Evidence map›Paper›PMID 27003179›Full record

ArticlePloS one2016

Multimodal MRI Evaluation of the MitoPark Mouse Model of Parkinson's Disease.

Linlin Cong, Eric R Muir, Cang Chen, Yusheng Qian, Jingwei Liu, K C Biju, Robert A Clark, Senlin Li, Timothy Q Duong

Abstract read
In one paragraph

Article in PloS one, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed, 1 pooled it
–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.

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, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Article
  3. Article
  4. Article
  5. Review
  6. Article
  7. Review
  8. Reduced cerebral blood flow in anJournal of cerebral blood flow and metabolism : official journal of the International Society of Cerebral Blood Flow and Metabolism · 2020
    Article
  9. Article
  10. Review
  11. Article
  12. The Aging of Iron Man.Frontiers in aging neuroscience · 2018
    Review
  13. Article
  14. 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.

Linlin CongResearch Imaging Institute, University of Texas Health Science Center, San Antonio, Texas, United States of America.
Eric R MuirResearch Imaging Institute, University of Texas Health Science Center, San Antonio, Texas, United States of America.
Cang ChenDepartment of Medicine, University of Texas Health Science Center, San Antonio, Texas, United States of America.
Yusheng QianDepartment of Medicine, University of Texas Health Science Center, San Antonio, Texas, United States of America.
Jingwei LiuDepartment of Medicine, University of Texas Health Science Center, San Antonio, Texas, United States of America.
K C BijuDepartment of Medicine, University of Texas Health Science Center, San Antonio, Texas, United States of America.
Robert A ClarkDepartment of Medicine, University of Texas Health Science Center, San Antonio, Texas, United States of America.
Senlin LiDepartment of Medicine, University of Texas Health Science Center, San Antonio, Texas, United States of America.
Timothy Q DuongResearch Imaging Institute, University of Texas Health Science Center, San Antonio, Texas, United States of America.

Funding

Institute for Integration of Medicine & Science: A Partnership to Improve HealthUL1TR001120 · NCATS · UNIVERSITY OF TEXAS HLTH SCIENCE CENTER · PI CLARK, ROBERT A, HARGREAVES, KENNETH M · 2013 to 2017
$16.5M
BLRD VA I01 BX000737NCATS NIH HHS UL1 TR001120
6 · The paper itself

Abstract

The MitoPark mouse, a relatively new genetic model of Parkinson's disease (PD), has a dopaminergic neuron-specific knock-out that inactivates the mitochondrial transcription factor A (Tfam), a protein essential for mitochondrial DNA expression and maintenance. This study used multimodal MRI to characterize the neuroanatomical correlates of PD-related deficits in MitoPark mice, along with functional behavioral tests. Compared with age-matched wild-type animals, MitoPark mice at 30 weeks showed: i) reduced whole-brain volume and increased ventricular volume, indicative of brain atrophy, ii) reduced transverse relaxation time (T2*) of the substantia nigra and striatum, suggestive of abnormal iron accumulation, iii) reduced apparent diffusion coefficient in the substantia nigra, suggestive of neuronal loss, iv) reduced fractional anisotropy in the corpus callosum and substantia nigra, indicative of white-matter damages, v) cerebral blood flow was not significantly affected, and vi) reduced motor activity in open-field tests, reduced memory in novel object recognition tests, as well as decreased mobility in tail suspension tests, an indication of depression. In sum, MitoPark mice recapitulate changes in many MRI parameters reported in PD patients. Multimodal MRI may prove useful for evaluating neuroanatomical correlates of PD pathophysiology in MitoPark mice, and for longitudinally monitoring disease progression and therapeutic interventions for PD.

Indexed as

AnimalsAtrophyBehavior, AnimalCorpus StriatumDisease Models, AnimalDisease ProgressionDNA-Binding ProteinsDNA, MitochondrialFemaleHigh Mobility Group ProteinsMagnetic Resonance ImagingMaleMiceMice, Inbred C57BLMice, KnockoutMotor ActivityDNA-Binding ProteinsDNA, MitochondrialHigh Mobility Group ProteinsTfam protein, mouse

Identifiers

PMID27003179
PMCPMC4803323

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.