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[医学科学与制药委员会放射性同位素体外检测小组委员会及日本放射性同位素协会在过去30年进行的免疫测定对照调查的报告]

[Report of immunoassay control surveys conducted in the past 30 years by the Subcommittee for Radioisotope in vitro Test, the Medical Science and Pharmaceutical Committee, and the Japan Radioisotope Association].

作者信息

Odagiri Emi, Kuwa Katsuhiko, Katakami Hideki, Takeda Kyoko, Takeoka Keiko, Hidaka Yoh, Ieiri Tamio, Ikeda Hitoshi, Kameko Mitsuaki

机构信息

Central Clinical Laboratories, Department of Clinical Laboratory, Tokyo Women's Medical University School of Medicine, Shinjuku-ku, Tokyo 162-8666, Japan.

出版信息

Rinsho Byori. 2012 Oct;60(10):932-54.

Abstract

Immunoassay control surveys, were conducted by the Subcommittee for Radioisotope in vitro Test, the Medical Science and Pharmaceutical Committee, and the Japan Radioisotope Association, between 1978 to 2008. A total of 40 analytes for 26 hormones, 14 tumor markers and pharmaceutical drugs were investigated in participating facilities. In the first immunoassay control survey in 1978, samples were measured using only RI kits, however, non-RI kits increased gradually during the next 30 years. In the 30th immunoassay control survey, more than 90% samples were measured using non-RI kits. Coefficient variation (CV) of intra-kits has been decreasing yearly in all analytes for hormones as well as tumor markers. However, improvement of CV in inter-kits has not been seen in the past 30 years by a lack of international standards, although there has been continuous effort over the years for the standardization of immunoassay. Growth hormone (GH) deficiency has been diagnosed using various loading tests. However, the clinical diagnosis varies according to the GH kit used. Standardization for GH measurement has been possible by using recombinant GH as the standard among commercial GH kits. The diagnosis of subclinical Cushing's syndrome also varies according to the cortisol kits being used. Candidate reference measurement procedure and low level cortisol standards have been developed by the Biomedical Standard Section, of the National Metrology Institute of Japan. Standardization of measurement is necessary for improvement of immunoassay.

摘要

免疫测定对照调查由放射性同位素体外检测小组委员会、医学与制药委员会以及日本放射性同位素协会在1978年至2008年期间开展。在参与调查的机构中,共对26种激素、14种肿瘤标志物和药物的40种分析物进行了研究。在1978年的首次免疫测定对照调查中,样本仅使用放射性免疫试剂盒进行检测,然而,在接下来的30年里,非放射性免疫试剂盒逐渐增多。在第30次免疫测定对照调查中,超过90%的样本使用非放射性免疫试剂盒进行检测。试剂盒内的变异系数(CV)在所有激素和肿瘤标志物分析物中逐年下降。然而,由于缺乏国际标准,试剂盒间CV的改善在过去30年中未见成效,尽管多年来一直在为免疫测定的标准化不断努力。生长激素(GH)缺乏症通过各种负荷试验进行诊断。然而,临床诊断因所使用的GH试剂盒而异。通过在商用GH试剂盒中使用重组GH作为标准,实现了GH测量的标准化。亚临床库欣综合征的诊断也因所使用的皮质醇试剂盒而异。日本国家计量院生物医学标准科已开发出候选参考测量程序和低水平皮质醇标准。为改进免疫测定,测量的标准化是必要的。

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