Department of Obstetrics and Gynecology, University of California, Los Angeles, Los Angeles, CA, USA.
J Assist Reprod Genet. 2021 Apr;38(4):957-963. doi: 10.1007/s10815-021-02084-6. Epub 2021 Jan 27.
When undergoing expanded carrier screening (ECS), couples are often screened sequentially to reduce need for a second individual's test. It is unknown how often partners of individuals found to be carriers complete the recommended testing with a sequential approach and what factors contribute to decision-making regarding partner testing. Additionally, the economic burden placed on individuals by ECS testing and its effect on partner testing has not been evaluated.
In part 1, all individuals at a university-affiliated reproductive endocrinology and infertility practice identified to be carriers of a recessively inherited mutation using the Counsyl/Foresight ECS were included. Conditions were categorized by severity according to a previously described classification system. In part 2, all individuals who underwent ECS with a single test provider between September 1, 2013 and February 1, 2020 were contacted via email to complete a confidential and anonymized online survey.
In part 1, a total of 2061 patients were screened. 36.9% were carriers of one or more recessively inherited disorders. Twenty-seven percent of positively screened individuals did not have their partner screened. Carriers of a moderate condition had a trend towards a reduced odds for having their partner screened compared to a profound condition (OR 0.36, 95% CI 0.12-1.05, p = 0.06). Number of conditions was not predictive of subsequent partner screening (OR 0.95, 95% CI 0.72-1.25, p = 0.72). In part 2, the cost of ECS was not covered by insurance for 54.5% (103/189) and most paid over $300 out-of-pocket for testing (47.6%). The most common reason for not completing partner testing was that the results would not alter their course when seeking conception (33.3%). 73.5% of patients knew that the largest benefit of ECS comes from knowing a partner's results as well as their own.
Not all carriers of recessively inherited disorders choose to undergo partner screening. Patients found to be carrier of more debilitating genetic disorders may be more likely to screen their reproductive partners. For many, ECS testing is not covered by insurance, and this test may impose a significant economic burden. For some patients, the results of ECS would not change what they would do when seeking conception. Providers should evaluate whether a patient's ECS result would change their treatment course prior to testing.
在进行扩展携带者筛查(ECS)时,通常会对夫妻双方进行顺序筛查,以减少对第二个人测试的需求。目前尚不清楚,当发现一方为携带者时,其伴侣以顺序方式完成推荐检测的频率是多少,以及哪些因素会影响伴侣检测的决策。此外,尚未评估 ECS 检测给个人带来的经济负担及其对伴侣检测的影响。
在第一部分中,纳入了在一所大学附属生殖内分泌和不孕不育诊所使用 Counsyl/Foresight ECS 检测出隐性遗传突变的所有个体。根据先前描述的分类系统,根据严重程度对条件进行分类。在第二部分中,联系了 2013 年 9 月 1 日至 2020 年 2 月 1 日期间在单一测试提供商处接受 ECS 的所有个体,以通过电子邮件完成一份机密且匿名的在线调查。
在第一部分中,共筛查了 2061 名患者。36.9%的患者携带一种或多种隐性遗传疾病。27%的阳性筛查个体未对其伴侣进行筛查。与严重程度的条件相比,中度条件携带者对伴侣筛查的可能性降低(OR 0.36,95%CI 0.12-1.05,p=0.06)。条件数量并不能预测随后的伴侣筛查(OR 0.95,95%CI 0.72-1.25,p=0.72)。在第二部分中,54.5%(103/189)的 ECS 费用未被保险覆盖,大多数人自费支付超过 300 美元用于检测(47.6%)。未完成伴侣检测的最常见原因是检测结果不会改变他们寻求受孕的方式(33.3%)。73.5%的患者知道 ECS 的最大益处是了解伴侣和自己的结果。
并非所有隐性遗传疾病的携带者都选择进行伴侣筛查。发现为更具致残性遗传疾病的携带者可能更有可能对其生殖伴侣进行筛查。对于许多人来说,ECS 检测未被保险覆盖,并且该检测可能会带来重大的经济负担。对于某些患者来说,ECS 的结果不会改变他们在寻求受孕时的做法。在进行检测之前,医生应该评估患者的 ECS 结果是否会改变他们的治疗方案。