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IDS iSYS 全自动完整型原胶原 1-N 端前肽检测:成人和儿童的方法评估及参考区间。

IDS iSYS automated intact procollagen-1-N-terminus pro-peptide assay: method evaluation and reference intervals in adults and children.

出版信息

Clin Chem Lab Med. 2013 Oct;51(10):2009-18. doi: 10.1515/cclm-2012-0531.

Abstract

BACKGROUND

We carried out a technical evaluation of the Immunodiagnostic Systems (IDS) automated intact procollagen-I N-terminus propeptide (PINP) assay on the iSYS platform, and established reference intervals for PINP in both adults and children.

METHODS

Assay imprecision, recovery and interference were studied. Serum and plasma values were compared, and PINP stability was assessed. Using 828 specimens, IDS iSYS intact PINP and Roche E170 total PINP values were compared. Specimens from 597 adults and 485 children and adolescents were used to establish reference intervals for intact PINP.

RESULTS

The method demonstrated good recovery and acceptable imprecision. The assay was unaffected by icterus and lipaemia, but haemolysis decreased measured PINP. Serum and plasma values were comparable. There was a non-linear relation between IDS intact and Roche total PINP values. Pre- and post-menopausal women had comparable PINP values, but there was a difference between women of different age groups. Serum PINP in men showed a decline in young age up to 45 years, but remained steady thereafter. Separate reference intervals were established for four age groups in women and for two age groups in men. Data for children were partitioned into four-year age groups, and these showed PINP to be high with no major gender differences until 12 years of age. Thereafter, values in females decreased in 13-16 years age groups and further in 17-20 years age groups, whereas PINP increased in boys of 13-16 years of age with a subsequent decline at 17-20 years.

CONCLUSIONS

The IDS iSYS PINP intact assay appears to be reliable. We have established gender- and age-related reference intervals for children and adults based on a relatively large healthy North European population.

摘要

背景

我们对 Immunodiagnostic Systems(IDS)在 iSYS 平台上的全自动完整型前胶原 I N 端前肽(PINP)检测进行了技术评估,并建立了成人和儿童 PINP 的参考区间。

方法

研究了检测的不精密度、回收率和干扰情况。比较了血清和血浆值,并评估了 PINP 的稳定性。使用 828 份标本,比较了 IDS iSYS 完整型 PINP 和罗氏 E170 总 PINP 的结果。使用 597 名成年人和 485 名儿童和青少年的标本建立了完整型 PINP 的参考区间。

结果

该方法显示出良好的回收率和可接受的不精密度。该检测不受黄疸和脂血的影响,但溶血会降低测量的 PINP 值。血清和血浆值具有可比性。IDS 完整型和罗氏总 PINP 值之间存在非线性关系。绝经前和绝经后妇女的 PINP 值相当,但不同年龄组的妇女之间存在差异。男性的血清 PINP 在 45 岁之前的年轻年龄呈下降趋势,但此后保持稳定。为女性建立了四个年龄组的单独参考区间,为男性建立了两个年龄组的单独参考区间。儿童的数据分为四个年龄组,直到 12 岁,PINP 一直较高且性别差异不大。此后,13-16 岁年龄组的女性 PINP 值下降,17-20 岁年龄组进一步下降,而 13-16 岁的男性 PINP 值增加,随后在 17-20 岁年龄组下降。

结论

IDS iSYS PINP 完整型检测似乎可靠。我们根据相对较大的北欧健康人群建立了儿童和成人的性别和年龄相关参考区间。

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