Department of Urology, Miller School of Medicine, University of Miami, Miami, FL, USA.
Department of Urology, Miller School of Medicine, University of Miami, Miami, FL, USA; Department of Urology, Dalhousie University, Halifax NS, Canada.
J Pediatr Urol. 2022 Jun;18(3):288.e1-288.e5. doi: 10.1016/j.jpurol.2022.04.008. Epub 2022 Apr 20.
Klinefelter Syndrome (KS) is the most common genetic condition cause of non-obstructive azoospermia (NOA). KS also often results in decreased testicular growth and testosterone production. Because of this, exogenous testosterone therapy is commonly prescribed for KS patients to treat hypogonadism, but this may have additional impacts to future fertility potential. KS adolescent patients may be asked to provide multiple semen samples to identify potential sperm for early cryopreservation.
To develop a multi-institutional database to evaluate the prevalence of sperm in the ejaculate of adolescent KS patients.
A retrospective study was performed of all adolescent KS patients seen at two high-volume tertiary male infertility clinics between 2015 and 2020. Adolescence was defined as individuals aged 12-19 years, as per the World Health Organization. Demographic information data including weight, height, medical comorbidities, and concurrent medications were collected. Serum hormone levels including FSH, LH, and testosterone were collected, as well as any available semen analysis data.
A total of 116 patients were identified and included in the database. A total of 100 (86.2%) had hormone data available and 48 (41.3%) had semen analysis data. Of the 48 patients with semen analyses, only 4 (8.3%) patients had rare sperm in the ejaculate while the remaining had azoospermia (91.7%). None of the specimens were suitable for cryopreservation. The average serum total testosterone level of adolescent KS patients was 181 ± 216 ng/dL. FSH levels were 14.3 ± 18.8 IU/L (normal 0.3-10.0 IU/L) and LH levels were 7.8 ± 12.4 IU/L (normal 1.2-7.8 IU/L). A total of 17 patients repeated a semen analysis, and in no instance did this result in sperm where there was none previously.
The findings from a large multicenter retrospective cohort of adolescent KS patients suggest that a single semen analysis is sufficient for attempted cryopreservation purposes, and that multiple semen analyses is not needed.
克氏综合征(KS)是导致非梗阻性无精子症(NOA)的最常见遗传病症。KS 还常常导致睾丸生长和睾酮产生减少。正因为如此,通常会为 KS 患者开具外源性睾酮治疗来治疗性腺功能减退症,但这可能会对未来的生育潜力产生额外影响。KS 青少年患者可能需要提供多次精液样本,以鉴定早期冷冻保存的潜在精子。
建立一个多机构数据库,以评估青少年 KS 患者精液中精子的出现率。
对 2015 年至 2020 年间在两家高容量男性不育症三级诊所就诊的所有青少年 KS 患者进行回顾性研究。根据世界卫生组织的定义,青春期为 12-19 岁的个体。收集了包括体重、身高、合并症和同时服用的药物在内的人口统计学信息数据。收集了包括 FSH、LH 和睾酮在内的血清激素水平,以及任何可用的精液分析数据。
共确定并纳入数据库 116 例患者。共有 100 例(86.2%)患者有激素数据,48 例(41.3%)患者有精液分析数据。在 48 例进行精液分析的患者中,只有 4 例(8.3%)患者的精液中罕见精子,其余均为无精子症(91.7%)。没有一个标本适合冷冻保存。青少年 KS 患者的平均血清总睾酮水平为 181±216ng/dL。FSH 水平为 14.3±18.8IU/L(正常值 0.3-10.0IU/L),LH 水平为 7.8±12.4IU/L(正常值 1.2-7.8IU/L)。共有 17 例患者重复进行了精液分析,但此前没有精子的情况下,这次也没有出现精子。
一项针对大量青少年 KS 患者的多中心回顾性队列研究的结果表明,单次精液分析足以满足尝试冷冻保存的目的,不需要多次进行精液分析。