Literature DB >> 26599997

Cerebellar neuronal loss in amyotrophic lateral sclerosis cases with ATXN2 intermediate repeat expansions.

Rachel H Tan1,2, Jillian J Kril3, Ciara McGinley3, Mohammad Hassani1, Masami Masuda-Suzukake4, Masato Hasegawa4, Remika Mito3, Matthew C Kiernan5, Glenda M Halliday1,2.   

Abstract

OBJECTIVE: Despite evidence suggesting that the cerebellum may be targeted in amyotrophic lateral sclerosis (ALS), particularly in cases with repeat expansions in the ATXN2 and C9ORF72 genes, the integrity of cerebellar neurons has yet to be examined. The present study undertakes a histopathological analysis to assess the impact of these repeat expansions on cerebellar neurons and determine whether similar cerebellar pathology occurs in sporadic disease.
METHODS: Purkinje and granule cells were quantified in the vermis and lateral cerebellar hemispheres of ALS cases with repeat expansions in the ATXN2 and C9ORF72 genes, sporadic disease, and sporadic progressive muscular atrophy with only lower motor neuron degeneration.
RESULTS: ALS cases with intermediate repeat expansions in the ATXN2 gene demonstrate a significant loss in Purkinje cells in the cerebellar vermis only. Despite ALS cases with expansions in the C9ORF72 gene having the highest burden of inclusion pathology, no neuronal loss was observed in this group. Neuronal numbers were also unchanged in sporadic ALS and sporadic PMA cases.
INTERPRETATION: The present study has established a selective loss of Purkinje cells in the cerebellar vermis of ALS cases with intermediate repeat expansions in the ATXN2 gene, suggesting a divergent pathogenic mechanism independent of upper and lower motor neuron degeneration in ALS. We discuss these findings in the context of large repeat expansions in ATXN2 and spinocerebellar ataxia type 2, providing evidence that intermediate repeats in ATXN2 cause significant, albeit less substantial, spinocerebellar damage compared with longer repeats in ATXN2.
© 2016 American Neurological Association.

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Year:  2016        PMID: 26599997     DOI: 10.1002/ana.24565

Source DB:  PubMed          Journal:  Ann Neurol        ISSN: 0364-5134            Impact factor:   10.422


  9 in total

1.  Conserved DNA methylation combined with differential frontal cortex and cerebellar expression distinguishes C9orf72-associated and sporadic ALS, and implicates SERPINA1 in disease.

Authors:  Mark T W Ebbert; Christian A Ross; Luc J Pregent; Rebecca J Lank; Cheng Zhang; Rebecca B Katzman; Karen Jansen-West; Yuping Song; Edroaldo Lummertz da Rocha; Carla Palmucci; Pamela Desaro; Amelia E Robertson; Ana M Caputo; Dennis W Dickson; Kevin B Boylan; Rosa Rademakers; Tamas Ordog; Hu Li; Veronique V Belzil
Journal:  Acta Neuropathol       Date:  2017-08-14       Impact factor: 17.088

Review 2.  Polyglutamine spinocerebellar ataxias - from genes to potential treatments.

Authors:  Henry L Paulson; Vikram G Shakkottai; H Brent Clark; Harry T Orr
Journal:  Nat Rev Neurosci       Date:  2017-08-17       Impact factor: 34.870

3.  Artificial intelligence in neurodegenerative disease research: use of IBM Watson to identify additional RNA-binding proteins altered in amyotrophic lateral sclerosis.

Authors:  Nadine Bakkar; Tina Kovalik; Ileana Lorenzini; Scott Spangler; Alix Lacoste; Kyle Sponaugle; Philip Ferrante; Elenee Argentinis; Rita Sattler; Robert Bowser
Journal:  Acta Neuropathol       Date:  2017-11-13       Impact factor: 17.088

4.  In-depth clinico-pathological examination of RNA foci in a large cohort of C9ORF72 expansion carriers.

Authors:  Mariely DeJesus-Hernandez; NiCole A Finch; Xue Wang; Tania F Gendron; Kevin F Bieniek; Michael G Heckman; Aliaksei Vasilevich; Melissa E Murray; Linda Rousseau; Rachael Weesner; Anthony Lucido; Meeia Parsons; Jeannie Chew; Keith A Josephs; Joseph E Parisi; David S Knopman; Ronald C Petersen; Bradley F Boeve; Neill R Graff-Radford; Jan de Boer; Yan W Asmann; Leonard Petrucelli; Kevin B Boylan; Dennis W Dickson; Marka van Blitterswijk; Rosa Rademakers
Journal:  Acta Neuropathol       Date:  2017-05-15       Impact factor: 17.088

5.  Interrupted CAG expansions in ATXN2 gene expand the genetic spectrum of frontotemporal dementias.

Authors:  Clémence Fournier; Vincent Anquetil; Agnès Camuzat; Sandrine Stirati-Buron; Véronique Sazdovitch; Laura Molina-Porcel; Sabrina Turbant; Daisy Rinaldi; Raquel Sánchez-Valle; Mathieu Barbier; Morwena Latouche; Giovanni Stevanin; Danielle Seilhean; Alexis Brice; Charles Duyckaerts; Isabelle Le Ber
Journal:  Acta Neuropathol Commun       Date:  2018-05-30       Impact factor: 7.801

Review 6.  Elucidating the Role of Cerebellar Synaptic Dysfunction in C9orf72-ALS/FTD - a Systematic Review and Meta-Analysis.

Authors:  Aleksandra Kaliszewska; Joseph Allison; Tarik-Tarkan Col; Christopher Shaw; Natalia Arias
Journal:  Cerebellum       Date:  2021-09-07       Impact factor: 3.648

7.  Clusters of anatomical disease-burden patterns in ALS: a data-driven approach confirms radiological subtypes.

Authors:  Peter Bede; Aizuri Murad; Jasmin Lope; Orla Hardiman; Kai Ming Chang
Journal:  J Neurol       Date:  2022-03-25       Impact factor: 6.682

8.  Cell-type specific differences in promoter activity of the ALS-linked C9orf72 mouse ortholog.

Authors:  Abraham J Langseth; Juhyun Kim; Janet E Ugolino; Yajas Shah; Ho-Yon Hwang; Jiou Wang; Dwight E Bergles; Solange P Brown
Journal:  Sci Rep       Date:  2017-07-18       Impact factor: 4.379

9.  Genotype-associated cerebellar profiles in ALS: focal cerebellar pathology and cerebro-cerebellar connectivity alterations.

Authors:  Peter Bede; Rangariroyashe H Chipika; Foteini Christidi; Jennifer C Hengeveld; Efstratios Karavasilis; Georgios D Argyropoulos; Jasmin Lope; Stacey Li Hi Shing; Georgios Velonakis; Léonie Dupuis; Mark A Doherty; Alice Vajda; Russell L McLaughlin; Orla Hardiman
Journal:  J Neurol Neurosurg Psychiatry       Date:  2021-06-24       Impact factor: 10.154

  9 in total

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