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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...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
The American Society of Hematology
2022
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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. |
format | Online Article Text |
id | pubmed-9618778 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | The American Society of Hematology |
record_format | MEDLINE/PubMed |
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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