Department of Biomedical and Neuromotor Sciences, University of Bologna, Bologna, Italy.
Department of Mental Health and Substance Abuse, Local Health Trust of Bologna, BolognaItaly.
Sleep. 2024 Nov 8;47(11). doi: 10.1093/sleep/zsad234.
Pseudocataplexy is a rare functional neurological disorder that mimics cataplexy, pathognomonic for narcolepsy type 1 (NT1). We describe the psychiatric comorbidity and personality traits of patients with pseudocataplexy versus NT1 cases.
The case-control observational study enrolled consecutive patients with pseudocataplexy and a control group of age-matched consecutive NT1 patients. The diagnostic work-up included a structured interview, 48-hour polysomnography, multiple sleep latency test, cataplexy provoking test, and hypocretin-1 measurement in cerebrospinal fluid. All participants were administered Beck Depression Inventory, State-Trait Anxiety Inventory, Patient Health Questionnaire-15 (PHQ-15), Personality Inventory for DSM-5 brief form, and quality-of-life (QoL) measurement by 36-item Short Form health survey (SF-36).
Fifteen patients with pseudocataplexy and 30 with NT1 were included. Despite the suspicion of possible cataplexy, none of the pseudocataplexy participants fulfilled international diagnostic criteria for NT1. Pseudocataplexy patients presented higher rates of moderate state anxiety (40% vs. 10%, p = 0.018), medium level of somatic symptoms, defined by PHQ-15 score > 10 (66.7% vs. 16.7%, p = 0.003), and a trend towards moderate-to-severe depressive symptoms (33.3% vs. 10%, p = 0.054) compared to NT1. No significant differences in personality traits emerged. Pseudocataplexy patients had worse QoL profiles in almost all SF-36 domains including physical (mean ± SD: 37.7 ± 9.88 vs. 51.13 ± 7.81, p < 0.001) and mental (mean ± SD: 33.36 ± 12.69 vs.42.76 ± 11.34, p = 0.02) summary scores.
Patients with pseudocataplexy present more severe psychiatric symptoms and a lower QoL profile in comparison with patients with NT1. The severe somatoform and affection impairment in pseudocataplexy may explain the poorer QoL and should require a tailored therapeutic approach.
假性猝倒症是一种罕见的功能性神经障碍,模仿猝倒症,是 1 型发作性睡病(NT1)的特征性表现。我们描述了假性猝倒症患者与 NT1 病例的精神共病和人格特征。
这项病例对照观察性研究纳入了连续的假性猝倒症患者和一组年龄匹配的连续 NT1 患者作为对照组。诊断性评估包括结构性访谈、48 小时多导睡眠图、多次睡眠潜伏期试验、猝倒诱发试验和脑脊液中下丘脑泌素-1 测量。所有参与者均接受贝克抑郁量表、状态特质焦虑量表、患者健康问卷-15(PHQ-15)、DSM-5 简明人格量表和 36 项简明健康调查(SF-36)的生活质量(QoL)测量。
纳入了 15 名假性猝倒症患者和 30 名 NT1 患者。尽管怀疑可能存在猝倒症,但假性猝倒症患者无一例符合 NT1 的国际诊断标准。假性猝倒症患者表现出更高的中度状态焦虑发生率(40%比 10%,p=0.018)、更高的躯体症状水平,定义为 PHQ-15 评分>10(66.7%比 16.7%,p=0.003),以及中度至重度抑郁症状的趋势(33.3%比 10%,p=0.054),与 NT1 相比。在人格特征方面没有出现显著差异。假性猝倒症患者在 SF-36 几乎所有领域的 QoL 评分都较差,包括身体(平均±标准差:37.7±9.88 比 51.13±7.81,p<0.001)和心理(平均±标准差:33.36±12.69 比 42.76±11.34,p=0.02)综合评分。
与 NT1 患者相比,假性猝倒症患者的精神症状更严重,QoL 评分更低。假性猝倒症严重的躯体形式和情感障碍可能解释了较差的 QoL,并需要有针对性的治疗方法。