Thalamic pulvinar metabolism, sleep disturbances, and hallucinations in dementia with Lewy bodies: Positron emission tomography and actigraphy study.


Journal

International journal of geriatric psychiatry
ISSN: 1099-1166
Titre abrégé: Int J Geriatr Psychiatry
Pays: England
ID NLM: 8710629

Informations de publication

Date de publication:
08 2020
Historique:
received: 21 07 2019
revised: 04 04 2020
accepted: 24 04 2020
pubmed: 30 4 2020
medline: 4 3 2021
entrez: 30 4 2020
Statut: ppublish

Résumé

Although sleep disturbances are prevalent among patients with dementia with Lewy bodies (DLB), their neural substrates remain unclear. We aimed to clarify the neural substrates of sleep disturbances in patients with DLB. We evaluated sleep disturbances, neuropsychiatric symptoms, and brain glucose metabolism in 22 patients with probable DLB using actigraphy, the Neuropsychiatric Inventory (NPI), and TST exhibited a significant positive association with FDG uptake in the bilateral orbitofrontal cortex and left thalamus, while AAC exhibited a significant negative association with FDG uptake in the left thalamus and the left parieto-occipital region. FDG uptake in the left pulvinar was associated with both TST and AAC. In addition, TST exhibited a significant negative association with the NPI hallucinations score (r = -0.66, P = .001), while AAC exhibited significant positive associations with the NPI delusions (r = 0.70, P < .001) and hallucinations (r = 0.63, P = .002) scores. TST and bodily activity during sleep are associated with dysfunction of the left pulvinar and the severity of hallucinations in patients with DLB.

Identifiants

pubmed: 32346907
doi: 10.1002/gps.5315
doi:

Substances chimiques

Fluorodeoxyglucose F18 0Z5B2CJX4D

Banques de données

ClinicalTrials.gov
['NCT00776347']

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

934-943

Informations de copyright

© 2020 John Wiley & Sons Ltd.

