The role of megestrol acetate as an alternative to conventional hormone replacement therapy
| Autor: | JF Barnes, E. Farish, F O'Donoghue, C. D. Fletcher, David M. Hart, K Ekevall |
|---|---|
| Rok vydání: | 2000 |
| Předmět: |
Adult
medicine.medical_specialty Very low-density lipoprotein Lipoproteins medicine.medical_treatment Antithrombin III Lipoproteins VLDL Bone and Bones Protein S Bone remodeling chemistry.chemical_compound Bone Density Internal medicine medicine Humans Femur Prospective Studies Blood Coagulation Triglycerides Bone mineral Vasomotor Cholesterol business.industry Megestrol Acetate Cholesterol HDL Estrogen Replacement Therapy Fibrinogen Obstetrics and Gynecology Plasminogen Hormone replacement therapy (menopause) Fasting General Medicine Middle Aged Alkaline Phosphatase Spine Lipoproteins LDL Endocrinology chemistry Megestrol acetate Female lipids (amino acids peptides and proteins) Menopause business Lipoprotein(a) Protein C Lipoprotein medicine.drug |
| Zdroj: | Climacteric. 3:125-134 |
| ISSN: | 1473-0804 1369-7137 |
| Popis: | To investigate the effect of megestrol acetate on menopausal symptoms, lipid metabolism, bone metabolism and coagulation.In a prospective observational study, 71 postmenopausal women, for whom conventional hormone replacement therapy (HRT) was unsuitable, were treated with megestrol acetate 40 mg per day. At 0, 3, 6 and 12 months, fasting lipoproteins, bone biochemistry and thrombophilia profiles were measured and symptom score cards (Greene climacteric scale) completed. Bone mineral density measurement was performed at 0 and 12 months.Forty-one women completed the study. Treatment produced significant decreases in psychological (p0.001), vasomotor (p0.001) and somatic (p0.01) symptoms. There were significant reductions in triglycerides (p0.001), total cholesterol (p0.001), very-low-density lipoprotein (VLDL) (p0.05), low-density lipoprotein (LDL) (p0.001), high-density lipoprotein (HDL) cholesterol (p0.001) and lipoprotein(a) (p0.001). Levels of protein C were reduced (p0.05) and fibrinogen increased (p0.05). Protein S, plasminogen and antithrombin III levels showed an upward trend, which did not reach statistical significance. Biochemical markers of bone turnover did not change, apart from a significant decrease in alkaline phosphatase. Spinal bone density decreased significantly after 12 months, while femoral neck density remained unchanged.Megestrol acetate controls menopausal symptoms, has equivocal effects on cardiovascular risk markers and does not increase bone density. It is useful where estrogen is contraindicated. |
| Databáze: | OpenAIRE |
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