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Published in: Respiratory Research 1/2023

Open Access 01-12-2023 | COVID-19 | Research

Ultra-rare RTEL1 gene variants associate with acute severity of COVID-19 and evolution to pulmonary fibrosis as a specific long COVID disorder

Authors: Laura Bergantini, Margherita Baldassarri, Miriana d’Alessandro, Giulia Brunelli, Gaia Fabbri, Kristina Zguro, Andrea Degl’Innocenti, Chiara Fallerini, Elena Bargagli, Alessandra Renieri, GEN-COVID Multicenter study

Published in: Respiratory Research | Issue 1/2023

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Abstract

Background

Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) is a novel coronavirus that caused an ongoing pandemic of a pathology termed Coronavirus Disease 19 (COVID-19). Several studies reported that both COVID-19 and RTEL1 variants are associated with shorter telomere length, but a direct association between the two is not generally acknowledged. Here we demonstrate that up to 8.6% of severe COVID-19 patients bear RTEL1 ultra-rare variants, and show how this subgroup can be recognized.

Methods

A cohort of 2246 SARS-CoV-2-positive subjects, collected within the GEN-COVID Multicenter study, was used in this work. Whole exome sequencing analysis was performed using the NovaSeq6000 System, and machine learning methods were used for candidate gene selection of severity. A nested study, comparing severely affected patients bearing or not variants in the selected gene, was used for the characterisation of specific clinical features connected to variants in both acute and post-acute phases.

Results

Our GEN-COVID cohort revealed a total of 151 patients carrying at least one RTEL1 ultra-rare variant, which was selected as a specific acute severity feature. From a clinical point of view, these patients showed higher liver function indices, as well as increased CRP and inflammatory markers, such as IL-6. Moreover, compared to control subjects, they present autoimmune disorders more frequently. Finally, their decreased diffusion lung capacity for carbon monoxide after six months of COVID-19 suggests that RTEL1 variants can contribute to the development of SARS-CoV-2-elicited lung fibrosis.

