Agenesis and microdontia of permanent teeth as late adverse effects after stem cell transplantation in young children

BACKGROUND The objective of the current study was to examine the occurrence of tooth agenesis and microdontia in pediatric stem cell transplantation (SCT) recipients. METHODS The impact of total body irradiation (TBI) and age at SCT on agenesis and microdontia of permanent teeth was examined in 55 p...

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Veröffentlicht in:Cancer 2005-01, Vol.103 (1), p.181-190
Hauptverfasser: Hölttä, Päivi, Alaluusua, Satu, Saarinen‐Pihkala, Ulla M., Peltola, Jaakko, Hovi, Liisa
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container_issue 1
container_start_page 181
container_title Cancer
container_volume 103
creator Hölttä, Päivi
Alaluusua, Satu
Saarinen‐Pihkala, Ulla M.
Peltola, Jaakko
Hovi, Liisa
description BACKGROUND The objective of the current study was to examine the occurrence of tooth agenesis and microdontia in pediatric stem cell transplantation (SCT) recipients. METHODS The impact of total body irradiation (TBI) and age at SCT on agenesis and microdontia of permanent teeth was examined in 55 patients from panoramic radiographs. Assessment A1 (for tooth agenesis and microdontia) excluded the third molars, and assessment A2 (for tooth agenesis) included the third molars. Patients were grouped according to TBI status (the TBI group vs. the non‐TBI group) and age at SCT (patients age ≤ 3.0 years [Group Y], patients ages 3.1–5.0 years [Group M], and patients age ≥ 5.1 years [Group O]). RESULTS From 1 to 12 teeth were missing in 77%, 40%, and 0% of patients (assessment A1) in Groups Y, M, and O, respectively (Group Y vs. Group M, P = 0.055; Group Y vs. Group O, P < 0.001; and Group M vs. Group O, P = 0.002), increasing to 83%, 78%, and 43%, respectively, when the third molars were included (assessment A2; P values were not significant). Correspondingly, 75%, 60%, and 13%, respectively, of patients had 1–12 microdontic teeth (assessment A1: Group Y vs. Group M, P = 0.306; Group Y vs. Group O, P < 0.001; and Group M vs. Group O, P = 0.003). Recipient age at the time of SCT was found to have a negative correlation with the number of missing teeth (P = 0.001) and microdontic teeth (P = 0.005). TBI appeared to have little effect on the prevalence of tooth agenesis (assessment A1: TBI group, 32%; non‐TBI group, 29%; assessment A2: TBI group, 72%; non‐TBI group, 46%; P values were not significant) or on the prevalence of microdontia (assessment A1: TBI, 41%; non‐TBI, 50%; P value was not significant). A tendency toward an increased number of affected teeth was noticed in the group of patients who received TBI. CONCLUSIONS Depending on their age at SCT, 50–100% of pediatric SCT recipients will later present with agenesis and/or microdontia of permanent teeth that may jeopardize occlusal development. Young age (≤ 5.0 years) at SCT was found to be a stronger risk factor than TBI, although TBI caused additive impairment. Cancer, 2005. © 2004 American Cancer Society. Depending on their age at the time of stem cell transplantation (SCT), 50–100% of pediatric SCT recipients are reported to present with permanent tooth agenesis and/or microdontia at a later date, which may jeopardize occlusal development. Young age (≤ 5.0 years) at the time of SCT was the strongest risk
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METHODS The impact of total body irradiation (TBI) and age at SCT on agenesis and microdontia of permanent teeth was examined in 55 patients from panoramic radiographs. Assessment A1 (for tooth agenesis and microdontia) excluded the third molars, and assessment A2 (for tooth agenesis) included the third molars. Patients were grouped according to TBI status (the TBI group vs. the non‐TBI group) and age at SCT (patients age ≤ 3.0 years [Group Y], patients ages 3.1–5.0 years [Group M], and patients age ≥ 5.1 years [Group O]). RESULTS From 1 to 12 teeth were missing in 77%, 40%, and 0% of patients (assessment A1) in Groups Y, M, and O, respectively (Group Y vs. Group M, P = 0.055; Group Y vs. Group O, P &lt; 0.001; and Group M vs. Group O, P = 0.002), increasing to 83%, 78%, and 43%, respectively, when the third molars were included (assessment A2; P values were not significant). Correspondingly, 75%, 60%, and 13%, respectively, of patients had 1–12 microdontic teeth (assessment A1: Group Y vs. Group M, P = 0.306; Group Y vs. Group O, P &lt; 0.001; and Group M vs. Group O, P = 0.003). Recipient age