Literature DB >> 12489566

Bio-available testosterone levels fall acutely following myocardial infarction in men: association with fibrinolytic factors.

Peter J Pugh1, Kevin S Channer, Helen Parry, Tom Downes, T Hugh Jone.   

Abstract

The effect of acute myocardial infarction on plasma levels of testosterone in men is unclear. No previous studies have evaluated the bio-available fraction of testosterone. Low plasma testosterone levels have been associated with several risk factors for myocardial infarction, including an unfavorable fibrinolytic profile. In a prospective, case control study, we examined changes in plasma levels of sex hormones, including bio-available testosterone, in patients with acute myocardial infarction and in control subjects. In addition, changes in hormone levels in patients were compared with alterations in the fibrinolytic profile. Thirty male patients admitted with chest pain were studied. Twenty two had acute myocardial infarction and eight had non-specific chest pain. Plasma levels of total and bio-available testosterone, 17beta-estradiol, sex hormone binding globulin and insulin were measured at baseline and throughout admission. In addition, fibrinolytic factors (plasminogen activator inhibitor-1 (PAI-1), tissue plasminogen activator (tPA) and fibrinogen) were measured in patients who received fibrinolysis. Height and weight, and the subsequent development of heart failure or myocardial dysfunction were also recorded. Patients had lower levels of bio-available testosterone (2.07 +/- 0.75 nmol/L vs. 5.3 +/- 1.7 nmol/L, p < 0.05) and higher levels of 17beta-estradiol (87.9 +/- 39.5 pmol/L vs. 48.1 +/- 18.4 pmol/L, p < 0.001) than controls. Total and bio-available testosterone levels fell acutely following myocardial infarction (11.9 +/- 3.8 nmol/L to 9.7 +/- 3.3 nmol/L, p < 0.05; 1.95 +/- 0.76 nmol/L to 1.55 +/- 0.67 nmol/L, p < 0.05). This reduction was associated with elevation of PAI-I activity and reduction of tPA activity, independent of changes in plasma insulin levels. Patients with lower baseline levels of testosterone and higher levels of 17beta-estradiol had a relatively pro-thrombotic fibrinolytic profile and increased risk of complications. In conclusion, total and bio-available levels of testosterone fall following acute myocardial infarction in men, in association with adverse changes in fibrinolytic profile. It is not clear whether this association represents a direct effect of testosterone on thrombotic tendency but warrants further investigation.

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Year:  2002        PMID: 12489566     DOI: 10.1081/erc-120015055

Source DB:  PubMed          Journal:  Endocr Res        ISSN: 0743-5800            Impact factor:   1.720


  9 in total

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2.  Role of endogenous testosterone in TNF-induced myocardial injury in males.

Authors:  Meijing Wang; Hongmei Gu; Benjamin D Brewster; Chunyan Huang
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Review 7.  Androgen deficiency as a predictor of metabolic syndrome in aging men: an opportunity for intervention?

Authors:  Dheeraj Kapoor; T Hugh Jones
Journal:  Drugs Aging       Date:  2008       Impact factor: 4.271

Review 8.  Are the adverse effects of glitazones linked to induced testosterone deficiency?

Authors:  M Carruthers; T R Trinick; E Jankowska; A M Traish
Journal:  Cardiovasc Diabetol       Date:  2008-10-15       Impact factor: 9.951

9.  Association of admission testosterone level with ST-segment resolution in male patients with ST-segment elevation myocardial infarction undergoing primary percutaneous coronary intervention.

Authors:  Ahmad Separham; Samad Ghaffari; Bahram Sohrabi; Naser Aslanabadi; Mozhgan Hadavi Bavil; Hasanali Lotfollahi
Journal:  Basic Clin Androl       Date:  2017-07-21
  9 in total

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