Evidence map›Paper›PMID 27477323›Full record

ArticleHuman brain mapping2016

Natural variation in sensory-motor white matter organization influences manifestations of Huntington's disease.

Michael Orth, Sarah Gregory, Rachael I Scahill, Isabella Sm Mayer, Lora Minkova, Stefan Klöppel, Kiran K Seunarine, Lara Boyd, Beth Borowsky, Ralf Reilmann and 9 more

Open access · greenAbstract readMulticenter Study
In one paragraph

Article in Human brain mapping, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed, 1 pooled it
2.0field-weighted citation impact, top 15% 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

7 citing papers in PubMed, 1 synthesis or guideline pooled it, 25 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Longitudinal Structural MRI in Neurologically Healthy Adults.Journal of magnetic resonance imaging : JMRI · 2020
    Article
  4. Diffusion imaging in Huntington's disease: comprehensive review.Journal of neurology, neurosurgery, and psychiatry · 2020
    Review
  5. Characterizing White Matter in Huntington's Disease.Movement disorders clinical practice · 2020
    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

19 authors at 11 institutions in 6 countries.

Michael OrthDepartment of Neurology, Ulm University Hospital, Ulm, Germany.
Sarah GregoryWellcome Trust Centre for Neuroimaging, University College London, London, United Kingdom.
Rachael I ScahillHD Research Group, UCL Institute of Neurology, Queen Square, London, United Kingdom.
Isabella Sm MayerDepartment of Neurology, Ulm University Hospital, Ulm, Germany.
Lora MinkovaDepartment of Psychiatry and Psychotherapy, Freiburg Brain Imaging, University Medical Center, Albert-Ludwigs-University Freiburg, Freiburg, Germany.ORCID 0000-0003-0945-0553
Stefan KlöppelDepartment of Psychiatry and Psychotherapy, Freiburg Brain Imaging, University Medical Center, Albert-Ludwigs-University Freiburg, Freiburg, Germany.
Kiran K SeunarineDevelopmental Imaging and Biophysics Section, UCL Institute of Child Health, London, United Kingdom.
Lara BoydCentre for Brain Health, University of British Columbia, Vancouver, Canada.
Beth BorowskyCHDI Foundation Inc, Princeton, New Jersey.
Ralf ReilmannGeorge-Huntington-Institute, Technology-Park Muenster, Muenster, Germany.
G Bernhard LandwehrmeyerDepartment of Neurology, Ulm University Hospital, Ulm, Germany.
Blair R LeavittCenter for Molecular Medicine and Therapeutics and Department of Medical Genetics, Child and Family Research Institute, University of British Columbia, Vancouver, Canada.
Raymund Ac RoosDepartment of Neurology, Leiden University Medical Centre, Leiden, Netherlands.
Alexandra DurrAPHP Department of Genetics, Groupe Hospitalier Pitié-Salpêtrière, and Institut Du Cerveau Et De La Moelle, INSERM U1127, CNRS UMR7225, UPMC Université Paris VI UMR_S1127, Paris, France.
Geraint ReesWellcome Trust Centre for Neuroimaging, University College London, London, United Kingdom.
John C RothwellSobell Department of Motor Neuroscience and Movement Disorders, University College London Institute of Neurology, Queen Square, London, United Kingdom.
Douglas LangbehnDepartments of Psychiatry and Biostatistics, University of Iowa, Iowa City, Iowa.
Sarah J TabriziDepartment of Neurodegenerative Disease, University College London, Institute of Neurology, Queen Square, London, United Kingdom.
TRACK-On Investigators
National Hospital for Neurology and Neurosurgery · GBQueen Mary University of London · GBUniversity Hospital Ulm · DEUniversity of British Columbia · CAWellcome Centre for Human Neuroimaging · GBCentre National de la Recherche Scientifique · FRCHDI Foundation · USGeorge Huntington Institute · DELeiden University Medical Center · NLUniversity College London · GBUniversity of Iowa · US

Funding

Medical Research Council MR/L012936/1Wellcome Trust 091593Wellcome Trust 200181/Z/15/Z
6 · The paper itself

Abstract

While the HTT CAG-repeat expansion mutation causing Huntington's disease (HD) is highly correlated with the rate of pathogenesis leading to disease onset, considerable variance in age-at-onset remains unexplained. Therefore, other factors must influence the pathogenic process. We asked whether these factors were related to natural biological variation in the sensory-motor system. In 243 participants (96 premanifest and 35 manifest HD; 112 controls), sensory-motor structural MRI, tractography, resting-state fMRI, electrophysiology (including SEP amplitudes), motor score ratings, and grip force as sensory-motor performance were measured. Following individual modality analyses, we used principal component analysis (PCA) to identify patterns associated with sensory-motor performance, and manifest versus premanifest HD discrimination. We did not detect longitudinal differences over 12 months. PCA showed a pattern of loss of caudate, grey and white matter volume, cortical thickness in premotor and sensory cortex, and disturbed diffusivity in sensory-motor white matter tracts that was connected to CAG repeat length. Two further major principal components appeared in controls and HD individuals indicating that they represent natural biological variation unconnected to the HD mutation. One of these components did not influence HD while the other non-CAG-driven component of axial versus radial diffusivity contrast in white matter tracts were associated with sensory-motor performance and manifest HD. The first component reflects the expected CAG expansion effects on HD pathogenesis. One non-CAG-driven component reveals an independent influence on pathogenesis of biological variation in white matter tracts and merits further investigation to delineate the underlying mechanism and the potential it offers for disease modification. Hum Brain Mapp 37:4615-4628, 2016. © 2016 Wiley Periodicals, Inc.

Indexed as

AdultBiological Variation, IndividualBrain MappingCross-Sectional StudiesDiffusion Tensor ImagingEvoked Potentials, SomatosensoryFemaleGray MatterHand StrengthHumansHuntington DiseaseLongitudinal StudiesMagnetic Resonance ImagingMaleMiddle AgedMotor Activitybiological traitbiological variationcortical thicknesseffective connectivitygrip forceprincipal component analysissomatosensory evoked potentials

Identifiers

PMID27477323
PMCPMC6867476
OpenAlexW2487156940

What OpenQuestion holds

Textmetadata
Read underepoch 390

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.