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1.
Reprod Biomed Online ; 48(1): 103572, 2024 Jan.
Article in English | MEDLINE | ID: mdl-37979227

ABSTRACT

RESEARCH QUESTION: Do live birth rates differ between recipients matched with donors using conventional ovarian stimulation compared with those using random-start protocols? DESIGN: Retrospective analysis of 891 ovarian stimulations in egg donors (January-December 2018) and clinical outcomes in matched recipients (n = 935). Donors commenced ovarian stimulation on day 1-3 of the menstrual cycle (n = 223) or in the mid/late-follicular (n = 388) or luteal phase (n = 280) under a conventional antagonist protocol. Live birth rate of matched recipients was the main outcome. RESULTS: Duration of stimulation and total gonadotrophin dose were comparable between conventional versus random-start groups. The number of collected eggs were similar (17.6 ± 8.8 versus 17.2 ± 8.5, P = 0.6, respectively). Sub-group analysis showed that stimulation length (10.2 ± 1.8 versus 9.8 ± 1.7 versus 10.4 ± 1.7, P < 0.001) and gonadotrophin consumption (2041.5 ± 645.3 versus 2003.2 ± 647.3 versus 2158.2 ± 685.7 IU, P = 0.01) differed significantly between the conventional, mid/late follicular and luteal phase groups, respectively. In matched recipients receiving fresh oocytes and undergoing fresh embryo transfer, the biochemical pregnancy (63.8% and 63.3%; P = 0.9), clinical pregnancy (54.6% and 56.1%; P = 0.8) and live birth rates (47.7% and 46.6%; P = 0.7) per embryo-transfer were similar between conventional versus random groups. Similar results were obtained in recipients receiving vitrified eggs. Euploidy rate was also comparable. CONCLUSIONS: No notable variations were found in clinical outcomes using oocytes obtained from random-start protocols and those proceeding from conventional ovarian stimulation in oocyte donation treatments. Luteal-phase stimulation seems to require longer stimulation and higher FSH consumption. Random-start stimulation strategy does not impair the potential of the oocyte yield or clinical outcomes in oocyte donation cycles.


Subject(s)
Fertilization in Vitro , Oocyte Donation , Pregnancy , Female , Humans , Fertilization in Vitro/methods , Retrospective Studies , Embryo Transfer/methods , Ovulation Induction/methods , Gonadotropins , Pregnancy Rate
2.
Gynecol Oncol Rep ; 50: 101304, 2023 Dec.
Article in English | MEDLINE | ID: mdl-38033360

ABSTRACT

Placental-site trophoblastic tumor (PSTT) is a rare pathological entity included in the spectrum of gestational trophoblastic neoplasia (GTN). It is a neoplasia with metastatic potential that, once metastasized, has poor prognosis because the tumor tends to be less sensitive to chemotherapy. We present a rare case of gestational trophoblastic neoplasia, in which hysterectomy for persistent gestational trophoblastic disease after hydatidiform mole, revealed a primary PSTT in the uterus. Subsequently, a slight persistent elevation of the beta fraction of human chorionic gonadotropin hormone (B-hCG) during follow-up revealed the presence of bone metastases. This location is not usual from this tumor, being even more rare the case of PSTT with isolated bone metastases. Metastasic foci were only identified with PET-CT since the usual diagnostic resources were not able to do it. Finally, it is also remarkable in our case that the treatment required the confluence of chemotherapy together with immunotherapy to achieve a favorable response.

3.
Menopause ; 30(8): 873-880, 2023 08 01.
Article in English | MEDLINE | ID: mdl-37449718

ABSTRACT

IMPORTANCE AND OBJECTIVE: Menopausal hormone therapy (HT) is widely used, and there are several statements of international scientific societies to guide prescribers; however, a summary of existing literature about possible drug interactions with HT does not exist, although many midlife women take medications for other conditions. Therefore, our objective was to create a document that presents and synthesizes the most relevant interactions. The impact of the interaction itself and the number of candidates for HT who are likely to use other treatments are considered based on the best available evidence. METHODS: A systematic review was performed to determine the best evidence of interaction effects on relevant outcomes of interest for decision making. A working framework was developed to formulate explicit and reasoned recommendations according to four predefined categories for coadministration: (1) can be used without expected risks, (2) acceptable use (no evidence of negative interaction), (3) alternative treatment should be considered, and (4) nonuse without express justification. The project protocol was registered in the Open Science Framework platform (doi: 10.17605/OSF.IO/J6WBC ) and in PROSPERO (registration number CRD42020166658). RESULTS: Studies targeting our objective are scarce, but 23 pharmacological groups were assigned to one of the predefined categories of recommendation for concomitant use of HT. Vaginal HT was assigned to category 1 for 21 of the analyzed pharmacological groups. For oral and transdermal HT (estrogen-only or combined) and tibolone, there were 12 pharmacological groups assigned to category 1, 12 to category 2, 5 to category 3, and 4 to category 4. Results are shown in crossed-tables that are useful for counseling and prescription. DISCUSSION AND CONCLUSIONS: Available evidence of HT interactions with other drugs is scarce and mainly indirect. It comes from biological plausibility, knowledge of extensive concomitant use without reported incidents, and/or extrapolation from hormonal contraception, but there are pharmacological groups in all categories showing that information is useful. These eligibility criteria summarize it and can help in the decision process of HT coadministration with other drugs. Decisions should be taken based on these recommendations but also individualized risk/benefit evaluation, according to underlying pathology, patient's clinical requirements, and the existence or nonexistence of alternatives.


