Ceruloplasmin and Lipofuscin Serum Concentrations Are Associated with Presence of Hypertrophic Cardiomyopathy

Wiktoria Smyła-Gruca1, Wioletta Szczurek-Wasilewicz2, Michał Skrzypek3

  • 1Student's Scientific Society, 3rd Department of Cardiology, Faculty of Medical Sciences in Zabrze, Medical University of Silesia, 40-055 Katowice, Poland.

Biomedicines
|August 29, 2024
PubMed

Insights

Oxidative stress markers, ceruloplasmin (CER) and lipofuscin (LPS), show promise in detecting hypertrophic cardiomyopathy (HCM). Superoxide dismutase (SOD) had limited utility for HCM diagnosis.

Area of Science:

  • Cardiology
  • Biochemistry
  • Pathophysiology

Background:

  • Oxidative stress, an imbalance between reactive oxygen species and antioxidant defenses, is implicated in various diseases.
  • Its specific role in hypertrophic cardiomyopathy (HCM) remains unclear, necessitating further investigation.

Purpose of the Study:

  • To investigate selected oxidative stress markers in patients diagnosed with HCM compared to a healthy control group.
  • To evaluate the diagnostic potential of these markers for HCM detection.

Main Methods:

  • The study included 85 HCM patients and 97 controls, matched for age, sex, and body mass index.
  • Key oxidative stress markers measured were superoxide dismutase (SOD), ceruloplasmin (CER), and lipofuscin (LPS).
  • Receiver operating characteristic (ROC) curve analysis was employed to assess discriminatory power.

Main Results:

  • HCM patients exhibited significantly elevated levels of CER and LPS compared to controls.
  • CER demonstrated strong discriminatory power for HCM (AUC 0.924), while LPS showed acceptable power (AUC 0.740).
  • SOD displayed poor discriminatory ability (AUC 0.556) in detecting HCM.

Conclusions:

  • Ceruloplasmin and lipofuscin show potential as biomarkers for detecting hypertrophic cardiomyopathy.
  • Superoxide dismutase has limited clinical utility for diagnosing HCM.
  • These findings contribute to understanding oxidative stress in HCM pathophysiology.