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骨髓增殖性肿瘤患者外周血内皮祖细胞数变化及临床意义

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目的 观察骨髓增殖性肿瘤(MPN)患者外周血内皮祖细胞(EPC)数变化,探讨其与血细胞计数、白细胞介素-6(IL-6)、肿瘤坏死因子-α(TNF-α)、高敏C反应蛋白(hs-CRP)和JAK2V617F突变的关系。方法 2013年6月-2020年12月北京安贞医院初诊的105例MPN患者为MPN组,45例非MPN血液恶性肿瘤患者为恶性肿瘤组,52例良性血液病患者为对照组。MPN组中真性红细胞增多症(PV)38例,原发性血小板增多症(ET)61例,原发性骨髓纤维化(PMF)6例。比较3组入院时血红蛋白(Hb)、白细胞计数(WBC)、红细胞计数(RBC)、血小板计数(PLT)、红细胞比容(Hct)、总胆固醇(TC)、三酰甘油(TG)、高密度脂蛋白胆固醇(HDL-C)、低密度脂蛋白胆固醇(LDL-C)、hs-CRP水平及心血管危险因素(CVRF)>1个比率、EPC数;分析不同临床特征MPN患者EPC数差异;Spearman相关法分析MPN患者EPC数与血细胞计数、IL-6、TNF-α、hs-CRP的相关性。结果 (1)MPN组入院时Hb[152(57,235)g/L]、WBC[9。14(2。91,30。56)× 109/L]、RBC[5。05(1。68,9。99)X 1012/L]、PLT[557(82,2 126)× 109/L]、Hct[(45。39± 10。60)%]均高于恶性肿瘤组[99(40,165)g/L、6。55(1。50,146。03)× 109/L、3。12(1。24,5。13)× 1012/L、137(4,1 305)×109/L、(29。96±13。17)%]和对照组[137(62,237)g/L、5。60(2。27,15。12)× 109/L、4。62(1。62,6。84)× 1012/L、208(32,658)× 109/L、(39。31±16。68%)](P<0。05);恶性肿瘤组 Hct、PLT 均低于对照组(P<0。05);MPN 组、恶性肿瘤组CVRF>1个比率(64。76%、62。22%)均高于对照组(38。46%)(P<0。05)。(2)MPN组、恶性肿瘤组外周血EPC 数[306(0,4 303)、193(0,2 920)个/mL]均多于对照组[87(0,2 616)个/mL](U=-4。251,P<0。001;U=-2。031,P=0。042),MPN组与恶性肿瘤组比较差异无统计学意义(U=-1。267,P=0。205)。(3)男性[435(0,4 303)个/mL]、>60 岁伴 JAK2V617F 突变阳性[363(0,4 303)个/mL]、CVRF>1 个[375(0,4 303)个/mL]、PV[404(0,2 622)个/mL]患者外周血EPC数分别多于女性[227(0,3 300)个/mL]、>60岁伴JAK2V617F突变阴性[248(0,2 639)个/mL]、1个CVRF[165(0,3 330)个/mL]、PMF 和 ET 患者[328(0,2 478)、240(0,4 303)个/mL](P<0。05),>60 岁、JAK2V617F突变阳性者外周血EPC数与≤60岁、JAK2V617F突变阴性者比较差异均无统计学意义(P>0。05)。(4)MPN患者外周血 IL-6 为[16。50(3。60,36。70)ng/L],TNF-α 为[12。45(0。40,199。00)ng/L]。MPN 患者外周血 EPC 数与 PLT(r=0。094,P=0。342)、hs-CRP(r=0。011,P=0。914)无相关性,与 WBC(r=0。196,P=0。046)、RBC(r=0。198,P=0。043)、Hb(r=0。205,P=0。036)、Hct(r=0。215,P=0。028)、IL-6(r=0。322,P=0。004)和 TNF-α(r=0。252,P=0。036)均呈正相关。结论 血液恶性肿瘤患者外周血EPC数增多,其中MPN患者外周血EPC数增多明显,且男性、PV、>60岁伴JAK2V617F突变和CVRF>1个者EPC数更多;外周血EPC数量增多可能与干细胞克隆性增殖和炎症有关。
Change and clinical significance of peripheral blood endothelial progenitor cells in patients with myeloproliferative neoplasms
Objective To observe the change of peripheral blood endothelial progenitor cells(EPCs)in patients with myeloproliferative neoplasms(MPNs),and to investigate its relationships with blood cell count,interleukin-6(IL-6),tumor necrosis factor-α(TNF-α),high-sensitivity C-reactive protein(hs-CRP)and JAK2V617F mutation.Methods From June 2013 to December 2020,105 patients with MPNs(MPNs group),45 patients with non-MPNs hematologic malignancies(malignancy group)and 52 patients with benign hematologic diseases(control group)were initially diagnosed and treated in Beijing Anzhen Hospital.In MPNs group,there were 38 patients with polycythemia vera(PV),61 patients with essential thrombocythemia(ET)and 6 patients with primary myelofibrosis(PMF).The hemoglobin(Hb),white blood cell count(WBC),red blood cell count(RBC),platelet(PLT),hematocrit(Hct),total cholesterol(TC),triglyceride(TG),high-density lipoprotein cholesterol(HDL-C),low-density lipoprotein cholesterol(LDL-C),hs-CRP,proportion of>1 cardiovascular risk