at the time of SCT was found to have a negative correlation with the number of missing teeth (P = 0.001) and microdontic teeth (P = 0.005). TBI appeared to have little effect on the prevalence of tooth agenesis (assessment A1: TBI group, 32%; non‐TBI group, 29%; assessment A2: TBI group, 72%; non‐TBI group, 46%; P values were not significant) or on the prevalence of microdontia (assessment A1: TBI, 41%; non‐TBI, 50%; P value was not significant). A tendency toward an increased number of affected teeth was noticed in the group of patients who received TBI. CONCLUSIONS Depending on their age at SCT, 50–100% of pediatric SCT recipients will later present with agenesis and/or microdontia of permanent teeth that may jeopardize occlusal development. Young age (≤ 5.0 years) at SCT was found to be a stronger risk factor than TBI, although TBI caused additive impairment. Cancer, 2005. © 2004 American Cancer Society. Depending on their age at the time of stem cell transplantation (SCT), 50–100% of pediatric SCT recipients are reported to present with permanent tooth agenesis and/or microdontia at a later date, which may jeopardize occlusal development. Young age (≤ 5.0 years) at the time of SCT was the strongest risk factor, and total body irradiation caused additive impairment.</description><identifier>ISSN: 0008-543X</identifier><identifier>EISSN: 1097-0142</identifier><identifier>DOI: 10.1002/cncr.20762</identifier><identifier>PMID: 15540242</identifier><identifier>CODEN: CANCAR</identifier><language>eng</language><publisher>Hoboken: Wiley Subscription Services, Inc., A Wiley Company</publisher><subject>Age Factors ; Biological and medical sciences ; Child ; Child, Preschool ; dental development ; Dental Enamel Hypoplasia - etiology ; Female ; Follow-Up Studies ; Humans ; hypodontia ; Infant ; Infant, Newborn ; late adverse effects ; Male ; Medical sciences ; microdontia ; Prevalence ; Risk Factors ; stem cell transplantation ; Stem Cell Transplantation - adverse effects ; Tooth - growth &amp; development ; Tooth Abnormalities - epidemiology ; Tooth Abnormalities - etiology ; tooth agenesis ; Tumors ; Whole-Body Irradiation - adverse effects</subject><ispartof>Cancer, 2005-01, Vol.103 (1), p.181-190</ispartof><rights>Copyright © 2004 American Cancer Society</rights><rights>2005 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4232-7de6ae2123929c37555ee990fdf2ebd440e4bc11a53919e90c1b8e9dcaa1cb3b3</citedby><cites>FETCH-LOGICAL-c4232-7de6ae2123929c37555ee990fdf2ebd440e4bc11a53919e90c1b8e9dcaa1cb3b3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fcncr.20762$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fcncr.20762$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,778,782,1414,1430,27913,27914,45563,45564,46398,46822</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=16541796$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/15540242$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Hölttä, Päivi</creatorcontrib><creatorcontrib>Alaluusua, Satu</creatorcontrib><creatorcontrib>Saarinen‐Pihkala, Ulla M.</creatorcontrib><creatorcontrib>Peltola, Jaakko</creatorcontrib><creatorcontrib>Hovi, Liisa</creatorcontrib><title>Agenesis and microdontia of permanent teeth as late adverse effects after stem cell transplantation in young children</title><title>Cancer</title><addtitle>Cancer</addtitle><description>BACKGROUND The objective of the current study was to examine the occurrence of tooth agenesis and microdontia in pediatric stem cell transplantation (SCT) recipients. METHODS The impact of total body irradiation (TBI) and age at SCT on agenesis and microdontia of permanent teeth was examined in 55 patients from panoramic radiographs. Assessment A1 (for tooth agenesis and microdontia) excluded the third molars, and assessment A2 (for tooth agenesis) included the third molars. Patients were grouped according to TBI status (the TBI group vs. the non‐TBI group) and age at SCT (patients age ≤ 3.0 years [Group Y], patients ages 3.1–5.0 years [Group M], and patients age ≥ 5.1 years [Group O]). RESULTS From 1 to 12 teeth were missing in 77%, 40%, and 0% of patients (assessment A1) in Groups Y, M, and O, respectively (Group Y vs. Group M, P = 0.055; Group Y vs. Group O, P &lt; 0.001; and Group M vs. Group O, P = 0.002), increasing to 83%, 78%, and 43%, respectively, when the third molars were included (assessment A2; P values were not significant). Correspondingly, 75%, 60%, and 13%, respectively, of patients had 1–12 microdontic teeth (assessment A1: Group