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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.
Afiliación
  • 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 en 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.

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Risk_factors_studies País/Región como asunto: Mexico Idioma: En Revista: Int J Impot Res Asunto de la revista: MEDICINA REPRODUTIVA / UROLOGIA Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Risk_factors_studies País/Región como asunto: Mexico Idioma: En Revista: Int J Impot Res Asunto de la revista: MEDICINA REPRODUTIVA / UROLOGIA Año: 2022 Tipo del documento: Article País de afiliación: Estados Unidos Pais de publicación: Reino Unido