Markers of inflammation in women on different hormone replacement therapies

被引:24
作者
Fröhlich, M
Mühlberger, N
Hanke, H
Imhof, A
Döring, A
Pepys, MB
Koenig, W
机构
[1] Univ Ulm, Med Ctr, Dept Internal Med 2, Ulm, Germany
[2] Univ Heidelberg Hosp, Dept Internal Med 6, Heidelberg, Germany
[3] GSF, Natl Res Ctr Environm & Hlth, IGM Inst, Neuherberg, Germany
[4] GSF, Natl Res Ctr Environm & Hlth, Inst Epidemiol, Neuherberg, Germany
[5] UCL Royal Free & Univ Coll Med Sch, Dept Med, London, England
关键词
coronary disease; C-reactive protein; fibrinogen; hormone;
D O I
10.1080/07853890310007090
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background and Aim. To measure inflammatory markers in postmenopausal women on different forms of hormone replacement therapy (HRT). Method. C-reactive protein (CRP). fibrinogen, plasma viscosity (PV), albumin and white blood cell (WBC) count were determined in 749 postmenopausal women. Results. CRP concentration was significantly higher in women on estrogen monotherapy (difference of the median (d) 0.96 mg/l, P=0.013). compared to those without HRT, but there was no difference in women on combined HRT. Fibrinogen concentration was significantly lower in women on estrogen monotherapy (d 0.25 g/l, P=0.004) and combined HRT (d 0.4 g/l, P<0.001), compared to women without HRT. Similarly, PV was significantly lower in women on estrogen monotherapy (d 0.017 mPa.s, P=0.007) and women on combined HRT (d 0.039 mPa.s, P<0.001), compared to those without HRT. No differences were found for WBC count and the negative acute phase marker albumin in the various treatment groups. In contrast to oral estrogen administration, levels of CRP, fibrinogen and PV in women on transdermal estrogen therapy did not differ from the no-HRT group. There was no association between these markers of inflammation and plasma estrogen levels. Conclusion. Oral estrogen monotherapy was associated with highest concentrations of CRP. In contrast, other markers of inflammation were either similar or lower in the oral HRT group, compared to the group of women without HRT, suggesting that higher CRP concentrations reflect estrogen effects on CRP expression rather than a systemic pro-inflammatory effect.
引用
收藏
页码:353 / 361
页数:9
相关论文
共 69 条
[1]   ESTROGEN AND CORONARY HEART-DISEASE IN WOMEN [J].
BARRETTCONNOR, E ;
BUSH, TL .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 1991, 265 (14) :1861-1867
[2]   THE ACUTE-PHASE RESPONSE [J].
BAUMANN, H ;
GAULDIE, J .
IMMUNOLOGY TODAY, 1994, 15 (02) :74-80
[3]   Complement and atherogenesis - Binding of CRP to degraded, nonoxidized LDL enhances complement activation [J].
Bhakdi, S ;
Torzewski, M ;
Klouche, M ;
Hemmes, M .
ARTERIOSCLEROSIS THROMBOSIS AND VASCULAR BIOLOGY, 1999, 19 (10) :2348-2354
[4]  
BOETHIG S, 1989, INT J EPIDEMIOL S1, V18, P29
[5]   ALCOHOL-CONSUMPTION AS A RISK FACTOR FOR HIGH BLOOD-PRESSURE - MUNICH BLOOD-PRESSURE STUDY [J].
CAIRNS, V ;
KEIL, U ;
KLEINBAUM, D ;
DOERING, A ;
STIEBER, J .
HYPERTENSION, 1984, 6 (01) :124-131
[6]   C-REACTIVE PROTEIN INDUCES HUMAN PERIPHERAL-BLOOD MONOCYTES TO SYNTHESIZE TISSUE FACTOR [J].
CERMAK, J ;
KEY, NS ;
BACH, RR ;
BALLA, J ;
JACOB, HS ;
VERCELLOTTI, GM .
BLOOD, 1993, 82 (02) :513-520
[7]  
Chae CU, 1997, THROMB HAEMOSTASIS, V78, P770
[8]   HAMSTER FEMALE PROTEIN - A DIVERGENT ACUTE PHASE PROTEIN IN MALE AND FEMALE SYRIAN-HAMSTERS [J].
COE, JE ;
ROSS, MJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 1983, 157 (05) :1421-1433
[9]  
Crosignani PG, 1996, THROMB HAEMOSTASIS, V75, P476
[10]  
Cucuianu M, 1996, Rom J Intern Med, V34, P13