The study on relationship between age and cytogenetic subgroups in 640 patients with de novo acute myeloid leukemia
To analyze the cytogenetic characteristics of different age subgroups in patients with acute myeloid leukemia (AML), and to explore the relationship between age and cytogenetics. Between January 2004 and December 2011, Bone marrow (BM) samples from 640 patients with de novo AML were analyzed retrosp...
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| Veröffentlicht in: | Zhōnghuá xuèyèxué zázhì 2013-02, Vol.34 (2), p.133-137 |
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| container_title | Zhōnghuá xuèyèxué zázhì |
| container_volume | 34 |
| creator | Su, Long Gao, Su-jun Li, Wei Tan, Ye-hui Yao, Cheng Song, Yan-qui Yang, Yan Liu, Zi-ling Bai, Ou Lin, Hai Yang, Lei Wang, Chang Cui, Jiu-wei Wang, Guan-jun |
| description | To analyze the cytogenetic characteristics of different age subgroups in patients with acute myeloid leukemia (AML), and to explore the relationship between age and cytogenetics.
Between January 2004 and December 2011, Bone marrow (BM) samples from 640 patients with de novo AML were analyzed retrospectively. The analyses were performed according to standard culturing and banding techniques, and clonal abnormalities were defined and described according to the International System for Human Cytogenetic Nomenclature (ISCN 2009). The cytogenetic subtypes were performed as normal, balanced, and unbalanced karyotypes. In the last group, the age distribution of complex and monosome karyotypes were further analyzed. The patients were divided into 8 age groups: 0 - 9, 10 - 19, 20 - 29, 30 - 39, 40 - 49, 50 - 59, 60 - 69, and ≥ 70 year old groups.
The distribution of normal, balanced, and unbalanced karyotypes showed age specific characteristics. The incidence of normal karyotype increased from 6.67% (0 ∼ 9 year old) t |
| format | Article |
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Between January 2004 and December 2011, Bone marrow (BM) samples from 640 patients with de novo AML were analyzed retrospectively. The analyses were performed according to standard culturing and banding techniques, and clonal abnormalities were defined and described according to the International System for Human Cytogenetic Nomenclature (ISCN 2009). The cytogenetic subtypes were performed as normal, balanced, and unbalanced karyotypes. In the last group, the age distribution of complex and monosome karyotypes were further analyzed. The patients were divided into 8 age groups: 0 - 9, 10 - 19, 20 - 29, 30 - 39, 40 - 49, 50 - 59, 60 - 69, and ≥ 70 year old groups.
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Between January 2004 and December 2011, Bone marrow (BM) samples from 640 patients with de novo AML were analyzed retrospectively. The analyses were performed according to standard culturing and banding techniques, and clonal abnormalities were defined and described according to the International System for Human Cytogenetic Nomenclature (ISCN 2009). The cytogenetic subtypes were performed as normal, balanced, and unbalanced karyotypes. In the last group, the age distribution of complex and monosome karyotypes were further analyzed. The patients were divided into 8 age groups: 0 - 9, 10 - 19, 20 - 29, 30 - 39, 40 - 49, 50 - 59, 60 - 69, and ≥ 70 year old groups.
The distribution of normal, balanced, and unbalanced karyotypes showed age specific characteristics. The incidence of normal karyotype increased from 6.67% (0 ∼ 9 year old) t</description><subject>Adolescent</subject><subject>Adult</subject><subject>Age Factors</subject><subject>Aged</subject><subject>Aged, 80 and over</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Female</subject><subject>Humans</subject><subject>Infant</subject><subject>Karyotype</subject><subject>Karyotyping</subject><subject>Leukemia, Myeloid, Acute - genetics</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Retrospective Studies</subject><subject>Young Adult</subject><issn>0253-2727</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2013</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNo1kL1qwzAURj20NCHNK5Q7dglIV7bkjCX0DwJd0tlI1nUiakuuJTX47RtoOn3L-c5wboolw0psUKFaFOsYnWEVF7IWgt0VCxSSc0S2LOLhRBBTtjMEDxP1Orng48mNYCidiTzoI4H2Fto5hSN5Sq6FmM1xCnmM4DzIksF4-ZFPEc4uncAS-PATQLc5EQwz9cFZ6Cl_0eD0fXHb6T7S-rqr4vPl-bB72-w_Xt93T_vNyFGmjWlNrTl2ciuEaZXiVc14WUlusTPKlttyy0TF0La1KlF2ipG1skQlpUCDQqyKxz_vOIXvTDE1g4st9b32FHJsuCgvGeoK-QV9uKLZDGSbcXKDnubmP5T4BfkMZEE</recordid><startdate>201302</startdate><enddate>201302</enddate><creator>Su, Long</creator><creator>Gao, Su-jun</creator><creator>Li, Wei</creator><creator>Tan, Ye-hui</creator><creator>Yao, Cheng</creator><creator>Song, Yan-qui</creator><creator>Yang, Yan</creator><creator>Liu, Zi-ling</creator><creator>Bai, Ou</creator><creator>Lin, Hai</creator><creator>Yang, Lei</creator><creator>Wang, Chang</creator><creator>Cui, Jiu-wei</creator><creator>Wang, Guan-jun</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>201302</creationdate><title>The