Loading…

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...

Full description

Saved in:
Bibliographic Details
Published in:Bone marrow transplantation (Basingstoke) 2020-07, Vol.55 (7), p.1438-1446
Main Authors: Uziel, Orit, Lahav, Meir, Shargian, Liat, Beery, Einat, Pasvolsky, Oren, Rozovski, Uri, Raanani, Pia, Yeshurun, Moshe
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c541t-a141ea454b802c3a2eff3d2499bf7643a2db34374d4688e425acc771cee1a8233
cites cdi_FETCH-LOGICAL-c541t-a141ea454b802c3a2eff3d2499bf7643a2db34374d4688e425acc771cee1a8233
container_end_page 1446
container_issue 7
container_start_page 1438
container_title Bone marrow transplantation (Basingstoke)
container_volume 55
creator Uziel, Orit
Lahav, Meir
Shargian, Liat
Beery, Einat
Pasvolsky, Oren
Rozovski, Uri
Raanani, Pia
Yeshurun, Moshe
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
fullrecord <record><control><sourceid>gale_proqu</sourceid><recordid>TN_cdi_proquest_miscellaneous_2364032995</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A628316927</galeid><sourcerecordid>A628316927</sourcerecordid><originalsourceid>FETCH-LOGICAL-c541t-a141ea454b802c3a2eff3d2499bf7643a2db34374d4688e425acc771cee1a8233</originalsourceid><addsrcrecordid>eNp9kstu1DAUhi0EokPhAdigSEgVmxRfTux4WVXlIrWCBawtj3OSSZXYg-0I0afH0ZRCUUFe2D7-_nOxfkJeMnrKqGjfJmBAdU05rWkrdH3ziGwYKFk3QjaPyYZy2dZCSH1EnqV0TSkDoM1TciQ41QBMbcjV54izzUvEyg44-qHqwzSF7-vJlsOAHkdX7VYo7MOIudxSxrlyOE1Vjtan_WR9tnkM_jl50tsp4Yvb_Zh8fXfx5fxDffnp_cfzs8vaNcBybRkwtNDAtqXcCcux70XHQettrySUQLcVIBR0INsWgTfWOaWYQ2S25UIckzeHvPsYvi2YspnHtDZkPYYlGS4kUMG1bgr6-i_0OizRl-4MB9VQ4IrJ_1NMcwq61L2jBjuhGX0fyvxuLW3OJG8Fk5qrQp0-QJXV4Ty64LEfS_ye4OQPwQ7tlHcpTMv6o-k-yA6giyGliL3Zx3G28Ydh1KyOMAdHmOIIszrC3BTNq9vJlu2M3Z3ilwUKwA9AKk9-wPh79H9n_QmFpb40</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2419204982</pqid></control><display><type>article</type><title>Premature ageing following allogeneic hematopoietic stem cell transplantation</title><source>Nexis UK</source><source>Springer Nature</source><creator>Uziel, Orit ; Lahav, Meir ; Shargian, Liat ; Beery, Einat ; Pasvolsky, Oren ; Rozovski, Uri ; Raanani, Pia ; Yeshurun, Moshe</creator><creatorcontrib>Uziel, Orit ; Lahav, Meir ; Shargian, Liat ; Beery, Einat ; Pasvolsky, Oren ; Rozovski, Uri ; Raanani, Pia ; Yeshurun, Moshe</creatorcontrib><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.</description><identifier>ISSN: 0268-3369</identifier><identifier>EISSN: 1476-5365</identifier><identifier>DOI: 10.1038/s41409-020-0839-z</identifier><identifier>PMID: 32094417</identifier><language>eng</language><publisher>London: Nature Publishing Group UK</publisher><subject>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 &amp; Public Health ; Medicine, Experimental ; Methylation ; p16 Protein ; Public Health ; Serum levels ; Stem cell transplantation ; Stem Cells ; Survival ; Telomeres ; Transplantation ; Transplants &amp; implants</subject><ispartof>Bone marrow transplantation (Basingstoke), 2020-07, Vol.55 (7), p.1438-1446</ispartof><rights>The Author(s), under exclusive licence to Springer Nature Limited 2020</rights><rights>COPYRIGHT 2020 Nature Publishing Group</rights><rights>The Author(s), under exclusive licence to Springer Nature Limited 2020.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c541t-a141ea454b802c3a2eff3d2499bf7643a2db34374d4688e425acc771cee1a8233</citedby><cites>FETCH-LOGICAL-c541t-a141ea454b802c3a2eff3d2499bf7643a2db34374d4688e425acc771cee1a8233</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32094417$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Uziel, Orit</creatorcontrib><creatorcontrib>Lahav, Meir</creatorcontrib><creatorcontrib>Shargian, Liat</creatorcontrib><creatorcontrib>Beery, Einat</creatorcontrib><creatorcontrib>Pasvolsky, Oren</creatorcontrib><creatorcontrib>Rozovski, Uri</creatorcontrib><creatorcontrib>Raanani, Pia</creatorcontrib><creatorcontrib>Yeshurun, Moshe</creatorcontrib><title>Premature ageing following allogeneic hematopoietic stem cell transplantation</title><title>Bone marrow transplantation (Basingstoke)</title><addtitle>Bone Marrow Transplant</addtitle><addtitle>Bone Marrow Transplant</addtitle><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.