Conclusion

RTEL1 ultra-rare variants can be considered as a predictive marker of COVID-19 severity, as well as a marker of pathological evolution in pulmonary fibrosis in the post-COVID phase. This notion can be used for a rapid screening in hospitalized infected people, for vaccine prioritization, and appropriate follow-up assessment for subjects at risk.
Trial Registration NCT04549831 (www.​clinicaltrial.​org)
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Literature
1.
go back to reference Croci S, Venneri MA, Mantovani S, Fallerini C, Benetti E, Picchiotti N, et al. The polymorphism L412F in TLR3 inhibits autophagy and is a marker of severe COVID-19 in males. Autophagy. 2022;18:1662–72.CrossRefPubMed Croci S, Venneri MA, Mantovani S, Fallerini C, Benetti E, Picchiotti N, et al. The polymorphism L412F in TLR3 inhibits autophagy and is a marker of severe COVID-19 in males. Autophagy. 2022;18:1662–72.CrossRefPubMed
3.
go back to reference COVID-19 Host Genetics Initiative. Mapping the human genetic architecture of COVID-19. Nature. 2021;600:472–7. COVID-19 Host Genetics Initiative. Mapping the human genetic architecture of COVID-19. Nature. 2021;600:472–7.
5.
go back to reference Sanchez-Vazquez R, Guío-Carrión A, Zapatero-Gaviria A, Martínez P, Blasco MA. Shorter telomere lengths in patients with severe COVID-19 disease. Aging (Albany NY). 2021;13:1–15.CrossRefPubMed Sanchez-Vazquez R, Guío-Carrión A, Zapatero-Gaviria A, Martínez P, Blasco MA. Shorter telomere lengths in patients with severe COVID-19 disease. Aging (Albany NY). 2021;13:1–15.CrossRefPubMed
6.
go back to reference Mongelli A, Barbi V, Gottardi Zamperla M, Atlante S, Forleo L, Nesta M, et al. Evidence for biological age acceleration and telomere shortening in COVID-19 survivors. Int J Mol Sci [Internet]. 2021;22:6151.CrossRefPubMedPubMedCentral Mongelli A, Barbi V, Gottardi Zamperla M, Atlante S, Forleo L, Nesta M, et al. Evidence for biological age acceleration and telomere shortening in COVID-19 survivors. Int J Mol Sci [Internet]. 2021;22:6151.CrossRefPubMedPubMedCentral
7.
go back to reference Blasco MA, Lee HW, Hande MP, Samper E, Lansdorp PM, DePinho RA, et al. Telomere shortening and tumor formation by mouse cells lacking telomerase RNA. Cell. 1997;91:25–34.CrossRefPubMed Blasco MA, Lee HW, Hande MP, Samper E, Lansdorp PM, DePinho RA, et al. Telomere shortening and tumor formation by mouse cells lacking telomerase RNA. Cell. 1997;91:25–34.CrossRefPubMed
9.
go back to reference Stuart BD, Choi J, Zaidi S, Xing C, Holohan B, Chen R, et al. Exome sequencing links mutations in PARN and RTEL1 with familial pulmonary fibrosis and telomere shortening. Nat Genet [Internet]. 2015;47:512–7.CrossRefPubMedPubMedCentral Stuart BD, Choi J, Zaidi S, Xing C, Holohan B, Chen R, et al. Exome sequencing links mutations in PARN and RTEL1 with familial pulmonary fibrosis and telomere shortening. Nat Genet [Internet]. 2015;47:512–7.CrossRefPubMedPubMedCentral
10.
go back to reference Kannengiesser C, Borie R, Ménard C, Réocreux M, Nitschké P, Gazal S, et al. Heterozygous RTEL1 mutations are associated with familial pulmonary fibrosis. Eur Respir J. 2015;46:474–85.CrossRefPubMed Kannengiesser C, Borie R, Ménard C, Réocreux M, Nitschké P, Gazal S, et al. Heterozygous RTEL1 mutations are associated with familial pulmonary fibrosis. Eur Respir J. 2015;46:474–85.CrossRefPubMed
11.
go back to reference Juge P-A, Borie R, Kannengiesser C, Gazal S, Revy P, Wemeau-Stervinou L, et al. Shared genetic predisposition in rheumatoid arthritis-interstitial lung disease and familial pulmonary fibrosis. Eur Respir J. 2017;49:1602314.CrossRefPubMed Juge P-A, Borie R, Kannengiesser C, Gazal S, Revy P, Wemeau-Stervinou L, et al. Shared genetic predisposition in rheumatoid arthritis-interstitial lung disease and familial pulmonary fibrosis. Eur Respir J. 2017;49:1602314.CrossRefPubMed
12.
