Citation: | WAN Jiangwei, CHENG Dongru, WANG Tao, GAO Ping. Value of serum lactate dehydrogenase, β2 microglobulin and ferritin combined with modified WHO-based Prognostic Scoring System in predicting poor prognosis of myelodysplastic syndrome[J]. Journal of Clinical Medicine in Practice, 2024, 28(5): 79-84. DOI: 10.7619/jcmp.20233107 |
To investigate the value of serum lactate dehydrogenase (LDH), β2-microglobulin (β2-MG) and serum ferritin (SF) combined with the modified WHO-based Prognostic Scoring System (WPSS) score in predicting poor prognosis of patients with myelodysplastic syndrome (MDS).
A total of 110 patients with MDS were selected as the research objects, and serum levels of LDH, β2-MG and SF were detected. The patients were divided into death group and survival group according to their survival status, and the serum levels of LDH, β2-MG and SF as well as the modified WPSS score were compared between the two groups. The risk factors for poor prognosis in MDS patients and the predictive values of serum LDH, β2-MG, SF and modified WPSS score alone and their combination for poor prognosis in MDS patients were analyzed.
The incidence of poor prognosis in MDS patients was 40.20% (41/102). The serum levels of LDH, β2-MG and SF, the modified WPSS score, and the ratio of adverse karyotype prognosis in the death group were significantly higher than those in the survival group (P < 0.05). The results of Cox regression model analysis showed that elevated serum levels of LDH, β2-MG and SF, elevated modified WPSS score, and adverse karyotype prognosis were risk factors for poor prognosis in MDS patients (P < 0.05). The results of receiver operating characteristic (ROC) curve analysis showed that the combination of serum LDH, β2-MG, SF levels and modified WPSS score had a sensitivity of 95.12% and an area under the curve (AUC) of 0.918 for predicting poor prognosis in MDS patients, which were significantly higher than those of each indicator alone (P < 0.05).
Serum LDH, β2-MG, SF levels and modified WPSS score have certain predictive value for poor prognosis in MDS patients, but the combined prediction value of the four indicators is higher.
[1] |
YANG X C, MA L, ZHANG X Y, et al. Targeting PD-1/PD-L1 pathway in myelodysplastic syndromes and acute myeloid leukemia[J]. Exp Hematol Oncol, 2022, 11(1): 11. doi: 10.1186/s40164-022-00263-4
|
[2] |
SAUTA E, ROBIN M, BERSANELLI M, et al. Real-world validation of molecular international prognostic scoring system for myelodysplastic syndromes[J]. J Clin Oncol, 2023, 41(15): 2827-2842. doi: 10.1200/JCO.22.01784
|
[3] |
李璘, 聂玲, 于明华, 等. 基于常规实验室检查指标的改良WPSS预后积分系统对骨髓增生异常综合征预后判断意义的初步研究[J]. 中华血液学杂志, 2009, 30(5): 313-317. doi: 10.3760/cma.j.issn.0253-2727.2009.05.008
|
[4] |
