<em>C9orf72</em> Intermediate Repeats Confer Genetic Risk for Severe COVID-19 Pneumonia Independently of Age

oleh: Isabella Zanella, Eliana Zacchi, Simone Piva, Massimiliano Filosto, Giada Beligni, Diana Alaverdian, Sara Amitrano, Francesca Fava, Margherita Baldassarri, Elisa Frullanti, Ilaria Meloni, Alessandra Renieri, GEN-COVID Multicenter Study, GEVACOBA Study Group, Francesco Castelli, Eugenia Quiros-Roldan

Format: Article
Diterbitkan: MDPI AG 2021-06-01

Deskripsi

A cytokine storm, autoimmune features and dysfunctions of myeloid cells significantly contribute to severe coronavirus disease 2019 (COVID-19), caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection. Genetic background of the host seems to be partly responsible for severe phenotype and genes related to innate immune response seem critical host determinants. The <i>C9orf72</i> gene has a role in vesicular trafficking, autophagy regulation and lysosome functions, is highly expressed in myeloid cells and is involved in immune functions, regulating the lysosomal degradation of mediators of innate immunity. A large non-coding hexanucleotide repeat expansion (HRE) in this gene is the main genetic cause of frontotemporal dementia (FTD) and amyotrophic lateral sclerosis (ALS), both characterized by neuroinflammation and high systemic levels of proinflammatory cytokines, while HREs of intermediate length, although rare, are more frequent in autoimmune disorders. <i>C9orf72</i> full mutation results in haploinsufficiency and intermediate HREs seem to modulate gene expression as well and impair autophagy. Herein, we sought to explore whether intermediate HREs in <i>C9orf72</i> may be a risk factor for severe COVID-19. Although we found intermediate HREs in only a small portion of 240 patients with severe COVID-19 pneumonia, the magnitude of risk for requiring non-invasive or mechanical ventilation conferred by harboring intermediate repeats >10 units in at least one <i>C9orf72</i> allele was more than twice respect to having shorter expansions, when adjusted for age (odds ratio (OR) 2.36; 95% confidence interval (CI) 1.04–5.37, <i>p</i> = 0.040). The association between intermediate repeats >10 units and more severe clinical outcome (<i>p</i> = 0.025) was also validated in an independent cohort of 201 SARS-CoV-2 infected patients. These data suggest that <i>C9orf72</i> HREs >10 units may influence the pathogenic process driving more severe COVID-19 phenotypes.