Kelsey Thomas W, McConville Lauren, Edgar Angela B, Ungurianu Alex I, Mitchell Rod T, Anderson Richard A, Wallace W Hamish B
School of Computer Science, University of St. Andrews, St. Andrews, United Kingdom.
School of Medicine, University of Edinburgh, Edinburgh, United Kingdom.
PLoS One. 2017 Jul 20;12(7):e0181377. doi: 10.1371/journal.pone.0181377. eCollection 2017.
The accuracy of Follicle Stimulating Hormone as a predictor of azoospermia in adult survivors of childhood cancer is unclear, with conflicting results in the published literature. A systematic review and post hoc analysis of combined data (n = 367) were performed on all published studies containing extractable data on both serum Follicle Stimulating Hormone concentration and semen concentration in survivors of childhood cancer. PubMed and Medline databases were searched up to March 2017 by two blind investigators. Articles were included if they contained both serum FSH concentration and semen concentration, used World Health Organisation certified methods for semen analysis, and the study participants were all childhood cancer survivors. There was no evidence for either publication bias or heterogeneity for the five studies. For the combined data (n = 367) the optimal Follicle Stimulating Hormone threshold was 10.4 IU/L with specificity 81% (95% CI 76%-86%) and sensitivity 83% (95% CI 76%-89%). The AUC was 0.89 (95%CI 0.86-0.93). A range of threshold FSH values for the diagnosis of azoospermia with their associated sensitivities and specificities were calculated. This study provides strong supporting evidence for the use of serum Follicle Stimulating Hormone as a surrogate biomarker for azoospermia in adult males who have been treated for childhood cancer.
促卵泡激素作为儿童癌症成年幸存者无精子症预测指标的准确性尚不清楚,已发表文献中的结果相互矛盾。对所有已发表的、包含儿童癌症幸存者血清促卵泡激素浓度和精液浓度可提取数据的研究进行了系统评价和合并数据的事后分析(n = 367)。两名盲法研究者检索了截至2017年3月的PubMed和Medline数据库。如果文章同时包含血清促卵泡激素浓度和精液浓度、使用世界卫生组织认证的精液分析方法且研究参与者均为儿童癌症幸存者,则纳入该文章。五项研究均未发现发表偏倚或异质性的证据。对于合并数据(n = 367),促卵泡激素的最佳阈值为10.4 IU/L,特异性为81%(95%CI 76%-86%),敏感性为83%(95%CI 76%-89%)。曲线下面积为0.89(95%CI 0.86-0.93)。计算了一系列用于诊断无精子症的促卵泡激素阈值及其相关的敏感性和特异性。本研究为将血清促卵泡激素用作接受过儿童癌症治疗的成年男性无精子症替代生物标志物提供了有力的支持证据。