Evidence map›Paper›PMID 20417959›Full record

ArticleBrain and language2010

Longitudinal cerebral blood flow changes during speech in hereditary ataxia.

John J Sidtis, Stephen C Strother, Ansam Groshong, Ansam Naoum, David A Rottenberg, Christopher Gomez

Erratum issuedAbstract read
In one paragraph

Article in Brain and language, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.9field-weighted citation impact, top 30% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

14 citing papers in PubMed, 23 citations in OpenAlex.

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4 · The record

Corrections and comments

  • Erratum issued
    Naoum, Ansam [corrected to Groshong, Ansam]
5 · Who and what money

Authors and funding

6 authors at 5 institutions in 2 countries.

John J SidtisBrain and Behavior Laboratory, Geriatrics Division, Nathan Kline Institute, 140 Old Orangeburg Road, Orangeburg, NY 10962, United States. john.sidtis@nyu.edu
Stephen C Strother
Ansam Groshong
Ansam Naoum
David A Rottenberg
Christopher Gomez
Minneapolis VA Medical Center · USNathan Kline Institute for Psychiatric Research · USUniversity of Chicago Medical Center · USUniversity of Minnesota · USUniversity of Toronto · CA

Funding

CORTICAL-SUBCORTICAL INTERACTION IN PD AND NORMAL SPEECHR01DC007658 · NIDCD · NATHAN S. KLINE INSTITUTE FOR PSYCH RES · PI SIDTIS, DIANA L, SIDTIS, JOHN J · 2006 to 2016
$4.3M
SPATIAL AND TEMPORAL PATTERNS OF FUNCTIONAL ACTIVATIONP20MH057180 · NIMH · UNIVERSITY OF MINNESOTA TWIN CITIES · PI ROTTENBERG, DAVID ALLAN · 1996 to 2003
$3.6M
TRINUCLEOTIDE REPEAT INSTABILITY IN ATAXIAP01NS033718 · NINDS · UNIVERSITY OF MINNESOTA TWIN CITIES · PI ORR, HARRY T. · 1995 to 1999
–
NIDCD NIH HHS R01 DC007658NIMH NIH HHS P20 MH057180NIMH NIH HHS P20 MH57180NINDS NIH HHS P01NS33718
6 · The paper itself

Abstract

The hereditary ataxias constitute a group of degenerative diseases that progress over years or decades. With principal pathology involving the cerebellum, dysarthria is an early feature of many of the ataxias. Positron emission tomography was used to study regional cerebral blood flow changes during speech production over a 21 month period in a group of seven right-handed subjects with hereditary ataxia (6 females and 1 male, 3 SCA1 and 4 SCA5, aged 38.3+/-18.9 years). The decline in blood flow was greatest in cerebellar regions. In contrast, blood flow actually increased during speech production in the classic speech area (Broca's area) but not in its right-hemisphere homologue at the second evaluation. This increase in cortical flow may have been compensatory for cerebellar degeneration as speech intelligibility did not decline significantly during this period. Compensation was not complete, though, as syllable timing shifted in the direction of equal syllable duration, one of the characteristics of ataxic dysarthria. These results are consistent with previous functional imaging studies of ataxia demonstrating a pattern of brain activity that reflects both loss of function and relative compensation when clinical signs and symptoms are still mild. The combination of disease-relevant tasks, behavioral measurement, and functional imaging may provide insight into the early changes associated with neurodegenerative disease.

Indexed as

AdolescentAdultAgedBrainBrain MappingCerebrovascular CirculationDisease ProgressionFemaleHumansLongitudinal StudiesMaleMiddle AgedNeurologic ExaminationPositron-Emission TomographySpeechSpinocerebellar Degenerations

Identifiers

PMID20417959
PMCPMC2935851
OpenAlexW2046768129

What OpenQuestion holds

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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.