A comparison of asymmetric dimethylarginine, arginine, galectin-3, and echocardiographic data with bipolar disorder

Gökçe Kavak Sinanoğlu1, Memduha Aydın2,3, Kürşat Altınbaş2,3

  • 1ALKU Alanya Education and Research Hospital, Department of Psychiatry - Antalya, Türkiye.

Revista Da Associacao Medica Brasileira (1992)
|July 10, 2025
PubMed

Insights

Biomarkers like arginine and galectin 3 may indicate cardiovascular disease risk in schizophrenia and bipolar disorder patients. Cardiac structure also differs between these patient groups, suggesting complex interactions.

Area of Science:

  • Psychiatry
  • Cardiology
  • Biochemistry

Background:

  • Schizophrenia and bipolar disorder patients face double the cardiovascular mortality risk compared to the general population.
  • Cardiovascular diseases and these psychiatric disorders exhibit a dual effect, with inflammation and oxidative stress contributing to cardiac remodeling and worsening psychiatric symptoms.

Purpose of the Study:

  • To investigate potential biomarkers for cardiovascular disease risk in patients with bipolar disorder and schizophrenia.
  • To compare echocardiographic and serum metabolite profiles between these patient groups.

Main Methods:

  • Echocardiography and serum analysis for arginine metabolites (asymmetric dimethylarginine, symmetric dimethylarginine, monomethyl-L-arginine) and galectin 3.
  • Study included 80 euthymic bipolar disorder patients and 69 treated schizophrenia patients.

Main Results:

  • Significantly higher levels of monomethyl-L-arginine and arginine were observed in bipolar disorder patients versus schizophrenia patients.
  • Galectin 3 levels were higher in bipolar disorder patients with psychotic symptoms.
  • Significant differences in echocardiographic parameters (diastolic diameter, systolic diameter, interventricular septum, left atrium, posterior wall) were noted between the groups.

Conclusions:

  • Arginine metabolites and galectin 3 may serve as crucial biomarkers for cardiovascular disease risk.
  • Observed biochemical and cardiac structural changes were not explained by disease severity in this study.
Abstract

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