Literature DB >> 28672395

Association Between Motor Symptoms and Brain Metabolism in Early Huntington Disease.

Véronique Gaura1,2,3, Sonia Lavisse1,2, Pierre Payoux4,5, Serge Goldman6, Christophe Verny7, Pierre Krystkowiak8, Philippe Damier9,10, Frédéric Supiot6, Anne-Catherine Bachoud-Levi11,12,13,14,15, Philippe Remy1,2,12,14,16.   

Abstract

Importance: Brain hypometabolism is associated with the clinical consequences of the degenerative process, but little is known about regional hypermetabolism, sometimes observed in the brain of patients with clinically manifest Huntington disease (HD). Studying the role of regional hypermetabolism is needed to better understand its interaction with the motor symptoms of the disease. Objective: To investigate the association between brain hypometabolism and hypermetabolism with motor scores of patients with early HD. Design, Setting, and Participants: This study started in 2001, and analysis was completed in 2016. Sixty symptomatic patients with HD and 15 healthy age-matched control individuals underwent positron emission tomography to measure cerebral metabolism in this cross-sectional study. They also underwent the Unified Huntington's Disease Rating Scale motor test, and 2 subscores were extracted: (1) a hyperkinetic score, combining dystonia and chorea, and (2) a hypokinetic score, combining bradykinesia and rigidity. Main Outcomes and Measures: Statistical parametric mapping software (SPM5) was used to identify all hypo- and hypermetabolic regions in patients with HD relative to control individuals. Correlation analyses (P < .001, uncorrected) between motor subscores and brain metabolic values were performed for regions with significant hypometabolism and hypermetabolism.
Results: Among 60 patients with HD, 22 were women (36.7%), and the mean (SD) age was 44.6 (7.6) years. Of the 15 control individuals, 7 were women (46.7%), and the mean (SD) age was 42.2 (7.3) years. In statistical parametric mapping, striatal hypometabolism was significantly correlated with the severity of all motor scores. Hypermetabolism was negatively correlated only with hypokinetic scores in the cuneus (z score = 3.95, P < .001), the lingual gyrus (z score = 4.31, P < .001), and the crus I/II of the cerebellum (z score = 3.77, P < .001), a region connected to associative cortical areas. More severe motor scores were associated with higher metabolic values in the inferior parietal lobule, anterior cingulate, inferior temporal lobule, the dentate nucleus, and the cerebellar lobules IV/V, VI, and VIII bilaterally corresponding to the motor regions of the cerebellum (z score = 3.96 and 3.42 in right and left sides, respectively; P < .001). Conclusions and Relevance: Striatal hypometabolism is associated with clinical disease severity. Conversely, hypermetabolism is likely compensatory in regions where it is associated with decreasing motor scores. Hypermetabolism might be detrimental in other structures in which it is associated with more severe motor symptoms. In the cerebellum, both compensatory and detrimental contributions seem to occur. This study helps to better understand the motor clinical relevance of hypermetabolic brain regions in HD.

Entities:  

Mesh:

Year:  2017        PMID: 28672395      PMCID: PMC5710184          DOI: 10.1001/jamaneurol.2017.1200

Source DB:  PubMed          Journal:  JAMA Neurol        ISSN: 2168-6149            Impact factor:   18.302


  44 in total

Review 1.  Brain networks in Huntington disease.

Authors:  David Eidelberg; D James Surmeier
Journal:  J Clin Invest       Date:  2011-02-01       Impact factor: 14.808

2.  Monochorea caused by a striatal lesion.

Authors:  M Ikeda; H Tsukagoshi
Journal:  Eur Neurol       Date:  1991       Impact factor: 1.710

3.  A comparison of neurological, metabolic, structural, and genetic evaluations in persons at risk for Huntington's disease.