Subject(s)
Estrogen Replacement Therapy , Estrogens , Humans , Female , Estrogens/therapeutic use , Estrogen Replacement Therapy/adverse effects , Estrogen Replacement Therapy/methods , Hormone Replacement Therapy , Risk Assessment , Menopause
4.
Maturitas ; 166: 65-85, 2022 Dec.
Article in English | MEDLINE | ID: mdl-36081216

ABSTRACT

This project aims to develop eligibility criteria for menopausal hormone therapy (MHT). The tool should be similar to those already established for contraception A consortium of scientific societies coordinated by the Spanish Menopause Society met to formulate recommendations for the use of MHT by women with medical conditions based on the best available evidence. The project was developed in two phases. As a first step, we conducted 14 systematic reviews and 32 metanalyses on the safety of MHT (in nine areas: age, time of menopause onset, treatment duration, women with thrombotic risk, women with a personal history of cardiovascular disease, women with metabolic syndrome, women with gastrointestinal diseases, survivors of breast cancer or of other cancers, and women who smoke) and on the most relevant pharmacological interactions with MHT. These systematic reviews and metanalyses helped inform a structured process in which a panel of experts defined the eligibility criteria according to a specific framework, which facilitated the discussion and development process. To unify the proposal, the following eligibility criteria have been defined in accordance with the WHO international nomenclature for the different alternatives for MHT (category 1, no restriction on the use of MHT; category 2, the benefits outweigh the risks; category 3, the risks generally outweigh the benefits; category 4, MHT should not be used). Quality was classified as high, moderate, low or very low, based on several factors (including risk of bias, inaccuracy, inconsistency, lack of directionality and publication bias). When no direct evidence was identified, but plausibility, clinical experience or indirect evidence were available, "Expert opinion" was categorized. For the first time, a set of eligibility criteria, based on clinical evidence and developed according to the most rigorous methodological tools, has been defined. This will provide health professionals with a powerful decision-making tool that can be used to manage menopausal symptoms.


Subject(s)
Breast Neoplasms , Estrogen Replacement Therapy , Menopause , Female , Humans , Breast Neoplasms/chemically induced , Estrogen Replacement Therapy/adverse effects , Health Personnel , Societies, Scientific
5.
Gynecol Endocrinol ; 34(10): 826-832, 2018 Oct.
Article in English | MEDLINE | ID: mdl-29790381

ABSTRACT

Tissue-selective estrogen complex (TSEC) is projected as a progestogen-free option for the treatment of estrogen deficiency symptoms in postmenopausal, non-hysterectomized women. TSEC combines the benefits of estrogen with a selective estrogen receptor modulator (SERM), in this case bazedoxifene acetate (BZA), which has an antagonistic effect on the endometrium, thus avoiding the use of progestins. The authorized TSEC combination (conjugated estrogens [CE] 0.45 mg/BZA 20 mg) for the alleviation of vasomotor symptoms has been demonstrated in randomized clinical trials compared with placebo or menopausal hormone therapy (MHT). In addition, TSEC has shown improvements in quality of life and vaginal atrophy. In respect to MHT using progestins, the benefits of TSEC are found mainly in the bleeding pattern, amenorrhea rate, and reduction in mammary repercussion (i.e., breast tenderness and radiological density). The objective of this guide will be to analyze the efficacy and safety of TSEC consisting of CE/BZA in postmenopausal women.


Subject(s)
Hormone Replacement Therapy , Hot Flashes/drug therapy , Menopause/drug effects , Osteoporosis, Postmenopausal/drug therapy , Selective Estrogen Receptor Modulators/therapeutic use , Vaginal Diseases/drug therapy , Bone Density/drug effects , Female , Humans , Quality of Life , Selective Estrogen Receptor Modulators/pharmacology
6.
Maturitas ; 79(1): 117-21, 2014 Sep.
Article in English | MEDLINE | ID: mdl-25042873

ABSTRACT

Denosumab is a new drug developed for the treatment of osteoporosis. Moreover, increasing evidences link denosumab with benefits in cancer, an area of interest for those in charge of the postmenopausal health. Denosumab has shown efficacy in the control of bone loss associated with hypogonadic states created by chemotherapy in breast and other cancers. Moreover, some studies reveal efficacy in reducing the progression of metastases. A panel of experts from the Spanish Menopause Society has met to develop usage recommendations based on the best available evidence.


