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1.
Rev Med Inst Mex Seguro Soc ; 50(5): 537-40, 2012.
Artículo en Español | MEDLINE | ID: mdl-23282268

RESUMEN

BACKGROUND: it is known that vitamin D increases the population of superficial cells, so the objective of the present work was to evaluate the effect in Mexican postmenopausal women who were using or not oral calcitriol. METHODS: postmenopausal women with vaginal dryness that received at random: calcium 500 mg orally every 24 h or calcitriol 0.25 µg every 24 h during two months. At the beginning of treatment and at two months a vaginal Pap smear was performed. The maturation index was determined and the estrogenic value was calculated. Vaginal dryness was evaluated using an analog visual scales and vaginal by the moistening of a pH test strip. Student's t test was used for statistical analysis. RESULTS: 23 postmenopausal women were studied and divided as follows: group I (calcium) = 11 women and group II (calcitriol) = 12 women. In the analyzed parameters only the average of superficial cells was significantly greater at the end of treatment in the calcitriol group. CONCLUSION: calcitriol use increased the average of superficial cells in vaginal cytology, but didn't modify vaginal dryness.


Asunto(s)
Calcitriol/uso terapéutico , Posmenopausia , Vagina/citología , Vagina/fisiopatología , Femenino , Humanos , Persona de Mediana Edad , Vagina/efectos de los fármacos
2.
Ginecol Obstet Mex ; 73(10): 521-4, 2005 Oct.
Artículo en Español | MEDLINE | ID: mdl-16583831

RESUMEN

OBJECTIVE: To evaluate the effect of conjugated equine estrogens (CEE) plus medroxyprogesterone acetate (MPA) and raloxifene on serum levels of complement C3 and C4 fractions in postmenopausal women. PATIENTS AND METHOD: Twenty healthy postmenopausal women were studied. In all weight, height and body mass index (BMI) were documented. FSH and estradiol levels were measured. They were randomly divided into two groups, according to the treatment they received: group I, CEE 0.625 mg/day plus MPA 2.5 mg/day (n = 7); group II, raloxifene 60 mg/day (n = 13), both treatments were continuous. Serum levels of C3 and C4 complement fractions were measured by immunonephelometry at baseline and six months after start of treatment. Differences among groups of baseline and final C3 and C4 levels were measured with Student's t test for independent and paired samples, respectively. RESULTS: There were no differences among groups in age, weight, height and body mass index, neither in C3 and C4 levels among baseline and final levels when comparing each group separately. CONCLUSIONS: Complement may not intervene significantly in the atherosclerotic inflammatory process in women receiving CEE plus MPA or raloxifene.


Asunto(s)
Complemento C3/análisis , Complemento C3/efectos de los fármacos , Complemento C4/análisis , Complemento C4/efectos de los fármacos , Terapia de Reemplazo de Estrógeno , Estrógenos Conjugados (USP)/administración & dosificación , Medroxiprogesterona/administración & dosificación , Posmenopausia , Clorhidrato de Raloxifeno/administración & dosificación , Moduladores Selectivos de los Receptores de Estrógeno/administración & dosificación , Quimioterapia Combinada , Estrógenos Conjugados (USP)/farmacología , Femenino , Humanos , Medroxiprogesterona/farmacología , Persona de Mediana Edad , Clorhidrato de Raloxifeno/farmacología , Moduladores Selectivos de los Receptores de Estrógeno/farmacología
3.
Int J Fertil Womens Med ; 49(3): 120-2, 2004.
Artículo en Inglés | MEDLINE | ID: mdl-15303313

RESUMEN

OBJECTIVE: To assess the differences in effect between raloxifene and continuous combined estrogen plus progestin therapy on Hamilton Depression Rating Scale (HDRS) score. METHODS: Fifteen post-menopausal patients who had not received, and were not receiving, hormone therapy were studied. They were divided into two groups according to the therapy they received, as follows: group I, conjugated equine estrogens (CEE) 0.625 mg/day plus medroxyprogesterone 2.5 mg/day (n = 6), group II, raloxifene 60 mg/day (n = 9). The Hamilton Depression Rating Scale was used at baseline and after 6 months of treatment for mood assessment. Student's t test for independent samples was used for comparison among the groups; Student's t test for paired samples was used to assess differences between baseline and final Hamilton Depression Rating Scale scores. RESULTS: No differences were found in age or in anthropometric variables, in final Hamilton Depression Rating Scale score between the groups. In analyzing each group independently, no significant difference was found between baseline and final scores in Hamilton Depression Rating Scale in group I, while in group II a significant decrease was found. CONCLUSIONS: Raloxifene induces a greater decrease in Hamilton Depression Rating Scale, which indicates an amelioration of depressive mood during the climacteric.


