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1.
Eur J Obstet Gynecol Reprod Biol ; 250: 235-240, 2020 Jul.
Article in English | MEDLINE | ID: mdl-32497923

ABSTRACT

Polycystic Ovary Syndrome is a very complex syndrome, with typical hormonal and metabolic features. In adolescent girls, this condition shows particular characteristics which are in common with adult sign and symptoms, often making the diagnosis difficult. On the other side, treatment strategy aims to manage the different aspects of this syndrome, and is generally based on lifestyle/diet modifications possibly associated with use of estroprogestins, anti-androgens and insulin-sensitizing agents. In this article, we will briefly review both diagnosis and clinical approach to polycystic ovary syndrome in adolescence which still remain a matter of debate in view of the peculiar hormonal milieu of that critical period.


Subject(s)
Insulin Resistance , Metformin , Polycystic Ovary Syndrome , Adolescent , Adult , Female , Humans , Hypoglycemic Agents , Insulin , Polycystic Ovary Syndrome/diagnosis , Polycystic Ovary Syndrome/therapy
2.
Gynecol Endocrinol ; 36(3): 185-189, 2020 Mar.
Article in English | MEDLINE | ID: mdl-32093515

ABSTRACT

The scientific interest and the number of papers dealing with vitamin D supplementation has greatly grown in the last decades. Unfortunately, expert consensus on many clinical aspects of this topic is still lacking. In addition, data coming from recent clinical trials and meta-analyses seem to strongly put into doubt the real benefit of vitamin D supplementation, on both skeletal and extra-skeletal outcomes. This is further confusing since they seem to completely contradict the considerable body of evidence provided from previous epidemiological studies. This paper aims to analyze these new data in order to shed light onto the debated issues.


Subject(s)
Cardiovascular Diseases/prevention & control , Diabetes Mellitus, Type 2/prevention & control , Fractures, Bone/prevention & control , Neoplasms/prevention & control , Vitamin D Deficiency/drug therapy , Vitamin D/therapeutic use , Vitamins/therapeutic use , Accidental Falls/prevention & control , Dietary Supplements , Humans , Meta-Analysis as Topic , Randomized Controlled Trials as Topic
3.
Gynecol Endocrinol ; 36(4): 285-288, 2020 Apr.
Article in English | MEDLINE | ID: mdl-31711322

ABSTRACT

Vitamin K2 (vit K2) belongs to a large group of fat-soluble compounds whose formulation is MK (menaquinone) (MK-2 to MK-14), that seem to be involved in different biological functions. In particular, vit K2 has been recently recognized as efficacious and safe in treatment of bone loss, as it contributes to structural integrity of osteocalcin (OC), the major non-collagenous protein typically found in bone matrix. Several studies proved low vit K2 intake is linked to bone loss and to increased fracture risk in both sexes. Nowadays, vit K2 supplementation is considered a significant manner to enhance the association of calcium and vitamin D whose role on bone health is largely recognized. On the other hand, vit K2 may be used alone or with other drugs to preserve bone quality/strength from skeletal degradation after menopause and/or in patients affected by secondary osteoporosis. In this paper, we review the most recent data about vit K2 on skeleton.


Subject(s)
Bone and Bones/drug effects , Bone and Bones/metabolism , Vitamin K 2/pharmacology , Bone Density/drug effects , Bone Density/physiology , Bone Diseases, Metabolic/epidemiology , Bone Diseases, Metabolic/etiology , Bone Diseases, Metabolic/therapy , Calcium/blood , Dietary Supplements , Female , Humans , Male , Osteoporosis/epidemiology , Osteoporosis/etiology , Osteoporosis/prevention & control , Osteoporosis, Postmenopausal/epidemiology , Osteoporosis, Postmenopausal/etiology , Osteoporosis, Postmenopausal/prevention & control , Risk Factors , Vitamin D/blood , Vitamin K 2/blood
4.
Climacteric ; 22(3): 303-306, 2019 06.
Article in English | MEDLINE | ID: mdl-30626218

