Evidence map›Paper›PMID 25380582›Full record

Observational studyJournal of neurology2015

Factors influencing the clinical expression of intermediate CAG repeat length mutations of the Huntington's disease gene.

Peter K Panegyres, Chen-Chun Shu, Huei-Yang Chen, Jane S Paulsen

Registry-linked trialAbstract readMulticenter StudyObservational Study
PubMed Publisher
In one paragraph

Observational study in Journal of neurology, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00313495 (Cooperative Huntington's Observational Research Trial), which is not on this map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
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.

NCT00313495 unknown statusnot on this map

Cooperative Huntington's Observational Research Trial

TypeobservationalSponsorHP Therapeutics FoundationRan2006 to 2020Enrolled5,000ConditionsHuntington Disease
3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

  1. Review
  2. Article
  3. Article
  4. Selected health and lifestyle factors, cytosine-adenine-guanine status, and phenoconversion in Huntington's disease.Movement disorders : official journal of the Movement Disorder Society · 2018
    Article
  5. Article
  6. Review
  7. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

4 authors.

Peter K PanegyresNeurodegenerative Disorders Research Pty Ltd, 4 Lawrence Avenue, 6005, West Perth, WA, Australia, research@ndr.org.au.
Chen-Chun Shu
Huei-Yang Chen
Jane S Paulsen

Funding

NEUROBIOLOGICAL PREDICTORS OF HUNTINGTON'S DISEASER01NS040068 · NINDS · UNIVERSITY OF IOWA · PI PAULSEN, JANE S · 2001 to 2013
$48.5M
Response of a Sample Population with the Deleterious HD allele RESPOND-HDR01HG003330 · NHGRI · UNIVERSITY OF IOWA · PI PAULSEN, JANE S. · 2005 to 2007
$1.1M
NHGRI NIH HHS R01 HG003330NINDS NIH HHS R01 NS040068
6 · The paper itself

Abstract

Our aim is to elucidate the clinical variables associated with the development of manifest HD in patients with intermediate CAG repeat lengths. 2,167 participants were seen throughout 44 research sites in the United States, Canada or Australia over a five-year natural history observational study (2006-2011) (Trial # NCT00313495). The Chi-square test and a generalised linear model were used to examine the differences in demographics and cognitive tests among three groups of CAG repeat length. The mixed model was then used to examine the time effect on cognitive assessments by CAG groups. No patient with CAG repeat length 27-35 developed manifest HD, whereas three patients with 36-39 did. Total motor score, maximal chorea score and maximal dystonia score were significantly different at baseline (p < 0.001) for each measure between those patients with a repeat length 27-35 versus those 36-39; as were total functional assessment, independence scale and total functional capacity (p < 0.001). Being aged 65 years or more (OR 5.81, 95 % CI 0.37-90.58, p = 0.02) and smoking (OR 13.99, 95 % CI 2.03-96.44, p = 0.007) were related to manifest HD in patients with CAG 36-39; those with an associated university degree or higher education were less frequently diagnosed as manifest HD (OR 0.10, 95 % CI 0.02-0.54, p = 0.007). Age, smoking and lower education achievement were found to be significantly associated with higher odds of manifest HD in patients with intermediate CAG repeat length mutations.

Indexed as

AdultAgedDisease ProgressionFemaleHumansHuntingtin ProteinHuntington DiseaseMaleMiddle AgedNerve Tissue ProteinsTrinucleotide Repeat ExpansionHTT protein, humanHuntingtin ProteinNerve Tissue Proteins

Identifiers

What OpenQuestion holds

Textmetadata
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Registered trials

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.