The Chilean COVID-19 Genomics Network Biorepository: A Resource for Multi-Omics Studies of COVID-19 and Long COVID in a Latin American Population

Iskra A. Signore, Gerardo Donoso, Pamela Bocchieri, Eduardo A. Tobar-Calfucoy, Cristian E. Yáñez, Laura Carvajal-Silva, Andrea X. Silva, Carola Otth, Claudio Cappelli, Héctor Valenzuela Jorquera, Daniela Zapata-Contreras, Yolanda Espinosa-Parrilla, Paula Zúñiga-Pacheco, Macarena Fuentes-Guajardo, Virginia A. Monardes-Ramírez, Pia Kochifas Velasquez, Christian A. Muñoz, Cristina Dorador, Jonathan García-Araya, Claudia P. Campillay-VélizCesar Echeverria, Rodolfo Alejandro Santander, Leslie C. Cerpa, Matías F. Martínez, Luis Abel Quiñones, Eduardo Roberto Lamoza Galleguillos, Juan Saez Hidalgo, Estefanía Nova-Lamperti, Sergio Sanhueza, Annesi Giacaman, Gerardo Acosta-Jamett, Cristóbal Verdugo, Anita Plaza, Claudio Verdugo, Carolina Selman, Ricardo Alejandro Verdugo, Alicia Colombo

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2 Citas (Scopus)

Resumen

Although a lack of diversity in genetic studies is an acknowledged obstacle for personalized medicine and precision public health, Latin American populations remain particularly understudied despite their heterogeneity and mixed ancestry. This gap extends to COVID-19 despite its variability in susceptibility and clinical course, where ethnic background appears to influence disease severity, with non-Europeans facing higher hospitalization rates. In addition, access to high-quality samples and data is a critical issue for personalized and precision medicine, and it has become clear that the solution lies in biobanks. The creation of the Chilean COVID-19 Biorepository reported here addresses these gaps, representing the first nationwide multicentric Chilean initiative. It operates under rigorous biobanking standards and serves as one of South America’s largest COVID cohorts. A centralized harmonization strategy was chosen and included unified standard operating procedures, a sampling coding system, and biobanking staff training. Adults with confirmed SARS-CoV-2 infection provided broad informed consent. Samples were collected to preserve blood, plasma, buffy coat, and DNA. Quality controls included adherence to the standard preanalytical code, incident reporting, and DNA concentration and absorbance ratio 260/280 assessments. Detailed sociodemographic, health, medication, and preexisting condition data were gathered. In five months, 2262 participants were enrolled, pseudonymized, and sorted by disease severity. The average Amerindian ancestry considering all participant was 44.0% [SD 15.5%], and this value increased to 61.2% [SD 19.5%] among those who self-identified as Native South Americans. Notably, 279 participants self-identified with one of 12 ethnic groups. High compliance (>90%) in all assessed quality controls was achieved. Looking ahead, our team founded the COVID-19 Genomics Network (C19-GenoNet) focused on identifying genetic factors influencing SARS-CoV-2 outcomes. In conclusion, this bottom-up collaborative effort aims to promote the integration of Latin American populations into global genetic research and welcomes collaborations supporting this endeavor. Interested parties are invited to explore collaboration opportunities through our catalog, accessible online.

Idioma originalInglés
Número de artículo1352
PublicaciónGenes
Volumen15
N.º11
DOI
EstadoPublicada - nov. 2024
Publicado de forma externa

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