ABSTRACT

Nowadays, postmenopausal women are largely undertreated. Analysis of conflicting results among different studies suggests that hormone replacement therapy (HRT) can prevent osteoporosis and cardiovascular disease in symptomatic, early postmenopausal women. In fact, climacteric symptoms are related to an increased risk of chronic conditions, including hypertension and cardiovascular disease. Different scientific societies have pointed out that patient selection, timing of initiation, and the choice of the type and dose of HRT used are the major determinants of the ultimate effect of HRT on women's health and quality of life in selected women. HRT may prevent chronic conditions when started in symptomatic women before the age of 60 years or within 10 years of the onset of the menopause, taking into consideration the characteristics and risk profiles of each given woman. The bulk of scientific evidence from preclinical, clinical, epidemiological, and also randomized studies indicates that wisely selected HRT is generally useful and rarely dangerous. Following simple and well-established rules, HRT benefits outweigh all of the possible risks. Progestogen choice can make the difference in terms of cardiovascular disease benefits.


Subject(s)
Chronic Disease/prevention & control , Estrogen Replacement Therapy , Postmenopause/physiology , Age Factors , Cardiovascular Diseases/prevention & control , Estrogen Replacement Therapy/methods , Female , Humans , Middle Aged , Osteoporosis, Postmenopausal/prevention & control , Progestins/administration & dosage , Quality of Life
6.
Climacteric ; 20(4): 306-312, 2017 Aug.
Article in English | MEDLINE | ID: mdl-28453310

ABSTRACT

Menopausal disorders may include shorter-term symptoms, such as hot flushes and night sweats (vasomotor symptoms, VMS) and longer-term chronic conditions such as cardiovascular disease (CVD), osteoporosis, and cognitive impairment. Initially, no clear link between the shorter-term symptoms and longer-term chronic conditions was evident and these disorders seemed to occur independently from each other. However, there is a growing body of evidence demonstrating that VMS may be a biomarker for chronic disease. In this review, the association between VMS and a range of chronic postmenopausal conditions including CVD, osteoporosis, and cognitive decline is discussed. Prevention of CVD in women, as for men, should be started early, and effective management of chronic disease in postmenopausal women has to start with the awareness that VMS during menopause are harbingers of things to come and should be treated accordingly.


Subject(s)
Biomarkers , Cardiovascular Diseases/epidemiology , Chronic Disease/epidemiology , Hot Flashes/epidemiology , Menopause/physiology , Vasomotor System/physiopathology , Adult , Aged , Bone Density , Cognition Disorders/epidemiology , Estrogens/deficiency , Female , Hot Flashes/physiopathology , Humans , Middle Aged , Osteoporosis, Postmenopausal/epidemiology , Risk Factors , Sweating/physiology
7.
Gynecol Endocrinol ; 31(8): 590-4, 2015.
Article in English | MEDLINE | ID: mdl-26036806

ABSTRACT

Osteoporosis (OP) and cardiovascular diseases (CVD) are the most important causes of mortality and morbility in the elderly. Lots of studies showed a correlation between bone loss and cardiovascular risk mediated by the vascular calcification. The relationship between OP and CVD could be firstly explained by their common risk factors such as age, smoking, alcohol consumption, physical activity and menopause. However, other different hypotheses were proposed to clarify this link. Multiple factors, for example bone morphogenetic proteins, osteoprotegerin, receptor activator of nuclear factor κB ligand, parathyroid hormone, phosphate, oxidized lipids and vitamins D and K seemed to be involved in both conditions, indicating a possible common pathophysiologic mechanism. We review and discuss the available data describing this association. Further studies are necessary to better investigate similarities between OP and CVD.


Subject(s)
Cardiovascular Diseases/complications , Osteoporosis/complications , Bone Morphogenetic Proteins/metabolism , Cardiovascular Diseases/metabolism , Cardiovascular Diseases/physiopathology , Humans , Osteoporosis/metabolism , Osteoporosis/physiopathology , Parathyroid Hormone/metabolism , RANK Ligand/metabolism , Risk Factors
8.
J Food Prot ; 75(10): 1859-61, 2012 Oct.
Article in English | MEDLINE | ID: mdl-23043838