Références

Mckeith IG, Galasko D, Kosaka K, et al. Consensus guidelines for the clinical and pathologic diagnosis of dementia with Lewy bodies (DLB): report of the consortium on DLB international workshop. Neurology. 1996;47:1113-1124.
Terzaghi M, Arnaldi D, Rizzetti MC, et al. Analysis of video-polysomnographic sleep findings in dementia with Lewy bodies. Mov Disord. 2013;28:1416-1423.
Pao WC, Boeve BF, Ferman TJ, et al. Polysomnographic findings in dementia with lewy bodies. Neurologist. 2013;19:1-6.
Mckeith IG, Boeve BF, Dickson DW, et al. Diagnosis and management of dementia with Lewy bodies fourth consensus report of the DLB consortium. Neurology. 2017;89:88-100.
Van Dongen HPA, Maislin G, Mullington JM, Dinges DF. The cumulative cost of additional wakefulness: dose-response effects on neurobehavioral functions and sleep physiology from chronic sleep restriction and total sleep deprivation. Sleep. 2003;2:117-126.
Kazui H, Adachi H, Kanemoto H, et al. Effects of donepezil on sleep disturbances in patients with dementia with Lewy bodies: an open-label study with actigraphy. Psychiatry Res. 2017;251:312-318.
Chiba Y, Iseki E, Fujishiro H, et al. Primary visual cortical metabolism and rapid eye movement sleep behavior disorder in dementia with Lewy bodies. Psychiatry Clin Neurosci. 2014;68:137-144.
Iaccarino L, Marelli S, Iannaccone S, Magnani G, Ferini-Strambi L, Perani D. Severe brain metabolic decreases associated with REM sleep behavior disorder in dementia with Lewy bodies. J Alzheimers Dis. 2016;52:989-997.
Kabeshita Y, Adachi H, Matsushita M, et al. Sleep disturbances are key symptoms of very early stage Alzheimer disease with behavioral and psychological symptoms: a Japan multi-center cross-sectional study (J-BIRD). Int J Geriatr Psychiatry. 2016;32:222-230. https://doi.org/10.1002/gps.4470.
Folstein M, Folstein S, McHugh P. Mini-mental state. A Practical Method for Grading the Cognitive State of Patients for the Clinician J Psychiatr Res. 1975;12:189-198.
Gelb DJ, St Laurent RT. Alternative calculation of the global clinical dementia rating. Alzheimer Dis Assoc Disord. 1993;7:202-211.
Wechsler D. WMS-R Manual. Psychological Corporation, 1987.
Ito E, Hatta T, Ito Y, Kogure T, Watanabe H. Performance of verbal fluency tasks in Japanese healthy adults-Effect of gender, age and education on the performance. Japanese J Neuropsychol. 2004;20:254-263.
Japan Society for Higher Brain Dysfunction, editor. Visual Perception Test for Agnosia: VPTA. Shinko-igaku, 2003.
Fahn S, Elton R, Members of the UPDRS Development Committee. Unified Parkinson's Disease Rating Scale. In: Fahn S, Marsden C, Calne D, Goldstein M, eds. Recent development in Parkinson's Disease. Vol 2. Florham Park, NJ: Macmillan Health Care Information; 1987:153-164.
Mori E, Ikeda M, Kosaka K. Donepezil for dementia with Lewy bodies: a randomized, placebo-controlled trial. Ann Neurol. 2012;72:41-52.
Cummings JL, Mega M, Gray K, Rosenverg-Thompson S, Carusi D, Gornvein J. The neuropsychiatric inventory: comprehensive assessment of psyhopathology in dementia. Neurology. 1994;44:2308-2314.
Cummings JL. The neuropsychiatric inventory: assessing psychopathology in dementia patients. Neurology. 1997;48:10S-16S.
Mori S, Mori E, Iseki E, Kosaka K. Efficacy and safety of donepezil in patients with dementia with Lewy bodies: preliminary findings from an open-label study. Psychiatry Clin Neurosci. 2006;60:190-195.
Escandon A, Al-Hammadi N, Galvin JE. Effect of cognitive fluctuation on neuropsychological performance in aging and dementia. Neurology. 2010;74:210-217.
Ancoli-Israel S, Cole R, Alessi C, Chambers M, Moorcroft W, Pollak CP. The role of actigraphy in the study of sleep and circadian rhythms. Sleep. 2003;26:342-392.
Natale V, Léger D, Martoni M, Bayon V, Erbacci A. The role of actigraphy in the assessment of primary insomnia: a retrospective study. Sleep Med. 2014;15:111-115.
Benson K, Friedman L, Noda A, Wicks D, Wakabayashi E, Yesavage J. The measurement of sleep by actigraphy: direct comparison of 2 commercially available actigraphs in a nonclinical population. Sleep. 2004;27:986-989.
Matsumoto K, Kitamura K, Mizuta T, et al. Performance characteristics of a new high-resolution PET camera evaluated with the NEMA NU 2-2001 standard. J Nucl Med. 2006;47:83-90.
Ishikawa A, Kitamura K, Mizuta T, Tanaka K, Amano M, Inoue Y, et al. Implementation of on-the-fly scatter correction using dual energy window method in continuous 3D whole body PET scanning. In IEEE Nuclear Science Symposium Conference Record, 2005: 2497-500. 2005.
Eskian M, Alavi A, Khorasanizadeh M, Viglianti BL, Jacobsson H. Effect of blood glucose level on standardized uptake value ( SUV ) in 18 F- FDG PET-scan: a systematic review and meta-analysis of 20, 807 individual SUV measurements. Eur J Nucl Med Mol Imaging. 2019;46:224-237.
Lancaster JL, Woldorff MG, Parsons LM, et al. Automated Talairach atlas labels for functional brain mapping. Hum Brain Mapp. 2000;10:120-131.
Lancaster JL, Rainey LH, Summerlin JL, et al. Automated labeling of the human brain: a preliminary report on the development and evaluation of a forward-transform method. Hum Brain Mapp. 1997;5:238-242.
Maldjian JA, Laurienti PJ, Kraft RA, Burdette JH. An automated method for neuroanatomic and cytoarchitectonic atlas-based interrogation of fMRI data sets. Neuroimage. 2003;19:1233-1239.
