The influence of testosterone on the risk of cardiovascular events after percutaneous coronary intervention

Cheng-Hung Chiang1,2, Wan-Ting Hung3, En-Shao Liu1

  • 1Cardiovascular Medical Center, Kaohsiung Veterans General Hospital, Kaohsiung, Taiwan.

Insights

Low testosterone levels in men increase the risk of major adverse cardiovascular events (MACE) and target lesion revascularization (TLR/TVR) after percutaneous coronary intervention (PCI). This finding highlights the importance of monitoring testosterone in cardiovascular patient care.

Area of Science:

  • Cardiology
  • Endocrinology
  • Men's Health

Background:

  • Testosterone plays a crucial role in male physiology, and low levels have been implicated in various health issues.
  • Percutaneous coronary intervention (PCI) is a common procedure for treating coronary artery disease, but post-procedural complications remain a concern.

Purpose of the Study:

  • To investigate the association between low serum testosterone levels and the risk of major adverse cardiovascular events (MACE) following PCI.
  • To evaluate the impact of testosterone levels on specific cardiovascular outcomes, including target lesion revascularization/target vessel revascularization (TLR/TVR) and myocardial infarction.

Main Methods:

  • A cohort of 580 men undergoing PCI between 2015 and 2018 was divided into low (<3.25 ng/mL) and normal (≥3.25 ng/mL) serum testosterone groups.
  • Major adverse cardiovascular event (MACE) was defined as a composite of cardiovascular death, myocardial infarction, and TLR/TVR.
  • Statistical analyses, including logistic and Cox regression, were employed to assess the association between testosterone levels and MACE, adjusting for relevant variables.

Main Results:

  • Patients with low testosterone exhibited a significantly higher overall MACE rate (26.13%) compared to those with normal testosterone (13.01%, p=0.0006).
  • Low testosterone was associated with increased rates of TLR/TVR (20.72% vs. 11.73%, p=0.0125) and myocardial infarction (3.6% vs. 0.85%, p=0.0255).
  • Event-free survival for MACE was shorter in the low testosterone group (25.22 months) versus the normal testosterone group (35.09 months, log-rank p=0.0004). Logistic regression showed low testosterone as an independent predictor of MACE (OR: 2.06, p=0.0081), and Cox regression confirmed higher HRs for MACE (HR: 1.88, p=0.0058) and TLR/TVR (HR: 1.73, p=0.0290).

Conclusions:

  • Low serum testosterone concentrations are significantly associated with an elevated risk of MACE and TLR/TVR after PCI.
  • These findings suggest that testosterone levels may be an important prognostic factor in men undergoing PCI.
Abstract

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