用改良的第II代或自动测定法测定血清抗勒氏杆菌激素:在不同血液/血清储存条件下的可重复性

IF 1.8 Q3 OBSTETRICS & GYNECOLOGY Clinical and Experimental Reproductive Medicine-CERM Pub Date : 2023-06-01 DOI:10.5653/cerm.2022.05687
Joong Yeup Lee, Chung Hyon Kim, Seung-Ah Choe, Soyeon Seo, Seok Hyun Kim
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摘要

目的:研究修订的Gen II (rev-Gen II)和自动AMH (Access)测定法测定的抗勒氏杆菌激素(AMH)水平之间的一致性,并评估每种方法在不同血液/血清储存条件下的重复性。方法:采用rev-Gen II和Access法检测74例志愿者血样中AMH水平,检测条件包括:立即血清分离和AMH测定(新鲜对照);-20°C保存血清,48小时、1周和2年后测定AMH;0 ~ 4℃保存血清,48小时和1周后测定AMH;室温保存48小时和1周后延迟血清分离,立即测定AMH。结果:在新鲜对照中,所有rev-Gen II-AMH值均高于可比较的Access-AMH值(差异为8.3%至19.7%)。两种方法测定的AMH水平在所有样品条件下均呈强相关性(r=0.977 ~ 0.995)。结论:rev-Gen II和Access-AMH检测在不同的血液/血清储存条件下具有不同的重复性,但自动Access对rev-Gen II具有更好的稳定性。
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Measurement of serum anti-Müllerian hormone by revised Gen II or automated assay: Reproducibility under various blood/serum storage conditions.

Objective: We investigated the agreement between anti-Müllerian hormone (AMH) levels measured with revised Gen II (rev-Gen II) and automated AMH (Access) assays and evaluated the reproducibility of each method under various blood/serum storage conditions.

Methods: AMH levels in blood samples from 74 volunteers were measured by rev-Gen II and Access assays under various conditions: immediate serum separation and AMH measurement (fresh control); serum stored at -20 °C and AMH measured after 48 hours, 1 week, and 2 years; serum stored at 0 to 4 °C and AMH measured after 48 hours and 1 week; and blood kept at room temperature and delayed serum separation after 48 hours and 1 week, with immediate AMH measurement.

Results: In fresh controls, all rev-Gen II-AMH values were higher than comparable Access-AMH values (difference, 8.3% to 19.7%). AMH levels measured with the two methods were strongly correlated for all sample conditions (r=0.977 to 0.995, all p<0.001). For sera stored at -20 °C or 0 to 4 °C for 48 hours, Access-AMH values were comparable to control measurements, but rev-Gen II-AMH values were significantly lower. AMH levels in sera stored at -20 °C or 0 to 4 °C for 1 week were significantly lower than in fresh controls, irrespective of method. Across methods, long-term storage at -20 °C for 2 years yielded AMH measurements significantly higher than control values. When serum separation was delayed, rev-Gen II-AMH values were significantly lower than control measurements, but Access-AMH values varied.

Conclusion: The rev-Gen II and Access-AMH assays showed varying reproducibility across blood/serum storage conditions, but automated Access yielded superior stability to rev-Gen II.

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