Relation of total and free testosterone and sex hormone-binding globulin with cardiovascular risk factors in men aged 24–45 years. The Cardiovascular Risk in Young Finns Study

2012 ◽  
Vol 222 (1) ◽  
pp. 257-262 ◽  
Author(s):  
Sonja Firtser ◽  
Markus Juonala ◽  
Costan G. Magnussen ◽  
Antti Jula ◽  
Britt-Marie Loo ◽  
...  
Metabolism ◽  
2001 ◽  
Vol 50 (8) ◽  
pp. 882-888 ◽  
Author(s):  
Jesper Gyllenborg ◽  
Susanne L. Rasmussen ◽  
Knut Borch-Johnsen ◽  
Berit L. Heitmann ◽  
Niels E. Skakkeb[aelig ]k ◽  
...  

2018 ◽  
Vol 26 (8) ◽  
pp. 847-854 ◽  
Author(s):  
Anne Wang ◽  
Stefan Arver ◽  
Kurt Boman ◽  
Hertzel C Gerstein ◽  
Shun Fu Lee ◽  
...  

Aims: Testosterone and its binding protein sex hormone-binding globulin have been associated with cardiovascular disease and dysglycaemia. However, information on the prognostic implication in patients at high cardiovascular risk with dysglycaemia is inconsistent. The study objective was to determine whether testosterone and/or sex hormone-binding globulin predict cardiovascular events or death in dysglycaemic patients. Methods: Dysglycaemic males at high cardiovascular risk ( n = 5553) who participated in the Outcome Reduction with an Initial Glargine Intervention (ORIGIN) trial and provided baseline blood samples were studied. Testosterone and sex hormone-binding globulin were measured at baseline and used to estimate free testosterone. Low levels of total and free testosterone were defined as ≤300 ng/dl and ≤7 ng/dl, respectively. Patients were followed for six years for cardiovascular events (defined as the composite of cardiovascular death, non-fatal myocardial infarction or stroke) and all-cause mortality. Results: The mean total and free testosterone levels were 416.6 ng/dl and 8.4 ng/dl, and low levels were present in 13% and 37% of the patients. The median sex hormone-binding globulin level was 35 nmol/l. In Cox regression models adjusted for age, previous diseases and pharmacological treatment, neither total nor free testosterone predicted cardiovascular events. However, a one-standard-deviation increase in sex hormone-binding globulin predicted both cardiovascular events (hazard ratio 1.07; 95% confidence interval 1.00–1.14; p = 0.03) and all-cause mortality (hazard ratio 1.13; 95% confidence interval 1.06–1.21; p < 0.01). Conclusion: Sex hormone-binding globulin, but not total testosterone, predicts cardiovascular disease and all-cause mortality in dysglycaemic males at high cardiovascular risk.


2021 ◽  
Vol 18 (2) ◽  
pp. 147916412110024
Author(s):  
Anne Wang ◽  
Hertzel C Gerstein ◽  
Shun Fu Lee ◽  
Sibylle Hess ◽  
Guillaume Paré ◽  
...  

Aims: Total and free testosterone and sex hormone-binding globulin may affect cardiovascular prognosis in women. The objective was to study the association between sex hormones and prognosis in women with dysglycemia and high cardiovascular risk. Methods: This epidemiological report included dysglycemic women from the Outcome Reduction with an Initial Glargine Intervention trial ( n = 2848) with baseline total testosterone and sex hormone-binding globulin. Free testosterone was calculated with the Vermeulen formula. Cox regression analyses adjusted for variables including age, previous diseases and pharmacological treatments were used to estimate the association between these levels and the composite cardiovascular outcome (death from cardiovascular causes, nonfatal myocardial infarction or nonfatal stroke) and all-cause mortality per one standard deviation. Results: Patients (73% post-menopausal) were followed for a median of 6.1 years during which 377 cardiovascular events and 389 deaths occurred. In Cox analyses, total and free testosterone were not associated with any outcomes, but sex hormone-binding globulin was related to all-cause mortality in age adjusted (HR 1.15; 95% CI 1.06–1.24; p < 0.01) and fully adjusted analyses (HR 1.14; 95% CI 1.05–1.24; p < 0.01). Conclusions: Increasing levels of baseline sex hormone-binding globulin were associated with an increased risk of all-cause mortality in dysglycemic women at high cardiovascular risk. Trial registration ClinicalTrials.gov no. NCT00069784.


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