Inquiries About Biomarkers of Acute Liver Failure in Patients Who Underwent Living Donor Liver Transplantation Using a Protein Chip Array.

Y. Yamashita, T. Yoshizumi, T. Ikegami, H. Uchiyama, E. Tsujita, S. Itoh, N. Harimoto, Y. Soejima, A. Taketomi, H. Baba, Y. Maehara
{"title":"Inquiries About Biomarkers of Acute Liver Failure in Patients Who Underwent Living Donor Liver Transplantation Using a Protein Chip Array.","authors":"Y. Yamashita, T. Yoshizumi, T. Ikegami, H. Uchiyama, E. Tsujita, S. Itoh, N. Harimoto, Y. Soejima, A. Taketomi, H. Baba, Y. Maehara","doi":"10.15017/1784634","DOIUrl":null,"url":null,"abstract":"The causative agent of hepatic encephalopathy (HE) has not been identified with certainty. The\nrecovery of consciousness in patients with acute liver failure (ALF) who underwent liver\ntransplantation (LT) is sometimes drastic ; therefore, we thought that the causative agents of HE\nwould change markedly peri-operatively in these patients. We examined the biomarkers including\nnew agents in the serum of patients using the ProteinChip® System 4000 (Ciphergen Biosystems,\nYokohama, JAPAN). Sixteen samples were obtained from four patients with ALF who underwent living donor LT\n(LDLT) at four time points ; pre-operative, one post-operative day (1POD), 3POD, and 7POD. We used\nthree chips made by the Biomek2000 robot. All duplicated samples were assayed and analyzed using\nthe CiphergenExpressTM data manager. We divided the peri-operative changes in the intensity of\nidentified peaks into seven patterns. The number of peaks whose intensity shows significant changes\nperi-operatively reached 755. Of course, it is difficult to determine each structure in all 755 peaks ; therefore, we should narrow\ndown the candidates for causative agents of HE in further studies. Our own results suggest that many\ndifficulties lie ahead in determining the causative agent of HE.","PeriodicalId":12665,"journal":{"name":"Fukuoka igaku zasshi = Hukuoka acta medica","volume":"19 1","pages":"131-5"},"PeriodicalIF":0.0000,"publicationDate":"2016-07-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Fukuoka igaku zasshi = Hukuoka acta medica","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.15017/1784634","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0

Abstract

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.
查看原文
分享 分享
微信好友 朋友圈 QQ好友 复制链接
本刊更多论文
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。
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。
求助全文
约1分钟内获得全文 去求助
来源期刊
自引率
0.00%
发文量
0
期刊最新文献
[Sphingolipidosis]. Completely Responsive Multiple Liver Recurrence of Colon Cancer Treated Using Chemotherapy with Oral S-1 and Oxaliplatin Plus Bevacizumab : A Case Report. Completely Responsive Multiple Liver Recurrence of Colon Cancer Treated Using Chemotherapy with Oral S-1 and Oxaliplatin Plus Bevacizumab : A Case Report. Bone and Joint Diseases in Present and Future. Natural Immunity and Ocular Inflammation.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
已复制链接
已复制链接
快去分享给好友吧!
我知道了
×
扫码分享
扫码分享
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1