Worldwide distribution of genetic factors related to severity of COVID-19 infection

Genome-wide association studies of COVID-19 severity have been carried out mostly on European or East Asian populations with small representation of other world regions. Here we explore the worldwide distribution and linkage disequilibrium (LD) patterns of genetic variants previously associated with...

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Veröffentlicht in:Annals of human biology 2024-12, Vol.51 (1), p.2366248
Hauptverfasser: Esteban, María Esther, Pino, Débora, Romero-Lorca, Alicia, Novillo, Apolonia, Gaibar, María, Riancho, José A, Rojas-Martínez, Augusto, Flores, Carlos, Lapunzina, Pablo, Carracedo, Ángel, Athanasiadis, Georgios, Fernández-Santander, Ana
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Sprache:eng
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Zusammenfassung:Genome-wide association studies of COVID-19 severity have been carried out mostly on European or East Asian populations with small representation of other world regions. Here we explore the worldwide distribution and linkage disequilibrium (LD) patterns of genetic variants previously associated with COVID-19 severity. We followed up the results of a large Spanish genome-wide meta-analysis on 26 populations from the 1000 Genomes Project by calculating allele frequencies and LD scores of the nine most significant SNPs. We also used the entire set of summary statistics to compute polygenic risk scores (PRSs) and carried out comparisons at the population and continental level. We observed the strongest differences among continental regions for the five top SNPs in chromosome 3. European, American, and South Asian populations showed similar LD patterns. Average PRSs in South Asian and American populations were consistently higher than those observed in Europeans. While PRS distributions were similar among South Asians, the American populations showed striking differences among them. Considering the caveats of PRS transferability across ethnicities, our analysis showed that American populations present the highest genetic risk score, hence potentially higher propensity, for COVID-19 severity. Independent validation is warranted with additional summary statistics and phenotype data.
ISSN:0301-4460
1464-5033
1464-5033
DOI:10.1080/03014460.2024.2366248