Homocysteine, hopelessness, rumination, affective temperaments, and clinical course in patients with bipolar disorder-1

This study aimed to explore the associations between homocysteine, rumination, affective temperaments, clinical features, and hopelessness in bipolar disorder-1 (BD-1). In total, 57 euthymic patients with BD-1 and 57 healthy controls were included. The Beck Hopelessness Scale (BHS), Temperament Eval...

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Published in:Nordic journal of psychiatry Vol. 78; no. 6; pp. 465 - 476
Main Authors: Aydın, Esat Fahri, Özcan, Halil, Yılmaz, Sinan, Aşkın, Seda, Koca Laçin, Tuğba, Topu, Elif Nur
Format: Journal Article
Language:English
Published: England 01-08-2024
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Summary:This study aimed to explore the associations between homocysteine, rumination, affective temperaments, clinical features, and hopelessness in bipolar disorder-1 (BD-1). In total, 57 euthymic patients with BD-1 and 57 healthy controls were included. The Beck Hopelessness Scale (BHS), Temperament Evaluation of Memphis, Pisa, Paris, and San Diego-Autoquestionnaire (TEMPS-A), and Ruminative Responses Scale Short Form (RRS-SF) were administered. Homocysteine, folate, and vitamin B12 levels were measured. The BHS total (  = 0.047), TEMPS-A irritable (  = 0.007), and TEMPS-A cyclothymic ( = 0.001) scores were significantly higher than the control group in the BD-1 group. Hyperhomocysteinemia (HHcy) was found in 33.3% of the patients (  = 19). In the HHcy group, age of onset of disease (  = 0.020) was significantly lower than the non-HHcy group in patients. Previous suicide attempt number was significantly correlated with scores of reflective pondering, brooding, and global rumination in BD-1 (  ˂ 0.05). Except for hyperthymic temperament, all types of affective temperaments were correlated with the scores of RRS-SF brooding (  ˂ 0.05) in the BD-1 group. The RRS-SF brooding scores significantly correlated with the BHS total scores (  = 0.263,  < 0.05); the TEMPS-A hyperthymic (  = -0.351,  = 0.001) and TEMPS-A irritable (  = 0.536,  < 0.001) scores significantly predicted the BHS total scores in the BD-1 group. The findings may lead clinical efforts and future clinical trials to explore and intervene in related sources and presentations of BD-1's adverse consequences.
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ISSN:0803-9488
1502-4725
1502-4725
DOI:10.1080/08039488.2024.2347633