Evidence map›Paper›PMID 19408064›Full record

ArticleCerebellum (London, England)2009

MRI detection of the cerebellar syndrome in Creutzfeldt-Jakob disease.

Oren S Cohen, Chen Hoffmann, Hedok Lee, Joab Chapman, Robert K Fulbright, Isak Prohovnik

Abstract read
PubMed Publisher
In one paragraph

Article in Cerebellum (London, England), 2009. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed
1.2field-weighted citation impact, top 22% 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

16 citing papers in PubMed, 36 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Article
  5. Selective vulnerability to atrophy in sporadic Creutzfeldt-Jakob disease.Annals of clinical and translational neurology · 2021
    Article
  6. Article
  7. Clinical radiological correlation in E200K familial Creutzfeldt-Jakob disease.Journal of neural transmission (Vienna, Austria : 1996) · 2016
    Article
  8. Article
  9. Article
  10. Article
  11. Article
  12. Article
  13. Cerebral white matter disruption in Creutzfeldt-Jakob disease.AJNR. American journal of neuroradiology · 2012
    Article
  14. Article
  15. Article
  16. 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

6 authors at 3 institutions in 2 countries.

Oren S CohenDepartment of Neurology, The Sagol Neuroscience Center, Sheba Medical Center, Tel-Hashomer, Israel. oren.cohen@sheba.health.gov.il
Chen Hoffmann
Hedok Lee
Joab Chapman
Robert K Fulbright
Isak Prohovnik
Sheba Medical Center · ILIcahn School of Medicine at Mount Sinai · USYale University · US

Funding

Neuroimaging of Genetically-Defined Incipient CJDR01NS043488 · NINDS · MOUNT SINAI SCHOOL OF MEDICINE OF NYU · PI PROHOVNIK, ISAK · 2005 to 2007
$1.2M
NINDS NIH HHS NS043488
6 · The paper itself

Abstract

Creutzfeldt-Jakob Disease (CJD) is characterized by bilateral basal ganglia hyperintensities on T2W and diffusion-weighted imaging (DWI) magnetic resonance imaging (MRI) scans, consistent with its extrapyramidal neurological manifestations. MRI is diagnostically uninformative about the cerebellar symptoms, equally prominent in CJD. This study was undertaken to explain this apparent paradox. Eleven CJD patients with definite cerebellar or brain stem symptoms were selected from a large prospective study, as well as 11 healthy controls matched for age and gender. All subjects participated in a standardized MRI protocol, including SPGR, fluid-attenuated inversion recovery (FLAIR), DWI and diffusion tensor imaging (DTI). All subjects underwent detailed examination by a neurologist blinded to the radiological findings, who predicted the expected site of cerebral abnormalities. MRI showed good sensitivity for the abnormalities predicted in the cortex (80-90%) and basal ganglia (100%). None of the standard MRI sequences, including DWI, DTI, and FLAIR, revealed any tissue abnormalities in cerebellum or brain stem. Apparent diffusion coefficient (ADC) values, however, were substantially and significantly elevated in several cerebellar structures, where also the volumetric (VBM) analysis revealed elevated cerebrospinal fluid volume, suggesting focal cerebellar atrophy in these CJD patients. In patients with CJD, DWI appears sensitive to the reduced diffusivity in cortex and basal ganglia but insensitive to cerebellar involvement. We propose that the radiological hallmark of cerebellar pathology in CJD is atrophy, revealed quantitatively by both VBM and elevated diffusivity, which is identifiable on ADC maps but poorly visualized in nonquantitative DWI images.

Indexed as

Magnetic Resonance ImagingAgedBrain MappingCerebellar DiseasesCreutzfeldt-Jakob SyndromeDiffusion Magnetic Resonance ImagingFemaleHumansMaleMiddle Aged

Identifiers

PMID19408064
OpenAlexW2045945767

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.