前交叉韧带重建后尿II型胶原c端交联末端肽测定的测定间变异性。

Lachlan M. Batty , Kate E. Webster , Natasha Vassileff , Jereme G. Spiers , Haydn J. Klemm , Brian Devitt , Timothy S. Whitehead , Andrew F. Hill , Julian A. Feller
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引用次数: 0

摘要

目的:比较两种不同的市售酶联免疫吸附试验(ELISA)在前交叉韧带(ACL)重建后第一年患者尿c端交联II型胶原末端肽(u-CTX-II)的浓度和趋势。设计:22例接受重建手术的acl损伤患者(平均年龄25.2岁(SD 8.0);12例(54.5%)男性患者在手术当天(基线)、术后6个月和12个月采集尿样。使用CloudClone®和软骨酶联免疫吸附测定u-CTX-II的浓度。u-CTX-II浓度与尿肌酐(Cr)归一化。结果:各时间点u-CTX-II浓度在两种检测方法间差异有统计学意义(p≤0.01)。使用CloudClone®Assay测定时,基线、6个月和12个月时间点的u-CTX-II平均(标准误差)浓度分别为26.5 (2.5)ng/mmol Cr、29.4 (3.8)ng/mmol Cr和40.6 (6.9)ng/mmol Cr。在同一时间点,使用软骨法测定u-CTX-II浓度分别为981.2 (256.5)ng/mmol Cr、867.0 (234.3)ng/mmol Cr和764.3 (220.3)ng/mmol Cr。使用CloudClone®法测定u-CTX-II浓度随时间增加(p = 0.04)。使用软骨法检测u-CTX-II的浓度随时间降低(p = 0.2)。结论:使用两种市售的检测方法,u-CTX-II在ACL重建后的第一年的浓度和趋势都有显著差异。在解释结果时,所使用的特定测定方法至关重要,并且对汇集数据和荟萃分析具有影响。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Inter-assay variability in the measurement of urinary C-terminal cross-linked telopeptide of type II collagen following anterior cruciate ligament reconstruction

Objective

To compare urinary C-terminal cross-linked telopeptide of type II collagen (u-CTX-II) concentrations and trends as measured by two different commercially available enzyme-linked immunosorbent assays (ELISA) in a cohort of patients in the first year following anterior cruciate ligament (ACL) reconstruction.

Design

22 ACL-injured patients undergoing reconstructive surgery (mean age 25.2 (SD 8.0) years; 12 (54.5 ​%) male) had urine samples taken on the day of surgery (baseline) and at 6 and 12 months post-operatively. Concentrations of u-CTX-II were measured using the CloudClone® and the CartiLaps® ELISA. u-CTX-II concentrations were normalized to urinary creatinine (Cr).

Results

The u-CTX-II concentrations were significantly different between the 2 assays at each timepoint (p ​≤ ​0.01). When measured using the CloudClone® Assay, mean (standard error) u-CTX-II concentrations were 26.5 (2.5) ng/mmol Cr, 29.4 (3.8) ng/mmol Cr and 40.6 (6.9) ng/mmol Cr at the baseline, 6-month and 12-month timepoints respectively. When measured using the CartiLaps® Assay, at the same respective timepoints, u-CTX-II concentrations were 981.2 (256.5) ng/mmol Cr, 867.0 (234.3) ng/mmol Cr and 764.3 (220.3) ng/mmol Cr. Concentrations of u-CTX-II using the CloudClone® Assay increased with time (p ​= ​0.04). Concentrations of u-CTX-II using the CartiLaps® Assay decreased over time (p ​= ​0.2).

Conclusion

Using two commercially available assays, u-CTX-II differed significantly in terms of both concentration and trends in the first year following ACL reconstruction. The specific assay used is critical to consider when interpreting results and has implications for pooling data and meta-analysis.
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来源期刊
Osteoarthritis and cartilage open
Osteoarthritis and cartilage open Orthopedics, Sports Medicine and Rehabilitation
CiteScore
3.30
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