医学
内科学
骨髓增生异常综合症
三体8
胃肠病学
白塞病
血沉
三体
中性粒细胞绝对计数
疾病
骨髓
细胞遗传学
化疗
染色体
中性粒细胞减少症
生物化学
化学
遗传学
生物
基因
作者
Yanxia Ding,Wenlu Hu,Li Li,Wenjuan Guan,Kelei Guan,Shengyun Liu,Tian-Fang Li
出处
期刊:Clinical and Experimental Rheumatology
日期:2022-08-15
被引量:1
标识
DOI:10.55563/clinexprheumatol/04us5e
摘要
ObjectiveTo investigate the correlation of Behçet's disease (BD) with myelodysplastic syndrome (MDS) and identify the predictive risk factors in Chinese patients. Methods A retrospective study of BD associated with MDS (BD-MDS) patients from the First Affiliated Hospital of ZhengzhouUniversity was conducted. ResultsAmong 15 BD-MDS patients, 10 were females and 5 males.While 13 (86.7%)patients had abnormal karyotype, 11 patients with trisomy 8. 10 (66.7%) had gastrointestinal (GI) involvement.Compared with 60 general BD patients without MDS, the BD-MDS patients were significantly older.In addition, fever and GI involvement were more common in BD-MDS patients, whereas these patients had lower levels of leukocyte count, haemoglobin, and platelet count (p<0.05).Logistic regression analysis showed that GI involvement, low haemoglobin, and high ESR level were independently associated with the development of MDS in BD patients.BD-MDS patients with GI involvement (IBD-MDS) were usually much older and have more fever than IBD patients without MDS, as well as lower leukocyte count, haemoglobin level, platelet count, and higher erythrocyte sedimentation rate (ESR) and C-reactive protein levels (p<0.05).By comparison with 60 primary MDS patients without BD, the BD-MDS patients had more abnormal karyotypes and more trisomy 8 (p<0.05),while the distribution of 2016 WHO subtypes of MDS and IPSS-R categories were similar. ConclusionOur findings suggest that cytogenetic abnormalities, especially trisomy 8, may play a role in the association of GI involvement, BD, and MDS.GI involvement, low haemoglobin, and high ESR level were independent predictors for MDS development in BD patients.
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