The objective of the research proposed in this Project is to evaluate a potential nutritional alternative to CEE replacement therapy that would provide a beneficial effect on postmenopausal CHD and osteoporosis but would be free of adverse effects on the breast and uterus. We have chosen to focus on the phytoestrogens of soybeans (genistein and daidzein) because: Asian women who consume diets relatively high in the soybean estrogens (SBE) have a low occurrence of postmenopausal CHD. An extensive literature exists suggesting that genistein has important inhibitory effects at several levels of atherogenesis. Data obtained in our laboratory indicate favorable effects of SBE on plasma lipid and lipoprotein profiles. The literature to date suggests a protective effect of SBE against the development of breast cancer and a lack of effect on the endometrium. Epidemiologic and experimental evidence suggests that phytoestrogens prevent bone loss postmenopausally. Nutritional supplements rich in these phytoestrogens are available. One hundred eighty-nine surgically postmenopausal monkeys were randomized into three groups (all fed a moderately atherogenic diet): one group fed a soy isolate with only trace amounts of genistein and daidzein as the source of dietary protein (Group 1); one fed the same diet with conjugated equine estrogens added at a dose equivalent for a woman of 0.625 mg/day (Group 2); and one fed a soy isolate with the naturally occurring amounts of genistein and daidzein (1.7 mg/g) (Group 3).
The aims of the research are to quantify the relative effectiveness of CEE and SBE in inhibiting the progression of postmenopausal coronary artery atherosclerosis, the effects of treatment with CEE and SBE on mammary gland and endometrial hyperplasia, the relative effectiveness of CEE and SBE in inhibiting postmenopausal bone loss, and whether CEE and SBE treatment results in a disassociation of the relationship between cardiac hyperactivity and exacerbated coronary artery atherosclerosis we have observed for estradiol.

Agency
National Institute of Health (NIH)
Institute
National Heart, Lung, and Blood Institute (NHLBI)
Type
Research Program Projects (P01)
Project #
5P01HL045666-08
Application #
6110062
Study Section
Project Start
1998-01-01
Project End
2000-03-31
Budget Start
1997-10-01
Budget End
1998-09-30
Support Year
8
Fiscal Year
1998
Total Cost
Indirect Cost
Name
Wake Forest University Health Sciences
Department
Type
DUNS #
041418799
City
Winston-Salem
State
NC
Country
United States
Zip Code
27106
Register, Thomas C; Appt, Susan E; Clarkson, Thomas B (2016) Atherosclerosis and Vascular Biologic Responses to Estrogens: Histologic, Immunohistochemical, Biochemical, and Molecular Methods. Methods Mol Biol 1366:517-532
Meléndez, Giselle C; Register, Thomas C; Appt, Susan E et al. (2015) Beneficial effects of soy supplementation on postmenopausal atherosclerosis are dependent on pretreatment stage of plaque progression. Menopause 22:289-96
Eyster, K; Appt, S; Chalpe, A et al. (2014) Effects of equol on gene expression in female cynomolgus monkey iliac arteries. Nutr Metab Cardiovasc Dis 24:423-7
Eyster, Kathleen M; Appt, Susan; Chalpe, Abha et al. (2014) Effects of estradiol on transcriptional profiles in atherosclerotic iliac arteries in ovariectomized cynomolgus macaques. Menopause 21:143-52
Silverstein, Marnie G; Kaplan, Jay R; Appt, Susan E et al. (2014) Effect of soy isoflavones on thyroid hormones in intact and ovariectomized cynomolgus monkeys (Macaca fascicularis). Menopause 21:1136-42
Sophonsritsuk, Areepan; Appt, Susan E; Clarkson, Thomas B et al. (2013) Differential effects of estradiol on carotid artery inflammation when administered early versus late after surgical menopause. Menopause 20:540-7
Schnatz, Peter F; Nudy, Matthew; O'Sullivan, David M et al. (2012) The quantification of vitamin D receptors in coronary arteries and their association with atherosclerosis. Maturitas 73:143-7
Schnatz, Peter F; Vila-Wright, Sharon; Jiang, Xuezhi et al. (2012) The association between plasma 25-hydroxyvitamin D3 concentrations, C-reactive protein levels, and coronary artery atherosclerosis in postmenopausal monkeys. Menopause 19:1074-80
Schnatz, Peter F; Nudy, Matthew; O'Sullivan, David M et al. (2012) Coronary artery vitamin D receptor expression and plasma concentrations of 25-hydroxyvitamin D: their association with atherosclerosis. Menopause 19:967-73
Wood, Charles E; Stavisky, Ronda C; Nowak, Jette et al. (2012) Stimulatory adrenocortical effects of a selective estrogen receptor modulator in ovariectomized female macaques. Toxicol Pathol 40:55-61

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