Subject(s)
Bone Density Conservation Agents/therapeutic use , Denosumab/therapeutic use , Osteoporosis, Postmenopausal/drug therapy , Bone Density/drug effects , Bone Density Conservation Agents/administration & dosage , Bone Density Conservation Agents/economics , Bone Neoplasms/prevention & control , Bone Neoplasms/secondary , Bone Remodeling/drug effects , Breast Neoplasms/pathology , Denosumab/administration & dosage , Denosumab/economics , Disease Progression , Female , Fractures, Bone/economics , Fractures, Bone/prevention & control , Humans , Injections, Subcutaneous , Postmenopause/drug effects , Safety
7.
Int J Womens Health ; 5: 449-55, 2013.
Article in English | MEDLINE | ID: mdl-23935389

ABSTRACT

BACKGROUND: The purpose of this paper is to report the long-term results of surgery without bowel resection in patients suffering from deep infiltrating endometriosis with rectovaginal or colorectal involvement. METHODS: This retrospective observational study identified 42 patients suffering with deep infiltrating endometriosis who underwent surgery. Conservative surgery was performed in 23 women (only one of them with bowel resection), and 19 women underwent a hysterectomy and bilateral salpingo-oophorectomy (HBSO). In the conservative surgery group, a later HBSO was performed in eight patients as a second operation. Pregnancies, recurrences, reoperations, use of hormone replacement therapy, and outcomes during long-term follow-up were analyzed. RESULTS: The average follow-up duration was 7 ± 5.7 years in conservative surgery cases. Only one patient was treated with sigmoid bowel resection in 1997 and had complications. In this conservative surgery group, 13 patients (56%) received medical treatment after surgery, 10 patients wanted to get pregnant (of whom seven [70%] were successful), and eight patients underwent a subsequent HBSO because of recurrent symptoms and/or endometrioma. Therefore, HBSO was performed in 27 patients, of whom 14 (51.8%) used hormone replacement therapy for 5.6 ± 3.6 years. No recurrences or complications were observed in patients after HBSO with or without hormone replacement therapy. CONCLUSION: Good clinical results can be obtained by performing only conservative surgery and/or HBSO without bowel resection, an alternative that could reduce the number of colorectal resections that are performed very frequently nowadays. After HBSO, patients may use hormone replacement therapy for several years with total satisfaction and well-being.

8.
Menopause ; 20(7): 754-60, 2013 Jul.
Article in English | MEDLINE | ID: mdl-23793166

ABSTRACT

Tibolone is a drug with complex tissue-specific action that exhibits a combination of estrogenic, progestogenic, and slight androgenic activity. Its variable profile explains its clinical effects, depending on the target tissue where it is metabolized, its metabolites' affinity for and potency in hormone receptors, and probable enzymatic activity modulation.In recent reviews and clinical trials, the effectiveness of tibolone in alleviating different hot flush menopause symptoms, mainly in mood and sexuality disorders, has been noted. In Spain, tibolone is the most prescribed hormonal treatment, and one of the most common complaints among postmenopausal women is change in sexual drive. For such reason, a panel of experts from the Spanish Menopause Society met to develop usage recommendations based on the best evidence available.


Subject(s)
Norpregnenes/therapeutic use , Postmenopause , Aged , Bone Density/drug effects , Cardiovascular Diseases/prevention & control , Estrogen Replacement Therapy , Female , Hot Flashes/drug therapy , Humans , Middle Aged , Norpregnenes/adverse effects , Osteoporosis, Postmenopausal/drug therapy , Osteoporosis, Postmenopausal/prevention & control , Quality of Life , Randomized Controlled Trials as Topic , Sexual Dysfunction, Physiological/drug therapy , Societies, Medical , Spain
9.
Maturitas ; 75(3): 294-300, 2013 Jul.
Article in English | MEDLINE | ID: mdl-23706280

ABSTRACT

Breast cancer is the most common female cancer in Spain. Its high prevalence, its high survival rate, and its incidence are the reasons treatment is increasingly sought for common problems by young women who have survived it. Besides the contraception and fertility issues, many breast cancer survivors develop sexual disorders and menopausal symptoms, whether as a consequence of treatment-induced menopause or side effects of treatment. For such reasons, a panel of experts from the Spanish Menopause Society has met to develop usage recommendations for the relief of vasomotor symptoms and for sexual and reproductive health in patients with breast cancer based on the best evidence available.


