Role of intra-individual variation in the detection of thresholds for DFI and for misclassification rates: A retrospective analysis of 14,775 SCSA® tests.

IF 3.2 2区 医学 Q1 ANDROLOGY Andrology Pub Date : 2024-11-15 DOI:10.1111/andr.13801
Preben Christensen, Robert Fischer, Wolfgang Schulze, Vera Baukloh, Kimberly Kienast, Graham Coull, Erik T Parner
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Abstract

Background: Sperm DNA damage is associated with reduced male fertility after natural conception and intrauterine insemination. However, the impact on in vitro fertilization (IVF) and especially intracytoplasmic sperm injection (ICSI) treatments is still unclear. Few studies have focused on the intra-individual variation in DFI even though it may have an important role to play in terms of detection of thresholds and for misclassification rates.

Methods: Results for Sperm Chromatin Structure Assay (SCSA®) tests performed for 70 European fertility clinics between January 1st, 2008 and December 31st, 2022 were examined. A small retrospective study included 406 couples receiving their first treatment with IVF or ICSI. These results were then used for a mathematical simulation to investigate the role of intra-individual variation. The large retrospective study included a total of 14,138 diagnostic tests and 637 tests from an IUI study. The distribution of DFI was assessed for the IUI cohort and cohorts of patients attending Sims IVF and Fertility Center Hamburg (FCH). Descriptive analysis of the data was performed regarding time of year, male age, and year.

Results: When DFI was above the thresholds of 15 and 25, a significant reduction in ongoing pregnancies after 12 weeks of gestation was observed for IVF and ICSI treatments, respectively. For IVF treatments, the pregnancy rate was reduced from 45.1% to 24.6%, odds ratio = 2.58 (p = 0.004). For ICSI treatments, the pregnancy rate was reduced from 48.6% to 29.6%, odds ratio = 2.00 (p = 0.032). Intra-individual variation was significantly related to the misclassification rate and the sample size required to identify a threshold. The percentage of patients with a DFI below 15 was 64.8% for the IUI cohort and 51.7% and 41.6% for cohorts of patients attending Sims IVF and FCH, respectively. The median DFI for these cohorts differed significantly and was 11.6, 15.0 and 17.2, respectively. DFI shows a seasonal variation, and increases with male age. During the past 15 years, the median DFI has increased by 0.05% per year (p = 0.02).

Discussion and conclusions: Ongoing pregnancy rates are reduced significantly for both IVF and ICSI treatments when DFI is above the thresholds of 15 and 25, respectively. The misclassification rate and the required sample size increase with increasing intra-individual variation. Couples with a DFI above 15 are more likely to experience failed assisted reproductive technology (ART) cycles. DFI appears to have increased during the past 15 years.

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个体内差异在检测 DFI 临界值和误诊率中的作用:对 14,775 次 SCSA® 检测的回顾性分析。
背景:精子 DNA 损伤与男性自然受孕和宫内人工授精后生育能力下降有关。然而,对体外受精(IVF),尤其是卵胞浆内单精子显微注射(ICSI)治疗的影响仍不清楚。很少有研究关注 DFI 的个体内变异,尽管它在检测阈值和误判率方面可能起着重要作用:方法: 对 2008 年 1 月 1 日至 2022 年 12 月 31 日期间欧洲 70 家不孕不育诊所进行的精子染色质结构检测(SCSA®)结果进行了研究。一项小型回顾性研究包括 406 对首次接受试管婴儿或卵胞浆内单精子显微注射(ICSI)治疗的夫妇。这些结果被用于数学模拟,以研究个体内部变异的作用。大型回顾性研究共包括 14 138 次诊断测试和 637 次人工授精研究测试。对人工授精队列和Sims IVF及汉堡不孕不育中心(FCH)就诊患者队列的DFI分布情况进行了评估。对数据进行了时间、男性年龄和年份的描述性分析:结果:当DFI超过15和25的临界值时,试管婴儿和卵胞浆内单精子显微注射治疗在妊娠12周后的持续妊娠率明显下降。试管婴儿治疗的妊娠率从 45.1%降至 24.6%,几率比 = 2.58(P = 0.004)。对于卵胞浆内单精子显微注射治疗,妊娠率从 48.6% 降至 29.6%,几率比 = 2.00(p = 0.032)。个体内差异与误诊率和确定阈值所需的样本量有显著关系。IUI队列中DFI低于15的患者比例为64.8%,Sims IVF和FCH队列中DFI低于15的患者比例分别为51.7%和41.6%。这些组群的 DFI 中位数差别很大,分别为 11.6、15.0 和 17.2。DFI 呈季节性变化,并随男性年龄的增长而增加。在过去 15 年中,DFI 中位数每年增加 0.05%(p = 0.02):当 DFI 分别超过 15 和 25 的阈值时,IVF 和 ICSI 治疗的持续妊娠率都会显著降低。随着个体内部差异的增加,误诊率和所需样本量也会增加。DFI超过15的夫妇更有可能经历失败的辅助生殖技术(ART)周期。在过去 15 年中,DFI 似乎有所上升。
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来源期刊
Andrology
Andrology ANDROLOGY-
CiteScore
9.10
自引率
6.70%
发文量
200
期刊介绍: Andrology is the study of the male reproductive system and other male gender related health issues. Andrology deals with basic and clinical aspects of the male reproductive system (gonads, endocrine and accessory organs) in all species, including the diagnosis and treatment of medical problems associated with sexual development, infertility, sexual dysfunction, sex hormone action and other urological problems. In medicine, Andrology as a specialty is a recent development, as it had previously been considered a subspecialty of urology or endocrinology
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