</description><subject>13</subject><subject>13/106</subject><subject>631/67/1990</subject><subject>631/80</subject><subject>Age determination</subject><subject>Aging</subject><subject>Blood cells</subject><subject>Bone marrow</subject><subject>Cell Biology</subject><subject>Chronology</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>DNA methylation</subject><subject>Epithelial cells</subject><subject>Epithelium</subject><subject>Gene expression</subject><subject>Hematology</subject><subject>Hematopoietic stem cells</subject><subject>INK4a protein</subject><subject>Interleukin 6</subject><subject>Internal Medicine</subject><subject>Medical research</subject><subject>Medicine</subject><subject>Medicine &amp; Public Health</subject><subject>Medicine, Experimental</subject><subject>Methylation</subject><subject>p16 Protein</subject><subject>Public Health</subject><subject>Serum levels</subject><subject>Stem cell transplantation</subject><subject>Stem Cells</subject><subject>Survival</subject><subject>Telomeres</subject><subject>Transplantation</subject><subject>Transplants &amp; implants</subject><issn>0268-3369</issn><issn>1476-5365</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><recordid>eNp9kstu1DAUhi0EokPhAdigSEgVmxRfTux4WVXlIrWCBawtj3OSSZXYg-0I0afH0ZRCUUFe2D7-_nOxfkJeMnrKqGjfJmBAdU05rWkrdH3ziGwYKFk3QjaPyYZy2dZCSH1EnqV0TSkDoM1TciQ41QBMbcjV54izzUvEyg44-qHqwzSF7-vJlsOAHkdX7VYo7MOIudxSxrlyOE1Vjtan_WR9tnkM_jl50tsp4Yvb_Zh8fXfx5fxDffnp_cfzs8vaNcBybRkwtNDAtqXcCcux70XHQettrySUQLcVIBR0INsWgTfWOaWYQ2S25UIckzeHvPsYvi2YspnHtDZkPYYlGS4kUMG1bgr6-i_0OizRl-4MB9VQ4IrJ_1NMcwq61L2jBjuhGX0fyvxuLW3OJG8Fk5qrQp0-QJXV4Ty64LEfS_ye4OQPwQ7tlHcpTMv6o-k-yA6giyGliL3Zx3G28Ydh1KyOMAdHmOIIszrC3BTNq9vJlu2M3Z3ilwUKwA9AKk9-wPh79H9n_QmFpb40</recordid><startdate>20200701</startdate><enddate>20200701</enddate><creator>Uziel, Orit</creator><creator>Lahav, Meir</creator><creator>Shargian, Liat</creator><creator>Beery, Einat</creator><creator>Pasvolsky, Oren</creator><creator>Rozovski, Uri</creator><creator>Raanani, Pia</creator><creator>Yeshurun, Moshe</creator><general>Nature Publishing Group UK</general><general>Nature Publishing Group</general><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7QO</scope><scope>7QP</scope><scope>7T5</scope><scope>7U9</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FD</scope><scope>8FE</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FR3</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>H94</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M7N</scope><scope>M7P</scope><scope>P64</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope></search><sort><creationdate>20200701</creationdate><title>Premature ageing following allogeneic hematopoietic stem cell transplantation</title><author>Uziel, Orit ; Lahav, Meir ; Shargian, Liat ; Beery, Einat ; Pasvolsky, Oren ; Rozovski, Uri ; Raanani, Pia ; Yeshurun, Moshe</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c541t-a141ea454b802c3a2eff3d2499bf7643a2db34374d4688e425acc771cee1a8233</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>13</topic><topic>13/106</topic><topic>631/67/1990</topic><topic>631/80</topic><topic>Age determination</topic><topic>Aging</topic><topic>Blood cells</topic><topic>Bone marrow</topic><topic>Cell Biology</topic><topic>Chronology</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>DNA methylation</topic><topic>Epithelial cells</topic><topic>Epithelium</topic><topic>Gene expression</topic><topic>Hematology</topic><topic>Hematopoietic stem