May high mobility group box protein-1 be a biomarker for major depressive disorder?
High Mobility Group Box Protein-1 (HMGB1), which has proinflammatory properties, is known to be involved in psychiatric disorders as far as we know, there are only one clinical studies investigating the role of HMGB1 in major depressive disorder (MDD). In this study, we aimed to investigate the role...
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Veröffentlicht in: | Journal of neuroimmunology 2024-11, Vol.396, p.578466, Article 578466 |
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Sprache: | eng |
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Zusammenfassung: | High Mobility Group Box Protein-1 (HMGB1), which has proinflammatory properties, is known to be involved in psychiatric disorders as far as we know, there are only one clinical studies investigating the role of HMGB1 in major depressive disorder (MDD). In this study, we aimed to investigate the role of HMGB1 in the etiopathogenesis of MDD and whether HMGB1 can be used as a biomarker in MDD by measuring the serum HMGB1 levels of depressed patients in the episode and remission periods. This study included 30 patients diagnosed with MDD in episode, 30 patients in remission and 30 healthy controls. Each group comprised 20 female and 10 male participants. In this study, serum HMGB1 levels were found to be lower in the patient group in the episode compared to the patient group in the remission period and the healthy control group. There was no significant difference between the patient group in remission and the healthy control group in terms of serum HMGB1 levels. The fact that serum HMGB1 levels were lower in the patient group in the episode compared to the patient group in the remission period and the control group may be related to the neuroprotective effects of HMGB1. HMGB1 may be used as a biomarker for MDD.
•HMGB1 levels are significantly lower in patients with MDD during an episode.•There is no statistical difference between MDD patients in remission and healthy controls in terms of HMGB1 levels.•HMGB1 may be used as a biomarker for MDD.•HMGB1 may have neuroprotective effects in MDD. |
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ISSN: | 0165-5728 1872-8421 1872-8421 |
DOI: | 10.1016/j.jneuroim.2024.578466 |