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84例骨髓增生异常综合征细胞遗传学特点及预后评估分析
  • ISSN号:1004-2806
  • 期刊名称:临床血液学杂志
  • 时间:2013
  • 页码:315-318
  • 分类:R551.3[医药卫生—血液循环系统疾病;医药卫生—临床医学;医药卫生—内科学]
  • 作者机构:[1]中南大学湘雅二医院血液科,长沙410011
  • 相关基金:国家自然科学基金项目(No:81100360); 中华医学会分子生物学应用研究专项资金(No:CAMB042010); 卫生部临床重点建设专科建设项目
  • 相关项目:c-Myb介导的MLL/AF4对HOXA9/MEIS1的调控及其在难治性急性淋巴细胞白血病中的作用机制研究
中文摘要:

目的:分析中国人种骨髓增生异常综合征(MDS)患者的骨髓细胞染色体异常特点,探讨细胞遗传学检测在我国MDS诊断及预后评估中的应用价值。方法:采用染色体核型分析结合荧光原位杂交(FISH)技术,检测84例MDS确诊病例的骨髓细胞染色体异常,将患者的骨髓细胞遗传学结合临床特点进行综合分析。结果:84例MDS患者中,存在骨髓细胞染色体异常者38例,占45.2%,其中+8、-7/7q-和20q-最常见,无单纯5q-者。具有预后良好染色体者55例,具有预后中等染色体者14例,具有预后不良染色体者15例。16例三系病态造血患者中染色体异常者10例(62.5%),其余68例患者中染色体异常者28例(41.2%),三系病态造血患者中染色体异常者比例似乎较高,但差异无统计学意义(P〉0.05)。经随访6~24个月,84例患者中已死亡29例。预后良好染色体组患者的生存时间高于预后不良染色体组(P〈0.01)。结论:中国人种MDS患者中,+8、-7/7q-和20q-为常见的染色体异常,单纯5q-罕见。细胞遗传学分析不仅应作为中国人种MDS诊断的重要依据,同时也是不可替代的预后评估指标。

英文摘要:

Objective: To analyze the cytogenetic features of Chinese patiens with myelodysplastic syndromes (MDS) and explore the value of cytogenetic analysis for the diagnosis and prognostic stratification in Chinese MDS patients. Method: Karyotyping and fluorescent in situ hybridization (FISH) analysis were performed in 84 MDS patients. Their cytogenetic features in correlation with clinical manifestations were analyzed. Result: Among the eighty-four patients, thirty-eight (45.2 % ) showed cytogenetic abnormalities. Incidence of trisomy 8,-7/7q- and 20q-- were common but no sole 5q-- was found. Fifty-five patients showed good karyotypes, fourteen patients showed intermediate karyotypes,and fifteen patients showed poor karyotypes. Ten of sixteen patients with trilincage dysplasia(62.5 % ) showed cytogenetie abnormalities, while twenty-eight of the else sixty eight patients (41. 2 ) showed cytogenetic abnormalities. The proportion of patients with abnormal karyotypes seemed higher in the patients with trilineage dysplasia than that in other patients, but the difference was not statistically significant (P〉0.05). During the follow up belween six months and twenty-four months, twenty-nine patients died. The survival time of the good karyotypic group was longer than that of poor karyotypic group (P〈0.01). Conclusion:Occurrence of trisomy 8,--7/7q and 20q-- was common but sole 5q-- was rare in Chinese MDS patients. Cytogenetic feature is not only indispensable for diagnosis, but also an independent prognostic factor in Chinese MDS patients.

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期刊信息
  • 《临床血液学杂志》
  • 中国科技核心期刊
  • 主管单位:中华人民共和国教育部
  • 主办单位:华中科技大学同济医学院附属协和医院 北京大学医学院血研所
  • 主编:宋善俊 陆道培 胡丽华
  • 地址:武汉市解放大道1277号
  • 邮编:430022
  • 邮箱:lcxyxzz@qq.com
  • 电话:027-85726342-8806
  • 国际标准刊号:ISSN:1004-2806
  • 国内统一刊号:ISSN:42-1284/R
  • 邮发代号:38-169
  • 获奖情况:
  • 中国科技论文统计源期刊
  • 国内外数据库收录:
  • 美国化学文摘(网络版),中国中国科技核心期刊
  • 被引量:7788