| Literature DB >> 30682553 |
Leo Gotoh1, Misa Yamada2, Kotaro Hattori3, Daimei Sasayama4, Takamasa Noda5, Sumiko Yoshida6, Hiroshi Kunugi7, Mitsuhiko Yamada8.
Abstract
It is suggested that lysophosphatidic acid (LPA) plays a key role in the pathophysiology of schizophrenia. In this study, we measured LPA levels by enzyme-linked immunosorbent assay in cerebrospinal fluid (CSF) and plasma samples. The participants were 49 patients with schizophrenia and 49 normal healthy controls for CSF study, and 42 patients and 44 controls for plasma study. We found that LPA levels in the patients were not significantly different from those of controls in CSF (controls: 0.189 ± 0.077 µM, patients: 0.175 ± 0.067 µM; P = 0.318) and plasma samples (controls: 0.131 ± 0.067 µM, patients: 0.120 ± 0.075 µM; P = 0.465). On the other hand, CSF levels in medicated patients (0.162 ± 0.061 µM) were significantly lower than those observed in unmedicated patients (0.224 ± 0.067 µM, P = 0.038), suggesting that our findings could be masked by the influence of medication with antipsychotics. Interestingly, we detected significant negative correlation between PANSS scores and plasma LPA levels, especially in males and in unmedicated patients. Our result suggests that LPA levels in CSF and plasma samples would not serve as a diagnostic biomarker, but plasma levels could be used for symptomatic assessment of schizophrenia.Entities:
Keywords: Biomarker; Lysophosphatidic acid; PANSS score; Schizophrenia
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Year: 2019 PMID: 30682553 DOI: 10.1016/j.psychres.2019.01.052
Source DB: PubMed Journal: Psychiatry Res ISSN: 0165-1781 Impact factor: 3.222