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New oral agents for erectile dysfunction: what is changing in our practice? 被引量:4
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作者 antonio aversa Andrea Fabbri 《Asian Journal of Andrology》 SCIE CAS CSCD 2001年第3期175-179,共5页
Erectile dysfunction (ED) is a highly prevalent disorder affecting an estimated 152 million men worldwide and isassociated with a variety of behavioral risk factors, such as cigarette smoking and excessive alcohol con... Erectile dysfunction (ED) is a highly prevalent disorder affecting an estimated 152 million men worldwide and isassociated with a variety of behavioral risk factors, such as cigarette smoking and excessive alcohol consumption, aswell as numerous age - related medical conditions, notably type-2 diabetes mellitus and cardiovascular disease. A ratio-nal step - wise approach which includes comprehensive medical and sexual history, a focused physical examination andessential laboratory tests such as fasting glucose, lipid profile and testosterone assay is to be preferred. Current diagnos-tic work - up does not recommend any of the specialized tests which were previously considered mandatory-i. e. penilepharmacotesting, Duplex ultrasound and nocturnal penile tumescence. Hormonal replacement therapy is appropriate onlyin the hypogonadal male with ED. Prior to direct intervention, the physician should consider altering modifiable riskfactors or causes, although frequently insufficient to reverse ED completely. When indicated, oral therapy with newmolecules (phosphodiesterase inhibitors or apomorphine) is the first - line treatment for the majority of patients becauseof potential benefits and lack of invasiveness. (Asian J Androl 2001 Sep; 3: 175-179 ) 展开更多
关键词 erectile dysfunction oral medicine THERAPY phosphodiesterase inhibitors APOMORPHINE nitric oxide
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Negative association between trunk fat, insulin resistance and skeleton in obese women
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作者 Emanuela A Greco Davide Francomano +9 位作者 Rachele Fornari Chiara Marocco Carla Lubrano Vincenza Papa Francesca Wannenes Luigi Di Luigi Lorenzo M Donini Andrea Lenzi antonio aversa Silvia Migliaccio 《World Journal of Diabetes》 SCIE CAS 2013年第2期31-39,共9页
AIM: To evaluate the potential interference of trunk fat (TF) mass on metabolic and skeletal metabolism. METHODS: In this cross-sectional study, 340 obese women (mean age: 44.8 ± 14 years; body mass index: 36.0 &... AIM: To evaluate the potential interference of trunk fat (TF) mass on metabolic and skeletal metabolism. METHODS: In this cross-sectional study, 340 obese women (mean age: 44.8 ± 14 years; body mass index: 36.0 ± 5.9 kg/m 2 ) were included. Patients were evaluated for serum vitamin D, osteocalcin (OSCA), inflammatory markers, lipids, glucose and insulin (homeostasis model assessment of insulin resistance, HOMA-IR) levels, and hormones profile. Moreover, all patients underwent measurements of bone mineral density (BMD;at lumbar and hip site) and body composition (lean mass, total and trunk fat mass) by dual-energy X-ray absorptiometry. RESULTS: Data showed that: (1) high TF mass was inversely correlated with low BMD both at lumbar (P < 0.001) and hip (P < 0.01) sites and with serum vitamin D (P < 0.0005), OSCA (P < 0.0001) and insulin-like growth factor-1 (IGF-1; P < 0.0001) levels; (2) a positive correlation was found between TF and HOMA-IR (P < 0.01), fibrinogen (P < 0.0001) and erythrocyte sedimentation rate (P < 0.0001); (3) vitamin D levels were directly correlated with IGF-1 (P < 0.0005), lumbar (P < 0.006) and hip (P < 0.01) BMD; and (4) inversely with HOMA-IR (P < 0.001) and fibrinogen (P < 0.0005). Multivariate analysis demonstrated that only vitamin D was independent of TF variable. CONCLUSION: In obese women, TF negatively correlates with BMD independently from vitamin D levels. Reduced IGF-1 and increased inflammatory markers might be some important determinants that account for this relationship. 展开更多
关键词 Obesity SKELETON VITAMIN D OSTEOCALCIN Insulin resistance TRUNK FAT Inflammation
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Systemic and metabolic effects of PDE5-inhibitor drugs
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作者 antonio aversa 《World Journal of Diabetes》 SCIE CAS 2010年第1期3-7,共5页
Phosphodiesterase type-5 inhibitor(PDE5-i) drugs were first marketed in 1998(sildenafil) for 'on-demand' treatment of male erectile dysfunction(ED) of any origin.They selectively inhibit intrapenile PDE5 isoen... Phosphodiesterase type-5 inhibitor(PDE5-i) drugs were first marketed in 1998(sildenafil) for 'on-demand' treatment of male erectile dysfunction(ED) of any origin.They selectively inhibit intrapenile PDE5 isoenz yme which in turn increases intracellular cyclic guanosine monophosphate levels,thus resulting in prolonged relaxation of cavernosum smooth muscle cells and facilitating the erectile proce ss.Since 2003,two new molecules(tadalafil and vard e na fil) have been introduced,resulting in greater interest in these compounds and leading patients to ask for more prescriptions from their doctors.The vast use of PDE5-i in diabetic and cardiovascular ED patients led resea rchers to investigate their possible extra sexual effects.Several studies investigating their effects on endothelium,coronary and pulmonary circulation,inf erior oesophageal sphincter and kidney functions have appeared and,finally,sildenafil was approved for the treatment of pulmonary arterial hyperten s ion.Recent animal studies highlighted a possible interaction between chronic PDE5 inhibition and glucose homeostasis which occurs through a marked improvem ent of high fat diet induced insulin resistance.If this data is extended to humans,a new scenario will be opened for the chronic use of PDE5-i for sexual rehabilit ation along with cardiovascular and metabolic benefits. 展开更多
关键词 ENDOTHELIUM INSULIN Cardio protection Diabetes ATHEROSCLEROSIS Erectile DYSFUNCTION
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