Serum of transthyretin as a treatment-responsive biomarker for schizophrenia

Nobuaki Nakagawa, Hiroshi Yao, Tatsuo Nakahara, Shinsaku Inomata, Kijiro Hashimoto, Toshihide Kuroki

研究成果: Contribution to journalArticle査読

2 被引用数 (Scopus)

抄録

We investigated the changes in protein profiles of treatment responsive biomarkers in three subjects with first-onset schizophrenia using the surface enhanced laser desorption/ionization time-of-flight mass spectrometry (SELDI-TOF-MS) technology. Our results showed that eight protein peaks were down-regulated or up-regulated during the acute phase, and returned toward the control values during the recovery phase. In particular, a 13,761Da protein peak was markedly down-regulated during the acute phase, and returned during the recovery phase. This protein was identified as unmodified transthyretin using two-dimensional electrophoresis followed by peptide mass fingerprinting based on matrix assisted laser desorption/ionization time-of-flight mass spectrometry (MALDI-TOF-MS). However, we failed to show transthyretin changes with the treatment using enzyme-linked immunosorbent assay (ELISA) and two-dimensional electrophoresis. The distinction between unmodified and modified subtypes of transthyretin was difficult with these methods because of similar molecular weights and isoelectric points in these subtypes. The present study showed that the application of SELDI-TOF-MS technology has higher precision for the distinction of detailed molecular weight than conventional proteomics techniques such as ELISA and two-dimensional electrophoresis. The dynamic changes in transthyretin have been reported to be associated with acute-psychosis condition; the present study suggested that unmodified transthyretin has the potential to be a treatment responsive biomarker for schizophrenia.

本文言語英語
ページ(範囲)1093-1099
ページ数7
ジャーナルBrain and Nerve
65
9
出版ステータス出版済み - 9 1 2013
外部発表はい

All Science Journal Classification (ASJC) codes

  • Clinical Neurology

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