[VEGF表达与多发性骨髓瘤患者浆液积液的相关性]。

Ping-Ping Zhang, Feng Zhang
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引用次数: 0

摘要

目的:探讨血管内皮生长因子(VEGF)在多发性骨髓瘤(MM)患者血清中的表达水平及其可能的临床意义。方法:收集2019年7月至2020年6月蚌埠医学院第一附属医院收治的MM患者68例。采用VEGF酶联免疫吸附法检测VEGF表达水平,探讨VEGF表达与MM浆液积液的相关性,分析VEGF表达水平与MM患者临床特征及预后的关系。结果:68例MM中VEGF阳性率为36.76%(25/68),17例MM合并浆液积液中VEGF阳性10例(58.82%,10/17)。血管内皮生长因子在浆液积液阳性患者中的表达水平明显高于浆液积液阴性患者(P0.05)。68例MM患者中,48例行FISH检查,核型正常28例(58.33%),核型异常20例(41.67%)。异常核型以IgH重排为主,共10例(20.83%);其他:1q21+、del (13q14)、del (17p13)分别为3例(6.25%)、2例(4.17%)、7例(14.58%)。与VEGF-组比较,VEGF+组的IgH重排和del (17p13)发生率更高[IgH重排:35% vs 10.71%, P=0.043;del(17p13): 30% vs 3.57%, P=0.011]。与阴性浆液积液组相比,阳性浆液积液组del (17p13)的发生率更高(31.25% vs 6.25%, P=0.021)。VEGF阳性伴浆液积液的比例为14.71% (10/68),VEGF阴性伴浆液积液的比例为52.94%(36/68)。浆液积液与VEGF表达有相关性(r=0.264, P=0.029)。结论:MM合并浆液积液患者预后较差,且血清中VEGF表达明显增高。VEGF升高可能参与浆液积液的发生和发展。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
[Correlation of VEGF Expression with Serous Effusion in Multiple Myeloma Patients].

Objective: To investigate the expression level of vascular endothelial growth factor (VEGF) in serum of patients with multiple myeloma (MM) and its possible clinical significance.

Methods: 68 patients with MM who were admitted to The First Affiliated Hospital of Bengbu Medical College from July 2019 to June 2020 were collected. The expression level of VEGF was detected by VEGF enzyme-linked immunosorbent assay, the correlation of VEGF expression with serous effusion in MM was explored, and the relationship between VEGF expression level and clinical features and prognosis of patients with MM was analyzed.

Results: The positive rate of VEGF was 36.76% (25/68) in 68 patients with MM, 10 cases (58.82%, 10/17) were VEGF positive in 17 MM patients with serous effusion. The expression level of VEGF in patients with positive serous effusion was significantly higher than that in patients with negative serous effusion (P<0.05); the expression level of VEGF in MM patients of the newly diagnosed and untreated group was significantly higher than that in the remission group after treatment (P<0.05), but there was no significant difference in the expression level of VEGF between the newly diagnosed group and the refractory/relapsed (R/R) group (P>0.05). Among 68 patients with MM, 48 patients underwent FISH examination, 28 cases had normal karyotype (58.33%), and 20 cases had abnormal karyotype (41.67%). The abnormal karyotype was mainly IgH rearrangement, with a total of 10 cases (20.83%); other cases: 1q21+, del (13q14), del (17p13) were 3 cases (6.25%), 2 cases (4.17%), 7 cases (14.58%), respectively. Compared with VEGF- group, the incidence of IgH rearrangement and del (17p13) in VEGF+ group was higher [IgH rearrangement: 35% vs 10.71%, P=0.043; del(17p13): 30% vs 3.57%, P=0.011]. Compared with negative serous effusion group, the incidence of del (17p13) in positive serous effusion group was higher (31.25% vs 6.25%, P=0.021). The proportion of patients with positive VEGF and serous effusion was 14.71% (10/68), and the proportion of patients with negative VEGF and negative serous effusion was 52.94% (36/68). There was a correlation between serous effusion and VEGF expression (r=0.264, P=0.029).

Conclusion: The prognosis of MM patients with serous effusion is poor, and the expression of VEGF in serum of these patients is significantly high. The increased VEGF may be involved in the occurrence and development of serous effusion.

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