Asunto(s)
Afecto/efectos de los fármacos , Depresión/tratamiento farmacológico , Antagonistas de Estrógenos/administración & dosificación , Estrógenos Conjugados (USP)/administración & dosificación , Medroxiprogesterona/administración & dosificación , Clorhidrato de Raloxifeno/administración & dosificación , Moduladores Selectivos de los Receptores de Estrógeno/administración & dosificación , Depresión/prevención & control , Femenino , Humanos , Persona de Mediana Edad , Posmenopausia , Escalas de Valoración Psiquiátrica , Factores de Tiempo , Salud de la Mujer
4.
Int J Fertil Womens Med ; 49(2): 88-90, 2004.
Artículo en Inglés | MEDLINE | ID: mdl-15188835

RESUMEN

OBJECTIVE: To compare vaginal dryness in two groups of postmenopausal women according to hormone replacement therapy schedule using pH test strip. METHODS: Twenty-two healthy postmenopausal women were divided into two groups according to the treatment they received: Group I, conjugated equine estrogens (CEE) 0.625 mg/day (n = 15); Group II, CEE 0.625 mg/day plus medroxyprogesterone 2.5 mg/day (n = 7). Vaginal dryness intensity was analyzed using an analog visual scale and vaginal humidity by measuring the moistening, in millimeters, of a pH test strip. Both were evaluated at baseline and 3 months after the beginning of treatment. The comparison among groups and between baseline and final results was done with Student's t test for paired and independent samples, respectively. RESULTS: No differences were found in age and in anthropometric variables among the groups. In both groups, vaginal dryness intensity significantly decreased and the pH test strip moistening significantly increased, but the magnitude of the moistening was greater in the group with medroxyprogesterone. CONCLUSIONS: When medroxyprogesterone was added to estrogen therapy, a greater vaginal moistening of pH test strip was observed than when estrogen was used alone.


Asunto(s)
Estrógenos Conjugados (USP)/administración & dosificación , Concentración de Iones de Hidrógeno , Medroxiprogesterona/administración & dosificación , Vagina/efectos de los fármacos , Esquema de Medicación , Terapia de Reemplazo de Estrógeno , Femenino , Humanos , Persona de Mediana Edad , Posmenopausia , Factores de Tiempo , Enfermedades Vaginales/diagnóstico
5.
Maturitas ; 45(1): 55-8, 2003 May 30.
Artículo en Inglés | MEDLINE | ID: mdl-12753944

RESUMEN

OBJECTIVE: To objectively analyze vaginal dryness in postmenopausal women. METHODS: Forty healthy postmenopausal women, were divided in three groups according to the treatment they received. Group I, conjugated equine estrogens (CEE) 0.625 mg/day (n=20), group II, CEE 0.625 mg/day plus chlormadinone 1 mg/day (n=13), and group III, CEE 0.625 mg/day plus medroxyprogesterone 2.5 mg/day (n=7). Vaginal dryness intensity was analyzed using an analog visual scale, and vaginal humidity measuring the moistening in mm of a pH test strip. Both were evaluated at baseline and 3 months after the beginning of treatment. The comparison among groups and between the baseline and final results was done with Student's t-test for paired and independent samples, respectively. Pearson correlation analysis was carried out between final vaginal dryness intensity and the final moistening of the pH test strip. RESULTS: No statistically significant differences were found in age neither in somatometric variables among the groups. In the three groups, vaginal dryness intensity significantly decreased and the pH test strip moistening significantly increased. A significant negative correlation was only found in group II (-0.690 P<0.009). CONCLUSIONS: Vaginal dryness evaluation assessing the pH test strip moistening is an objective method to evaluate this symptom in postmenopausal women, and the results are independent of the hormone replacement therapy schedule.


Asunto(s)
Concentración de Iones de Hidrógeno , Vagina/fisiología , Enfermedades Vaginales/diagnóstico , Atrofia/diagnóstico , Atrofia/patología , Acetato de Clormadinona/administración & dosificación , Acetato de Clormadinona/farmacología , Esquema de Medicación , Terapia de Reemplazo de Estrógeno , Estrógenos Conjugados (USP)/administración & dosificación , Estrógenos Conjugados (USP)/farmacología , Femenino , Humanos , Medroxiprogesterona/administración & dosificación , Medroxiprogesterona/farmacología , Persona de Mediana Edad , Dimensión del Dolor , Posmenopausia , Valor Predictivo de las Pruebas , Vagina/efectos de los fármacos , Enfermedades Vaginales/patología
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