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Association of total and free testosterone with cardiovascular disease in a nationally representative sample of white, black, and Mexican American men.
Lopez, David S; Taha, Shaden; Gutierrez, Sirena; Villasante-Tezanos, Alejandro; Khalife, Wissam I; Alzweri, Laith; Markides, Kyriakos; Baillargeon, Jacques; Tsilidis, Konstantinos K.
Affiliation
  • Lopez DS; School of Public and Population Health, University of Texas Medical Branch, Galveston, TX, USA. davlopez@utmb.edu.
  • Taha S; School of Public and Population Health, University of Texas Medical Branch, Galveston, TX, USA.
  • Gutierrez S; School of Public and Population Health, University of Texas Medical Branch, Galveston, TX, USA.
  • Villasante-Tezanos A; Department of Epidemiology and Biostatistics, University of California, San Francisco, CA, USA.
  • Khalife WI; School of Public and Population Health, University of Texas Medical Branch, Galveston, TX, USA.
  • Alzweri L; Division of Cardiology, Internal Medicine- University of Texas Medical Branch, Galveston, TX, USA.
  • Markides K; Division of Urology, Department of Surgery, University of Texas Medical Branch, Galveston, TX, USA.
  • Baillargeon J; School of Public and Population Health, University of Texas Medical Branch, Galveston, TX, USA.
  • Tsilidis KK; School of Public and Population Health, University of Texas Medical Branch, Galveston, TX, USA.
Int J Impot Res ; 2022 Dec 29.
Article in En | MEDLINE | ID: mdl-36581758
Associations of total testosterone (T) and calculated free T with cardiovascular disease (CVD) remain poorly understood. Particularly how these associations vary according to race and ethnicity in a nationally representative sample of men. Data included 7058 men (≥20 years) from NHANES. CVD was defined as any reported diagnosis of heart failure (HF), coronary artery disease (CAD), myocardial infarction (MI), and stroke. Total T (ng/mL) was obtained among males who participated in the morning examination. Weighted multivariable-adjusted logistic regression models were conducted. We found associations of low T (OR = 1.57, 95% CI = 1.17-2.11), low calculated free T (OR = 1.53, 95% CI = 1.10-2.17), total T (Q1 vs Q5), and calculated free T (Q1 vs Q5) with CVD after adjusting for estradiol and SHBG. In disease specific analysis, low T increased prevalence of MI (OR = 1.72, 95% CI = 1.08-2.75) and HF (OR = 1.74, 95% CI = 1.08-2.82), but a continuous increment of total T reduced the prevalence of CAD. Similar inverse associations were identified among White and Mexican Americans, but not Blacks (OR = 0.93, 95% CI = 0.49-1.76). Low levels of T and calculated free T were associated with an increased prevalence of overall CVD and among White and Mexican Americans. Associations remained in the same direction with specific CVD outcomes in the overall population.

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Risk_factors_studies Country/Region as subject: Mexico Language: En Journal: Int J Impot Res Journal subject: MEDICINA REPRODUTIVA / UROLOGIA Year: 2022 Document type: Article Affiliation country: United States Country of publication: United kingdom

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Risk_factors_studies Country/Region as subject: Mexico Language: En Journal: Int J Impot Res Journal subject: MEDICINA REPRODUTIVA / UROLOGIA Year: 2022 Document type: Article Affiliation country: United States Country of publication: United kingdom