ABSTRACT

The aim of this study was to investigate the hygiene performance of a camel (Camelus dromedarius) slaughtering process as carried out with the traditional method in the Sahrawi refugee camps located in southwestern Algeria. The camel slaughtering process in this region differs significantly from that carried out in commercial abattoirs. Slaughtering is performed outdoors in desert areas, and dehiding of the carcass is approached via the dorsoventral route rather than the classic ventrodorsal route. Samples were taken from 10 camel carcasses from three different areas: the hide, the carcass meat immediately after dehiding, and the meat after final cutting. Enterobacteriaceae counts (EC) were enumerated employing conventional laboratory techniques. Carcass meat samples resulted in EC below the detection limit more frequently if the hide samples from the same carcass had also EC counts below the detection limit. Because of the low number of trials, the calculation of statistical significance of the results was not possible. Further experimental research is needed in order to validate the results presented in this study. The comparison of the microbiological hygiene performance between dorsal dehiding and traditional ventral dehiding of slaughtered animals could serve to validate the hypothesis of the potential positive impact of the dorsal dehiding method in carcass meat hygiene.


Subject(s)
Camelus , Enterobacteriaceae/isolation & purification , Euthanasia, Animal/methods , Food Contamination/analysis , Food Handling/methods , Meat/microbiology , Abattoirs , Algeria , Animals , Camelus/microbiology , Colony Count, Microbial , Food Contamination/prevention & control , Humans , Hygiene , Meat/standards , Risk Assessment
9.
Br Dent J ; 212(1): 4, 2012 Jan 13.
Article in English | MEDLINE | ID: mdl-22240669
10.
J Eur Acad Dermatol Venereol ; 26(11): 1364-71, 2012 Nov.
Article in English | MEDLINE | ID: mdl-22011217

ABSTRACT

BACKGROUND: Despite it is accepted that acne is mostly caused by an hyper-responsiveness of the pilo-sebaceous unit to normal circulating androgen hormones, in a few patients, especially women, acneic lesions can be associated with increased serum androgen levels (hyperandrogenism), of which polycystic ovary syndrome (PCOS) is the most common cause. In women with acne and proven PCOS therapy with estroprogestins (EPs) can be an excellent option. OBJECTIVE: The aim of the study was to assess the effects of two estroprogestins (EPs), ethinyl-estradiol (EE) 30 mcg/drospirenone (DRSP) 3 mg, and ethinyl-estradiol (EE) 30 mcg/chlormadinone acetate (CMA) 2 mg, both on increased serum androgen levels and on several skin parameters in women affected by mild to severe acne and polycystic ovary syndrome (PCOS). METHODS: Fifty-nine women were randomized to receive EE/DRSP (n = 32) or EE/CMA (n = 27) for six months. Evaluation of serum androgen levels, grading of acne and hirsutism (respectively with Pillsbury and Ferriman-Gallwey score) and non-invasive assessment of skin hydration, transepidermal water loss (TEWL) and skin homogeneity were performed at baseline, at 3 and 6 months (end of treatment). RESULTS: Both treatments were well tolerated and showed a significant improvement of skin and hormonal parameters, although EE/DRSP showed a more potent effect on acne and seborrhea. CONCLUSIONS: Estroprogestins represent an effective and safe treatment in women with acne and polycystic ovary syndrome (PCOS). Nevertheless, the combination EE 30 mcg/DRSP 3 mg appears to be a more potent therapeutic option.


Subject(s)
Acne Vulgaris/drug therapy , Contraceptives, Oral, Combined/therapeutic use , Estrogens/therapeutic use , Polycystic Ovary Syndrome/drug therapy , Progestins/therapeutic use , Acne Vulgaris/complications , Adolescent , Adult , Estrogens/administration & dosage , Female , Humans , Polycystic Ovary Syndrome/complications , Progestins/administration & dosage
11.
Minerva Ginecol ; 63(3): 305-14, 2011 Jun.
Article in Italian | MEDLINE | ID: mdl-21654615

ABSTRACT

Prevention of osteopenia/osteoporosis in postmenopausal patients can reduce fracture risk. In this view, the use of Selective Estrogen Receptor Modulators (SERMs) appear to be important in managing this condition. Bazedoxifene Acetate (BZA) is a third-generation SERM that showed to protect bone mass in postmenopausal women with osteopenia, and to reduce vertebral fracture risk in osteoporotic postmenopausal women; moreover, BZA decreased the non-vertebral fracture risk in a subgroup of patients at high-risk for fracture in comparison to placebo. BZA showed no stimulating effects on endometrium and breast. BZA can be a valid option in management of osteopenia/osteoporosis in postmenopause.


