Literature DB >> 25592070

Substantia nigra echogenicity in hereditary ataxias with and without nigrostriatal pathology: a pilot study.

Patricia Martínez-Sánchez1, Rubén Cazorla-García, Irene Sanz-Gallego, Elisa Correas-Callero, Irene Pulido-Valdeolivas, Javier Arpa.   

Abstract

Our objective was to determine whether substantia nigra (SN) hyperechogenicity is greater in spinocerebellar ataxias (SCA) with nigrostriatal affectation than in ataxias without it. A cross-sectional case-control study analyzing four groups of patients was conducted: 1) nigrostriatal ataxias (SCA3 and SCA6), 2) nigrostriatal healthy controls matched by age and sex, 3) non-nigrostriatal ataxias (FRDA and SCA7), and 4) non-nigrostriatal healthy controls matched by age and sex. All the patients underwent a transcranial ultrasound performed by an experienced sonographer blinded to the clinical, genetic, and neuroimaging data. The SN area was measured and compared in the four groups. The SN area was also correlated with clinical features and genetic data in the two ataxia groups. We examined 12 patients with nigrostriatal ataxia (11 SCA3 and 1 SCA6), 12 nigrostriatal healthy control patients, 7 patients with non-nigrostriatal ataxia (5 FRDA and 2 SCA7), and 7 non-nigrostriatal healthy control patients. The median (IQR) SN area (cm(2)) was greater in the nigrostriatal ataxias compared with the controls (right SN, 0.43 [0.44] vs. 0.11 [0.25]; P=0.001; left SN, 0.32 [0.25] vs. 0.11 [0.16]; P=0.001), but was similar among the non-nigrostriatal ataxias and controls. There were no statistically significant differences in the SN area between the nigrostriatal and non-nigrostriatal ataxias, although there was a tendency for a greater left SN area in the nigrostriatal compared with the non-nigrostriatal ataxias (0.32 [0.25] vs. 0.16 [0.24], P=0.083). SN echogenicity is markedly greater in ataxias with nigrostriatal pathology than in controls. The role of SN hyperechogenicity in differentiating ataxias with and without nigrostriatal pathology should be elucidated in future studies.

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Year:  2015        PMID: 25592070     DOI: 10.1007/s12311-014-0642-8

Source DB:  PubMed          Journal:  Cerebellum        ISSN: 1473-4222            Impact factor:   3.847


  37 in total

1.  Transcranial sonography in spinocerebellar ataxia type 3.

Authors:  Th Postert; J Eyding; D Berg; H Przuntek; G Becker; M Finger; L Schöls
Journal:  J Neural Transm Suppl       Date:  2004

2.  Restless legs and substantia nigra hypoechogenicity are common features in Friedreich's ataxia.

Authors:  Matthis Synofzik; Jana Godau; Tobias Lindig; Ludger Schöls; Daniela Berg
Journal:  Cerebellum       Date:  2011-03       Impact factor: 3.847

Review 3.  Friedreich's ataxia: pathology, pathogenesis, and molecular genetics.

Authors:  Arnulf H Koeppen
Journal:  J Neurol Sci       Date:  2011-04-15       Impact factor: 3.181

4.  Substantia nigra echogenicity in Friedreich's ataxia patients.

Authors:  María Sierra; Jon Infante; José Berciano
Journal:  Cerebellum       Date:  2013-08       Impact factor: 3.847

5.  Microglia activation is related to substantia nigra echogenicity.

Authors:  D Berg; J Godau; P Riederer; M Gerlach; T Arzberger
Journal:  J Neural Transm (Vienna)       Date:  2010-11-06       Impact factor: 3.575

6.  Autosomal dominant cerebellar ataxia: clinical analysis of 263 patients from a homogeneous population in Holguín, Cuba.

Authors:  G Orozco Diaz; A Nodarse Fleites; R Cordovés Sagaz; G Auburger
Journal:  Neurology       Date:  1990-09       Impact factor: 9.910

7.  Severity of restless legs syndrome is inversely correlated with echogenicity of the substantia nigra in different neurodegenerative movement disorders. a preliminary observation.

Authors:  José Luiz Pedroso; Edson Bor-Seng-Shu; Andre C Felicio; Pedro Braga-Neto; Lívia A Dutra; Camila C de Aquino; Henrique B Ferraz; Gilmar F do Prado; Manoel J Teixeira; Orlando G Barsottini
Journal:  J Neurol Sci       Date:  2012-05-24       Impact factor: 3.181

Review 8.  Thalamic involvement in a spinocerebellar ataxia type 2 (SCA2) and a spinocerebellar ataxia type 3 (SCA3) patient, and its clinical relevance.

Authors:  U Rüb; D Del Turco; K Del Tredici; R A I de Vos; E R Brunt; G Reifenberger; C Seifried; C Schultz; G Auburger; H Braak
Journal:  Brain       Date:  2003-07-07       Impact factor: 13.501

9.  The parkinsonian phenotype of spinocerebellar ataxia type 2.

Authors:  Chin-Song Lu; Yah-Huei Wu Chou; Pei-Chi Kuo; Hsiu-Chen Chang; Yi-Hsin Weng
Journal:  Arch Neurol       Date:  2004-01

10.  The sensory neuropathy of Friedreich's ataxia: an autopsy study of a case with prolonged survival.

Authors:  S Jitpimolmard; J Small; R H King; J Geddes; P Misra; J McLaughlin; J R Muddle; M Cole; A E Harding; P K Thomas
Journal:  Acta Neuropathol       Date:  1993       Impact factor: 17.088

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