Mahmoud Abd El-Mawla, A. Kandil, A. Hashim, A. Zidan
{"title":"Assessment of the effect of psoriasis on male sexual function","authors":"Mahmoud Abd El-Mawla, A. Kandil, A. Hashim, A. Zidan","doi":"10.21608/HA.2018.4550.1032","DOIUrl":null,"url":null,"abstract":"There is increasing evidence that psoriasis is associated with metabolic syndrome[4]. It was reported that there is a significant increased risk of metabolic syndrome in patients with psoriasis compared with controls even after adjustment for age, sex, race/ ethnicity, smoking, and C-reactive protein levels[5]. Genetic susceptibility and overlapping inflammatory pathways may be potential biological links underlying this association. The chronic and systemic T-helper-1-mediated and T-helper-17mediated inflammation of psoriasis characterized by increased levels of proinflammatory cytokines, such as tumor necrosis factor-α and interleukin-6, not only promotes epidermal hyperplasia in psoriasis but also antagonizes insulin signaling, alters adipokine expression, and mediates insulin resistance and obesity[6].","PeriodicalId":13018,"journal":{"name":"Human Andrology","volume":"11 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2019-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"1","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Human Andrology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.21608/HA.2018.4550.1032","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 1
Abstract
There is increasing evidence that psoriasis is associated with metabolic syndrome[4]. It was reported that there is a significant increased risk of metabolic syndrome in patients with psoriasis compared with controls even after adjustment for age, sex, race/ ethnicity, smoking, and C-reactive protein levels[5]. Genetic susceptibility and overlapping inflammatory pathways may be potential biological links underlying this association. The chronic and systemic T-helper-1-mediated and T-helper-17mediated inflammation of psoriasis characterized by increased levels of proinflammatory cytokines, such as tumor necrosis factor-α and interleukin-6, not only promotes epidermal hyperplasia in psoriasis but also antagonizes insulin signaling, alters adipokine expression, and mediates insulin resistance and obesity[6].