Subject(s)
Indoles/therapeutic use , Osteoporosis, Postmenopausal/prevention & control , Selective Estrogen Receptor Modulators/therapeutic use , Female , Humans , Raloxifene Hydrochloride/therapeutic use
12.
Minerva Ginecol ; 62(6): 509-13, 2010 Dec.
Article in Italian | MEDLINE | ID: mdl-21079572

ABSTRACT

AIM: evaluate the efficacy of an estroprogestin EP containing 20 mcg ethinilestradiol (EE) and 3 mg drospirenone (DRSP) in the treatment of hyperandrogenism. METHODS: In this study, twenty hyperandrogenic patients were treated with an EP containing EE 20 mcg and DRSP 3 mg in 24+4 regimen for three months. Skin evaluation was performed both quantitatively and qualitatively. RESULTS AND CONCLUSION: This EP combination showed, after a short-term treatment (three months) to decrease significantly seborrhea, acne, and circulating androgens (testosterone, deidroepiandrosterone sulphate, and androstenedione), while increased sex hormone binding globulin levels. Moreover, this EE 20 mcg/DRSP 3mg EP combination changed some parameters of skin quality, increasing corneometry (a parameter related to skin hydration), and reduced trans epidermal water loss (TEWL, a parameter related to skin evaporation), and erythema (a parameter related to skin inflammation). These results could be taken into account in individualizing the treatment of hyperandrogenic patients.


Subject(s)
Androstenes/administration & dosage , Estrogens/administration & dosage , Ethinyl Estradiol/administration & dosage , Hyperandrogenism/drug therapy , Mineralocorticoid Receptor Antagonists/administration & dosage , Norpregnenes , Administration, Oral , Adolescent , Adult , Drug Combinations , Female , Humans , Hyperandrogenism/diagnosis , Severity of Illness Index , Time Factors , Treatment Outcome
13.
Minerva Ginecol ; 62(5): 483-95, 2010 Oct.
Article in Italian | MEDLINE | ID: mdl-20938431

ABSTRACT

Progestins are a group of different compounds sharing the ability to induce secretory changes on a endometrium pretreated with estrogen, while they are different in some abilities, for example the interaction with receptors other than progestin receptor, as androgenic or mineralocorticoid receptor. Some progestins have antiandrogenic properties and are used in treating hyperandrogenic manifestations (seborrhea, acne, hirsutism). The different clinical pharmacology of the various progestins is the basis for an individualized treatment in different clinical conditions. Key words.


Subject(s)
Progestins , Female , Humans , Hyperandrogenism/drug therapy , Progesterone/physiology , Progestins/metabolism , Progestins/pharmacology , Progestins/therapeutic use
14.
Climacteric ; 12(6): 533-40, 2009 Dec.
Article in English | MEDLINE | ID: mdl-19905905

ABSTRACT

OBJECTIVES: To assess perception of sexuality and awareness of the impact of testosterone on sexual desire in a clinical sample of Italian women with surgical menopause. METHODS: In the present cross-sectional study, a structured interview on sexuality-related menopausal symptoms, attitudes towards sexuality and menopausal profile was administered to 568 women (age range 35-69 years) with bilateral oophorectomy with and without hysterectomy for benign conditions. RESULTS: The majority of women (58% yes; 36% most of the time) reported they were satisfied with their sexual life before surgical menopause. After oophorectomy, 79.3% noted the appearance/worsening of vaginal dryness, whereas the reduction of sexual desire was reported by 78.7%. Women with low sexual desire (n = 436) were significantly distressed (59.7%) and reported an impairment (24.8% yes/yes, very much) in the relationship with their partner. Sexual reactions of the partner reported by women included reduced sexual desire (17.8%), sexual dysfunction (5.1%) and fears of giving pain/lack of pleasure (28.3%). A high number of women (88.2%) would be willing to discuss sexual matters with their doctors and would consider therapeutic options. Only 36.8% were aware that a lack of testosterone might impact on sexual desire but 71% would like to know more about the role of testosterone. Hormone replacement therapy was used by 38.4% of the women. CONCLUSIONS: These data suggest that women experience significant vaginal dryness and low sexual desire and report a significant distress in the relationship with their partner after surgical menopause. Sexual counseling is mandatory in order to discuss potential therapeutic strategies, including testosterone use.


