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1 Department of Cardiology and 2 Atherosclerosis Research Unit, King Gustaf V Research Institute, Karolinska University Hospital, and 3 Department of Medicine, Danderyd Hospital, Karolinska Institute, Stockholm, Sweden
aaddress correspondence to this author at: Department of Cardiology, Karolinska University Hospital, S-17176 Stockholm, Sweden; fax 46-8-311044, e-mail per.tornvall@karolinska.se
| The first 20% of the full text of this article appears below. |
The plasma concentration of C-reactive protein (CRP), measured by high-sensitivity methods, is a reliable marker of risk of future coronary heart disease (CHD) in healthy individuals (1)(2) and of CHD death in patients with unstable angina pectoris or non-Q-wave myocardial infarction (3). The possibility of hormonal regulation of circulating CRP is of great interest because male gender is considered an independent risk factor for CHD and estrogen has many beneficial cardiovascular effects in women (4).
Both in vivo and in vitro data support the hypothesis that interleukin-6 (IL-6) is the main inducer of the acute-phase CRP response, but other factors such as IL-1ß might potentiate IL-6 stimulation of CRP (5). The factors determining unstimulated CRP expression are less known.
Because of the strong association between CRP and CHD and the fact that previous studies have shown that CRP to a large extent is regulated on the transcriptional level (5), it is of great interest to identify factors that regulate CRP production. A study of randomized treatment of prostate cancer by orchidectomy or estrogen allowed us to investigate the hormonal influence on circulating CRP concentrations in middle-aged and elderly men.
A total of 100 consecutive patients with prostate cancer suitable for hormonal therapy were enrolled in the study. Patients were randomized to either orchidectomy or estrogen treatment. The estrogen regimen was 160 mg of polyestradiol phosphate intramuscularly every month during the first 3 months, then
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