go back to reference Cogan JD, Kropski JA, Zhao M, Mitchell DB, Rives L, Markin C, et al. Rare variants in RTEL1 are associated with familial interstitial pneumonia. Am J Respir Crit Care Med. 2015;191:646–55.CrossRefPubMedPubMedCentral Cogan JD, Kropski JA, Zhao M, Mitchell DB, Rives L, Markin C, et al. Rare variants in RTEL1 are associated with familial interstitial pneumonia. Am J Respir Crit Care Med. 2015;191:646–55.CrossRefPubMedPubMedCentral
13.
go back to reference García-Carmona S, Falfán-Valencia R, Verónica-Aguilar A, Buendía-Roldán I, Chávez-Galán L, Hernández-Zenteno RJ, et al. COVID-19 survivor patients carrying the Rs35705950 risk allele in MUC5B have higher plasma levels of mucin 5B. Curr Issues Mol Biol. 2022;44:3283–90.CrossRefPubMedPubMedCentral García-Carmona S, Falfán-Valencia R, Verónica-Aguilar A, Buendía-Roldán I, Chávez-Galán L, Hernández-Zenteno RJ, et al. COVID-19 survivor patients carrying the Rs35705950 risk allele in MUC5B have higher plasma levels of mucin 5B. Curr Issues Mol Biol. 2022;44:3283–90.CrossRefPubMedPubMedCentral
14.
go back to reference Bergantini L, Mainardi A, d’Alessandro M, Cameli P, Bennett D, Bargagli E, et al. Common molecular pathways between post-COVID19 syndrome and lung fibrosis: a scoping review. Front Pharmacol. 2022;13: 748931.CrossRefPubMedPubMedCentral Bergantini L, Mainardi A, d’Alessandro M, Cameli P, Bennett D, Bargagli E, et al. Common molecular pathways between post-COVID19 syndrome and lung fibrosis: a scoping review. Front Pharmacol. 2022;13: 748931.CrossRefPubMedPubMedCentral
15.
go back to reference Fallerini C, Picchiotti N, Baldassarri M, Zguro K, Daga S, Fava F, et al. Common, low-frequency, rare, and ultra-rare coding variants contribute to COVID-19 severity. Hum Genet. 2022;141:147–73.CrossRefPubMed Fallerini C, Picchiotti N, Baldassarri M, Zguro K, Daga S, Fava F, et al. Common, low-frequency, rare, and ultra-rare coding variants contribute to COVID-19 severity. Hum Genet. 2022;141:147–73.CrossRefPubMed
16.
go back to reference Jiang L, Tang B-S, Guo J-F, Li J-C. Telomere length and COVID-19 outcomes: a two-sample bidirectional Mendelian randomization study. Front Genet. 2022;13: 805903.CrossRefPubMedPubMedCentral Jiang L, Tang B-S, Guo J-F, Li J-C. Telomere length and COVID-19 outcomes: a two-sample bidirectional Mendelian randomization study. Front Genet. 2022;13: 805903.CrossRefPubMedPubMedCentral
17.
go back to reference Victor J, Jordan T, Lamkin E, Ikeh K, March A, Frere J, et al. SARS-CoV-2 hijacks host cell genome instability pathways. Res Sq. 2022;rs.3.rs-1556634. Victor J, Jordan T, Lamkin E, Ikeh K, March A, Frere J, et al. SARS-CoV-2 hijacks host cell genome instability pathways. Res Sq. 2022;rs.3.rs-1556634.
19.
go back to reference Daga S, Fallerini C, Baldassarri M, Fava F, Valentino F, Doddato G, et al. Employing a systematic approach to biobanking and analyzing clinical and genetic data for advancing COVID-19 research. Eur J Hum Genet. 2021;29:745–59.CrossRefPubMedPubMedCentral Daga S, Fallerini C, Baldassarri M, Fava F, Valentino F, Doddato G, et al. Employing a systematic approach to biobanking and analyzing clinical and genetic data for advancing COVID-19 research. Eur J Hum Genet. 2021;29:745–59.CrossRefPubMedPubMedCentral
21.
go back to reference COVID-19 Host Genetics Initiative. A first update on mapping the human genetic architecture of COVID-19. Nature. 2022;608:E1–10. COVID-19 Host Genetics Initiative. A first update on mapping the human genetic architecture of COVID-19. Nature. 2022;608:E1–10.
22.
go back to reference Tarraso J, Safont B, Carbonell-Asins JA, Fernandez-Fabrellas E, Sancho-Chust JN, Naval E, et al. Lung function and radiological findings 1 year after COVID-19: a prospective follow-up. Respir Res. 2022;23:242.CrossRefPubMedPubMedCentral Tarraso J, Safont B, Carbonell-Asins JA, Fernandez-Fabrellas E, Sancho-Chust JN, Naval E, et al. Lung function and radiological findings 1 year after COVID-19: a prospective follow-up. Respir Res. 2022;23:242.CrossRefPubMedPubMedCentral
23.
