Platelet-rich plasma serotonin levels in chronic myeloproliferative disorders: evaluation of diagnostic use and comparison with the neutrophil PRV-1 assay

被引:16
作者
Koch, CA [1 ]
Lasho, TL [1 ]
Tefferi, A [1 ]
机构
[1] Mayo Clin & Mayo Fdn, Div Hematol, Rochester, MN 55905 USA
关键词
polycythaemia; myeloproliferative disorders; serotonin; diagnosis; polycythaemia rubra vera-1;
D O I
10.1111/j.1365-2141.2004.05149.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
In a prospective study of 109 subjects, an enzyme-linked immunosorbent assay (ELISA) was used to measure platelet-rich plasma (PRP) serotonin levels in patients with polycythaemia vera (PV; n = 27), essential thrombocythaemia (ET; n = 14), myelofibrosis with myeloid metaplasia (MMM; n = 30), secondary or spurious polycythaemia (SP; n = 22) and controls (n = 16). Nine study subjects who were taking a selective serotonin reuptake inhibitor (SSRI) all displayed a markedly decreased PRP serotonin level (median, 24.2 ng/10(9) platelets; range, 0-49.3) and were therefore excluded from further analysis. Among the remaining 100 subjects, the median and range of PRP serotonin levels, in ng/10(9) platelets, was significantly lower in MMM (89.5; 0-278.3), PV (204.8; 0-496.0) and ET (385.3; 136.8-1025.7) compared with both SP (608.8; 369.0-1780.1) and controls (567.2; 359.9-1071.1). Neutrophil polycythaemia rubra vera-1 (PRV-1) expression was concurrently assayed by real-time polymerase chain reaction in 69 patients (23 PV, 17 SP, 12 ET, seven MMM, 10 controls). PRP serotonin measurement performed as well as the PRV-1 assay in distinguishing PV from SP (93% vs. 86% test accuracy). The current study suggests that PRP serotonin concentration might be considered as one of the several biological markers that complement each other for the diagnosis of PV.
引用
收藏
页码:34 / 39
页数:6
相关论文
共 44 条
[1]  
ADAMS T, 1974, SCAND J HAEMATOL, V13, P215
[2]   DETERMINATION OF SEROTONIN IN WHOLE-BLOOD, PLATELET-RICH PLASMA, PLATELET-POOR PLASMA AND PLASMA ULTRAFILTRATE [J].
ANDERSON, GM ;
FEIBEL, FC ;
COHEN, DJ .
LIFE SCIENCES, 1987, 40 (11) :1063-1070
[3]   PLATELET-AGGREGATION IN PLATELET-RICH PLASMA AND WHOLE-BLOOD IN 120 PATIENTS WITH MYELOPROLIFERATIVE DISORDERS [J].
BALDUINI, CL ;
BERTOLINO, G ;
NORIS, P ;
PILETTA, GC .
AMERICAN JOURNAL OF CLINICAL PATHOLOGY, 1991, 95 (01) :82-86
[4]  
BERGER S, 1973, CANCER RES, V33, P2683
[5]  
BONEU B, 1980, SCAND J HAEMATOL, V25, P214
[6]  
CARANOBE C, 1984, THROMB HAEMOSTASIS, V51, P349
[7]   EVIDENCE FOR A PLATELET MEMBRANE DEFECT IN THE MYELOPROLIFERATIVE SYNDROMES [J].
CASTALDI, PA ;
BERNDT, MC ;
BOOTH, W ;
GREGORY, C ;
BULL, H ;
GREAVES, M .
THROMBOSIS RESEARCH, 1982, 27 (05) :601-609
[8]  
CHAUVEAU J, 1991, CLIN CHEM, V37, P1178
[9]  
CORTELLAZZO S, 1985, SCAND J HAEMATOL, V34, P146
[10]   Highly sensitive fluorescence in situ hybridization method to detect double BCR/ABL fusion and monitor response to therapy in chronic myeloid leukemia [J].
Dewald, GW ;
Wyatt, WA ;
Juneau, AL ;
Carlson, RO ;
Zinsmeister, AR ;
Jalal, SM ;
Spurbeck, JL ;
Silver, RT .
BLOOD, 1998, 91 (09) :3357-3365