Department of Biochemistry, PathWest Laboratory Medicine, Nedlands, Western Australia, Australia; School of Pathology and Laboratory Medicine, University of Western Australia, Crawley, Western Australia, Australia; Western Diagnostic Pathology, Myaree, Western Australia, Australia.
Department of Endocrinology, Sir Charles Gairdner Hospital, Nedlands, Western Australia, Australia.
Fertil Steril. 2016 Oct;106(5):1230-1237. doi: 10.1016/j.fertnstert.2016.06.009. Epub 2016 Jun 25.
To quantify intraindividual variability of antimüllerian hormone (AMH) as analytical and biological coefficients of variation and assess the effects of variation on clinical classification.
Retrospective cohort study.
Not applicable.
PATIENT(S): Thirty-eight women referred by general practitioners.
INTERVENTION(S): None.
MAIN OUTCOME MEASURE(S): Total intraindividual variability (CV), analytical (CV) and biological variability (CV) for each woman and for AMH ranges: low (<5 pmol/L), reduced (5-10), moderate (>10-30) and high (>30 pmol/L), with calculation of proportion of women crossing clinical cutoffs and expected variability around each cutoff.
RESULT(S): Cycling women (n = 38) contributed 238 blood samples (average 6 samples each). The average total intraindividual AMH variability was 20% (range: 2.1% to 73%). Biological variation was 19% (range: 0 to 71%) and at least twice the analytical variation of 6.9% (range: 4.5% to 16%). Reclassification rates were highest in women with low (33%) or reduced AMH (67%) levels. Expected variations around the 5, 10, and 30 pmol/L cutoffs were 3-7, 7-13, and 20-40 pmol/L, respectively. In a woman with mean AMH in the 10-30 pmol/L range, the span of results that could occur was 7-40 pmol/L.
CONCLUSION(S): Total variation in AMH was 20%, and the majority of this was biological. Changes in AMH resulted in reclassification in 29% of women and occurred most frequently in those with low and reduced AMH. In cycling women, the variability in AMH should be considered by clinicians, especially if a result is close to a clinical cutoff.
量化抗缪勒管激素(AMH)的个体内变异性,作为分析和生物学变异系数,并评估变异对临床分类的影响。
回顾性队列研究。
不适用。
38 名由全科医生转介的女性。
无。
每位女性的总个体内变异性(CV)、分析(CV)和生物学变异性(CV),以及 AMH 范围的变异性:低(<5 pmol/L)、降低(5-10)、中度(>10-30)和高(>30 pmol/L),计算跨越临床截止值的女性比例和每个截止值周围的预期变异性。
38 名月经周期女性(n=38)提供了 238 份血样(平均每人 6 份)。AMH 的个体内总变异平均为 20%(范围:2.1%-73%)。生物学变异性为 19%(范围:0-71%),至少是分析变异性 6.9%(范围:4.5%-16%)的两倍。AMH 水平较低(33%)或降低(67%)的女性重分类率最高。5、10 和 30 pmol/L 截止值周围的预期变化分别为 3-7、7-13 和 20-40 pmol/L。在 AMH 平均值处于 10-30 pmol/L 范围内的女性中,结果可能出现的范围为 7-40 pmol/L。
AMH 的总变异性为 20%,其中大部分为生物学变异性。AMH 的变化导致 29%的女性重新分类,在 AMH 水平较低和降低的女性中最常见。在月经周期女性中,临床医生应考虑 AMH 的变异性,特别是如果结果接近临床截止值。