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Prolactin levels and the risk of future coronary artery disease in apparently healthy men and women.

Authors :
Reuwer AQ
Twickler MT
Hutten BA
Molema FW
Wareham NJ
Dallinga-Thie GM
Bogorad RL
Goffin V
Smink-Bol M
Kastelein JJ
Boekholdt SM
Khaw KT
Source :
Circulation. Cardiovascular genetics [Circ Cardiovasc Genet] 2009 Aug; Vol. 2 (4), pp. 389-95. Date of Electronic Publication: 2009 Jun 23.
Publication Year :
2009

Abstract

Background: Prolactin is increasingly recognized to play a stimulatory role in the inflammatory response. Because inflammation is considered of crucial importance in the development of atherosclerosis, we aimed to evaluate whether prolactin levels are associated with the occurrence of coronary artery disease (CAD).<br />Methods and Results: We performed a nested case-control study in the prospective EPIC-Norfolk cohort. Cases were apparently healthy men and women, aged 45 to 79 years, who developed fatal or nonfatal CAD (n=882). Controls remained free of CAD (n=1490). Overall, systemic prolactin levels did not differ between cases and controls, and people in the highest prolactin tertile did not have a significantly increased risk of developing future CAD (in men, odds ratio, 1.21; 95% CI, 0.92 to 1.61; in women, odds ratio, 1.12; 95% CI, 0.76 to 1.64). However, in a separate immunohistochemical study, the presence of prolactin receptors could be demonstrated in postmortem human coronary artery plaques (preliminary data).<br />Conclusions: Elevated systemic prolactin levels do not predict CAD in the general population. However, prolactin receptors were found in human coronary artery plaques. This observation may indicate a role of prolactin within atherosclerotic plaques. More studies are needed to define the possible role of prolactin in atherosclerotic plaque development.

Details

Language :
English
ISSN :
1942-3268
Volume :
2
Issue :
4
Database :
MEDLINE
Journal :
Circulation. Cardiovascular genetics
Publication Type :
Academic Journal
Accession number :
20031611
Full Text :
https://doi.org/10.1161/CIRCGENETICS.109.853572