Consensus Paper: Cerebellum and Ageing

被引:43
作者
Arleo, Angelo [1 ]
Bares, Martin [2 ,3 ,4 ]
Bernard, Jessica A. [5 ,6 ]
Bogoian, Hannah R. [7 ]
Bruchhage, Muriel M. K. [8 ,9 ,10 ,11 ]
Bryant, Patrick [12 ]
Carlson, Erik S. [13 ,14 ]
Chan, Chetwyn C. H. [15 ]
Chen, Liang-Kung [16 ,17 ,18 ]
Chung, Chih-Ping [16 ,19 ]
Dotson, Vonetta M. [7 ,20 ]
Filip, Pavel [21 ,22 ,23 ]
Guell, Xavier [24 ,25 ,26 ]
Habas, Christophe [27 ,28 ]
Jacobs, Heidi I. L. [25 ,29 ,30 ,31 ]
Kakei, Shinji [32 ]
Lee, Tatia M. C. [33 ,34 ]
Leggio, Maria
Misiura, Maria [7 ,35 ,36 ]
Mitoma, Hiroshi [37 ]
Olivito, Giusy [35 ,36 ]
Ramanoel, Stephen [1 ,38 ]
Rezaee, Zeynab [39 ]
Samstag, Colby L. [13 ,14 ]
Schmahmann, Jeremy D. [24 ,25 ,26 ,40 ]
Sekiyama, Kaoru [41 ]
Wong, Clive H. Y. [15 ]
Yamashita, Masatoshi [42 ,43 ,44 ]
Manto, Mario [45 ,46 ]
机构
[1] Sorbonne Univ, Inst Vis, INSERM, CNRS, 17 Rue Moreau, F-75012 Paris, France
[2] Masaryk Univ, Fac Med, Dept Neurol 1, Brno, Czech Republic
[3] St Annes Teaching Hosp, Brno, Czech Republic
[4] Univ Minnesota, Sch Med, Dept Neurol, Minneapolis, MN USA
[5] Texas A&M Univ, Dept Psychol & Brain Sci, 4235 TAMU, College Stn, TX 77843 USA
[6] Texas A&M Univ, Texas A&M Inst Neurosci, College Stn, TX USA
[7] Georgia State Univ, Dept Psychol, Atlanta, GA USA
[8] Stavanger Univ, Inst Social Sci, Dept Psychol, Kjell Arholms Gate 41, N-4021 Stavanger, Norway
[9] Kings Coll London, Inst Psychiat Psychol & Neurosci, Ctr Neuroimaging Sci, Box 89,De Crespigny Pk, London SE5 8AF, England
[10] Rhode Isl Hosp, Dept Diagnost Imaging, 1 Hoppin St, Providence, RI 02903 USA
[11] Brown Univ, Dept Paediat, Warren Alpert Med Sch, 222 Richmond St, Providence, RI 02903 USA
[12] Free Univ Berlin, Fachbereich Math & Informat, Arnimallee 12, D-14195 Berlin, Germany
[13] Univ Washington, Dept Psychiat & Behav Sci, Seattle, WA USA
[14] Vet Affairs Med Ctr, Geriatr Res Educ & Clin Ctr, Puget Sound, Seattle, WA USA
[15] Educ Univ Hong Kong, Dept Psychol, Tai Po, Hong Kong, Peoples R China
[16] Natl Yang Ming Chiao Tung Univ, Ctr Hlth Longev & Aging Sci, Coll Med, Taipei, Taiwan
[17] Taipei Vet Gen Hosp, Ctr Geriatr & Gerontol, Taipei, Taiwan
[18] Taipei Vet Gen Hosp, Taipei Municipal Gan Dau Hosp, Taipei, Taiwan
[19] Taipei Vet Gen Hosp, Neurol Inst, Dept Neurol, Taipei, Taiwan
[20] Georgia State Univ, Gerontol Inst, Atlanta, GA USA
[21] Charles Univ Prague, Fac Med 1, Dept Neurol, Prague, Czech Republic
[22] Gen Univ Hosp, Prague, Czech Republic
[23] Univ Minnesota, Ctr Magnet Resonance Res CMRR, Minneapolis, MN USA
[24] Massachusetts Gen Hosp, Dept Neurol, Boston, MA USA
[25] Harvard Med Sch, Boston, MA USA
[26] Massachusetts Gen Hosp, Lab Neuroanat & Cerebellar Neurobiol, Boston, MA USA
[27] CHNO Quinze Vingts, INSERM DGOS CIC 1423, 28 Rue Charenton, F-75012 Paris, France
[28] Univ Versailles St Quentin En Yvelines, Paris, France
[29] Maastricht Univ, Alzheimer Ctr Limburg, Sch Mental Hlth & Neurosci, POB 616, NL-6200 MD Maastricht, Netherlands
[30] Maastricht Univ, Fac Psychol & Neurosci, Dept Cognit Neurosci, POB 616, NL-6200 MD Maastricht, Netherlands
[31] Massachusetts Gen Hosp, Gordon Ctr Med Imaging, Dept Radiol, Boston, MA USA
[32] Jissen Womens Univ, Tokyo, Japan
[33] Univ Hong Kong, State Key Lab Brain & Cognit Sci, Hong Kong, Peoples R China
[34] Univ Hong Kong, Dept Psychol, Lab Neuropsychol & Human Neurosci, Hong Kong, Peoples R China
[35] Sapienza Univ Rome, Dept Psychol, Rome, Italy
[36] IRCCS Santa Lucia Fdn, Ataxia Lab, Rome, Italy
[37] Tokyo Med Univ, Dept Med Educ, Tokyo, Japan
[38] Univ Cote Azur, LAMHESS, Nice, France
[39] NIMH, Noninvas Neuromodulat Unit, Expt Therapeut & Pathophysiol Branch, NIH, Bethesda, MD USA
[40] Massachusetts Gen Hosp, Ataxia Ctr, Cognit Behav Neurol Unit, Boston, MA USA
[41] Kyoto Univ, Grad Sch Adv Integrated Studies Human Survivabil, Kyoto, Japan
[42] Univ Fukui, Res Ctr Child Mental Dev, Fukui, Japan
[43] Osaka Univ, Kanazawa Univ, Hamamatsu Univ Sch Med, Chiba Univ,United Grad Sch Child Dev, Osaka, Japan
[44] Univ Fukui, Osaka, Japan
[45] CHU Charleroi, Serv Neurol, Mediatheque Jean Jacquy, Charleroi, Belgium
[46] Univ Mons, Serv Neurosci, Mons, Belgium
基金
日本学术振兴会; 美国国家科学基金会;
关键词
