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Premature ageing following allogeneic hematopoietic stem cell transplantation
Survivors of hematopoietic cell transplantation (HCT) have been shown to exhibit both clinical and biological features of accelerated ageing. Most studies used frailty measures, comorbidities for clinical assessment and several biological assessment of premature ageing. However, these tests are less...
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Published in: | Bone marrow transplantation (Basingstoke) 2020-07, Vol.55 (7), p.1438-1446 |
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description | Survivors of hematopoietic cell transplantation (HCT) have been shown to exhibit both clinical and biological features of accelerated ageing. Most studies used frailty measures, comorbidities for clinical assessment and several biological assessment of premature ageing. However, these tests are less suitable for age determination of individual patients. Recently, DNA methylation has emerged as a novel test to measure cellular age. In the present study, we assessed ageing in a cohort of 26 survivors of allogeneic HCT by frailty tests comprising the handgrip and 6 min walk tests and by biological tests including DNA methylation, telomere length and expression of p16INK
4A
and serum levels of IL-6. DNA methylation was evaluated both in blood and buccal epithelial cells. Physiological reserve was markedly reduced in transplant survivors, reflected by 6 min walk test. Increased IL-6 serum levels and p16
ink4A
correlated with accelerated ageing. Overall, the measured age of donor blood cells was significantly higher than these blood cells residing in their respective donors, as reflected by DNA methylation and by buccal epithelium methylation status. These clinical and biological observations suggest that allogeneic HCT is associated with accelerated ageing. |
doi_str_mv | 10.1038/s41409-020-0839-z |
format | article |
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4A
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4A
and serum levels of IL-6. DNA methylation was evaluated both in blood and buccal epithelial cells. Physiological reserve was markedly reduced in transplant survivors, reflected by 6 min walk test. Increased IL-6 serum levels and p16
ink4A
correlated with accelerated ageing. Overall, the measured age of donor blood cells was significantly higher than these blood cells residing in their respective donors, as reflected by DNA methylation and by buccal epithelium methylation status. 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Transplant</addtitle><date>2020-07-01</date><risdate>2020</risdate><volume>55</volume><issue>7</issue><spage>1438</spage><epage>1446</epage><pages>1438-1446</pages><issn>0268-3369</issn><eissn>1476-5365</eissn><abstract>Survivors of hematopoietic cell transplantation (HCT) have been shown to exhibit both clinical and biological features of accelerated ageing. Most studies used frailty measures, comorbidities for clinical assessment and several biological assessment of premature ageing. However, these tests are less suitable for age determination of individual patients. Recently, DNA methylation has emerged as a novel test to measure cellular age. In the present study, we assessed ageing in a cohort of 26 survivors of allogeneic HCT by frailty tests comprising the handgrip and 6 min walk tests and by biological tests including DNA methylation, telomere length and expression of p16INK
4A
and serum levels of IL-6. DNA methylation was evaluated both in blood and buccal epithelial cells. Physiological reserve was markedly reduced in transplant survivors, reflected by 6 min walk test. Increased IL-6 serum levels and p16
ink4A
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subjects | 13 13/106 631/67/1990 631/80 Age determination Aging Blood cells Bone marrow Cell Biology Chronology Deoxyribonucleic acid DNA DNA methylation Epithelial cells Epithelium Gene expression Hematology Hematopoietic stem cells INK4a protein Interleukin 6 Internal Medicine Medical research Medicine Medicine & Public Health Medicine, Experimental Methylation p16 Protein Public Health Serum levels Stem cell transplantation Stem Cells Survival Telomeres Transplantation Transplants & implants |
title | Premature ageing following allogeneic hematopoietic stem cell transplantation |
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