Subject(s)
Breast Neoplasms/complications , Hot Flashes/therapy , Menopause , Female , Hot Flashes/drug therapy , Hot Flashes/etiology , Humans , Reproductive Health , Societies, Medical , Spain , Survivors , Young Adult
10.
Eur J Obstet Gynecol Reprod Biol ; 167(2): 190-3, 2013 Apr.
Article in English | MEDLINE | ID: mdl-23369341

ABSTRACT

OBJECTIVE: A randomised and controlled experimental study was carried out to determine the effect of short and long series of treatment with recombinant human interferon-alpha-2b on surgically induced endometriosis in rats. STUDY DESIGN: Ninety-six Wistar adult female rats, which had undergone an autotransplant into the peritoneal cavity of four endometrial fragments measuring 4.5mm at the side, were randomly divided into three groups. One third of the animals were manipulated like the treated animals but were not given treatment and served as control (group C). Another third (group S) were treated with three doses (one every 48 h, 100,000 U per dose) of recombinant human interferon-alpha-2b (subcutaneous route), and the last third (group L) were treated with fifteen doses of interferon (100,000 U every 48 h). RESULTS: Before interferon was administered, there were no differences between groups in the average growth of experimental endometriosis per animal (17.3±6.7, 18.1±9.2, 16.4±5.6mm in groups C, S and L respectively). After the treatment, experimental endometriosis per animal was significantly smaller in the groups treated with interferon than in the control non-treated group (p<0.001), and in the group treated with 15 doses versus the group treated with 3 doses (p<0.05), (17.6±7.5, 14.0±9.5, 9.4±6.0mm in groups C, S, and L respectively). While the implants of the animals in the control group showed no change in size throughout the study (120 days) (+1.96% of variation), the mean size of the implants in the treated rats decreased, (22.7% with the short and 42.8% with the long series of treatment with interferon). Only one implant in group C (0.8%) disappeared, while this occurred in 27 cases (22.5%) in group S (p<0.001) and in 45 (37.5%) in group L (p<0.001 versus group C and p<0.05 versus group S). CONCLUSION: The long series of treatment with human interferon-alpha-2b was more effective than the short one in reducing the size of surgically induced endometriosis in the peritoneal cavity of the rat.


Subject(s)
Disease Models, Animal , Endometriosis/drug therapy , Immunologic Factors/therapeutic use , Interferon-alpha/therapeutic use , Peritoneal Diseases/drug therapy , Animals , Endometriosis/immunology , Endometriosis/pathology , Female , Humans , Immunologic Factors/administration & dosage , Immunologic Factors/genetics , Injections, Subcutaneous , Interferon alpha-2 , Interferon-alpha/administration & dosage , Interferon-alpha/genetics , Peritoneal Cavity/pathology , Peritoneal Diseases/immunology , Peritoneal Diseases/pathology , Random Allocation , Rats , Rats, Wistar , Recombinant Proteins/administration & dosage , Recombinant Proteins/genetics , Recombinant Proteins/therapeutic use , Time Factors
11.
Menopause Int ; 16(3): 111-4, 2010 Sep.
Article in English | MEDLINE | ID: mdl-20956685

ABSTRACT

AIM: The purpose of this study is to confirm in our population the decreasing secular trend in the age of menarche (AAM) observed in other European countries. Another aim is to investigate the association between early menarche and breast cancer, metabolic disorders risk or early menopause. MATERIALS AND METHODS: We conducted a nationwide population-based study of 1980 Caucasoid Spanish postmenopausal women from 2003 to 2006 to investigate the AAM, the duration of the fertile period and the relation of early menarche with breast cancer and some metabolic disorders. RESULTS: Regression analysis of AAM demonstrates a trend towards the younger AAM in our population during the past decades (P > 0.001). Parallel to this decrease we observe a significant increase in the fertility period and the height of our population (P < 0.001). In the women with AAM less than 11 years, there is an increased risk of hypercholesterolaemia, being overweight and obesity. However, early menarche does not raise the risk of adult onset diabetes, hypertension or breast cancer. CONCLUSIONS: These data indicate a decreasing secular trend of AAM in a Spanish population in the last decades. Furthermore, hypercholesterolaemia and obesity, but not breast cancer, appears to be influenced by younger AAM. Only women who have their menarche at the age of nine years or less are more likely to have an earlier menopause.


