Evidence map›Paper›PMID 32993765›Full record

ArticleOrphanet journal of rare diseases2020

Early detection of Niemann-pick disease type C with cataplexy and orexin levels: continuous observation with and without Miglustat.

A Imanishi, T Kawazoe, Y Hamada, T Kumagai, K Tsutsui, N Sakai, K Eto, A Noguchi, T Shimizu, T Takahashi and 4 more

Open access · goldAbstract read
In one paragraph

Article in Orphanet journal of rare diseases, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.6field-weighted citation impact, top 36% 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

2 citing papers in PubMed, 8 citations in OpenAlex.

  1. Article
  2. Central sleep apnea and daytime sleepiness in Niemann-Pick type C disease: a report of 2 cases.Journal of clinical sleep medicine : JCSM : official publication of the American Academy of Sleep Medicine · 2023
    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

14 authors at 8 institutions in 1 country.

A ImanishiDepartment of Psychiatry, Akita University Graduate School of Medicine, Akita, Japan.
T KawazoeDepartment of Neurology, National Center of Neurology and Psychiatry, Tokyo, Japan.
Y HamadaDepartment of Pediatrics, Toyonaka Municipal Hospital, Toyonaka, Japan.
T KumagaiNational Center for Child Health and Development, Tokyo, Japan.
K TsutsuiDepartment of Psychiatry, Akita University Graduate School of Medicine, Akita, Japan.
N SakaiDivision of Health Sciences, Osaka University Graduate School of Medicine, Osaka, Japan.
K EtoDepartment of Pediatrics, Tokyo Women's Medical University, Tokyo, Japan.
A NoguchiDepartment of Pediatrics, Akita University Graduate School of Medicine, Akita, Japan.
T ShimizuAkita Mental Health and Welfare Center, Akita, Japan.
T TakahashiDepartment of Pediatrics, Akita University Graduate School of Medicine, Akita, Japan.
G HanInternational Institute for Integrative Sleep Medicine (IIIS), University of Tsukuba, Tsukuba, 305-8575, Japan.
K MishimaDepartment of Psychiatry, Akita University Graduate School of Medicine, Akita, Japan.
T KanbayashiInternational Institute for Integrative Sleep Medicine (IIIS), University of Tsukuba, Tsukuba, 305-8575, Japan. kanbayashi.ta.fn@u.tsukuba.ac.jp.
H KondoInternational Institute for Integrative Sleep Medicine (IIIS), University of Tsukuba, Tsukuba, 305-8575, Japan.
Akita University · JPUniversity of Tsukuba · JPNational Center For Child Health and Development · JPNational Center of Neurology and Psychiatry · JPOsaka Health Science University · JPTokyo Women's Medical University · JPToyonaka Municipal Hospital · JPTsukuba International University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

STUDY

objectivesNiemann-Pick type C (NPC) is an autosomal recessive and congenital neurological disorder characterized by the accumulation of cholesterol and glycosphingolipids. Symptoms include hepatosplenomegaly, vertical supranuclear saccadic palsy, ataxia, dystonia, and dementia. Some cases frequently display narcolepsy-like symptoms, including cataplexy which was reported in 26% of all NPC patients and was more often recorded among late-infantile onset (50%) and juvenile onset (38%) patients. In this current study, we examined CSF orexin levels in the 10 patients of NPC with and without cataplexy, which supports previous findings.

methodsTen patients with NPC were included in the study (5 males and 5 females). NPC diagnosis was biochemically confirmed in all 10 patients, from which 8 patients with NPC1 gene were identified. We compared CSF orexin levels among NPC, narcoleptic and idiopathic hypersomnia patients.

resultsSix NPC patients with cataplexy had low or intermediate orexin levels. In 4 cases without cataplexy, their orexin levels were normal. In 5 cases with Miglustat treatment, their symptoms stabilized or improved. For cases without Miglustat treatment, their conditions worsened generally. The CSF orexin levels of NPC patients were significantly higher than those of patients with narcolepsy-cataplexy and lower than those of patients with idiopathic hypersomnia, which was considered as the control group with normal CSF orexin levels. DISCUSSION: Our study indicates that orexin level measurements can be an early alert of potential NPC. Low or intermediate orexin levels could further decrease due to reduction in the neuronal function in the orexin system, accelerating the patients' NPC pathophysiology. However with Miglustat treatment, the orexin levels stabilized or improved, along with other general symptoms. Although the circuitry is unclear, this supports that orexin system is indeed involved in narcolepsy-cataplexy in NPC patients.

conclusionThe NPC patients with cataplexy had low or intermediate orexin levels. In the cases without cataplexy, their orexin levels were normal. Our study suggests that orexin measurements can serve as an early alert for potential NPC; furthermore, they could be a marker of therapy monitoring during a treatment.

Indexed as

CataplexyNiemann-Pick Disease, Type C1-DeoxynojirimycinFemaleHumansMaleOrexins1-DeoxynojirimycinmiglustatOrexinsCataplexyMiglustatNarcolepsyNiemann-pick type C (NPC)Orexin (hypocretin)

Identifiers

PMID32993765
PMCPMC7523321
OpenAlexW3089993658

What OpenQuestion holds

Textmetadata
LicenceCC BY
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Registered trials

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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.