Cerebellum; Aging; Motor; Cognitive; Affective; Alzheimer's Disease; DIRECT-CURRENT STIMULATION; FUNCTIONAL CONNECTIVITY; GRAY-MATTER; ALZHEIMERS-DISEASE; MOTOR CORTEX; NEUROFIBRILLARY TANGLES; INDIVIDUAL-DIFFERENCES; PREFRONTAL CORTEX; AMYLOID PLAQUES; NEURAL-NETWORKS;
D O I
10.1007/s12311-023-01577-7
中图分类号
Q189 [神经科学];
学科分类号
071006 ;
摘要
Given the key roles of the cerebellum in motor, cognitive, and affective operations and given the decline of brain functions with aging, cerebellar circuitry is attracting the attention of the scientific community. The cerebellum plays a key role in timing aspects of both motor and cognitive operations, including for complex tasks such as spatial navigation. Anatomically, the cerebellum is connected with the basal ganglia via disynaptic loops, and it receives inputs from nearly every region in the cerebral cortex. The current leading hypothesis is that the cerebellum builds internal models and facilitates automatic behaviors through multiple interactions with the cerebral cortex, basal ganglia and spinal cord. The cerebellum undergoes structural and functional changes with aging, being involved in mobility frailty and related cognitive impairment as observed in the physio-cognitive decline syndrome (PCDS) affecting older, functionally-preserved adults who show slowness and/or weakness. Reductions in cerebellar volume accompany aging and are at least correlated with cognitive decline. There is a strongly negative correlation between cerebellar volume and age in cross-sectional studies, often mirrored by a reduced performance in motor tasks. Still, predictive motor timing scores remain stable over various age groups despite marked cerebellar atrophy. The cerebello-frontal network could play a significant role in processing speed and impaired cerebellar function due to aging might be compensated by increasing frontal activity to optimize processing speed in the elderly. For cognitive operations, decreased functional connectivity of the default mode network (DMN) is correlated with lower performances. Neuroimaging studies highlight that the cerebellum might be involved in the cognitive decline occurring in Alzheimer's disease (AD), independently of contributions of the cerebral cortex. Grey matter volume loss in AD is distinct from that seen in normal aging, occurring initially in cerebellar posterior lobe regions, and is associated with neuronal, synaptic and beta-amyloid neuropathology. Regarding depression, structural imaging studies have identified a relationship between depressive symptoms and cerebellar gray matter volume. In particular, major depressive disorder (MDD) and higher depressive symptom burden are associated with smaller gray matter volumes in the total cerebellum as well as the posterior cerebellum, vermis, and posterior Crus I. From the genetic/epigenetic standpoint, prominent DNA methylation changes in the cerebellum with aging are both in the form of hypo- and hyper-methylation, and the presumably increased/decreased expression of certain genes might impact on motor coordination. Training influences motor skills and lifelong practice might contribute to structural maintenance of the cerebellum in old age, reducing loss of grey matter volume and therefore contributing to the maintenance of cerebellar reserve. Non-invasive cerebellar stimulation techniques are increasingly being applied to enhance cerebellar functions related to motor, cognitive, and affective operations. They might enhance cerebellar reserve in the elderly. In conclusion, macroscopic and microscopic changes occur in the cerebellum during the lifespan, with changes in structural and functional connectivity with both the cerebral cortex and basal ganglia. With the aging of the population and the impact of aging on quality of life, the panel of experts considers that there is a huge need to clarify how the effects of aging on the cerebellar circuitry modify specific motor, cognitive, and affective operations both in normal subjects and in brain disorders such as AD or MDD, with the goal of preventing symptoms or improving the motor, cognitive, and affective symptoms.
引用
收藏
页码:802 / 832
页数:31
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