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MGUS and clonal hematopoiesis show unrelated clinical and biological trajectories in an older population cohort

Monoclonal gammopathy of undetermined significance (MGUS) and clonal hematopoiesis (CH) are 2 preclinical clonal expansions of hematopoietic cells whose prevalence rises with age, reaching almost 10% in people of aged 70 years and older. The increased risk of myeloid malignancies in patients with my...

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Autores principales: Da Vià, Matteo Claudio, Lionetti, Marta, Marella, Alessio, Matera, Antonio, Travaglino, Erica, Signaroldi, Elena, Galbussera, Alessia Antonella, Lucca, Ugo, Mandelli, Sara, Riva, Emma, Tettamanti, Mauro, Pettine, Loredana, Pompa, Alessandra, Baldini, Luca, Neri, Antonino, Della Porta, Matteo Giovanni, Bolli, Niccolò
Formato: Online Artículo Texto
Lenguaje:English
Publicado: The American Society of Hematology 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9618778/
https://www.ncbi.nlm.nih.gov/pubmed/35390146
http://dx.doi.org/10.1182/bloodadvances.2021006498
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author Da Vià, Matteo Claudio
Lionetti, Marta
Marella, Alessio
Matera, Antonio
Travaglino, Erica
Signaroldi, Elena
Galbussera, Alessia Antonella
Lucca, Ugo
Mandelli, Sara
Riva, Emma
Tettamanti, Mauro
Pettine, Loredana
Pompa, Alessandra
Baldini, Luca
Neri, Antonino
Della Porta, Matteo Giovanni
Bolli, Niccolò
author_facet Da Vià, Matteo Claudio
Lionetti, Marta
Marella, Alessio
Matera, Antonio
Travaglino, Erica
Signaroldi, Elena
Galbussera, Alessia Antonella
Lucca, Ugo
Mandelli, Sara
Riva, Emma
Tettamanti, Mauro
Pettine, Loredana
Pompa, Alessandra
Baldini, Luca
Neri, Antonino
Della Porta, Matteo Giovanni
Bolli, Niccolò
author_sort Da Vià, Matteo Claudio
collection PubMed
description Monoclonal gammopathy of undetermined significance (MGUS) and clonal hematopoiesis (CH) are 2 preclinical clonal expansions of hematopoietic cells whose prevalence rises with age, reaching almost 10% in people of aged 70 years and older. The increased risk of myeloid malignancies in patients with myeloma is well defined, and the study of the association between CH and MGUS could help explain this phenomenon. Here, we analyzed a fully clinically annotated dataset of 777 older subjects (median age, 91 years) previously screened for prevalence of CH. The prevalence of MGUS and CH was 9.6% and 17.3%, respectively. We detected CH in 9.7% of the patients with MGUS and MGUS in 5.5% of the patients with CH. We did not find a significant correlation between the presence of MGUS and CH. Furthermore, the 2 conditions showed a differential association with clinical and laboratory covariates, suggesting that MGUS and CH may represent age-associated unrelated clonal drifts of hematopoietic cells. Confirmatory studies are needed to assess the relevance of CH in plasma cell disorders. This trial was registered at www.clinicaltrials.gov as #NCT03907553.
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spelling pubmed-96187782022-11-01 MGUS and clonal hematopoiesis show unrelated clinical and biological trajectories in an older population cohort Da Vià, Matteo Claudio Lionetti, Marta Marella, Alessio Matera, Antonio Travaglino, Erica Signaroldi, Elena Galbussera, Alessia Antonella Lucca, Ugo Mandelli, Sara Riva, Emma Tettamanti, Mauro Pettine, Loredana Pompa, Alessandra Baldini, Luca Neri, Antonino Della Porta, Matteo Giovanni Bolli, Niccolò Blood Adv Stimulus Report Monoclonal gammopathy of undetermined significance (MGUS) and clonal hematopoiesis (CH) are 2 preclinical clonal expansions of hematopoietic cells whose prevalence rises with age, reaching almost 10% in people of aged 70 years and older. The increased risk of myeloid malignancies in patients with myeloma is well defined, and the study of the association between CH and MGUS could help explain this phenomenon. Here, we analyzed a fully clinically annotated dataset of 777 older subjects (median age, 91 years) previously screened for prevalence of CH. The prevalence of MGUS and CH was 9.6% and 17.3%, respectively. We detected CH in 9.7% of the patients with MGUS and MGUS in 5.5% of the patients with CH. We did not find a significant correlation between the presence of MGUS and CH. Furthermore, the 2 conditions showed a differential association with clinical and laboratory covariates, suggesting that MGUS and CH may represent age-associated unrelated clonal drifts of hematopoietic cells. Confirmatory studies are needed to assess the relevance of CH in plasma cell disorders. This trial was registered at www.clinicaltrials.gov as #NCT03907553. The American Society of Hematology 2022-04-09 /pmc/articles/PMC9618778/ /pubmed/35390146 http://dx.doi.org/10.1182/bloodadvances.2021006498 Text en © 2022 by The American Society of Hematology. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Stimulus Report
Da Vià, Matteo Claudio
Lionetti, Marta
Marella, Alessio
Matera, Antonio
Travaglino, Erica
Signaroldi, Elena
Galbussera, Alessia Antonella
Lucca, Ugo
Mandelli, Sara
Riva, Emma
Tettamanti, Mauro
Pettine, Loredana
Pompa, Alessandra
Baldini, Luca
Neri, Antonino
Della Porta, Matteo Giovanni
Bolli, Niccolò
MGUS and clonal hematopoiesis show unrelated clinical and biological trajectories in an older population cohort
title MGUS and clonal hematopoiesis show unrelated clinical and biological trajectories in an older population cohort
title_full MGUS and clonal hematopoiesis show unrelated clinical and biological trajectories in an older population cohort
title_fullStr MGUS and clonal hematopoiesis show unrelated clinical and biological trajectories in an older population cohort
title_full_unstemmed MGUS and clonal hematopoiesis show unrelated clinical and biological trajectories in an older population cohort
title_short MGUS and clonal hematopoiesis show unrelated clinical and biological trajectories in an older population cohort
title_sort mgus and clonal hematopoiesis show unrelated clinical and biological trajectories in an older population cohort
topic Stimulus Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9618778/
https://www.ncbi.nlm.nih.gov/pubmed/35390146
http://dx.doi.org/10.1182/bloodadvances.2021006498
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