Estrogen replacement therapy and coagulation: Relationship to lipid and lipoprotein changes
To examine the relationship of estrogen-induced changes in lipids and lipoproteins with alterations in the coagulation system. Coagulation and lipid indices were measured in 31 postmenopausal women, ages 40–60 years, after a 3-month course of 0.625-mg conjugated equine estrogen. We analyzed changes...
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Veröffentlicht in: | Obstetrics and gynecology (New York. 1953) 1997-03, Vol.89 (3), p.326-331 |
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Zusammenfassung: | To examine the relationship of estrogen-induced changes in lipids and lipoproteins with alterations in the coagulation system.
Coagulation and lipid indices were measured in 31 postmenopausal women, ages 40–60 years, after a 3-month course of 0.625-mg conjugated equine estrogen. We analyzed changes in variables from baseline to 3 months using
t tests for paired samples or the Wilcoxon matched-pairs signed-rank test.
Unopposed estrogen replacement therapy produced statistically significant decreases in antithrombin-III antigen (
P = .006) and activity (
P = .001) and total protein S (
P = .003) and a significant increase in protein C antigen (
P = .017). C4b-binding protein also decreased significantly from baseline to 3 months (
P < .001). Mean fibrinogen level decreased by 18.2 mg/dL, not a statistically significant change (
P = .213). Estrogen produced the expected statistically significant changes in lipids and lipoproteins. Several correlations between changes in lipids and lipoproteins and coagulation indices were statistically significant. Protein C antigen and activity changes correlated directly with high-density lipoprotein cholesterol changes (
r = .52,
P ≤ .005;
r = .38,
P ≤ .05; respectively), and protein C antigen also correlated directly with increases in apoprotein A-I (
r = .54,
P ≤ .005). Triglyceride changes correlated directly with changes in protein C antigen (
r = .36,
P ≤ .05) and activity (
r = .49,
P ≤ .005) and inversely with C4b-binding protein (
r = −.58,
P ≤ .01). Apoprotein B was correlated with free protein S (
r = .48,
P ≤ .01).
Although several estrogen-induced changes may decrease atherosclerotic potential and hypercoagulability, others may promote coagulability. These divergent effects may be manipulated pharmacologically by other estrogen compounds or by the addition of various progestins. |
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ISSN: | 0029-7844 1873-233X |
DOI: | 10.1016/S0029-7844(96)00530-3 |