Characterization of prevalent genetic variants in the Estonian Biobank body-mass index GWAS

Population-specific genome-wide association studies can reveal high-impact genomic variants that influence traits like body-mass index (BMI). Using the Estonian Biobank BMI dataset (n = 204,747 participants) we identified 214 genome-wide significant loci. Among those hits, we identified a common non-coding variant within the newly associated ADGRL3 gene (-0.18 kg/m²; P = 3.21 × 10⁻⁹). Moreover, the missense rare variant PTPRT:p.Arg1384His associated with lower BMI (-0.44 kg/m²; P = 2.51 × 10⁻¹⁰), while the protein-truncating variant POMC:p.Glu206* was associated with considerably higher BMI (+ 0.81 kg/m²; P = 1.48 × 10<sup>-12</sup>), both likely affecting the functioning of the leptin-melanocortin pathway. POMC:p.Glu206* was observed in different North-European populations, suggesting a broader, yet elusive, distribution of this damaging variant. These observations indicate the previously unrecognized roles of the ADGRL3 and PTPRT genes in body weight regulation and suggest an increased prevalence of the POMC:p.Glu206* variant in European populations, offering avenues for developing interventions in obesity management.

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Journal
Nature Communications
Published
2025-10-08
DOI
https://doi.org/10.1038/s41467-025-64006-9
Citations
1
Primary Topic
Regulation of Appetite and Obesity
Type
article
Field-Weighted Citation Impact
0.91

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article

Characterization of prevalent genetic variants in the Estonian Biobank body-mass index GWAS

Taavi Tillmann, Erik Abner, Mari Nelis, Mait Metspalu et al.
1 citations
Nature Communications
Regulation of Appetite and Obesity
0.91
article

Characterization of prevalent genetic variants in the Estonian Biobank body-mass index GWAS

Taavi Tillmann, Erik Abner, Mari Nelis, Mait Metspalu, Liis Haljasmägi, Kelli Lehto, Lili Milani, Kristi Läll, Georgi Hudjashov, Joel Rämö, Uku Vainik, Hanna M. Ollila, Hanna Maria Kariis, Kanwal Batool, Urmo Võsa, Anders Eriksson, Tiit Nikopensius, Andres Metspalu, Kai Kisand, Nele Taba, Hele Haapaniemi, Tõnu Esko, Anastasiia Alekseienko, Reedik Mägi
article en
1 citations

Abstract

Population-specific genome-wide association studies can reveal high-impact genomic variants that influence traits like body-mass index (BMI). Using the Estonian Biobank BMI dataset (n = 204,747 participants) we identified 214 genome-wide significant loci. Among those hits, we identified a common non-coding variant within the newly associated ADGRL3 gene (-0.18 kg/m²; P = 3.21 × 10⁻⁹). Moreover, the missense rare variant PTPRT:p.Arg1384His associated with lower BMI (-0.44 kg/m²; P = 2.51 × 10⁻¹⁰), while the protein-truncating variant POMC:p.Glu206* was associated with considerably higher BMI (+ 0.81 kg/m²; P = 1.48 × 10<sup>-12</sup>), both likely affecting the functioning of the leptin-melanocortin pathway. POMC:p.Glu206* was observed in different North-European populations, suggesting a broader, yet elusive, distribution of this damaging variant. These observations indicate the previously unrecognized roles of the ADGRL3 and PTPRT genes in body weight regulation and suggest an increased prevalence of the POMC:p.Glu206* variant in European populations, offering avenues for developing interventions in obesity management.

Nature CommunicationsVol. 16(1)
Montreal Neurological Institute and Hospital (CA), University of Helsinki (FI), Tallinn University (EE), Institute for Molecular Medicine Finland (FI), Estonian Biocentre (EE), McGill University (CA), University of Tartu (EE)
European Commission, Eesti Teadusagentuur, Tartu Ülikool, Research Executive Agency, European Regional Development Fund
Openalex Percentile: Top 22%
Regulation of Appetite and Obesity
0.91
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