Department of Psychiatry, Osaka University Graduate School of Medicine, Suita, Japan.
Department of Molecular Imaging in Medicine, Osaka University Graduate School of Medicine, Suita, Japan.
Int Psychogeriatr. 2024 Jan;36(1):64-77. doi: 10.1017/S1041610222001132. Epub 2023 Jan 30.
We aimed to investigate the association between very late-onset schizophrenia-like psychosis (VLOSLP), a schizophrenia spectrum disorder with an onset of ≥60 years, and Alzheimer's disease (AD) using biomarkers.
Retrospective cross-sectional study.
Neuropsychology clinic of Osaka University Hospital in Japan.
Thirty-three participants were classified into three groups: eight AD biomarker-negative VLOSLP (VLOSLP-AD), nine AD biomarker-positive VLOSLP (VLOSLP+AD), and sixteen amnestic mild cognitive impairment due to AD without psychosis (aMCI-P+AD) participants.
Phosphorylated tau levels in the cerebrospinal fluid and F-Florbetapir positron emission tomography results were used as AD biomarkers. Several scales (e.g. the Mini-Mental State Examination (MMSE), Wechsler Memory Scale-Revised (WMS-R) Logical Memory (LM) I and II, and Neuropsychiatric Inventory (NPI)-plus) were conducted to assess clinical characteristics.
Those in both VLOSLP-AD and +AD groups scored higher than those in aMCI-P+AD in WMS-R LM I. On the other hand, VLOSLP+AD participants scored in between the other two groups in the WMS-R LM II, with only VLOSLP-AD participants scoring significantly higher than aMCI-P+AD participants. There were no significant differences in sex distribution and MMSE scores among the three groups or in the subtype of psychotic symptoms between VLOSLP-AD and +AD participants. Four VLOSLP-AD and five VLOSLP+AD participants harbored partition delusions. Delusion of theft was shown in two VLOSLP-AD patients and five VLOSLP+AD patients.
Some VLOSLP patients had AD pathology. Clinical characteristics were different between AD biomarker-positive and AD biomarker-negative VLOSLP, which may be helpful for detecting AD pathology in VLOSLP patients.
我们旨在使用生物标志物研究发病年龄≥60 岁的极晚发性精神分裂样精神病(VLOSLP)——一种精神分裂症谱系障碍——与阿尔茨海默病(AD)之间的关联。
回顾性横断面研究。
日本大阪大学医院神经心理学诊所。
33 名参与者被分为三组:8 名 AD 生物标志物阴性 VLOSLP(VLOSLP-AD)、9 名 AD 生物标志物阳性 VLOSLP(VLOSLP+AD)和 16 名无精神病的 AD 所致遗忘性轻度认知障碍(aMCI-P+AD)参与者。
脑脊液中磷酸化 tau 水平和 F-Florbetapir 正电子发射断层扫描结果被用作 AD 生物标志物。使用了几个量表(例如,简易精神状态检查(MMSE)、韦氏记忆量表修订版(WMS-R)逻辑记忆(LM)I 和 II 以及神经精神病学问卷(NPI)-plus)来评估临床特征。
VLOSLP-AD 和 +AD 组的 WMS-R LM I 评分均高于 aMCI-P+AD 组。另一方面,VLOSLP+AD 组的 WMS-R LM II 评分在其他两组之间,只有 VLOSLP-AD 组的评分显著高于 aMCI-P+AD 组。三组之间的性别分布和 MMSE 评分或 VLOSLP-AD 和 +AD 组之间的精神病症状亚型均无显著差异。4 名 VLOSLP-AD 和 5 名 VLOSLP+AD 患者存在分裂妄想。2 名 VLOSLP-AD 患者和 5 名 VLOSLP+AD 患者存在盗窃妄想。
一些 VLOSLP 患者存在 AD 病理。AD 生物标志物阳性和 AD 生物标志物阴性 VLOSLP 之间的临床特征不同,这可能有助于在 VLOSLP 患者中检测 AD 病理。