Using human genetics to understand the disease impacts of testosterone in men and women.
Katherine S RuthFelix R DayJessica TyrrellDeborah J ThompsonAndrew R WoodAnubha MahajanRobin N BeaumontLaura WittemansSusan MartinAlexander Siegfried BuschAbdullah Mesut ErzurumluogluBenjamin HollisTracy A O'Maranull nullMark I McCarthyClaudia LangenbergDouglas F EastonNicholas J WarehamStephen BurgessAnna MurrayKen K OngTimothy M FraylingJohn R B PerryPublished in: Nature medicine (2020)
Testosterone supplementation is commonly used for its effects on sexual function, bone health and body composition, yet its effects on disease outcomes are unknown. To better understand this, we identified genetic determinants of testosterone levels and related sex hormone traits in 425,097 UK Biobank study participants. Using 2,571 genome-wide significant associations, we demonstrate that the genetic determinants of testosterone levels are substantially different between sexes and that genetically higher testosterone is harmful for metabolic diseases in women but beneficial in men. For example, a genetically determined 1 s.d. higher testosterone increases the risks of type 2 diabetes (odds ratio (OR) = 1.37 (95% confidence interval (95% CI): 1.22-1.53)) and polycystic ovary syndrome (OR = 1.51 (95% CI: 1.33-1.72)) in women, but reduces type 2 diabetes risk in men (OR = 0.86 (95% CI: 0.76-0.98)). We also show adverse effects of higher testosterone on breast and endometrial cancers in women and prostate cancer in men. Our findings provide insights into the disease impacts of testosterone and highlight the importance of sex-specific genetic analyses.
Keyphrases
- polycystic ovary syndrome
- replacement therapy
- genome wide
- body composition
- prostate cancer
- type diabetes
- insulin resistance
- dna methylation
- public health
- healthcare
- smoking cessation
- gene expression
- endothelial cells
- emergency department
- cardiovascular disease
- pregnancy outcomes
- copy number
- adipose tissue
- risk assessment
- cross sectional
- cervical cancer screening
- skeletal muscle
- social media
- postmenopausal women
- young adults
- electronic health record
- health promotion