Y vs. Group M, P = 0.306; Group Y vs. Group O, P &lt; 0.001; and Group M vs. Group O, P = 0.003). Recipient age at the time of SCT was found to have a negative correlation with the number of missing teeth (P = 0.001) and microdontic teeth (P = 0.005). TBI appeared to have little effect on the prevalence of tooth agenesis (assessment A1: TBI group, 32%; non‐TBI group, 29%; assessment A2: TBI group, 72%; non‐TBI group, 46%; P values were not significant) or on the prevalence of microdontia (assessment A1: TBI, 41%; non‐TBI, 50%; P value was not significant). A tendency toward an increased number of affected teeth was noticed in the group of patients who received TBI. CONCLUSIONS Depending on their age at SCT, 50–100% of pediatric SCT recipients will later present with agenesis and/or microdontia of permanent teeth that may jeopardize occlusal development. Young age (≤ 5.0 years) at SCT was found to be a stronger risk factor than TBI, although TBI caused additive impairment. Cancer, 2005. © 2004 American Cancer Society. Depending on their age at the time of stem cell transplantation (SCT), 50–100% of pediatric SCT recipients are reported to present with permanent tooth agenesis and/or microdontia at a later date, which may jeopardize occlusal development. Young age (≤ 5.0 years) at the time of SCT was the strongest risk factor, and total body irradiation caused additive impairment.</description><subject>Age Factors</subject><subject>Biological and medical sciences</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>dental development</subject><subject>Dental Enamel Hypoplasia - etiology</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Humans</subject><subject>hypodontia</subject><subject>Infant</subject><subject>Infant, Newborn</subject><subject>late adverse effects</subject><subject>Male</subject><subject>Medical sciences</subject><subject>microdontia</subject><subject>Prevalence</subject><subject>Risk Factors</subject><subject>stem cell transplantation</subject><subject>Stem Cell Transplantation - adverse effects</subject><subject>Tooth - growth &amp; development</subject><subject>Tooth Abnormalities - epidemiology</subject><subject>Tooth Abnormalities - etiology</subject><subject>tooth agenesis</subject><subject>Tumors</subject><subject>Whole-Body Irradiation - adverse effects</subject><issn>0008-543X</issn><issn>1097-0142</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2005</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kE1LAzEQhoMotn5c_AGSixdha5JNus1Ril9QFETB2zKbTDSymy1JqvTfu9pCb56GgWfm5X0IOeNswhkTVyaYOBGsmoo9MuZMVwXjUuyTMWNsVihZvo3IUUqfw1oJVR6SEVdKMiHFmKyu3zFg8olCsLTzJva2D9kD7R1dYuwgYMg0I-YPCom2kJGC_cKYkKJzaPJw6jJGmjJ21GDb0hwhpGULIUP2faA-0HW_Cu_UfPjWRgwn5MBBm_B0O4_J6-3Ny_y-WDzdPcyvF4WRohRFZXEKKLgotdCmrJRSiFozZ53AxkrJUDaGc1Cl5ho1M7yZobYGgJumbMpjcrn5O9RKKaKrl9F3ENc1Z_Wvu_rXXf3nboDPN_By1XRod-hW1gBcbAFIBlo3tDQ-7bipkrzS04HjG-7bt7j-J7KeP86fN-E_6CGJSA</recordid><startdate>20050101</startdate><enddate>20050101</enddate><creator>Hölttä, Päivi</creator><creator>Alaluusua, Satu</creator><creator>Saarinen‐Pihkala, Ulla M.</creator><creator>Peltola, Jaakko</creator><creator>Hovi, Liisa</creator><general>Wiley Subscription Services, Inc., A Wiley Company</general><general>Wiley-Liss</general><scope>IQODW</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope></search><sort><creationdate>20050101</creationdate><title>Agenesis and microdontia of permanent teeth as late adverse effects after stem cell transplantation in young children</title><author>Hölttä, Päivi ; Alaluusua, Satu ; Saarinen‐Pihkala, Ulla M. ; Peltola, Jaakko ; Hovi, Liisa</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4232-7de6ae2123929c37555ee990fdf2ebd440e4bc11a53919e90c1b8e9dcaa1cb3b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2005</creationdate><topic>Age Factors</topic><topic>Biological and medical sciences</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>dental development</topic><topic>Dental Enamel Hypoplasia - etiology</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Humans</topic><topic>hypodontia</topic><topic>Infant</topic><topic>Infant, Newborn</topic><topic>late adverse effects</topic><topic>Male</topic><topic>Medical sciences</topic><topic>microdontia</topic><topic>Prevalence</topic><topic>Risk Factors</topic><topic>stem cell transplantation</topic><topic>Stem Cell Transplantation - adverse effects</topic><topic>Tooth - growth &amp; development</topic><topic>Tooth Abnormalities - epidemiology</topic><topic>Tooth Abnormalities - etiology</topic><topic>tooth agenesis</topic><topic>Tumors</topic><topic>Whole-Body Irradiation - adverse effects</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Hölttä, Päivi</creatorcontrib><creatorcontrib>Alaluusua, Satu</creatorcontrib><creatorcontrib>Saarinen‐Pihkala, Ulla M.