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Cognitive impairment profile in adult patients with Niemann pick type C disease

Overview of attention for article published in Orphanet Journal of Rare Diseases, October 2017
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Title
Cognitive impairment profile in adult patients with Niemann pick type C disease
Published in
Orphanet Journal of Rare Diseases, October 2017
DOI 10.1186/s13023-017-0714-1
Pubmed ID
Authors

Camille Heitz, Stéphane Epelbaum, Yann Nadjar

Abstract

Cognitive impairment is one of the core symptoms of Niemann Pick type C (NPC) disease, but few data concerning the neuropsychological profile of NPC patients are available. The aim of our study was to characterize cognitive impairments in NPC disease and to assess the evolution of these symptoms and the impact of miglustat on cognitive follow-up. We conducted a retrospective study of 21 adult patients diagnosed with NPC disease. Neuropsychological data (global cognitive efficiency, language, attention, executive functions, praxis, and visuoconstructive functions tests) were retrieved to describe the cognitive profile of patients. Cognitive impairment scores over time were assessed under treatment by miglustat. The majority of patients (90%) were impaired in one or more cognitive function. Executive functions and attention were the most impaired cognitive functions. Conversely, storage in the episodic memory was preserved in 61.5% of cases. Mean neuropsychological scores were stable during the period under miglustat (mean of 3.8 years). This study is one of the first to assess the cognitive profile of adult NPC patients. This profile is not specific to attention and executive dysfunctions; however, the preservation of storage in the episodic memory is promising for cognitive remediation. Further studies are needed to confirm the role of miglustat on cognition, but in this study, patients were stable under this treatment.

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Mendeley readers

Mendeley readers

The data shown below were compiled from readership statistics for 62 Mendeley readers of this research output. Click here to see the associated Mendeley record.

Geographical breakdown

Country Count As %
Unknown 62 100%

Demographic breakdown

Readers by professional status Count As %
Other 7 11%
Researcher 7 11%
Student > Ph. D. Student 6 10%
Lecturer 4 6%
Student > Postgraduate 4 6%
Other 10 16%
Unknown 24 39%
Readers by discipline Count As %
Medicine and Dentistry 11 18%
Neuroscience 7 11%
Biochemistry, Genetics and Molecular Biology 3 5%
Nursing and Health Professions 2 3%
Agricultural and Biological Sciences 2 3%
Other 6 10%
Unknown 31 50%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 23 July 2018.
All research outputs
#18,574,814
of 23,006,268 outputs
Outputs from Orphanet Journal of Rare Diseases
#2,162
of 2,640 outputs
Outputs of similar age
#250,658
of 327,016 outputs
Outputs of similar age from Orphanet Journal of Rare Diseases
#23
of 24 outputs
Altmetric has tracked 23,006,268 research outputs across all sources so far. This one is in the 11th percentile – i.e., 11% of other outputs scored the same or lower than it.
So far Altmetric has tracked 2,640 research outputs from this source. They typically receive more attention than average, with a mean Attention Score of 7.6. This one is in the 5th percentile – i.e., 5% of its peers scored the same or lower than it.
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We're also able to compare this research output to 24 others from the same source and published within six weeks on either side of this one. This one is in the 1st percentile – i.e., 1% of its contemporaries scored the same or lower than it.