go back to reference Hama Amin BJ, Kakamad FH, Ahmed GS, Ahmed SF, Abdulla BA, Mohammed SH, et al. Post COVID-19 pulmonary fibrosis; a meta-analysis study. Ann Med Surg (Lond). 2022;77: 103590.PubMed Hama Amin BJ, Kakamad FH, Ahmed GS, Ahmed SF, Abdulla BA, Mohammed SH, et al. Post COVID-19 pulmonary fibrosis; a meta-analysis study. Ann Med Surg (Lond). 2022;77: 103590.PubMed
26.
go back to reference Cheng F, Carroll L, Joglekar MV, Januszewski AS, Wong KK, Hardikar AA, et al. Diabetes, metabolic disease, and telomere length. Lancet Diabetes Endocrinol. 2021;9:117–26.CrossRefPubMed Cheng F, Carroll L, Joglekar MV, Januszewski AS, Wong KK, Hardikar AA, et al. Diabetes, metabolic disease, and telomere length. Lancet Diabetes Endocrinol. 2021;9:117–26.CrossRefPubMed
27.
go back to reference M’Kacher R, Jaillet M, Colicchio B, Vasarmidi E, Mailleux A, Dieterlen A, et al. Lung fibroblasts from idiopathic pulmonary fibrosis patients harbor short and unstable telomeres leading to chromosomal instability. Biomedicines. 2022;10:310.CrossRefPubMedPubMedCentral M’Kacher R, Jaillet M, Colicchio B, Vasarmidi E, Mailleux A, Dieterlen A, et al. Lung fibroblasts from idiopathic pulmonary fibrosis patients harbor short and unstable telomeres leading to chromosomal instability. Biomedicines. 2022;10:310.CrossRefPubMedPubMedCentral
29.
go back to reference Borie R, Bouvry D, Cottin V, Gauvain C, Cazes A, Debray M-P, et al. Regulator of telomere length 1 (RTEL1) mutations are associated with heterogeneous pulmonary and extra-pulmonary phenotypes. Eur Respir J. 2019;53:1800508.CrossRefPubMed Borie R, Bouvry D, Cottin V, Gauvain C, Cazes A, Debray M-P, et al. Regulator of telomere length 1 (RTEL1) mutations are associated with heterogeneous pulmonary and extra-pulmonary phenotypes. Eur Respir J. 2019;53:1800508.CrossRefPubMed
30.
go back to reference Mank VMF, Mank J, Ogle J, Roberts J. Delayed, transient and self-resolving neutropenia following COVID-19 pneumonia. BMJ Case Reports CP [Internet]. 2021;14:e242596.CrossRef Mank VMF, Mank J, Ogle J, Roberts J. Delayed, transient and self-resolving neutropenia following COVID-19 pneumonia. BMJ Case Reports CP [Internet]. 2021;14:e242596.CrossRef
33.
go back to reference López-Pereira P, Iturrate I, de La Cámara R, Cardeñoso L, Alegre A, Aguado B. Can COVID-19 cause severe neutropenia? Clin Case Rep. 2020;8:3349–51.CrossRefPubMedPubMedCentral López-Pereira P, Iturrate I, de La Cámara R, Cardeñoso L, Alegre A, Aguado B. Can COVID-19 cause severe neutropenia? Clin Case Rep. 2020;8:3349–51.CrossRefPubMedPubMedCentral
34.
go back to reference Taha M, Sharma A, Soubani A. Clinical deterioration during neutropenia recovery after G-CSF therapy in patient with COVID-19. Respir Med Case Rep. 2020;31: 101231.PubMedPubMedCentral Taha M, Sharma A, Soubani A. Clinical deterioration during neutropenia recovery after G-CSF therapy in patient with COVID-19. Respir Med Case Rep. 2020;31: 101231.PubMedPubMedCentral
36.
go back to reference Tavakolpour S, Rakhshandehroo T, Wei EX, Rashidian M. Lymphopenia during the COVID-19 infection: what it shows and what can be learned. Immunol Lett. 2020;225:31–2.CrossRefPubMedPubMedCentral Tavakolpour S, Rakhshandehroo T, Wei EX, Rashidian M. Lymphopenia during the COVID-19 infection: what it shows and what can be learned. Immunol Lett. 2020;225:31–2.CrossRefPubMedPubMedCentral
37.
go back to reference Parthasarathi A, Padukudru S, Arunachal S, Basavaraj CK, Krishna MT, Ganguly K, et al. The role of neutrophil-to-lymphocyte ratio in risk stratification and prognostication of COVID-19: a systematic review and meta-analysis. Vaccines (Basel). 2022;10:1233.CrossRefPubMed Parthasarathi A, Padukudru S, Arunachal S, Basavaraj CK, Krishna MT, Ganguly K, et al. The role of neutrophil-to-lymphocyte ratio in risk stratification and prognostication of COVID-19: a systematic review and meta-analysis. Vaccines (Basel). 2022;10:1233.CrossRefPubMed
38.
