Research and Practice in Thrombosis and HaemostasisGenomicsPeer-reviewed journal article
PIK3R3 is a candidate regulator of platelet count in people of Bangladeshi ancestry
Kate BurleyiD, Lucy Fitzgibbon, David A. van HeeliD, Shaheen AkhtariD, Mohammad Anwar, Elena ArcieroiD, Omar Asgar, Samina Ashraf, Gerome D. BreeniD, Raymond ChungiD, Charles J. C. CurtisiD, Shabana Chaudhary, Maharun Chowdhury, Grainne ColliganiD, Panos DeloukasiD, Ceri Durham, Faiza Gul DurraniiD, Fabíola EtoiD, Sarah FineriD, Ana Angel Garcia, Chris GriffithsiD, Joanne Harvey, Teng Heng, Qin HuangiD, Matt E. Hurles, , Andrew David MumfordiD
Abstract
Platelets are mediators of cardiovascular disease and are regulated by complex sets of interacting genes. To reveal new regulatory loci for platelet count (PLT), we performed genome-wide association studies (GWAS) in 20,218 Bangladeshi (BAN) and 9,198 Pakistani (PAK) individuals from the Genes and Health study. Most significantly associated loci (p <5 x10-8) replicated findings in prior transethnic GWAS. However, the BAN locus defined by rs946528 (chr1:46019890) did not associate with PLT in the PAK analysis but was in the same linkage disequilibrium block as PLT-associated variants in prior East Asian GWAS. The single independent association signal was refined to a 95% credible set of 343 variants spanning eight coding genes. Functional annotation, mapping to megakaryocyte regulatory regions and colocalization with whole blood eQTLs identified the most likely mediator of the PLT phenotype to be PIK3R3 encoding a regulator of phosphoinositol 3-kinase, widely linked elsewhere to adverse cardiovascular phenotypes.
- organism: human
- assay: GWAS summary statistics
- research focus: GWAS / association mapping
- approach: statistical model
- Citations
- 3
- FWCI
- 0.61
- Field percentile
- top 32%
Reproducibility ledger
Nobody has reported trying to reproduce this paper yet. Did you replicate an experiment or run the code? Your report saves the next lab a week.
Sign in to file a reproducibility report.
Related papers
- Identification of functional variants for platelet CD36 expression by Massively Parallel Reporter Assay.
Namrata Madan, Andrew R. Ghazi, … Leonard C. Edelstein·PLoS GeneticsPeer-reviewed·Jul 25, 2019
- A genome-wide meta-analysis identifies a sex-specific genetic effect for platelet aggregation in response to agonists
Julius Suh Ngwa, Ming‐Huei Chen, … Ingo Ruczinski·medRxiv·May 18, 2026
- Genome Sequencing Unveils a New Regulatory Landscape of Platelet Reactivity
Ali Reza Keramati, Ming‐Huei Chen, … Paul S. de Vries·Nature CommunicationsPeer-reviewed·Jun 15, 2021
- Genetically determined platelet traits impact stroke risk through multiple mechanisms and cell types
Kim Ha, Katherine Hartmann, … Christopher S. Thom·medRxiv·Aug 1, 2025
- Integrative Genomic Analysis and Functional Studies Reveal GP5, GRN, MPO and MCAM as Causal Protein Biomarkers for Platelet Traits
Dong Heon Lee, Chen Yao, … Andrew D. Johnson·bioRxiv·Nov 29, 2019
- A Sardinian founder mutation in GP1BB that impacts thrombocytopenia.
Fabio Busonero, Maristella Steri, … Francesco Cucca·British Journal of HaematologyPeer-reviewed·Nov 20, 2020