Division of Endocrinology, University of Iowa Stead Family Children's Hospital, Iowa City, Iowa, USA.
Department of Pediatrics, University of Iowa, Iowa City, Iowa, USA.
Horm Res Paediatr. 2022;95(1):68-75. doi: 10.1159/000524169. Epub 2022 Mar 21.
Turner syndrome (TS) results from a complete or partial loss of the X chromosome and affects 25-50 per 100,000 females. These individuals have characteristic neurocognitive and psychological profiles with an increased lifetime prevalence of mood disorders, such as depression and anxiety. Consensus guidelines recommend the use of psychometrically robust tools to screen for these conditions [Eur J Endocrinol. 2017;177(3):G1-G70 and Gynecol Endocrinol. 2004;19(6):313-9]. We propose a sustainable and informative approach to routine anxiety screening in individuals with TS and describe the prevalence of anxiety, genotype-phenotype associations, and impact of comorbidities on anxiety.
We pilot the use of a self-administered version of the validated Pediatric, Parent Proxy, and Adult Patient-Reported Outcomes Measurement Information System (PROMIS®) Anxiety tool during routine visits to the Cincinnati Children's Hospital Medical Center (CCHMC) TS clinic from October 2019 to March 2020.
Ninety-two eligible TS females, ages 8-62 years, received the PROMIS® Anxiety measure. Elevated anxiety scores, ≥1 standard deviation above the T-score mean, were present in 65% of patients (38% mild, 19% moderate, and 8% severe). Results were discussed during the clinic visit, and referral for further evaluation and treatment was offered. There was no apparent genotype-phenotype association among females with anxiety; however, there appeared to be elevated anxiety symptoms (T-score >60) in those with hearing deficits and also in individuals with three or more medical comorbidities. Of the 55% of patients who filled out the acceptability survey, 88% found the process helpful and ∼50% felt that screening should be performed at least every 6 months.
Our study demonstrated a high prevalence of anxiety symptoms within a cohort of 92 females with TS. In alignment with current guidelines, these findings indicate the importance of routine neuropsychological assessments for timely recognition and subsequent management of anxiety, especially as milder presentations may otherwise go unnoticed. We have shown that screening tools, such as the PROMIS® Anxiety measure, can be easily utilized by nonmental health care providers (i.e., endocrinologists) who may see TS patients more frequently and be able to initiate impactful discussions surrounding mental health and further referral to subspecialists for expert management.
特纳综合征(TS)是由于 X 染色体完全或部分缺失引起的,影响每 10 万名女性中有 25-50 名。这些个体具有特征性的神经认知和心理特征,终生患心境障碍(如抑郁症和焦虑症)的患病率增加。共识指南建议使用心理测量学上可靠的工具来筛查这些疾病[Eur J Endocrinol. 2017;177(3):G1-G70 和 Gynecol Endocrinol. 2004;19(6):313-9]。我们提出了一种可持续且信息丰富的方法,用于对 TS 个体进行常规焦虑筛查,并描述焦虑的患病率、基因型-表型相关性以及合并症对焦虑的影响。
我们在 2019 年 10 月至 2020 年 3 月期间,在辛辛那提儿童医院医疗中心(CCHMC)TS 诊所的常规就诊期间,试用了经过验证的儿科、父母代理和成人患者报告的测量信息系统(PROMIS®)焦虑工具的自我管理版本。
92 名符合条件的 TS 女性,年龄 8-62 岁,接受了 PROMIS®焦虑测量。65%的患者存在焦虑评分升高,高于 T 评分平均值 1 个标准差(38%轻度、19%中度和 8%重度)。在就诊期间讨论了结果,并提供了进一步评估和治疗的转介。在有焦虑的女性中,没有明显的基因型-表型相关性;然而,在有听力缺陷的个体中,以及在有三种或更多种合并症的个体中,似乎存在焦虑症状升高(T 评分>60)。在填写可接受性调查的 55%的患者中,88%的患者认为该过程有帮助,约 50%的患者认为至少每 6 个月应进行一次筛查。
我们的研究在 92 名 TS 女性队列中显示出焦虑症状的高患病率。与当前指南一致,这些发现表明,为了及时识别和随后管理焦虑症,需要进行常规神经心理评估,尤其是因为轻度焦虑症可能会被忽视。我们已经表明,筛查工具,如 PROMIS®焦虑量表,可以由非心理健康护理提供者(即内分泌学家)轻松使用,他们可能更频繁地看到 TS 患者,并能够围绕心理健康问题展开有意义的讨论,并进一步转介给专家以进行专业管理。