Evidence map›Paper›PMID 26085965›Full record

ArticleBrain and behavior2015

Intraventricular cerebrospinal fluid temperature analysis using MR diffusion-weighted imaging thermometry in Parkinson's disease patients, multiple system atrophy patients, and healthy subjects.

Kaoru Sumida, Noriko Sato, Miho Ota, Koji Sakai, Yasumasa Nippashi, Daichi Sone, Kota Yokoyama, Kimiteru Ito, Norihide Maikusa, Etsuko Imabayashi and 5 more

Abstract read
In one paragraph

Article in Brain and behavior, 2015. 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
–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

13 citing papers in PubMed.

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  6. In Vivo Stability of Therapeutic Proteins.Pharmaceutical research · 2020
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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

15 authors.

Kaoru SumidaDepartment of Radiology, National Center Hospital of Neurology and Psychiatry 4-1-1 Ogawa-Higashi-Cho, Kodaira, Tokyo, 187-8502, Japan ; Department of Radiology, Graduate School of Medicine and Faculty of Medicine, The University of Tokyo 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8655, Japan.
Noriko SatoDepartment of Radiology, National Center Hospital of Neurology and Psychiatry 4-1-1 Ogawa-Higashi-Cho, Kodaira, Tokyo, 187-8502, Japan.
Miho OtaDepartment of Mental Disorder Research, National Institute of Mental Health 4-1-1 Ogawa-Higashi-Cho, Kodaira, Tokyo, 187-8502, Japan.
Koji SakaiDepartment of Human Health Science, Graduate School of Medicine, Kyoto University 53 Shogoin Kawahara-cho, Sakyo-ku, Kyoto, 606-8507, Japan.
Yasumasa NippashiDepartment of Radiology, National Center Hospital of Neurology and Psychiatry 4-1-1 Ogawa-Higashi-Cho, Kodaira, Tokyo, 187-8502, Japan ; Department of Radiology, Graduate School of Medicine and Faculty of Medicine, The University of Tokyo 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8655, Japan.
Daichi SoneDepartment of Psychiatry, National Center Hospital of Neurology and Psychiatry 4-1-1 Ogawa-Higashi-Cho, Kodaira, Tokyo, 187-8502, Japan.
Kota YokoyamaDepartment of Radiology, National Center Hospital of Neurology and Psychiatry 4-1-1 Ogawa-Higashi-Cho, Kodaira, Tokyo, 187-8502, Japan.
Kimiteru ItoDepartment of Radiology, Tokyo Metropolitan Geriatric Hospital 35-2 Sakae-Cho, Itabashi-ku, Tokyo, 173-0015, Japan.
Norihide MaikusaDepartment of Mental Disorder Research, National Institute of Mental Health 4-1-1 Ogawa-Higashi-Cho, Kodaira, Tokyo, 187-8502, Japan.
Etsuko ImabayashiIntegrative Brain Imaging Center, National Center of Neurology and Psychiatry 4-1-1 Ogawa-Higashi-Cho, Kodaira, Tokyo, 187-8551, Japan.
Hiroshi MatsudaIntegrative Brain Imaging Center, National Center of Neurology and Psychiatry 4-1-1 Ogawa-Higashi-Cho, Kodaira, Tokyo, 187-8551, Japan.
Kei YamadaDepartment of Radiology, Graduate School of Medical Science, Kyoto Prefectural University of Medicine 465 Kajii-cho, Kawaramachi-honmachi, Kamigyo-ku, Kyoto, 602-8566, Japan.
Miho MurataDepartment of Neurology, National Center Hospital of Neurology and Psychiatry 4-1-1 Ogawa-Higashi-Cho, Kodaira, Tokyo, 187-8502, Japan.
Akira KunimatsuDepartment of Radiology, Graduate School of Medicine and Faculty of Medicine, The University of Tokyo 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8655, Japan.
Kuni OhtomoDepartment of Radiology, Graduate School of Medicine and Faculty of Medicine, The University of Tokyo 7-3-1 Hongo, Bunkyo-ku, Tokyo, 113-8655, Japan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeWe examined the temperature of the intraventricular cerebrospinal fluid (Tv) in patients with Parkinson's disease (PD) and those with multiple system atrophy (MSA) in comparison with healthy subjects, and we examined normal changes in this temperature with aging.

methodsTv was estimated by magnetic resonance (MR) diffusion-weighted imaging (DWI) thermometry in 36 PD patients (19 males, 17 females), 34 MSA patients (17 males, 17 females), 64 age-matched controls (27 men, 37 women), and 114 all-age adult controls (47 men, 67 women; 28-89 years old). The volume of lateral ventricles was also estimated using FreeSurfer in all subjects. Tv and ventricular volume data were compared among the PD and MSA patients and age-matched controls. We also evaluated the relationship between Tv and age in the 114 all-age controls, controlling for ventricular volume. Men and women were analyzed separately.

resultsThe male PD and MSA patients had significantly higher Tv values compared to the male controls, with no significant difference in ventricular volume among them. There was no significant difference in Tv between the female patients and controls. In the all-age male controls, there was a significant negative correlation between Tv and age controlling for ventricular volume, and this was not observed in the women.

conclusionDWI thermometry is a useful and easy method for demonstrating an altered intracranial environment in male patients and healthy controls, but not in females. DWI thermometry can thus be used to help to explore the pathophysiology of Parkinsonian syndromes and to differentiate individuals affected by neurodegenerative disease with autonomic dysfunction from those without it.

Indexed as

Cerebral VentriclesCerebrospinal FluidMultiple System AtrophyParkinson DiseaseAdultAgedBody TemperatureDiagnosis, DifferentialDiffusion Magnetic Resonance ImagingFemaleHumansMaleMiddle AgedOrgan SizeReproducibility of ResultsSex FactorsCerebrospinal fluiddiffusion-weighted imaging thermometrymultiple system atrophyParkinson's diseasetemperature

Identifiers

PMID26085965
PMCPMC4467774

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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.