Plasma C-reactive protein is not elevated in physically active postmenopausal women taking hormone replacement therapy

2004 ◽  
Vol 96 (1) ◽  
pp. 143-148 ◽  
Author(s):  
Brian L. Stauffer ◽  
Greta L. Hoetzer ◽  
Derek T. Smith ◽  
Christopher A. DeSouza

We tested the hypothesis that hormone replacement therapy (HRT)-related increases in C-reactive protein (CRP) would either be blunted or absent in postmenopausal women who regularly perform endurance exercise. Plasma CRP is an independent predictor of future cardiovascular events in healthy men and women. Oral HRT increases plasma CRP concentrations in postmenopausal women. Regular aerobic exercise reduces the risk of cardiovascular events and is associated with lower CRP concentrations in adults. To date, no study has evaluated the influence of habitual physical activity on the elevation of CRP associated with HRT. Plasma CRP concentrations were measured in 114 postmenopausal women: 39 physically active (endurance trained) and 75 sedentary postmenopausal subjects. Sixty-five women were users of HRT (22 physically active and 43 sedentary), and 49 were nonusers (17 physically active and 32 sedentary). CRP levels were ∼75% higher ( P < 0.01) in the sedentary users vs. nonusers of HRT (1.9 ± 1.8 vs. 1.1 ± 1.0 mg/l). In contrast, there was no difference in CRP levels between the physically active users and nonusers of HRT (0.6 ± 0.4 vs. 0.4 ± 0.2 mg/l; P = 0.61). Regardless of HRT status, CRP concentrations were ∼65% lower in the physically active compared with sedentary women. In conclusion, physically active postmenopausal women exhibit lower plasma CRP concentrations compared with sedentary controls. Importantly, the HRT-related elevation in plasma CRP levels observed in sedentary women is absent in women who engage in regular endurance exercise. These data suggest that habitual physical activity may prevent the elevation in CRP concentrations due to HRT.

2003 ◽  
Vol 15 (1) ◽  
pp. 91-100 ◽  
Author(s):  
Patricia J. Manns ◽  
Daniel P. Williams ◽  
Christine M. Snow ◽  
Rosemary C. Wander

Maturitas ◽  
2003 ◽  
Vol 46 (4) ◽  
pp. 245-253 ◽  
Author(s):  
Mehmet Yilmazer ◽  
Veysel Fenkci ◽  
Semin Fenkci ◽  
Murat Sonmezer ◽  
Orhan Aktepe ◽  
...  

Metabolism ◽  
2005 ◽  
Vol 54 (1) ◽  
pp. 72-78 ◽  
Author(s):  
Hanna Bukowska ◽  
Stanisław Stanosz ◽  
Ewa Żochowska ◽  
Barbara Millo ◽  
Krzysztof Sieja ◽  
...  

1999 ◽  
Vol 81 (06) ◽  
pp. 925-928 ◽  
Author(s):  
Marchien van Baal ◽  
Peter Kenemans ◽  
Marius van der Mooren ◽  
Hilda Kessel ◽  
Jef Emeis ◽  
...  

Summary Objective: To study the short-term effect of unopposed oestradiol (E2) and sequentially combined hormone replacement therapy (E2 + P) on C-reactive protein (CRP) in healthy postmenopausal women. Design: Prospective, randomised, placebo-controlled 12-week study. Sixty healthy, normotensive, non-hysterectomised postmenopausal women received either placebo (N = 16) or daily 2 mg micronised oestradiol, either unopposed (N = 16, E2 group) or sequentially combined with a progestagen on 14 days of each cycle (N = 28, E2+P group). Data were collected at baseline and at 4 and 12 weeks. Results: CRP levels increased significantly during the 12 weeks in the E2 and the E2+P groups compared to placebo. No differences were found between the E2 group and the E2+P group [E2 and E2+P group together (N = 44) versus placebo: P = 0.01; E2 versus E2+P: P = 0.75]. To give a quantitative estimate of the increase, the median change calculated from baseline in both treatment groups together was +87% (P = 0.02) at 4 weeks, and +114% (P = 0.08) at 12 weeks, as compared to the placebo group. Conclusion: In healthy postmenopausal women, short-term treatment with E2 or E2+P was associated with a rapid rise in CRP concentrations. These observations raise the possibility that the increased risk of cardiovascular events is related to an initial increase in CRP levels after starting hormone replacement therapy.


2000 ◽  
Vol 85 (1) ◽  
pp. 214-218 ◽  
Author(s):  
Brian W. Walsh ◽  
Sofia Paul ◽  
Robert A. Wild ◽  
Robert A. Dean ◽  
Russell P. Tracy ◽  
...  

C-Reactive protein and homocysteine are independent risk factors for the development of cardiovascular disease. This study compared the effects of hormone replacement therapy (HRT) and raloxifene on serum C-reactive protein and homocysteine levels as markers of cardiovascular risk in healthy postmenopausal women. Healthy postmenopausal women (n = 390) were enrolled in a double blind, randomized, placebo-controlled, 6-month trial at eight out-patient sites in the United States. Women were randomly assigned to receive continuous combined HRT (0.625 mg/day conjugated equine estrogen and 2.5 mg/day medroxyprogesterone acetate), raloxifene (60 or 120 mg/day), or placebo for 6 months. C-Reactive protein and homocysteine were measured in baseline and 6-month serum samples. HRT increased C-reactive protein levels by 84% (P &lt; 0.001), whereas raloxifene (60 and 120 mg/day) had no significant effect (−6% and −4%, respectively; P &gt; 0.2). Raloxifene (60 and 120 mg/day) significantly lowered serum levels of homocysteine by 8% (P = 0.014) and 6% (P = 0.024), respectively, similar to the 7% (P = 0.014) reduction obtained with HRT. We conclude that HRT and raloxifene lower serum homocysteine levels to a comparable extent in postmenopausal women. Whereas cardiovascular risk predicted by C-reactive protein in healthy postmenopausal women is not influenced by raloxifene, the relationship between elevated C-reactive protein levels with HRT and cardiovascular disease events requires further study.


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