factors(CVRFs),and EPCs number on admission were compared among three groups.The differences in EPCs number were analyzed in MPN patients with different clinical characteristics.Spearman correlation method was used to analyze the correlations of EPCs number with blood cell count,IL-6,TNF-αand hs-CRP in MPNs patients.Results(1)The Hb,WBC,RBC,PLT and Hct were higher in MPNs group[152(57,235)g/L,9.14(2.91,30.56)×109/L,5.05(1.68,9.99)× 1012/L,557(82,2 126)× 109/L,(45.39± 10.60)%]than those in malignancy group[99(40,165)g/L,6.55(1.50,146.03)× 109/L,3.12(1.24,5.13)×1012/L,137(4,1 305)×109/L,(29.96±13.17)%]and control group[137(62,237)g/L,5.60(2.27,15.12)× 109/L,4.62(1.62,6.84)×1012/L,208(32,658)× 109/L,(39.31±16.68)%](P<0.05).The Hct and PLT were lower in malignancy group than those in control group(P<0.05).The proportion of>1 CVRFs was higher in MPNs group(64.76%)and malignancy group(62.22%)than that in control group(38.46%)(P<0.05).(2)The peripheral blood EPCs number was greater in MPNs group[306(0,4 303)cells/mL]and malignancy group[193(0,2 920)cells/mL]than that in control group[87(0,2 616)cells/mL](U=-4.251,P<0.001;U=-2.031,P=0.042),and showed no significant difference between MPNs group and malignancy group(U=-1.267,P=0.205).(3)The numbers of peripheral blood EPCs were greater in males,>60-year old patients with J AK2V617F mutation positive,>1 CVRFs and PV patients[435(0,4 303),363(0,4 303),375(0,4 303),404(0,2 622)cells/mL]than those in females,>60-year old patients with JAK2V617F mutation negative,1 CVRF,PMF patients and ET patients[227(0,3 300),248(0,2 639),165(0,3 330),328(0,2 478),240(0,4 303)cells/mL](P<0.05),and showed no significant differences between>60-year old patients with JAK2V617F mutation positive and≤60-year old patients with JAK2V617F mutation negative(P>0.05).(4)The IL-6 level in MPNs patients was[16.50(3.60,36.70)ng/L]and TNF-a was[12.45(0.40,199.00)ng/L].The EPCs number in MPN patients was not correlated with PLT(r=0.094,P=0.342)and hs-CRP(r=0.011,P=0.914),but was positively correlated with WBC(r=0.196,P=0.046),RBC(r=0.198,P=0.043),Hb(r=0.205,P=0.036),Hct(r=0.215,P=0.028),IL-6(r=0.322,P=0.004)and TNF-α(r=0.252,P=0.036).Conclusions The peripheral blood EPC increases in number in patients with hematologic malignancies,especially in patients with MPN,and it increases significantly in males,PV patients,>60-year old patients with JAK2V617F mutation,and patients with>1 CVRF.The increase of EPCs number in peripheral blood may be correlated with clonal proliferation and inflammation of stem cells.

myeloproliferative neoplasmsendothelial progenitor cellsblood cell countinterleukin-6tumor necrosis factor-αhigh-sensitivity C-reactive protein

韩雪、白贝贝、冯翠翠、赵森、王芳、王春键、陈烨

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首都医科大学附属北京安贞医院血液科,北京 100029

北京大学国际医院血液科,北京 102206

骨髓增殖性肿瘤 内皮祖细胞 血细胞计数 白细胞介素-6 肿瘤坏死因子-α 高敏C反应蛋白

2024

中华实用诊断与治疗杂志
中华预防医学会 河南省人民医院

中华实用诊断与治疗杂志

CSTPCD
影响因子:1.276
ISSN:1674-3474
年,卷(期):2024.38(5)
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