Common and rare variants in complement genes as biomarkers of COVID-19 infection and severity. A lesson to learn for emerging pathogens - Takeaways - MDSpire

Common and rare variants in complement genes as biomarkers of COVID-19 infection and severity. A lesson to learn for emerging pathogens

  • By

  • María Eugenia De La Morena-Barrio

  • Ana Van Den Rym

  • Olga Escorial Sanz

  • Fernando Corvillo

  • Rosario García-Sánchez

  • Laura González-Sánchez

  • Adrián Muñoz-Barrera

  • Rafaela González-Montelongo

  • José Miguel Lorenzo-Salazar

  • Carlos Flores

  • Ana de Andrés-Martín

  • Carlos Rodríguez-Gallego

  • Luis Allende

  • Laia Alsina

  • Silvia Sánchez-Ramón

  • Eduardo López-Collazo

  • Margarita López-Trascasa

  • Pilar Sánchez-Corral

  • Rebeca Pérez de Diego

  • Javier Corral de la Calle

  • Alberto López-Lera

  • June 11, 2026

  • 0 min

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  • 1

    The study analyzed genetic variants in complement pathway genes among 154 Spanish adults hospitalized with severe COVID-19.

  • 2

    Common polymorphisms CFHR4 rs7417769 and CFH rs1061170 were linked to protection against acute respiratory distress syndrome (ARDS).

  • 3

    Variants C3 rs2230199 and MASP2 rs7255087 correlated with C3 levels, indicating their role in COVID-19 severity.

  • 4

    Over-representation of C1R rs117402032 and C8A rs143523574 polymorphisms suggests defective complement activation increases SARS-CoV-2 infection rates.

  • 5

    The findings highlight potential genetic biomarkers for predicting COVID-19 severity and preparedness for future infectious threats.

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