Linking the plasma proteome to genetics in individuals from continental Africa provides insights into type 2 diabetes pathogenesis

Individuals of African ancestry remain largely underrepresented in genetic and proteomic studies. Here we measure the levels of 2,873 proteins in plasma samples from 163 individuals with type 2 diabetes (T2D) or prediabetes and 362 normoglycemic controls from the Ugandan population. We identify 88 differentially expressed proteins between the two groups. We link genome-wide data to protein expression levels and construct a protein quantitative trait locus (pQTL) map for this population. We identify 399 independent associations with 346 (86.7%) cis-pQTLs and 53 (13.3%) trans-pQTLs; 16.7% of the cis-pQTLs and all of the trans-pQTLs have not been previously reported in individuals of African ancestry. Of these, 37 pQTLs have not been previously reported in any population. We find evidence for colocalization between a pQTL and T2D genetic risk. Our findings reveal proteins causally implicated in the pathogenesis of T2D, which may be leveraged for personalized medicine tailored to individuals of African ancestry.

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Publication Details

Journal
Nature Genetics
Published
2026-01-01
DOI
https://doi.org/10.1038/s41588-025-02421-w
Citations
1
Primary Topic
Genetic Associations and Epidemiology
Type
article
Field-Weighted Citation Impact
30.93

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article

Linking the plasma proteome to genetics in individuals from continental Africa provides insights into type 2 diabetes pathogenesis

Moffat Nyirenda, Mauro Tutino, Allan Kalungi, Opeyemi Soremekun et al.
1 citations
Nature Genetics
Genetic Associations and Epidemiology
30.93
article

Linking the plasma proteome to genetics in individuals from continental Africa provides insights into type 2 diabetes pathogenesis

Moffat Nyirenda, Mauro Tutino, Allan Kalungi, Opeyemi Soremekun, Segun Fatumo, N. William Rayner, Young-Chan Park, Eleftheria Zeggini, Ana Luiza Arruda
article en
1 citations

Abstract

Individuals of African ancestry remain largely underrepresented in genetic and proteomic studies. Here we measure the levels of 2,873 proteins in plasma samples from 163 individuals with type 2 diabetes (T2D) or prediabetes and 362 normoglycemic controls from the Ugandan population. We identify 88 differentially expressed proteins between the two groups. We link genome-wide data to protein expression levels and construct a protein quantitative trait locus (pQTL) map for this population. We identify 399 independent associations with 346 (86.7%) cis-pQTLs and 53 (13.3%) trans-pQTLs; 16.7% of the cis-pQTLs and all of the trans-pQTLs have not been previously reported in individuals of African ancestry. Of these, 37 pQTLs have not been previously reported in any population. We find evidence for colocalization between a pQTL and T2D genetic risk. Our findings reveal proteins causally implicated in the pathogenesis of T2D, which may be leveraged for personalized medicine tailored to individuals of African ancestry.

Nature GeneticsVol. 58(1)
Queen Mary University of London (GB), Center for Environmental Health (US), Helmholtz Zentrum München (DE), London School of Hygiene & Tropical Medicine (GB), Technical University of Munich (DE), Makerere University (UG), Uganda Virus Research Institute (UG), University of KwaZulu-Natal (ZA)
Alexander von Humboldt-Stiftung, London School of Hygiene and Tropical Medicine, Wellcome Trust, Department for International Development, Medical Research Council, Helmholtz Zentrum München
Good health and well-being
Openalex Percentile: Top 2%
Genetic Associations and Epidemiology
30.93
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