Subject(s)
Breast Neoplasms/epidemiology , Diabetes Mellitus, Type 2/epidemiology , Hypercholesterolemia/epidemiology , Hypertension/epidemiology , Menarche/physiology , Postmenopause/psychology , Adult , Age Factors , Aged , Body Height , Female , Fertility , Humans , Middle Aged , Overweight/epidemiology , Retrospective Studies , Risk , Spain/epidemiology , White People
12.
Gynecol Obstet Invest ; 69(3): 203-11, 2010.
Article in English | MEDLINE | ID: mdl-20051692

ABSTRACT

BACKGROUND: To analyze the therapeutic results of recombinant interleukin-2 (rIL-2) left in the cysts after transvaginal ultrasound (US)-guided drainage of endometriomas as an alternative to surgery. METHODS: Prospective and randomized clinical trial. A total of 25 consecutive patients were included. Two transvaginal US-guided punctures were performed, and 3 million IU of rIL-2 were left in the aspirated cysts once (group I) or both (group II) times according to randomization. MAIN OUTCOME MEASURES: Clinical results, prevented surgeries, and recurrences. RESULTS: Results were moderate or good in only 16% of subjects at 3 months and in 33% of subjects at 6 months after treatment in group I; these numbers were 66 and 33%, respectively, in group II. Differences were not statistically significant. However, the evolution of symptoms, endometriomas, and CA-125 revealed the low efficacy of rIL-2 left intracyst as well as a poor control of the clinical manifestations. After 1 year, 20% (group I) and 73% (group II) of patients had to be operated; after 2 years, these numbers were 55 and 82%, respectively. CONCLUSIONS: Treatment of endometriomas with transvaginal US-guided drainage and rIL-2 left in the cysts, without using endometrial suppressive therapy with GnRH analogues as done in previous studies, has low efficacy. Recurrences are even more frequent after the use of two rIL-2 doses.


Subject(s)
Drainage/methods , Endometriosis/diagnostic imaging , Endometriosis/drug therapy , Interleukin-2/administration & dosage , Ultrasonography, Interventional , Adult , Combined Modality Therapy , Female , Follow-Up Studies , Humans , Immunologic Factors/administration & dosage , Injections, Intralesional , Prospective Studies , Recombinant Proteins/administration & dosage , Secondary Prevention , Treatment Outcome , Young Adult
13.
Prog. obstet. ginecol. (Ed. impr.) ; 52(12): 712-721, dic. 2009.
Article in Spanish | IBECS | ID: ibc-75054

ABSTRACT

Objetivo: Dado el creciente interés en los países occidentales acerca de la utilización de ciertas plantas para el tratamiento de los síntomas relacionados con la menopausia, la AsociaciónEspañola para el Estudio de la Menopausia (AEEM)ha evaluado el papel de la Cimicífuga racemosa en el tratamiento de los síntomas climatéricos sobre la base de las mejores evidencias disponibles. Material y métodos. Se reunió un panel de expertos, clínicos e investigadores, en el campo dela fitoterapia. Los estudios seleccionados se obtuvieron mediante una búsqueda electrónica que incluyó buscadores de Internet, MEDLINE (1985-mayo 2008) y el Registro de Ensayos Clínicos Controlados Cochrane. Resultados: La mayoría de los estudios publicados en los últimos años están realizados con el extractoisopropanólico de Cimicífuga racemosa. La dosis más estudiada ha sido 40 mg/día y ha demostrado obtener una reducción moderada de las sofocaciones, sobre todo en las mujeres con sofocos más intensos, y una mejoría del estado de ánimo. Utilizada a las dosis recomendadas, no hay riesgo relevante desde el punto de vista hepático. Los datos disponibles sobre su efecto en la enfermedad cardiovascular, el hueso, la función cognitiva y la piel son muy escasos o inexistentes. Conclusiones: La Cimic ífuga racemosa es un tratamiento eficaz en el alivio de los síntomas vasomotores, al menos en una población adecuada de mujeres peri y posmenopáusicas, si bien se precisan mejores ensayos clínicos con suficiente número de pacientes incluidas y mayor duración del estudio (AU)


Objective: Due to an increasing interest in the symptoms related to menopause in western countries, the Spanish Menopause Society (SMS)has assessed the role of cimicifuga racemosa in relieving those symptoms based on the mostreliable evidence available. Material and methods: A meeting was held with a panel of experts, health scientists and researchers specialised in the field of phytotherapy. The studies selected were obtained through electronic search which included INTERNET, MEDLINE (1985-May 2008), and the Cochrane Controlled Clinical Trials Register. Results: Most studies published in recent years have been carried out using an isopropanol extract of cimicifuga racemosa. The dose most commonly studied was 40mg/day and was shown to result ina moderate decrease in hot flushes, particularly in those women with the most intense hot flushes, and an improvement in their mood. When recommended doses are used there is no significant risk to the hepatic system. Available data on the effect of cimicifuga racemosa on cardiovascular disease, bones, cognitive function or skin are scarce or non-existent. Conclusions: Cimicifuga racemosa is an effective treatment for relief of vasomotor symptoms, at least within a suitable population of peri- and postmenopausal women. Nevertheless, more accurate clinical trials which include sufficient numbers of patients and a longer follow-up are required (AU)