cells</topic><topic>INK4a protein</topic><topic>Interleukin 6</topic><topic>Internal Medicine</topic><topic>Medical research</topic><topic>Medicine</topic><topic>Medicine &amp; Public Health</topic><topic>Medicine, Experimental</topic><topic>Methylation</topic><topic>p16 Protein</topic><topic>Public Health</topic><topic>Serum levels</topic><topic>Stem cell transplantation</topic><topic>Stem Cells</topic><topic>Survival</topic><topic>Telomeres</topic><topic>Transplantation</topic><topic>Transplants &amp; implants</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Uziel, Orit</creatorcontrib><creatorcontrib>Lahav, Meir</creatorcontrib><creatorcontrib>Shargian, Liat</creatorcontrib><creatorcontrib>Beery, Einat</creatorcontrib><creatorcontrib>Pasvolsky, Oren</creatorcontrib><creatorcontrib>Rozovski, Uri</creatorcontrib><creatorcontrib>Raanani, Pia</creatorcontrib><creatorcontrib>Yeshurun, Moshe</creatorcontrib><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Biotechnology Research Abstracts</collection><collection>Calcium &amp; Calcified Tissue Abstracts</collection><collection>Immunology Abstracts</collection><collection>Virology and AIDS Abstracts</collection><collection>PHMC-Proquest健康医学期刊库</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Technology Research Database</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>Biological Science Collection</collection><collection>ProQuest Central</collection><collection>ProQuest Natural Science Collection</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Engineering Research Database</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>SciTech Premium Collection</collection><collection>ProQuest Health &amp; Medical Complete (Alumni)</collection><collection>ProQuest Biological Science Collection</collection><collection>Health &amp; Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>ProQuest Biological Science Journals</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><jtitle>Bone marrow transplantation (Basingstoke)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Uziel, Orit</au><au>Lahav, Meir</au><au>Shargian, Liat</au><au>Beery, Einat</au><au>Pasvolsky, Oren</au><au>Rozovski, Uri</au><au>Raanani, Pia</au><au>Yeshurun, Moshe</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Premature ageing following allogeneic hematopoietic stem cell transplantation</atitle><jtitle>Bone marrow transplantation (Basingstoke)</jtitle><stitle>Bone Marrow Transplant</stitle><addtitle>Bone Marrow 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 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.</abstract><cop>London</cop><pub>Nature Publishing Group UK</pub><pmid>32094417</pmid><doi>10.1038/s41409-020-0839-z</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 0268-3369
ispartof Bone marrow transplantation (Basingstoke), 2020-07, Vol.55 (7), p.1438-1446
issn 0268-3369
1476-5365
language eng
recordid cdi_proquest_miscellaneous_2364032995
source Nexis UK; Springer Nature
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
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-23T06%3A05%3A32IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_proqu&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Premature%20ageing%20following%20allogeneic%20hematopoietic%20stem%20cell%20transplantation&rft.jtitle=Bone%20marrow%20transplantation%20(Basingstoke)&rft.au=Uziel,%20Orit&rft.date=2020-07-01&rft.volume=55&rft.issue=7&rft.spage=1438&rft.epage=1446&rft.pages=1438-1446&rft.issn=0268-3369&rft.eissn=1476-5365&rft_id=info:doi/10.1038/s41409-020-0839-z&rft_dat=%3Cgale_proqu%3EA628316927%3C/gale_proqu%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c541t-a141ea454b802c3a2eff3d2499bf7643a2db34374d4688e425acc771cee1a8233%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2419204982&rft_id=info:pmid/32094417&rft_galeid=A628316927&rfr_iscdi=true