Clinical features and independent predictors of Behçet's disease associated with myelodysplastic syndrome

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 化学 基因 生物 生物化学 遗传学
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 [Springer Vienna]
被引量:2
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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