study on relationship between age and cytogenetic subgroups in 640 patients with de novo acute myeloid leukemia</title><author>Su, Long ; Gao, Su-jun ; Li, Wei ; Tan, Ye-hui ; Yao, Cheng ; Song, Yan-qui ; Yang, Yan ; Liu, Zi-ling ; Bai, Ou ; Lin, Hai ; Yang, Lei ; Wang, Chang ; Cui, Jiu-wei ; Wang, Guan-jun</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p126t-bcb8a12f6933bc77158014561d2fb7d494903502dc87426f70edd64276632b233</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>chi</language><creationdate>2013</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Age Factors</topic><topic>Aged</topic><topic>Aged, 80 and over</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Female</topic><topic>Humans</topic><topic>Infant</topic><topic>Karyotype</topic><topic>Karyotyping</topic><topic>Leukemia, Myeloid, Acute - genetics</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Retrospective Studies</topic><topic>Young Adult</topic><toplevel>online_resources</toplevel><creatorcontrib>Su, Long</creatorcontrib><creatorcontrib>Gao, Su-jun</creatorcontrib><creatorcontrib>Li, Wei</creatorcontrib><creatorcontrib>Tan, Ye-hui</creatorcontrib><creatorcontrib>Yao, Cheng</creatorcontrib><creatorcontrib>Song, Yan-qui</creatorcontrib><creatorcontrib>Yang, Yan</creatorcontrib><creatorcontrib>Liu, Zi-ling</creatorcontrib><creatorcontrib>Bai, Ou</creatorcontrib><creatorcontrib>Lin, Hai</creatorcontrib><creatorcontrib>Yang, Lei</creatorcontrib><creatorcontrib>Wang, Chang</creatorcontrib><creatorcontrib>Cui, Jiu-wei</creatorcontrib><creatorcontrib>Wang, Guan-jun</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Zhōnghuá xuèyèxué zázhì</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Su, Long</au><au>Gao, Su-jun</au><au>Li, Wei</au><au>Tan, Ye-hui</au><au>Yao, Cheng</au><au>Song, Yan-qui</au><au>Yang, Yan</au><au>Liu, Zi-ling</au><au>Bai, Ou</au><au>Lin, Hai</au><au>Yang, Lei</au><au>Wang, Chang</au><au>Cui, Jiu-wei</au><au>Wang, Guan-jun</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The study on relationship between age and cytogenetic subgroups in 640 patients with de novo acute myeloid leukemia</atitle><jtitle>Zhōnghuá xuèyèxué zázhì</jtitle><addtitle>Zhonghua Xue Ye Xue Za Zhi</addtitle><date>2013-02</date><risdate>2013</risdate><volume>34</volume><issue>2</issue><spage>133</spage><epage>137</epage><pages>133-137</pages><issn>0253-2727</issn><abstract>To analyze the cytogenetic characteristics of different age subgroups in patients with acute myeloid leukemia (AML), and to explore the relationship between age and cytogenetics.
Between January 2004 and December 2011, Bone marrow (BM) samples from 640 patients with de novo AML were analyzed retrospectively. The analyses were performed according to standard culturing and banding techniques, and clonal abnormalities were defined and described according to the International System for Human Cytogenetic Nomenclature (ISCN 2009). The cytogenetic subtypes were performed as normal, balanced, and unbalanced karyotypes. In the last group, the age distribution of complex and monosome karyotypes were further analyzed. The patients were divided into 8 age groups: 0 - 9, 10 - 19, 20 - 29, 30 - 39, 40 - 49, 50 - 59, 60 - 69, and ≥ 70 year old groups.
The distribution of normal, balanced, and unbalanced karyotypes showed age specific characteristics. The incidence of normal karyotype increased from 6.67% (0 ∼ 9 year old) t</abstract><cop>China</cop><pmid>23611220</pmid><tpages>5</tpages></addata></record> |
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| ispartof | Zhōnghuá xuèyèxué zázhì, 2013-02, Vol.34 (2), p.133-137 |
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| language | chi |
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| source | MEDLINE; EZB Electronic Journals Library |
| subjects | Adolescent Adult Age Factors Aged Aged, 80 and over Child Child, Preschool Female Humans Infant Karyotype Karyotyping Leukemia, Myeloid, Acute - genetics Male Middle Aged Retrospective Studies Young Adult |
| title | The study on relationship between age and cytogenetic subgroups in 640 patients with de novo acute myeloid leukemia |
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