年轻发病痴呆综合征和原发性精神疾病的诊断挑战:来自20年回顾性横断面研究的结果

Paraskevi Tsoukra, Dennis Velakoulis, Pierre Wibawa, Charles B Malpas, Mark Walterfang, Andrew Evans, Sarah Farrand, Wendy Kelso, Dhamidhu Eratne, Samantha M Loi
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引用次数: 12

摘要

目的:在年轻患者中区分痴呆综合征与原发性精神疾病可能具有挑战性,并可能随着时间的推移导致诊断改变。研究人员旨在检查一组年轻发病的神经认知障碍患者的诊断稳定性。方法:回顾性分析2000年至2019年住院神经精神病学服务单元的患者的记录,这些患者至少随访了12个月,并且在任何时间点被诊断为早发性痴呆。初步诊断包括阿尔茨海默病型痴呆(N=30)、额颞叶痴呆(FTD)综合征(N=44)、血管性痴呆(N=7)、轻度认知障碍(N=10)、原发性精神疾病(N=6)和其他疾病,如路易体痴呆(N=30)。结果:127例患者中,49例(39%)在随访期间改变了最初的诊断。行为变异性FTD (bvFTD)是最不稳定的诊断,其次是未明确说明的痴呆和轻度认知障碍。与诊断稳定的患者相比,那些改变的患者在基线时表现出更高的认知评分,更长的随访期,更长的最终诊断延迟,并且没有痴呆家族史。从神经退行性疾病诊断变为精神疾病诊断的患者更有可能有较长的精神病史,而从精神疾病诊断变为神经退行性疾病诊断的患者最近有精神症状的表现。结论:年轻患者神经认知障碍的误诊并不罕见,特别是在bvFTD病例中。晚发性精神症状可能是神经退行性疾病的先兆。有必要对这些患者进行密切的随访和监测。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Diagnostic Challenge of Young-Onset Dementia Syndromes and Primary Psychiatric Diseases: Results From a Retrospective 20-Year Cross-Sectional Study.

Objective: Distinguishing a dementia syndrome from a primary psychiatric disease in younger patients can be challenging and may lead to diagnostic change over time. The investigators aimed to examine diagnostic stability in a cohort of patients with younger-onset neurocognitive disorders.

Methods: A retrospective review of records was conducted for patients who were admitted to an inpatient neuropsychiatry service unit between 2000 and 2019, who were followed up for at least 12 months, and who received a diagnosis of young-onset dementia at any time point. Initial diagnosis included Alzheimer's disease-type dementia (N=30), frontotemporal dementia (FTD) syndromes (N=44), vascular dementia (N=7), mild cognitive impairment (N=10), primary psychiatric diseases (N=6), and other conditions, such as Lewy body dementia (N=30).

Results: Among 127 patients, 49 (39%) had a change in their initial diagnoses during the follow-up period. Behavioral variant FTD (bvFTD) was the least stable diagnosis, followed by dementia not otherwise specified and mild cognitive impairment. Compared with patients with a stable diagnosis, those who changed exhibited a higher cognitive score at baseline, a longer follow-up period, greater delay to final diagnosis, and no family history of dementia. Patients whose diagnosis changed from a neurodegenerative to a psychiatric diagnosis were more likely to have a long psychiatric history, while those whose diagnosis changed from a psychiatric to a neurodegenerative one had a recent manifestation of psychiatric symptoms.

Conclusions: Misdiagnosis of younger patients with neurocognitive disorders is not uncommon, especially in cases of bvFTD. Late-onset psychiatric symptoms may be the harbinger to a neurodegenerative disease. Close follow-up and monitoring of these patients are necessary.

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