Ancoli-israel S. Sleep and its disorders in aging populations. Sleep Med. 2009;10:S7-11.
Desjardins S, Lapierre S, Hudon C, Desgagné A. Factors involved in sleep efficiency: a population-based study of community-dwelling elderly persons. Sleep. 2019;42:1-10.
Van Den Berg JF, Miedema HME, Tulen JHM, Hofman A, Neven AK, Tiemeier H. Sex differences in subjective and Actigraphic sleep measures: a population- based study of elderly persons. Sleep. 2009;32:1367-1375.
Willis MW, Ketter TA, Kimbrell TA, et al. Age, sex and laterality effects on cerebral glucose metabolism in healthy adults. Psychiatry Res-Neuroimaging. 2002;114:23-37.
Kalaitzakis ME, Gentleman SM, Pearce RKB. Disturbed sleep in Parkinson's disease: anatomical and pathological correlates. Neuropathol Appl Neurobiol. 2013;39:644-653.
Erskine D, Thomas AJ, Attems J, et al. Specific patterns of neuronal loss in the Pulvinar nucleus in dementia with Lewy bodies. Mov Disord. 2017;32:414-422.
Gent TC, Bassetti CLA, Adamantidis AR. Sleep-wake control and the thalamus. Curr Opin Neurobiol. 2018;52:188-197.
McKenna JT, Vertes RP. Afferent projections to nucleus reuniens of the thalamus. J Comp Neurol. 2004;480:115-142.
Vertes RP, Linley SB, Hoover WB. Limbic circuitry of the midline thalamus. Neurosci Biobehav Rev. 2015;54:89-107.
Van Der Werf YD, Witter MP, Groenewegen HJ. The intralaminar and midline nuclei of the thalamus. Anatomical and functional evidence for participation in processes of arousal and awareness. Brain Res Rev. 2002;39:107-140.
Baker R, Gent XTC, Yang XQ, et al. Altered activity in the central medial thalamus precedes changes in the neocortex during transitions into both sleep and propofol anesthesia. J Neurosci. 2014;34:13326-35.
Saalmann YB. Intralaminar and medial thalamic influence on cortical synchrony, information transmission and cognition. Front Syst Neurosci. 2014;8:1-8.
Magnin M, Rey M, Bastuji H, Guillemant P, Mauguière F, Garcia-larrea L. Thalamic deactivation at sleep onset precedes that of the cerebral cortex in humans. Proc Natl Acad Sci U S A. 2010;107:3829-3833.
Salsone M, Cerasa A, Arabia G, et al. Reduced thalamic volume in Parkinson disease with REM sleep behavior disorder: volumetric study. Park Relat Disord. 2014;20:1004-1008.
Boucetta S, Salimi A, Dadar M, Jones BE, Collins DL, Dang-Vu TT. Structural brain alterations associated with rapid eye movement sleep behavior disorder in Parkinson's disease. Sci Rep. 2016;6:26782.
Most EIS, Aboudan S, Scheltens P, Van Someren EJW. Discrepancy between subjective and objective sleep disturbances in early- and moderate-stage Alzheimer disease. Am J Geriatr Psychiatry. 2012;20:460-467.
Merrilees J, Hubbard E, Mastick J, Miller BL, Dowling GA. Sleep in persons with frontotemporal dementia and their family caregivers. Nurs Res. 2014;63:129-136.
Saalmann YB, Kastner S. Cognitive and perceptual functions of the visual thalamus. Neuron. 2011;71:209-223.
Komura Y, Nikkuni A, Hirashima N, Uetake T, Miyamoto A. Responses of pulvinar neurons reflect a subject's confidence in visual categorization. Nat Neurosci. 2013;16:749-755.
Magnin M, Bastuji H, Garcia-Larrea L, Mauguière F. Human thalamic medial pulvinar nucleus is not activated during paradoxical sleep. Cereb Cortex. 2004;14:858-862.
Delli Pizzi S, Franciotti R, Tartaro A, et al. Structural alteration of the dorsal visual network in DLB patients with visual hallucinations: a cortical thickness MRI study. PLoS One. 2014;9:e86624. https://doi.org/10.1371/journal.pone.0086624.
Nie S, Peng D-C, Gong H-H, Li H-J, Chen L-T, Ye C-L. Resting cerebral blood flow alteration in severe obstructive sleep apnoea: an arterial spin labelling perfusion fMRI study. Sleep Breath. 2017;21:487-495.
Innes CRH, Kelly PT, Hlavac M, Melzer TR, Jones RD. Decreased regional cerebral perfusion in moderate-severe obstructive sleep apnoea during wakefulness. Sleep. 2015;38:699-706.
Mckeith IG. Diagnosis and management of dementia with Lewy bodies: third report of the DLB consortium. Neurology. 2005;65:1863-1872.
Marino M, Li Y, Rueschman MN, et al. Measuring sleep: accuracy, sensitivity, and specificity of wrist actigraphy compared to polysomnography. Sleep. 2013;36:1747-1755.

Auteurs

Hideki Kanemoto (H)

Department of Psychiatry, Osaka University Graduate School of Medicine, Osaka, Japan.

Hiroaki Kazui (H)

Department of Psychiatry, Osaka University Graduate School of Medicine, Osaka, Japan.
Department of Neuropsychiatry, Kochi Medical School, Kochi University, Kochi, Japan.

Hiroyoshi Adachi (H)

Department of Psychiatry, Osaka University Graduate School of Medicine, Osaka, Japan.
Department of Psychiatry, Osaka University Health and Counseling Center, Osaka, Japan.

Kenji Yoshiyama (K)

Department of Psychiatry, Osaka University Graduate School of Medicine, Osaka, Japan.

Tamiki Wada (T)

Department of Psychiatry, Osaka University Graduate School of Medicine, Osaka, Japan.

Keiko T Nomura (KT)

Department of Psychiatry, Osaka University Graduate School of Medicine, Osaka, Japan.

Eku Shimosegawa (E)

Department of Molecular Imaging in Medicine, Osaka University Graduate School of Medicine, Osaka, Japan.

Manabu Ikeda (M)

Department of Psychiatry, Osaka University Graduate School of Medicine, Osaka, Japan.

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