go back to reference Rello AP, Martínez AM, Iturbe CV, Escolano-Pueyo A, Bayo EH, Lafarga IA. Assessment of the effectiveness of tocilizumab on mortality and progression to mechanical ventilation or intensive care in patients with COVID-19 admitted to a tertiary hospital. Eur J Hosp Pharm [Internet]. British Medical Journal Publishing Group; 2022 [cited 2023 Jan 14]; Available from: https://ejhp.bmj.com/content/early/2022/09/23/ejhpharm-2022-003366. Rello AP, Martínez AM, Iturbe CV, Escolano-Pueyo A, Bayo EH, Lafarga IA. Assessment of the effectiveness of tocilizumab on mortality and progression to mechanical ventilation or intensive care in patients with COVID-19 admitted to a tertiary hospital. Eur J Hosp Pharm [Internet]. British Medical Journal Publishing Group; 2022 [cited 2023 Jan 14]; Available from: https://​ejhp.​bmj.​com/​content/​early/​2022/​09/​23/​ejhpharm-2022-003366.
39.
go back to reference Besutti G, Pellegrini M, Ottone M, Bonelli E, Monelli F, Farì R, et al. Modifications of chest CT body composition parameters at three and six months after severe COVID-19 pneumonia: a retrospective cohort study. Nutrients. 2022;14:3764.CrossRefPubMedPubMedCentral Besutti G, Pellegrini M, Ottone M, Bonelli E, Monelli F, Farì R, et al. Modifications of chest CT body composition parameters at three and six months after severe COVID-19 pneumonia: a retrospective cohort study. Nutrients. 2022;14:3764.CrossRefPubMedPubMedCentral
40.
go back to reference Zinellu A, Mangoni AA. A systematic review and meta-analysis of the association between the neutrophil, lymphocyte, and platelet count, neutrophil-to-lymphocyte ratio, and platelet-to-lymphocyte ratio and COVID-19 progression and mortality. Expert Rev Clin Immunol. 2022;18:1187–202.CrossRefPubMed Zinellu A, Mangoni AA. A systematic review and meta-analysis of the association between the neutrophil, lymphocyte, and platelet count, neutrophil-to-lymphocyte ratio, and platelet-to-lymphocyte ratio and COVID-19 progression and mortality. Expert Rev Clin Immunol. 2022;18:1187–202.CrossRefPubMed
41.
go back to reference Yuan Z-Z, Fan L-L, Wang C-Y, Luo H, Liu L. Novel heterozygous mutation of RTEL1 in interstitial pneumonia with autoimmune feature. QJM. 2022;115:253–5.CrossRefPubMed Yuan Z-Z, Fan L-L, Wang C-Y, Luo H, Liu L. Novel heterozygous mutation of RTEL1 in interstitial pneumonia with autoimmune feature. QJM. 2022;115:253–5.CrossRefPubMed
42.
go back to reference Savage SA, Bertuch AA. The genetics and clinical manifestations of telomere biology disorders. Genet Med. 2010;12:753–64.CrossRefPubMed Savage SA, Bertuch AA. The genetics and clinical manifestations of telomere biology disorders. Genet Med. 2010;12:753–64.CrossRefPubMed
43.
go back to reference Hoffman TW, van der Vis JJ, Biesma DH, Grutters JC, van Moorsel CHM. Extrapulmonary manifestations of a telomere syndrome in patients with idiopathic pulmonary fibrosis are associated with decreased survival. Respirology. 2022;27:959–65.CrossRefPubMed Hoffman TW, van der Vis JJ, Biesma DH, Grutters JC, van Moorsel CHM. Extrapulmonary manifestations of a telomere syndrome in patients with idiopathic pulmonary fibrosis are associated with decreased survival. Respirology. 2022;27:959–65.CrossRefPubMed
44.
go back to reference Fortini A, Rosso A, Cecchini P, Torrigiani A, Lo Forte A, Carrai P, et al. One-year evolution of DLCO changes and respiratory symptoms in patients with post COVID-19 respiratory syndrome. Infection. 2022;50:513–7.CrossRefPubMedPubMedCentral Fortini A, Rosso A, Cecchini P, Torrigiani A, Lo Forte A, Carrai P, et al. One-year evolution of DLCO changes and respiratory symptoms in patients with post COVID-19 respiratory syndrome. Infection. 2022;50:513–7.CrossRefPubMedPubMedCentral
Metadata
Title
Ultra-rare RTEL1 gene variants associate with acute severity of COVID-19 and evolution to pulmonary fibrosis as a specific long COVID disorder
Authors
Laura Bergantini
Margherita Baldassarri
Miriana d’Alessandro
Giulia Brunelli
Gaia Fabbri
Kristina Zguro
Andrea Degl’Innocenti
Chiara Fallerini
Elena Bargagli
Alessandra Renieri
GEN-COVID Multicenter study
Publication date
01-12-2023
Publisher
BioMed Central
Published in
Respiratory Research / Issue 1/2023
Electronic ISSN: 1465-993X
DOI
https://doi.org/10.1186/s12931-023-02458-7

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