Authors:  S T Grafton; J C Mazziotta; J J Pahl; P St George-Hyslop; J L Haines; J Gusella; J M Hoffman; L R Baxter; M E Phelps
Journal:  Ann Neurol       Date:  1990-11       Impact factor: 10.422

4.  The temporal dynamics of tics in Gilles de la Tourette syndrome.

Authors:  B S Peterson; J F Leckman
Journal:  Biol Psychiatry       Date:  1998-12-15       Impact factor: 13.382

5.  Striatal metabolism and psychomotor speed as predictors of motor onset in Huntington's disease.

Authors:  Meike Herben-Dekker; Joost C H van Oostrom; Raymund A C Roos; Caroline K Jurgens; Marie-Noëlle W Witjes-Ané; Hubertus P H Kremer; Klaus L Leenders; Jacoba M Spikman
Journal:  J Neurol       Date:  2014-04-30       Impact factor: 4.849

6.  Rhythmic finger tapping reveals cerebellar dysfunction in essential tremor.

Authors:  A W G Buijink; M Broersma; A M M van der Stouwe; G A van Wingen; P F C Groot; J D Speelman; N M Maurits; A F van Rootselaar
Journal:  Parkinsonism Relat Disord       Date:  2015-02-11       Impact factor: 4.891

7.  Thalamic metabolism and symptom onset in preclinical Huntington's disease.

Authors:  A Feigin; C Tang; Y Ma; P Mattis; D Zgaljardic; M Guttman; J S Paulsen; V Dhawan; D Eidelberg
Journal:  Brain       Date:  2007-09-24       Impact factor: 13.501

8.  Neural correlates of tic generation in Tourette syndrome: an event-related functional MRI study.

Authors:  S Bohlhalter; A Goldfine; S Matteson; G Garraux; T Hanakawa; K Kansaku; R Wurzman; M Hallett
Journal:  Brain       Date:  2006-03-06       Impact factor: 13.501

9.  PET scan investigations of Huntington's disease: cerebral metabolic correlates of neurological features and functional decline.

Authors:  A B Young; J B Penney; S Starosta-Rubinstein; D S Markel; S Berent; B Giordani; R Ehrenkaufer; D Jewett; R Hichwa
Journal:  Ann Neurol       Date:  1986-09       Impact factor: 10.422

10.  Altered sensorimotor activation patterns in idiopathic dystonia-an activation likelihood estimation meta-analysis of functional brain imaging studies.

Authors:  Annemette Løkkegaard; Damian M Herz; Brian N Haagensen; Anne K Lorentzen; Simon B Eickhoff; Hartwig R Siebner
Journal:  Hum Brain Mapp       Date:  2015-11-09       Impact factor: 5.038

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  4 in total

1.  Abnormal development of cerebellar-striatal circuitry in Huntington disease.

Authors:  Alexander V Tereshchenko; Jordan L Schultz; Joel E Bruss; Vincent A Magnotta; Eric A Epping; Peg C Nopoulos
Journal:  Neurology       Date:  2020-04-07       Impact factor: 9.910

2.  Brain structure in juvenile-onset Huntington disease.

Authors:  Alexander Tereshchenko; Vincent Magnotta; Eric Epping; Katherine Mathews; Patricia Espe-Pfeifer; Erin Martin; Jeffrey Dawson; Wenzhen Duan; Peg Nopoulos
Journal:  Neurology       Date:  2019-04-10       Impact factor: 11.800

Review 3.  Glucose metabolic crosstalk and regulation in brain function and diseases.

Authors:  Shuai Zhang; Brittany Bolduc Lachance; Mark P Mattson; Xiaofeng Jia
Journal:  Prog Neurobiol       Date:  2021-06-10       Impact factor: 10.885

Review 4.  The Neurodevelopmental Hypothesis of Huntington's Disease.

Authors:  Ellen van der Plas; Jordan L Schultz; Peg C Nopoulos
Journal:  J Huntingtons Dis       Date:  2020
  4 in total

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