</creatorcontrib><creatorcontrib>Peltola, Jaakko</creatorcontrib><creatorcontrib>Hovi, Liisa</creatorcontrib><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><jtitle>Cancer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Hölttä, Päivi</au><au>Alaluusua, Satu</au><au>Saarinen‐Pihkala, Ulla M.</au><au>Peltola, Jaakko</au><au>Hovi, Liisa</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Agenesis and microdontia of permanent teeth as late adverse effects after stem cell transplantation in young children</atitle><jtitle>Cancer</jtitle><addtitle>Cancer</addtitle><date>2005-01-01</date><risdate>2005</risdate><volume>103</volume><issue>1</issue><spage>181</spage><epage>190</epage><pages>181-190</pages><issn>0008-543X</issn><eissn>1097-0142</eissn><coden>CANCAR</coden><abstract>BACKGROUND The objective of the current study was to examine the occurrence of tooth agenesis and microdontia in pediatric stem cell transplantation (SCT) recipients. METHODS The impact of total body irradiation (TBI) and age at SCT on agenesis and microdontia of permanent teeth was examined in 55 patients from panoramic radiographs. Assessment A1 (for tooth agenesis and microdontia) excluded the third molars, and assessment A2 (for tooth agenesis) included the third molars. Patients were grouped according to TBI status (the TBI group vs. the non‐TBI group) and age at SCT (patients age ≤ 3.0 years [Group Y], patients ages 3.1–5.0 years [Group M], and patients age ≥ 5.1 years [Group O]). RESULTS From 1 to 12 teeth were missing in 77%, 40%, and 0% of patients (assessment A1) in Groups Y, M, and O, respectively (Group Y vs. Group M, P = 0.055; Group Y vs. Group O, P &lt; 0.001; and Group M vs. Group O, P = 0.002), increasing to 83%, 78%, and 43%, respectively, when the third molars were included (assessment A2; P values were not significant). Correspondingly, 75%, 60%, and 13%, respectively, of patients had 1–12 microdontic teeth (assessment A1: Group Y vs. Group M, P = 0.306; Group Y vs. Group O, P &lt; 0.001; and Group M vs. Group O, P = 0.003). Recipient age at the time of SCT was found to have a negative correlation with the number of missing teeth (P = 0.001) and microdontic teeth (P = 0.005). TBI appeared to have little effect on the prevalence of tooth agenesis (assessment A1: TBI group, 32%; non‐TBI group, 29%; assessment A2: TBI group, 72%; non‐TBI group, 46%; P values were not significant) or on the prevalence of microdontia (assessment A1: TBI, 41%; non‐TBI, 50%; P value was not significant). A tendency toward an increased number of affected teeth was noticed in the group of patients who received TBI. CONCLUSIONS Depending on their age at SCT, 50–100% of pediatric SCT recipients will later present with agenesis and/or microdontia of permanent teeth that may jeopardize occlusal development. Young age (≤ 5.0 years) at SCT was found to be a stronger risk factor than TBI, although TBI caused additive impairment. Cancer, 2005. © 2004 American Cancer Society. Depending on their age at the time of stem cell transplantation (SCT), 50–100% of pediatric SCT recipients are reported to present with permanent tooth agenesis and/or microdontia at a later date, which may jeopardize occlusal development. Young age (≤ 5.0 years) at the time of SCT was the strongest risk factor, and total body irradiation caused additive impairment.</abstract><cop>Hoboken</cop><pub>Wiley Subscription Services, Inc., A Wiley Company</pub><pmid>15540242</pmid><doi>10.1002/cncr.20762</doi><tpages>10</tpages></addata></record>
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subjects Age Factors
Biological and medical sciences
Child
Child, Preschool
dental development
Dental Enamel Hypoplasia - etiology
Female
Follow-Up Studies
Humans
hypodontia
Infant
Infant, Newborn
late adverse effects
Male
Medical sciences
microdontia
Prevalence
Risk Factors
stem cell transplantation
Stem Cell Transplantation - adverse effects
Tooth - growth & development
Tooth Abnormalities - epidemiology
Tooth Abnormalities - etiology
tooth agenesis
Tumors
Whole-Body Irradiation - adverse effects
title Agenesis and microdontia of permanent teeth as late adverse effects after stem cell transplantation in young children
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