Subject(s)
Menopause , Ovariectomy/adverse effects , Sexual Dysfunction, Physiological/epidemiology , Testosterone/therapeutic use , Adult , Aged , Cross-Sectional Studies , Female , Humans , Middle Aged , Sexual Dysfunction, Physiological/drug therapy , Sexual Dysfunction, Physiological/etiology , Sexual Dysfunctions, Psychological/drug therapy , Sexual Dysfunctions, Psychological/epidemiology , Sexual Dysfunctions, Psychological/psychology , Surveys and Questionnaires , Testosterone/physiology , Vaginal Diseases/etiology
15.
Minerva Ginecol ; 61(5): 459-63, 2009 Oct.
Article in Italian | MEDLINE | ID: mdl-19749678

ABSTRACT

Progestogens are used in clinical practice in some conditions. Their effects depend on their chemical structure, pharmacokinetics, pharmacodynamics, with important differences among various progestogens. Generally, progestins are classified according to their parent molecule, of which often they keep some features. Derivatives of 19-nor-progesterone are characterized by high selectivity of action on progestin receptor. In particular, nomegestrol acetate (NomAc) shows an important progestational potency, neutral gluco-lipid profile, and antigonadotropic activity. It is used for treating menstrual cycle disorders and for hormone replacement therapy in menopause in association with an estrogen. In future, thanks to its antigonadotropic activity, NomAc will be used in estroprogestin combinations in fertile women, thus taking advantage of its tolerability profile and obtaining numerous non-contraceptive benefits as well.


Subject(s)
Megestrol/pharmacology , Norpregnadienes/pharmacology , Biological Availability , Breast Diseases/drug therapy , Drug Therapy, Combination , Estradiol/administration & dosage , Estradiol/analogs & derivatives , Female , Hormone Replacement Therapy , Humans , Hypothalamo-Hypophyseal System/drug effects , Inactivation, Metabolic , Megestrol/adverse effects , Megestrol/chemistry , Megestrol/pharmacokinetics , Megestrol/therapeutic use , Menopause , Menstruation Disturbances/drug therapy , Molecular Structure , Norpregnadienes/adverse effects , Norpregnadienes/chemistry , Norpregnadienes/pharmacokinetics , Norpregnadienes/therapeutic use , Ovulation Inhibition/drug effects , Protein Binding
16.
Minerva Ginecol ; 60(3): 239-43, 2008 Jun.
Article in Italian | MEDLINE | ID: mdl-18547986

ABSTRACT

AIM: This study evaluated hormonal and skin effects in hyperandrogenic women of an oral estroprogestin (EP) association containing ethynilestradiol 30 mcg plus drospirenone 3 mg. METHODS: Thirty two women with signs and symptoms of hyperandrogenism (seborrhea, acne, increased hair); hormonal assessment (follicle-stimulating hormone, [FSH]; luteinizing hormone, LH; 17-hydroxi-progesterone, 17OHP; androstenedione, A, testosterone, T; dehydroepiandrosterone sulfate, DHEAS; sex hormone binding globulin, [SHBG]; Free Androgen Index [FAI, Tx100/SHBG] was performed before the start of treatment, and after 3 and 6 months of administration of EP. The impact on seborrhea, acne, and hair pattern (Ferriman-Gallwey score) was assessed, and, by non-invasive technique, hydration, water transpiration, and homogeneity of the skin were evaluated. RESULTS: Treatment with this EP for 6 months decreased significantly circulating androgen levels (A, T, DHEAS) and FAI, and increased SHBG levels, also reducing seborrhea, acne and hirsutism. Moreover, EE/DRSP increased hydration and improved overall appearance of skin surface (homogeneity). CONCLUSION: Treatment with EE 30 mcg+DRSP 3 mg improves hormonal pattern and skin appearance in hyperandrogenic patients, potentially with subsequent, beneficial effects on quality of life of these women.


