| Literature DB >> 29925283 |
Nur-Vaizura Mohamad1, Sok Kuan Wong1, Wan Nuraini Wan Hasan1, James Jam Jolly1, Mohd Fozi Nur-Farhana1, Soelaiman Ima-Nirwana1, Kok-Yong Chin1.
Abstract
Testosterone is the predominant gonadal androgen in men. Low testosterone levels are found to be associated with an increased in metabolic risk and systematic inflammation. Since adipose tissue is a source of inflammatory cytokines, testosterone may regulate inflammation by acting on adipose tissue. This review aimed to explore the role of testosterone in inflammation and its mechanism of action. Both animal studies and human studies showed that (1) testosterone deficiency was associated with an increase in pro-inflammatory cytokines; (2) testosterone substitution reduced pro-inflammatory cytokines. The suppression of inflammation by testosterone were observed in patients with coronary artery disease, prostate cancer and diabetes mellitus through the increase in anti-inflammatory cytokines (IL-10) and the decrease in pro-inflammatory cytokines (IL-1β, IL-6, and TNF-α). Despite these, some studies also reported a non-significant relationship. In conclusion, testosterone may possess anti-inflammatory properties but its magnitude is debatable. More evidence is needed to validate the use of testosterone as a marker and in the management of chronic inflammatory diseases.Entities:
Keywords: Androgen; inflammation; inflammatory markers; interleukins
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Year: 2018 PMID: 29925283 DOI: 10.1080/13685538.2018.1482487
Source DB: PubMed Journal: Aging Male ISSN: 1368-5538 Impact factor: 5.892