power in Large-Scale Genome-Wide Association Study Meta-Analysis.

Archit Singh, Lorraine Southam, Konstantinos Hatzikotoulas, Nigel W Rayner, Ken Suzuki, Henry J Taylor, Xianyong Yin, Ravi Mandla, Alicia Huerta-Chagoya, Andrew P Morris and 2 more

Abstract readMeta-Analysis
In one paragraph

Synthesis in Genetic epidemiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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

2 citing papers in PubMed.

  1. Article
  2. 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

12 authors.

Archit SinghTechnical University of Munich (TUM), TUM School of Medicine and Health, Graduate School of Experimental Medicine, Munich, Germany.ORCID 0000-0002-3983-6126
Lorraine SouthamInstitute of Translational Genomics, Helmholtz Zentrum München- German Research Center for Environmental Health, Neuherberg, Germany.
Konstantinos HatzikotoulasInstitute of Translational Genomics, Helmholtz Zentrum München- German Research Center for Environmental Health, Neuherberg, Germany.
Nigel W RaynerInstitute of Translational Genomics, Helmholtz Zentrum München- German Research Center for Environmental Health, Neuherberg, Germany.
Ken SuzukiDepartment of Diabetes and Metabolic Diseases, Graduate School of Medicine, University of Tokyo, Tokyo, Japan.
Henry J TaylorCenter for Precision Health Research, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, USA.ORCID 0000-0003-2088-5240
Xianyong YinDepartment of Epidemiology, School of Public Health, Nanjing Medical University, Nanjing, China.
Ravi MandlaPrograms in Metabolism and Medical and Population Genetics, Broad Institute of Harvard and MIT, Cambridge, Massachusetts, USA.ORCID 0000-0002-0782-0138
Alicia Huerta-ChagoyaPrograms in Metabolism and Medical and Population Genetics, Broad Institute of Harvard and MIT, Cambridge, Massachusetts, USA.ORCID 0000-0001-6218-3904
Andrew P MorrisInstitute of Translational Genomics, Helmholtz Zentrum München- German Research Center for Environmental Health, Neuherberg, Germany.ORCID 0000-0002-6805-6014
Eleftheria ZegginiInstitute of Translational Genomics, Helmholtz Zentrum München- German Research Center for Environmental Health, Neuherberg, Germany.ORCID 0000-0003-4238-659X
Ozvan BocherInstitute of Translational Genomics, Helmholtz Zentrum München- German Research Center for Environmental Health, Neuherberg, Germany.ORCID 0000-0002-2467-9236

Funding

Archit Singh and Dr Ozvan Bocher have received funding from the European Union's Horizon 2020 research and innovation program under Grant Agreement No 101017802 (OPTOMICS).
6 · The paper itself

Abstract

Inflation in genome-wide association studies (GWAS) summary statistics represents a major challenge, for which correction methods have been developed. These include the genomic control (GC) method, which uses the λ-value to correct summary statistics, and the linkage disequilibrium score regression (LDSR) method, which uses the LDSR intercept. By using type 2 diabetes (T2D) as an exemplar, we explore factors influencing λ-values and the impact of these corrections on association signals. We find that larger sample sizes increase λ-values due to increased captured polygenicity, while including lower frequency variants decreases λ-values due to reduced power. Comparing T2D genetic associations described in overlapping GWAS meta-analyses of increasing sample size, we find that GC correction reduces the false positive rate and leads to the loss of robust associations. In one of the largest meta-analysis, GC correction results in 39.7% loss of independent loci, substantially reducing the number of detected associations. In comparison, the LDSR intercept correction leads to a loss of up to 25.2% of the independent loci, being therefore less conservative than the GC correction. We conclude that in large, well-powered GWAS meta-analysis of polygenic traits, both GC and LDSR intercept correction leads to power loss, highlighting the need for improved genomic inflation correction methods.

Indexed as

Genome-Wide Association StudyDiabetes Mellitus, Type 2HumansLinkage DisequilibriumMeta-Analysis as TopicModels, GeneticMultifactorial InheritancePolymorphism, Single NucleotideSample Sizegenetic associationsgenomic controlgenomic inflationGWAS meta‐analysisLD‐score regression

Identifiers

PMID40767503
PMCPMC12327166

What Socratic holds

Textmetadata
LicenceCC BY
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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 Socratic graph.