Subject(s)
Androstenes/therapeutic use , Dermatitis, Seborrheic/drug therapy , Ethinyl Estradiol/pharmacology , Hyperandrogenism/drug therapy , Hyperandrogenism/physiopathology , Mineralocorticoid Receptor Antagonists/therapeutic use , Norpregnenes/pharmacology , Skin/drug effects , Adolescent , Adult , Drug Combinations , Ethinyl Estradiol/administration & dosage , Ethinyl Estradiol/therapeutic use , Female , Humans , Hyperandrogenism/diagnosis , Norpregnenes/therapeutic use , Severity of Illness Index , Treatment Outcome
18.
Minerva Ginecol ; 56(4): 349-52, 2004 Aug.
Article in Italian | MEDLINE | ID: mdl-15377983

ABSTRACT

Urinary incontinence is a disease able to decrease the quality of life of affected women. It shows a prevalence of about 35% among adult women. Pharmacological treatment can be used when pelvic floor muscle training has failed or when it could be better to postpone or avoid surgery. Duloxetine, a selective serotonin and noradrenaline reuptake inhibitor (SNRI), can act effectively in treating stress urinary incontinence.


Subject(s)
Adrenergic Uptake Inhibitors/therapeutic use , Thiophenes/therapeutic use , Urinary Incontinence/drug therapy , Duloxetine Hydrochloride , Female , Humans , Treatment Outcome , Urinary Incontinence/diagnosis
19.
Neurology ; 62(2): 301-3, 2004 Jan 27.
Article in English | MEDLINE | ID: mdl-14745075

ABSTRACT

The authors investigated whether testosterone levels and testosterone availability differ between older lean subjects with and without Alzheimer's disease (AD). Sex hormone binding globulin (SHBG) and estradiol levels were higher, whereas the free androgenization index (FAI) was lower, in lean subjects with AD than in lean subjects without AD. Factors involved in the increase of SHBG secretion could have an important role in the lower testosterone availability of subjects with AD.


Subject(s)
Alzheimer Disease/blood , Testosterone/blood , Aged , Body Mass Index , Dehydroepiandrosterone Sulfate/blood , Estradiol/blood , Female , Humans , Hydrocortisone/blood , Male , Sex Hormone-Binding Globulin/analysis , Testosterone/deficiency , Thinness/blood
20.
Gynecol Endocrinol ; 15(4): 265-71, 2001 Aug.
Article in English | MEDLINE | ID: mdl-11560099

ABSTRACT

The attempt to decrease the hormonal components of combined estrogen/progestin-containing oral formulations has led to use of low-dose formulations. The monophasic formulation containing ethinyl estradiol 20 micrograms (EE20) plus gestodene 75 micrograms (GSD75) was studied in an open, non-comparative, multicenter, clinical trial investigating its efficacy, safety, effects on body weight, blood pressure and sexual function. To evaluate the impact on sexual function, the Golombok Rust Questionnaire on Sexual Satisfaction (GRISS) was used. The study population comprised 216 women treated for 1 year. The EE20/GSD75 formulation did not show any significant effect on blood pressure, hematological parameters, body weight or sexual function. The treatment was well tolerated with a high compliance rate by the patients, with a low rate of estrogen-dependent symptoms. Moreover, there was no overall effect on sexual function, with no disturbance of sexual behavior or activity. In conclusion, our data show that the EE20/GSD75 has a very good tolerability profile, without any significant side-effects.


Subject(s)
Contraceptives, Oral, Combined/therapeutic use , Ethinyl Estradiol/administration & dosage , Norpregnenes/administration & dosage , Adult , Blood Pressure , Body Weight , Contraceptives, Oral, Combined/administration & dosage , Drug Administration Schedule , Drug Combinations , Female , Humans , Italy , Patient Compliance , Sexuality , Surveys and Questionnaires , Treatment Outcome
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