{"title":"阿尔茨海默病导致的轻度认知障碍患者的睡眠片段和睡眠-觉醒周期失调与脑Tau负担有关:病例系列","authors":"Mariana Fernandes, Agostino Chiaravalloti, Emanuele Cassetta, Fabio Placidi, Nicola Biagio Mercuri, Claudio Liguori","doi":"10.3233/ADR-230187","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Although disturbed sleep is frequent in patients with mild cognitive impairment (MCI) and dementia due to Alzheimer's disease (AD), the association between sleep and tau pathology is unclear.</p><p><strong>Objective: </strong>This case series focused on measuring the sleep-wake rhythm over 7 days through actigraphy in patients diagnosed with MCI due to AD. Further, the association between sleep-wake cycle and tau deposition measured through positron emission tomography (PET) was explored.</p><p><strong>Methods: </strong>This case series included 6 MCI due to AD patients (2 women and 4 men, mean age 73.17±5.53 years), who completed neuropsychological testing, 7-day actigraphy, and tau PET imaging with radiolabeled compounds aimed to estimate the density and distribution of aggregated tau neurofibrillary tangles in the brain.</p><p><strong>Results: </strong>The case series indicated that patients with MCI due to AD who exhibited greater tau deposition in the frontal, parietal, and limbic regions, as well as in the precuneus and olfactory regions, also showed increased sleep fragmentation, as measured through actigraphy.</p><p><strong>Conclusion: </strong>The findings from this case series suggest a potential link between tau deposition in key brain regions associated with AD and both sleep fragmentation and sleep-wake cycle dysregulation in a small sample of patients with MCI due to AD. These preliminary results warrant further investigation in larger, more comprehensive studies to confirm and expand upon these findings.</p>","PeriodicalId":73594,"journal":{"name":"Journal of Alzheimer's disease reports","volume":"8 1","pages":"1275-1283"},"PeriodicalIF":2.8000,"publicationDate":"2024-09-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11491934/pdf/","citationCount":"0","resultStr":"{\"title\":\"Sleep Fragmentation and Sleep-Wake Cycle Dysregulation Are Associated with Cerebral Tau Burden in Patients with Mild Cognitive Impairment due to Alzheimer's Disease: A Case Series.\",\"authors\":\"Mariana Fernandes, Agostino Chiaravalloti, Emanuele Cassetta, Fabio Placidi, Nicola Biagio Mercuri, Claudio Liguori\",\"doi\":\"10.3233/ADR-230187\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Although disturbed sleep is frequent in patients with mild cognitive impairment (MCI) and dementia due to Alzheimer's disease (AD), the association between sleep and tau pathology is unclear.</p><p><strong>Objective: </strong>This case series focused on measuring the sleep-wake rhythm over 7 days through actigraphy in patients diagnosed with MCI due to AD. Further, the association between sleep-wake cycle and tau deposition measured through positron emission tomography (PET) was explored.</p><p><strong>Methods: </strong>This case series included 6 MCI due to AD patients (2 women and 4 men, mean age 73.17±5.53 years), who completed neuropsychological testing, 7-day actigraphy, and tau PET imaging with radiolabeled compounds aimed to estimate the density and distribution of aggregated tau neurofibrillary tangles in the brain.</p><p><strong>Results: </strong>The case series indicated that patients with MCI due to AD who exhibited greater tau deposition in the frontal, parietal, and limbic regions, as well as in the precuneus and olfactory regions, also showed increased sleep fragmentation, as measured through actigraphy.</p><p><strong>Conclusion: </strong>The findings from this case series suggest a potential link between tau deposition in key brain regions associated with AD and both sleep fragmentation and sleep-wake cycle dysregulation in a small sample of patients with MCI due to AD. 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引用次数: 0
摘要
背景:尽管轻度认知功能障碍(MCI)和阿尔茨海默病(AD)导致的痴呆症患者经常出现睡眠障碍,但睡眠与tau病理学之间的关系尚不清楚:虽然轻度认知障碍(MCI)和阿尔茨海默病(AD)导致的痴呆患者经常出现睡眠障碍,但睡眠与tau病理学之间的关系尚不清楚:本病例系列主要通过对确诊为轻度认知障碍(MCI)和阿尔兹海默症(AD)所致痴呆症(Dementia)的患者进行7天的睡眠-觉醒节律测量。此外,还探讨了睡眠-觉醒周期与正电子发射断层扫描(PET)测量的 tau 沉积之间的关联:该病例系列包括 6 名因 AD 引起的 MCI 患者(2 名女性和 4 名男性,平均年龄(73.17±5.53)岁),他们完成了神经心理测试、7 天动图仪和使用放射性标记化合物进行的 tau PET 成像,目的是估计大脑中聚集的 tau 神经纤维缠结的密度和分布:结果:病例系列显示,AD 引起的 MCI 患者在额叶、顶叶、边缘区以及楔前区和嗅区有较多的 tau 沉积,同时,通过行为记录仪测量,他们的睡眠片段也有所增加:本系列病例的研究结果表明,在小样本的AD导致的MCI患者中,与AD相关的关键脑区的tau沉积与睡眠片段和睡眠-觉醒周期失调之间存在潜在联系。这些初步结果值得在更大规模、更全面的研究中进一步调查,以证实和扩展这些发现。
Sleep Fragmentation and Sleep-Wake Cycle Dysregulation Are Associated with Cerebral Tau Burden in Patients with Mild Cognitive Impairment due to Alzheimer's Disease: A Case Series.
Background: Although disturbed sleep is frequent in patients with mild cognitive impairment (MCI) and dementia due to Alzheimer's disease (AD), the association between sleep and tau pathology is unclear.
Objective: This case series focused on measuring the sleep-wake rhythm over 7 days through actigraphy in patients diagnosed with MCI due to AD. Further, the association between sleep-wake cycle and tau deposition measured through positron emission tomography (PET) was explored.
Methods: This case series included 6 MCI due to AD patients (2 women and 4 men, mean age 73.17±5.53 years), who completed neuropsychological testing, 7-day actigraphy, and tau PET imaging with radiolabeled compounds aimed to estimate the density and distribution of aggregated tau neurofibrillary tangles in the brain.
Results: The case series indicated that patients with MCI due to AD who exhibited greater tau deposition in the frontal, parietal, and limbic regions, as well as in the precuneus and olfactory regions, also showed increased sleep fragmentation, as measured through actigraphy.
Conclusion: The findings from this case series suggest a potential link between tau deposition in key brain regions associated with AD and both sleep fragmentation and sleep-wake cycle dysregulation in a small sample of patients with MCI due to AD. These preliminary results warrant further investigation in larger, more comprehensive studies to confirm and expand upon these findings.