| Literature DB >> 34203982 |
Margherita Baldassarri1,2, Francesca Fava1,2,3, Chiara Fallerini1,2, Sergio Daga1,2, Elisa Benetti2, Kristina Zguro2, Sara Amitrano3, Floriana Valentino1,2, Gabriella Doddato1,2, Annarita Giliberti1,2, Laura Di Sarno1,2, Maria Palmieri1,2, Miriam Lucia Carriero1,2, Diana Alaverdian1,2, Giada Beligni1,2, Nicola Iuso1,2, Francesco Castelli4, Eugenia Quiros-Roldan4, Mario Umberto Mondelli5,6, Rosalba Miceli7, Elisa Frullanti1,2, Simone Furini2, Francesca Mari1,2,3, Alessandra Renieri1,2,3, Chiara Gabbi8.
Abstract
The clinical presentation of COVID-19 is extremely heterogeneous, ranging from asymptomatic to severely ill patients. Thus, host genetic factors may be involved in determining disease presentation and progression. Given that carriers of single cystic fibrosis (CF)-causing variants of the CFTR gene-CF-carriers-are more susceptible to respiratory tract infections, our aim was to determine their likelihood of undergoing severe COVID-19. We implemented a cohort study of 874 individuals diagnosed with COVID-19, during the first pandemic wave in Italy. Whole exome sequencing was performed and validated CF-causing variants were identified. Forty subjects (16 females and 24 males) were found to be CF-carriers. Among mechanically ventilated patients, CF-carriers were more represented (8.7%) and they were significantly (p < 0.05) younger (mean age 51 years) compared to noncarriers (mean age 61.42 years). Furthermore, in the whole cohort, the age of male CF-carriers was lower, compared to noncarriers (p < 0.05). CF-carriers had a relative risk of presenting an abnormal inflammatory response (CRP ≥ 20 mg/dL) of 1.69 (p < 0.05) and their hazard ratio of death at day 14 was 3.10 (p < 0.05) in a multivariate regression model, adjusted for age, sex and comorbidities. In conclusion, CF-carriers are more susceptible to the severe form of COVID-19, showing also higher risk of 14-day death.Entities:
Keywords: CF carrier screening; CFTR; COVID-19; host genetics
Year: 2021 PMID: 34203982 DOI: 10.3390/jpm11060558
Source DB: PubMed Journal: J Pers Med ISSN: 2075-4426