Wills Ben Curran, Matthews Margaret M, Johnston Josephine, Bolo Isabel, Ottman Ruth, Appelbaum Paul S
University of California San Diego, La Jolla, California; At the time of the study: The Hastings Center, Garrison, New York; At the time of the study: Georgia Institute of Technology, Atlanta, Georgia.
At the time of the study: The Hastings Center, Garrison, New York; Harvard University, Cambridge, Massachusetts.
J Am Acad Child Adolesc Psychiatry. 2025 Jul 3. doi: 10.1016/j.jaac.2025.06.024.
To perform a systematic literature review of the psychosocial impacts on parents and autistic people of receiving autism-related genetic test results.
Systematic searches of MEDLINE, PsycINFO, CINAHL, Web of Science Core Collection, Sociological Index, and Scopus were conducted for articles appearing through October 27, 2024. The authors screened 3,606 articles. The quality of the included articles was assessed with the QuADS appraisal tool.
Twenty-two articles met inclusion criteria. Across research and clinical settings, articles assessed impacts of receiving actual (n=18) or hypothetical (n=4) genetic test results. Twenty articles assessed impacts on parents and prospective parents, while two assessed impacts on autistic adults. Psychological impacts of receiving results varied and included relief, peace of mind, reduced guilt, disappointment, fear, frustration, stress, blame, and guilt. Comparison of the frequencies of these responses was limited by heterogeneous assessment methods, variable reporting formats, and inconsistent outcome measures across studies. Receiving results sometimes confirmed diagnoses, led to altered care plans, influenced family planning, or impacted the decision to end or continue a pregnancy. Most articles reported low-to-mild or highly variable satisfaction with the testing experience. Studies of autistic adults reported strong concerns about testing without consent and discriminatory uses of genetics.
Impacts on parents and prospective parents appear relatively modest, albeit with mixed valences-a finding broadly similar to return-of-results studies for other complex genetic conditions. Although the findings of the two studies of autistic adults differ substantially, they suggest that autistic people and current and prospective parents of autistic children may have significantly different experiences and perspectives. Clinicians should recognize these differences and help parents understand and weigh them in decision-making.
对自闭症相关基因检测结果对父母和自闭症患者的心理社会影响进行系统的文献综述。
对MEDLINE、PsycINFO、CINAHL、科学网核心合集、社会学索引和Scopus进行系统检索,查找截至2024年10月27日发表的文章。作者筛选了3606篇文章。使用QuADS评估工具对纳入文章的质量进行评估。
22篇文章符合纳入标准。在研究和临床环境中,文章评估了收到实际(n = 18)或假设(n = 4)基因检测结果的影响。20篇文章评估了对父母和准父母的影响,而两篇评估了对成年自闭症患者的影响。收到结果的心理影响各不相同,包括宽慰、安心、内疚感减轻、失望、恐惧、沮丧、压力、指责和内疚。由于评估方法各异、报告格式不同以及各研究结果测量不一致,这些反应频率的比较受到限制。收到结果有时会确诊,导致护理计划改变,影响计划生育,或影响终止或继续妊娠的决定。大多数文章报告对检测体验的满意度为低至中度或高度可变。对成年自闭症患者的研究报告了对未经同意进行检测和基因歧视性使用的强烈担忧。
对父母和准父母的影响似乎相对较小,尽管有积极和消极的不同影响——这一发现与其他复杂基因疾病的结果反馈研究大致相似。尽管对成年自闭症患者的两项研究结果差异很大,但它们表明自闭症患者以及自闭症儿童的现任和准父母可能有显著不同的经历和观点。临床医生应认识到这些差异,并帮助父母在决策过程中理解并权衡这些差异。