The effects of estrogen on cardiovascular risk factors have been less
well defined in men than in women. We measured lipid and lipoprotein c
oncentrations, lipoprotein particle size distributions, lipoprotein (a
), homocysteine, and markers of thrombosis and fibrinolysis in 22 heal
thy elderly men (age 74+/-3 years, mean +/-S.D.) before and after 9 we
eks of treatment with 0.5, 1 or 2 mg/day of oral micronized 17 beta-es
tradiol. LDL-C (-6%), apo B (-9%), triglyceride (-5%), and homocystein
e (-11%) concentrations decreased with estradiol, whereas HDL-C (+/-14
%) increased. Intermediate-size VLDL subclass concentrations were lowe
red and LDL and HDL subclass levels altered in such a way as to cause
average LDL and HDL particle size to increase. Lipoprotein (a) did not
change. Fibrinogen (-13%) and plasminogen activator inhibitor-1 (PAI-
1) concentrations (-26%) decreased, but there were no changes in throm
botic markers including thrombin-antithrombin III complex, prothrombin
fragment 1.2, D-dimer, antithrombin activity, protein-C and S and von
Willebrand factor antigen. Breast tenderness occurred in four men and
heartburn in five but did not require discontinuation of treatment. W
e conclude that oral estrogen in men reduces homocysteine, fibrinogen,
and PAI-1 concentrations and favorably influences VLDL, LDL and HDL s
ubclass levels without increasing markers of thrombotic risk. (C) 1998
Elsevier Science Ireland Ltd. All rights reserved.