YANAGISAWA H, KAWABATA H, UEDA Y, et al. Prognostic impacts of serum levels of C-reactive protein, albumin, and total cholesterol in patients with myelodysplastic syndromes[J]. Int J Hematol, 2022, 116(1): 81-88. doi: 10.1007/s12185-022-03321-z
|
[5] |
张佩芸, 蒋旭, 孙群英, 等. 骨髓增生异常综合征患儿血清LDH、β2-MG、SF和维生素B12的表达及意义[J]. 中国妇幼健康研究, 2022, 33(1): 19-23. https://www.cnki.com.cn/Article/CJFDTOTAL-SANE202201004.htm
|
[6] |
BAI Z M, LI L Y, GUAN T, et al. Clinical prognosis and bioinformatic analysis of primary thyroid lymphoma[J]. Medicine, 2021, 100(6): e24598. doi: 10.1097/MD.0000000000024598
|
[7] |
HU Y Z, LIN J, WANG Y, et al. Identification of serum feRRitin-specific nanobodies and development towards a diagnostic immunoassay[J]. Biomolecules, 2022, 12(8): 1080. doi: 10.3390/biom12081080
|
[8] |
何广胜. 世界卫生组织2016年骨髓增生异常综合征分类更新解读[J]. 中国实用内科杂志, 2016, 36(8): 643-646. https://www.cnki.com.cn/Article/CJFDTOTAL-SYNK201608008.htm
|
[9] |
王化泉, 杨丽艳, 邵宗鸿. 骨髓增生异常综合征最低诊断标准(2017)解读[J]. 天津医药, 2018, 46(8): 811-814. https://www.cnki.com.cn/Article/CJFDTOTAL-TJYZ201808007.htm
|
[10] |
肖志坚. 骨髓增生异常综合征诊断与治疗专家共识(解读)[J]. 临床内科杂志, 2014, 31(3): 210-211. doi: 10.3969/j.issn.1001-9057.2014.03.027
|
[11] |
冉俊丽, 韩伟. 地西他滨治疗骨髓增生异常综合征的疗效分析[J]. 实用临床医药杂志, 2020, 24(18): 103-105. doi: 10.7619/jcmp.202018027
|
[12] |
陈春平, 王娟, 徐徐. 骨髓增生异常综合征患者血清LDH、β2-MG、铁蛋白、维生素B12变化与预后的关系[J]. 标记免疫分析与临床, 2021, 28(4): 647-650, 691. https://www.cnki.com.cn/Article/CJFDTOTAL-BJMY202104026.htm
|
[13] |
LEE P, YIM R, YUNG Y, et al. Molecular targeted therapy and immunotherapy for myelodysplastic syndrome[J]. Int J Mol Sci, 2021, 22(19): 10232. doi: 10.3390/ijms221910232
|
[14] |
BERSANELLI M, TRAVAGLINO E, MEGGENDORFER M, et al. Classification and personalized prognostic assessment on the basis of clinical and genomic features in myelodysplastic syndromes[J]. J Clin Oncol, 2021, 39(11): 1223-1233. doi: 10.1200/JCO.20.01659
|
[15] |
叶佳鑫, 钱文斌. 老年骨髓增生异常综合征患者的临床预后及影响因素分析[J]. 中华老年医学杂志, 2017, 36(9): 983-986. doi: 10.3760/cma.j.issn.0254-9026.2017.09.011
|
[16] |
姚玉, 朱晖. 血清EPO、Hepcidin水平与骨髓增生异常综合征异基因造血干细胞移植预后的相关性[J]. 医学临床研究, 2022, 39(3): 335-339.
|
[17] |
李雯雯, 李燕, 王晓敏. 血清学指标联合骨髓形态学分析对骨髓增生异常综合征的预后判断价值[J]. 中国全科医学, 2013, 16(38): 3789-3793. https://www.cnki.com.cn/Article/CJFDTOTAL-QKYX201338011.htm
|
[18] |
王佩, 董照, 杨艳敏. 阿扎胞苷联合小剂量阿糖胞苷治疗中高危骨髓增生异常综合征患者的疗效及安全性[J]. 安徽医学, 2022, 43(10): 1126-1130. https://www.cnki.com.cn/Article/CJFDTOTAL-AHYX202210002.htm
|
[19] |
谢杨, 汪丹, 刘建会. 骨髓增生异常综合征贫血患者铁代谢、炎症指标与铁调素的关系及对病情转归的影响[J]. 临床误诊误治, 2022, 35(10): 58-62. https://www.cnki.com.cn/Article/CJFDTOTAL-LCWZ202210013.htm
|
[20] |
唐元艳, 张利铭, 张江召, 等. 细胞发育异常在骨髓增生异常综合征患者预后评估中的价值[J]. 现代肿瘤医学, 2018, 26(11): 1759-1761. doi: 10.3969/j.issn.1672-4992.2018.11.027
|
[21] |
邓琳, 刘文, 李英, 等. 骨髓增生异常综合征细胞遗传学特征与临床的关系[J]. 川北医学院学报, 2021, 36(6): 719-722. doi: 10.3969/j.issn.1005-3697.2021.06.09
|