Subject(s)
Humans , Female , Adult , Middle Aged , Menopause/physiology , Climacteric/physiology , Cimicifuga/administration & dosage , Cimicifuga/therapeutic use , Phytotherapy/methods , Phytotherapy , Menopause, Premature/physiology , Apoptosis/physiology
14.
Menopause Int ; 15(4): 150-6, 2009 Dec.
Article in English | MEDLINE | ID: mdl-19933466

ABSTRACT

OBJECTIVE: Age at natural menopause (ANM) can be considered a complex parameter that depends on the interaction of multiple factors. In the present study, the role of interaction between genetic variants within estrogen synthesis and signalling pathways in the ANM in Spanish women is studied. MATERIAL AND METHODS: Nine single nucleotide polymorphisms (SNPs) located at different candidate genes related to the estrogen signalling pathway were analysed in 1980 Spanish postmenopausal women. RESULTS: Independently, none of the nine markers were significantly associated with early ANM. Only heterozygosis at the NRIP rs2229741 locus could be associated with early menopause; however, this marker does not maintain statistical significance. In contrast, linear regression analysis suggests several epistatic interactions including these markers in relation to ANM, especially between ESR2, NRIP1 and BMP15. The genetic variant that appears most in these interactions is that of the BMP15 rs3897937. It was observed that AA-TC combined genotype for NRIP-BMP15 (rs3897937), respectively, appears to be associated with a lower ANM than other possible combinations of these SNP (46.1+/-5.9 versus 50.4+/-3.3; P = 0.002). In the multilocus analysis, the multigenic interaction formed by ESR2 (AA), BMP15 rs3897937 (TC) and NRIP1 (AA) has the lower ANM (45.37+/-6.8 versus 48.69+/-5; P = 0.038). CONCLUSIONS: The results suggest that epistatic interactions of estrogen-related alleles may contribute to variance in ANM in Spanish women. Moreover, BMP15 and NRIP1 also appear as attractive candidate genes for premature menopause but require further investigation to confirm them.


Subject(s)
Estrogens/genetics , Postmenopause/genetics , Age Factors , Age of Onset , Aged , Female , Gene Frequency , Genotype , Humans , Menopause/genetics , Middle Aged , Polymorphism, Single Nucleotide , Signal Transduction , Spain
15.
Prog. obstet. ginecol. (Ed. impr.) ; 52(10): 562-571, oct. 2009. tab
Article in Spanish | IBECS | ID: ibc-74483

ABSTRACT

Objetivo: Este estudio describe el perfil, las actitudes, conocimiento y expectativas de las pacientes con osteoporosis posmenopáusica. Sujetos y métodos: Estudio epidemiológico, transversal, realizado en España. Participaron pacientes en tratamiento para osteoporosis posmenopáusica > 45 años. Se recogieron antecedentes personales y familiares, enfermedades y fármacos concomitantes, hábitos tóxicos, dietéticos y de actividad física, tipo de diagnóstico, tratamiento y cumplimiento. Todas las pacientes cumplimentaron un cuestionario de 17 preguntas sobre las actitudes, el conocimiento y las expectativas en relación con su afección. Resultados: Se incluyó a 1.179 pacientes con osteoporosis posmenopáusica válidas, con una edad media ± desviación estándar de 59,89 ± 7,53 años. Sólo el 22,6% mostró un conocimiento aceptable sobre la osteoporosis. Al 74,6% de las pacientes les preocupaba su enfermedad mucho/ bastante. El 53,3% describió su estado de salud como excelente/bueno. No obstante, el 63,6% indicó que necesitaba más información sobre la osteoporosis. Conclusiones: Este estudio ha evidenciado la necesidad de promover el correcto conocimiento de las pacientes con osteoporosis posmenopáusica sobre su afección (AU)


Objective: This study describes the profile and attitudes, knowledge and expectations of patients with postmenopausal osteoporosis. Subjects and methods: Epidemiological and cross-sectional study carried out in Spain. Participating patients were aged over 45 years and receiving treatment for postmenopausal osteoporosis. Data on personal and family medical history, diseases and concomitant medications, smoking and drinking habits, diet and physical activity, treatment and compliance were recorded. All patients completed a 17 item questionnaire on attitudes, knowledge and expectations related to their condition. Results: A total of 1179 valid patients with postmenopausal osteoporosis were included, with a mean age of 59.89 ± 7.53 years. Only 22.6% of the patients showed acceptable knowledge of osteoporosis. A large majority (74.6%) of the patients were very/quite concerned about their condition, and 53.3% described their health status as excellent/good. However, 63.6% of the patients indicated that they need more information about osteoporosis. Conclusions: The results of this study prove the need to provide accurate knowledge of their disease to patients with postmenopausal osteoporosis (AU)


