| Literature DB >> 24448481 |
Narimasa Katsuta1, Tohru Ohnuma2, Hitoshi Maeshima1, Yuto Takebayashi1, Motoyuki Higa1, Mayu Takeda1, Toru Nakamura1, Shohei Nishimon1, Takahiro Sannohe1, Yuri Hotta1, Ryo Hanzawa1, Ryoko Higashiyama1, Nobuto Shibata1, Heii Arai1.
Abstract
Altered peripheral carbonyl stress markers, high levels of serum pentosidine, which accumulates following carbonyl stress, and low levels of pyridoxal (vitamin B6), which detoxifies reactive carbonyl compounds, have been reported in a cross-sectional study of chronic schizophrenia. However, changes in the levels of these compounds in patients with schizophrenia have not been investigated in a longitudinal study. To clarify whether these markers may be biological markers that reflect the clinical course of the disease, the serum levels of these compounds were investigated in a cross-sectional and a longitudinal study. One hundred and thirty-seven acute-stage Japanese patients were enrolled. Among these, 53 patients were followed from the acute stage to remission. A portion of patients in the acute stage (14 cases, 10.2%) showed extremely high pentosidine levels. These levels were not associated with the severity of symptoms but were associated with antipsychotic dose amounts. Pyridoxal levels were lower in schizophrenia and increased according to the clinical course of the illness. Furthermore, 18 patients with decreased pyridoxal levels according to the clinical course showed that the greater the decrease in pyridoxal levels, the lesser the improvement in symptoms. Thus, extremely high pentosidine levels in a portion of patients may be caused by higher daily antipsychotic doses, whereas pyridoxal levels were lower in schizophrenia and increased according to the clinical course. Patients with decreasing pyridoxal levels during the clinical course showed less improvement in symptoms. Carbonyl stress markers may also be therapeutic biological markers in some patients with schizophrenia.Entities:
Keywords: clinical course; pentosidine; pyridoxal; vitamin B6
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Year: 2014 PMID: 24448481 PMCID: PMC4193703 DOI: 10.1093/schbul/sbt234
Source DB: PubMed Journal: Schizophr Bull ISSN: 0586-7614 Impact factor: 9.306