Trends in the incidence of chronic Philadelphia chromosome negative (Ph-) myeloproliferative disorders in the city of Goteborg, Sweden, during 1983-99

被引:49
作者
Johansson, P
Kutti, J
Andréasson, B
Safai-Kutti, S
Vilén, L
Wedel, H
Ridell, B
机构
[1] Sahlgrens Univ Hosp, Dept Med, Sect Haematol & Coagulat, S-41345 Gothenburg, Sweden
[2] Nord Sch Publ Hlth, Gothenburg, Sweden
[3] Sahlgrens Univ Hosp, Dept Pathol & Cytol, S-41345 Gothenburg, Sweden
关键词
essential thrombocythaemia; idiopathic myelofibrosis; incidence; myeloproliferative disorders; polycythaemia vera;
D O I
10.1111/j.1365-2796.2004.01357.x
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective. In the literature the incidence rates for the chronic Philadelphia chromosome negative (Ph-) myeloproliferative disorders (MPD) are known to vary extensively; only a few studies have, however, been concerned with incidence trends over time. Therefore, the aim of the present work was to investigate possible trends as regards incidence rates over time for Ph-MPD. Design. Herein, we carried out a retrospective population-based survey on the incidence of polycythaemia vera (PV), essential thrombocythae-mia (ET) and chronic idiopathic myelofibrosis (IMF), in the city of Goteborg (Sweden), covering the years 1983-99. Results. The study comprised 416 patients with Ph-MPD. There were 205 patients with PV, 153 patients with ET, 34 with IMF and 24 with unclassified MPD. The annual incidence for PV was 1.97 per 10(5) inhabitants; the corresponding figures for ET and IMF were 1.55 per 10(5) and 0.30 per 10(5) inhabitants, respectively. There was a significant increase in the annual incidence rate for ET (P = 0.008); this increase was significant for male subjects (P = 0.015) but did not reach significance for females (P = 0.118). No such increase over time was recorded as regards PV and IMF. Conclusions. The increasing annual incidence rate for ET is most possibly explained by the more frequent use of automated platelet counts whenever a patient consults a doctor. Thereby, an increasing number of patients with overt thrombocytosis of unknown origin are discovered and will be referred to specialists within the field of haematology for a correct diagnosis.
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页码:161 / 165
页数:5
相关论文
共 27 条
[1]  
Altman DG, 1990, PRACTICAL STAT MED R
[2]   TRENDS IN THE INCIDENCE OF POLYCYTHEMIA-VERA AMONG OLMSTED COUNTY, MINNESOTA RESIDENTS, 1935-1989 [J].
ANIA, BJ ;
SUMAN, VJ ;
SOBELL, JL ;
CODD, MB ;
SILVERSTEIN, MN ;
MELTON, LJ .
AMERICAN JOURNAL OF HEMATOLOGY, 1994, 47 (02) :89-93
[3]  
BERGLUND S, 1992, EUR J HAEMATOL, V48, P20
[4]  
BERK PD, 1986, SEMIN HEMATOL, V23, P132
[5]  
CARLI PM, 1994, NOUV REV FR HEMATOL, V36, P147
[6]  
Carneskog J, 1996, EUR J HAEMATOL, V56, P158
[7]   HIGH-INCIDENCE OF MYELOPROLIFERATIVE DISORDERS IN ASHKENAZI JEWS IN NORTHERN ISRAEL [J].
CHAITER, Y ;
BRENNER, B ;
AGHAI, E ;
TATARSKY, I .
LEUKEMIA & LYMPHOMA, 1992, 7 (03) :251-255
[8]  
*COLL AM PATH, 1979, SYST NOM MED
[9]  
Doll R., 1966, CANC INC 5 CONT TECH
[10]  
DOUGAN LE, 1981, CANCER, V48, P866, DOI 10.1002/1097-0142(19810801)48:3<866::AID-CNCR2820480334>3.0.CO