Subject(s)
Humans , Female , Middle Aged , Health Knowledge, Attitudes, Practice , Postmenopause/physiology , Osteoporosis/diagnosis , Osteoporosis/epidemiology , Patient Participation/statistics & numerical data , Patient Participation/trends , Cross-Sectional Studies , Surveys and Questionnaires/standards , Surveys and Questionnaires , Patient Care/trends , Health Services/statistics & numerical data , Health Services/trends
16.
Menopause Int ; 15(3): 113-9, 2009 Sep.
Article in English | MEDLINE | ID: mdl-19723681

ABSTRACT

OBJECTIVE: The aim of this study was to evaluate the knowledge, attitudes and expectations of patients receiving treatment for postmenopausal osteoporosis, analysing the factors related to good compliance with treatment. METHODS: A national, epidemiological, cross-sectional study collected information on personal medical history, family history, bone densitometry, and treatment and compliance of patients over 45 years who were receiving treatment for osteoporosis and provided their informed consent. The patients anonymously completed a questionnaire about their knowledge of osteoporosis and the Morisky and Green treatment compliance evaluation test. RESULTS: Three hundred and fifteen specialists in gynaecology participated, recruiting 1179 patients with postmenopausal osteoporosis. The mean age was 59.9 years (standard deviation [SD] = 7.5). Only 22.6% of the patients showed an acceptable knowledge of osteoporosis (the criterion established was correct response to 80% of the questions). Treatment compliance was evaluated using a combination of Morisky-Green and Haynes-Sackett criteria. Of the patients 39.2% were classified as compliant, 74.6% of the patients were very or quite concerned about their condition and 53.3%; described their health status as excellent or good. However, 63.6% of the patients indicated that they needed more information about osteoporosis. The factors related to good compliance were the existence of one or no concomitant disease (odds ratio [OR] = 1.38, P = 0.025) and the type of knowledge about their disease (acceptable knowledge: OR = 1.33, P = 0.043). CONCLUSIONS: Correct knowledge about osteoporosis would increase the possibility of appropriate compliance with the prescribed treatment, thus reducing the risk of osteoporotic fractures.


Subject(s)
Bone Density Conservation Agents/therapeutic use , Health Knowledge, Attitudes, Practice , Medication Adherence , Osteoporosis, Postmenopausal/drug therapy , Aged , Cross-Sectional Studies , Female , Humans , Middle Aged , Osteoporosis, Postmenopausal/psychology
17.
Fertil Steril ; 92(6): 1947-52, 2009 Dec.
Article in English | MEDLINE | ID: mdl-18980762

ABSTRACT

OBJECTIVE: To investigate whether body mass index (BMI), abdominal obesity, and fat distribution in postmenopausal women influence quality of life. DESIGN: Cross-sectional survey. SETTING: Outpatient clinics in the hospital setting and private practices. PATIENT(S): 274 postmenopausal Spanish women, distributed by body phenotype, fat distribution (android or gynoid), and BMI. INTERVENTION(S): The Cervantes scale, a specific health-related quality of life (HRQOL) questionnaire. MAIN OUTCOME MEASURE(S): The quality of life of the obese and overweight patients was compared by age, sex, education, marriage, and municipality with matched healthy normal-weight controls. RESULT(S): Women of the pyknoid phenotype have worse general HRQOL, menopausal symptoms, and psychological and sexuality scores than athletic or lean women. Android fat distribution is also related to low global Cervantes scale scores. All scores on the Cervantes scale worsened with increasing BMI (>or=25). CONCLUSION(S): Pyknoid phenotype, android fat distribution, and a higher BMI are related to poor HRQOL.


Subject(s)
Body Fat Distribution/psychology , Body Mass Index , Menopause/psychology , Obesity, Abdominal/psychology , Quality of Life , Anthropometry , Cost of Illness , Cross-Sectional Studies , Female , Hot Flashes/psychology , Humans , Middle Aged , Surveys and Questionnaires
18.
Prog. obstet. ginecol. (Ed. impr.) ; 51(5): 265-270, mayo 2008. tab
Article in Spanish | IBECS | ID: ibc-139881

ABSTRACT

Objetivos: Conocer la distribución de los factores de riesgo asociados con la osteoporosis posmenopáusica en la población española. Pacientes y métodos: Estudio observacional multicéntrico de 1.779 mujeres posmenopáusicas. En función del diagnóstico densitométrico, se dividieron en 3 grupos: a) 450 mujeres con osteoporosis; b) 766 con osteopenia, y c) grupo control formado por 479 mujeres con valores de densidad mineral ósea normal. Resultados: Los factores de riesgo conocidos de osteoporosis se presentan en nuestras pacientes con similar distribución que en otros estudios. Además, se observa un efecto protector de la dieta basada en alimentos vegetales, junto al consumo moderado de alcohol, pescado y productos lácteos. Conclusión: Se confirmó la importancia de los factores de riesgo conocidos de osteoporosis. Además, en nuestra población se identificó el papel protector de la ingesta abundante de los alimentos que se incluyen en la llamada dieta mediterránea (AU)


