Do estroprogestinic hormones protect against chemotherapy-induced amenorrhea in multiple sclerosis?
| Autor: | T. C. Jackson Wu, Rhonda R. Voskuhl |
|---|---|
| Rok vydání: | 2008 |
| Předmět: |
musculoskeletal diseases
Adult Male endocrine system Multiple Sclerosis endocrine system diseases Bioinformatics Article Chemotherapy induced amenorrhea Young Adult Cellular and Molecular Neuroscience Risk Factors Surveys and Questionnaires Humans Medicine Amenorrhea Retrospective Studies Menarche business.industry Multiple sclerosis musculoskeletal system medicine.disease Female Neurology (clinical) Menopause Mitoxantrone medicine.symptom business Infertility Female Immunosuppressive Agents hormones hormone substitutes and hormone antagonists Follow-Up Studies Hormone |
| Zdroj: | Nature clinical practice. Neurology. 5(1) |
| ISSN: | 1745-8358 |
| Popis: | Improved prognosis in women with multiple sclerosis (MS) undergoing immunosuppressive treatment with mitoxantrone (MITO) has led to an increased interest in the effect of such treatments on fertility. FErtility and Mitoxantrone In MS (FEMIMS) is a collaborative retrospective study aimed at evaluating the impact of MITO treatment on fertility in women with MS.Occurrence of chemotherapy-induced amenorrhea (CIA) was evaluated in 189 women with MS treated with MITO before the age of 45. An "ad hoc" questionnaire, paying particular attention to onset of CIA either during or post-MITO treatment, was administered to each patient. The probability of CIA was calculated using a multivariate logistic regression analysis taking into account age at exposure, cumulative dose, and use of estroprogestinic (EP) drugs during treatment.Forty-eight (26%) patients presented CIA following MITO. The probability of CIA was increased by 2%/mg/m(2) of cumulative dose and by 18% for each year of age, whereas it was reduced by administration of EP during treatment.MITO treatment may affect reproductive capacity in women with MS. Patients of childbearing age should be properly counseled before MITO treatment and EP therapy should be administered to reduce the risk of CIA. |
| Databáze: | OpenAIRE |
| Externí odkaz: |
|
Full text from SpringerLink