Evidence map›Paper›PMID 20226865›Full record

ArticleNeuroImage2010

The contributions of myelin and axonal caliber to transverse relaxation time in shiverer and neurofilament-deficient mouse models.

Victor V Dyakin, Yuanxin Chen, Craig A Branch, Veeranna, Aidong Yuan, Mala Rao, Asok Kumar, Corrinne M Peterhoff, Ralph A Nixon

Abstract read
In one paragraph

Article in NeuroImage, 2010. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
2.7field-weighted citation impact, top 10% 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

13 citing papers in PubMed, 23 citations in OpenAlex.

  1. Review
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Reprint of "Quantitative evaluation of brain development using anatomical MRI and diffusion tensor imaging".International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience · 2014
    Article
  8. Quantitative evaluation of brain development using anatomical MRI and diffusion tensor imaging.International journal of developmental neuroscience : the official journal of the International Society for Developmental Neuroscience · 2013
    Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. 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

9 authors at 2 institutions in 1 country.

Victor V DyakinCenter for Dementia Research, Nathan Kline Institute Orangeburg, New York 10962, USA.
Yuanxin Chen
Craig A Branch
Veeranna
Aidong Yuan
Mala Rao
Asok Kumar
Corrinne M Peterhoff
Ralph A Nixon
Nathan Kline Institute for Psychiatric Research · USNew York University · US

Funding

DYNAMICS OF THE NEURONAL CYTOSKELETON IN AGING BRAINR01AG005604 · NIA · NEW YORK UNIVERSITY SCHOOL OF MEDICINE · PI NIXON, RALPH A. · 1985 to 2014
$4.5M
NIA NIH HHS 5R01AG005604NIA NIH HHS R01 AG005604
6 · The paper itself

Abstract

White matter disorders can involve injury to myelin or axons but the respective contribution of each to clinical course is difficult to evaluate non-invasively. Here, to develop a paradigm for further investigations of axonal pathology by MRI, we compared two genetic mouse models exhibiting relatively selective axonal or myelin deficits using quantitative MRI relaxography of the transverse relaxation times (T2) in vivo and ultrastructural morphometry. In HM-DKO mice, which lack genes encoding the heavy (NF-H) and medium (NF-M) subunits of neurofilaments, neurofilament content of large myelinated axons of the central nervous system (CNS) is markedly reduced in the absence of changes in myelin thickness and volume. In shiverer mutant mice, which lack functional myelin basic protein, CNS myelin sheath formation is markedly reduced but neurofilament content is normal. We observed increases in T2 in nearly all white matter in shiverer mice compared to their wild type, while more subtle increases in T2 were observed in HM-DKO in the corpus callosum. White matter T2 was generally greater in shiverer mice than HM-DKO mice. Ultrastructural morphometry of the corpus callosum, which exhibited the greatest T2 differences, confirmed that total cross-sectional area occupied by axons was similar in the two mouse models and that the major ultrastructural differences, determined by morphometry, were an absence of myelin and larger unmyelinated axons in shiverer mice and absence of neurofilaments in HM-DKO mice. Our findings indicate that T2 is strongly influenced by myelination state and axonal volume, while neurofilament structure within the intra-axonal compartment has a lesser effect upon single compartment T2 estimates.

Indexed as

Disease Models, AnimalAnimalsBrainDemyelinating DiseasesHumansMagnetic Resonance ImagingMiceMice, Inbred C3HMice, Inbred C57BLMice, KnockoutMice, Neurologic MutantsMyelin Basic ProteinNeurofilament ProteinsMyelin Basic ProteinNeurofilament Proteins

Identifiers

PMID20226865
PMCPMC2862816
OpenAlexW2154162084

What OpenQuestion holds

Textmetadata
LicenceTDM
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.