Objective: To determinate the distribution of risk factors for osteoporosis in a Spanish population of postmenopausal women. Patients and methods: An observational multicenter study was carried out in 1779 postmenopausal women. The women were divided into three groups depending on the results of densitometry: 450 women with osteoporosis, 766 women with osteopenia, and 479 controls. Results: The distribution of known risk factors for osteoporosis in our patients was similar to that in other studies. Moreover, a protective effect of a diet based on vegetables, fish, dairy products, and moderate alcohol intake against developing osteoporosis was found. Conclusions: Our study confirms the importance of known risk factors for osteoporosis. Moreover, in our population, the beneficial effects of moderate alcohol ingestion and abundant intake of food included in the Mediterranean diet is identified (AU)


Subject(s)
Adult , Female , Humans , Osteoporosis, Postmenopausal/epidemiology , Bone Diseases, Metabolic/epidemiology , Postmenopause , Diet, Mediterranean , Epidemiological Monitoring/trends , Risk Factors , Densitometry , Menopause, Premature , Life Style , Sedentary Behavior , Exercise , Quality of Life , Feeding Behavior , Observational Study , Spain/epidemiology
19.
Reprod Sci ; 15(3): 305-11, 2008 Apr.
Article in English | MEDLINE | ID: mdl-18421025

ABSTRACT

In the present study, the authors look at an association of genetic variants within estrogen synthesis and signaling pathways and age at menarche (AAM) in Spanish women. They analyzed 9 polymorphisms in 6 different genes in 714 well-characterized postmenopausal women from Spain. They performed a quantitative trait locus study of these markers individually or in digenic combinations in relation to AAM. None of the studied markers, with the exception of the follicle-stimulating hormone receptor (P = .013), were significantly associated with AAM in the Spanish population, and no marker demonstrated an association of statistical significance after multiple testing corrections (P > .0055). In contrast, linear regression analysis suggests epistatic interactions including ESR1 and ESR2 loci in relation to AAM in the series (P = .003). The results suggest that epistatic interactions of ESR1 and ESR2 alleles could be associated with advancing AAM among Spanish women.


Subject(s)
Aging/genetics , Epistasis, Genetic , Estrogen Receptor alpha/genetics , Estrogen Receptor beta/genetics , Menarche/genetics , Polymorphism, Genetic , Adolescent , Age Factors , Aged , Aging/metabolism , Child , Estrogen Receptor alpha/metabolism , Estrogen Receptor beta/metabolism , Estrogens/biosynthesis , Female , Gene Frequency , Genotype , Humans , Logistic Models , Menarche/metabolism , Middle Aged , Phenotype , Postmenopause/genetics , Signal Transduction/genetics , Spain
20.
Eur J Obstet Gynecol Reprod Biol ; 136(2): 243-8, 2008 Feb.
Article in English | MEDLINE | ID: mdl-17208346

ABSTRACT

OBJECTIVE: To evaluate the effect of interleukin-2 (IL-2) on an experimental model of endometriosis. STUDY DESIGN: Double blind and randomized experimental prospective placebo-controlled study. Experimental endometriosis was induced in 66 three-month-old female Wistar rats, by auto-transplanting fragments of endometrium to the peritoneum. After four weeks, the size of each implant was measured in millimeters by laparotomy (L2), and animals were randomly distributed for intraperitoneal administration of human-IL-2, rat-IL-2 or placebo. Four weeks later, the implants were measured (L3) and a second dose was given. After four weeks, endometriosis size was evaluated again (L4). RESULTS: We found a reduction of experimental endometriosis at L3 that was only significant in IL-2 treated groups: 20.1% and 30.3% with human-IL-2 and rat-IL-2, respectively (p<0.001 with respect to L2 size), versus a non-significant reduction of 9.0% found in placebo group, but the differences were not statistically significant between groups. The decrease after a second dose (L4) was: 49.8%, 41.8% and 11.4% with human-IL-2, rat-IL-2 and placebo, respectively (p<0.001 in IL-2 groups versus L2 and L3, and p<0.05 in both groups versus placebo at L4). CONCLUSION: Intraperitoneal administration of IL-2 reduces experimental endometriosis, and this effect is similar using rat-IL-2 or human IL-2 (non specie-specific effect).


Subject(s)
Antineoplastic Agents/administration & dosage , Endometriosis/drug therapy , Interleukin-2/administration & dosage , Peritoneal Diseases/drug therapy , Animals , Female , Injections, Intraperitoneal , Random Allocation , Rats , Rats, Wistar
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