使用蛋白质芯片阵列研究活体肝移植患者急性肝衰竭的生物标志物。

Yo-ichi Yamashita, Tomoharu Yoshizumi, Toru Ikegami, Hideaki Uchiyama, Eiji Tsujita, Shinji Itoh, Norifumi Harimoto, Yuji Soejima, Akinobu Taketomi, Hideo Baba, Yoshihiko Maehara
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引用次数: 0

摘要

肝性脑病(HE)的病因尚未确定。急性肝功能衰竭(ALF)患者接受肝移植(LT)后意识的恢复有时是剧烈的;因此,我们认为he的致病因子在这些患者围手术期会发生显著变化。我们使用ProteinChip®System 4000 (Ciphergen Biosystems,Yokohama, JAPAN)检测了患者血清中的生物标志物,包括新药。在四个时间点,从4名接受活体供体肝移植(LDLT)的ALF患者中获得16份样本;术前、术后1天(1POD)、3POD、7POD。我们使用了三个由Biomek2000机器人制造的芯片。使用CiphergenExpressTM数据管理器对所有重复的样本进行检测和分析。我们将围术期识别峰强度的变化分为7种模式。围手术期出现明显变化的峰数达到755个。当然,很难确定所有755个峰中的每个结构;因此,我们应该在进一步的研究中缩小HE致病因子的候选范围。我们自己的结果表明,在确定HE的致病因子方面还有许多困难。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Inquiries About Biomarkers of Acute Liver Failure in Patients Who Underwent Living Donor Liver Transplantation Using a Protein Chip Array.

The causative agent of hepatic encephalopathy (HE) has not been identified with certainty. The recovery of consciousness in patients with acute liver failure (ALF) who underwent liver transplantation (LT) is sometimes drastic ; therefore, we thought that the causative agents of HE would change markedly peri-operatively in these patients. We examined the biomarkers including new agents in the serum of patients using the ProteinChip® System 4000 (Ciphergen Biosystems, Yokohama, JAPAN). Sixteen samples were obtained from four patients with ALF who underwent living donor LT (LDLT) at four time points ; pre-operative, one post-operative day (1POD), 3POD, and 7POD. We used three chips made by the Biomek2000 robot. All duplicated samples were assayed and analyzed using the CiphergenExpressTM data manager. We divided the peri-operative changes in the intensity of identified peaks into seven patterns. The number of peaks whose intensity shows significant changes peri-operatively reached 755. Of course, it is difficult to determine each structure in all 755 peaks ; therefore, we should narrow down the candidates for causative agents of HE in further studies. Our own results suggest that many difficulties lie ahead in determining the causative agent of HE.

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