Evidence map›Paper›PMID 32592146›Full record

ArticleJournal of neurology2020

High diagnostic value of plasma Niemann-Pick type C biomarkers in adults with selected neurological and/or psychiatric disorders.

Daniele Mandia, Marion Plaze, Isabelle Le Ber, Claire Ewenczyk, Alexandre Morin, Guilhem Carle, Angèle Consoli, Adrian Degardin, Ali Amad, Caroline Moreau and 16 more

Abstract read
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In one paragraph

Article in Journal of neurology, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

0numbers the graph read from it
0cells of the map it votes in
6citing 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

6 citing papers in PubMed.

  1. Article
  2. Review
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  5. Article
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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

26 authors.

Daniele MandiaNeurology Department, Reference Center for Lysosomal Diseases, Neurogenetics and Metabolism Unit, Hôpital Pitié-Salpêtrière, 47-83 boulevard de l'Hôpital, 75013, Paris, France.
Marion PlazeInserm U894, Institute of Psychiatry and Neurosciences of Paris, University Paris Descartes, Service Hospitalo-Universitaire de Psychiatrie GHU Paris Psychiatrie et Neurosciences, Paris, France.
Isabelle Le BerInserm U1127, CNRS UMR 7225, Institut du Cerveau et la Moelle épinière (ICM), Sorbonne Universités, UPMC Université Paris 6, Hôpital Pitié-Salpêtrière, Paris, France.
Claire EwenczykDépartement de Génétique Clinique, Hôpital Pitié-Salpêtrière, 47-83 boulevard de l'Hôpital, 75013, Paris, France.
Alexandre MorinNational reference center for rare or early dementias, Institute of Memory and Alzheimer's Disease (IM2A), Department of Neurology, AP-HP-Hôpital Pitié-Salpêtrière, Paris, France.
Guilhem CarleBehavioral Neuropsychiatric Unit, Brain and Spine Institute, Pitié-Salpêtrière Hospital, Paris, France.
Angèle ConsoliDepartment of Child and Adolescent Psychiatry, Pitié-Salpêtrière Hospital, Sorbonne University, Paris, France.
Adrian DegardinDepartment of Neurology, Guy Chatiliez Hospital, 59200, Tourcoing, France.
Ali AmadCNRS, CHU LILLE, UMR9193-PsychiC-SCALab, Pôle de Psychiatrie, Univ. Lille, 59000, Lille, France.
Caroline MoreauDepartment of Neurology, Expert Center for Parkinson's Disease, CHU LILLE, INSERM UMR_S 1171, LICEND, University of Lille, Lille, France.
Mathieu AnheimDépartement de Neurologie, Hôpital de Hautepierre, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.
Christine TranchantDépartement de Neurologie, Hôpital de Hautepierre, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.
Nicolas MéléService de Neurologie, Centre Hospitalier Sainte-Anne, Paris, France.
Carole Roue-JagotUnité de Neurologie de la Mémoire et du Langage, GHU Paris Psychiatrie et Neurosciences, Hôpital Sainte-Anne, Paris, France.
Julien LagardeUnité de Neurologie de la Mémoire et du Langage, GHU Paris Psychiatrie et Neurosciences, Hôpital Sainte-Anne, Paris, France.
Marie SarazinUnité de Neurologie de la Mémoire et du Langage, GHU Paris Psychiatrie et Neurosciences, Hôpital Sainte-Anne, Paris, France.
Lorraine HamelinUnité de Neurologie de la Mémoire et du Langage, GHU Paris Psychiatrie et Neurosciences, Hôpital Sainte-Anne, Paris, France.
Pierre EllulChild and Adolescent Psychiatry Department, Robert Debré Hospital, APHP, 48 Boulevard Sérurier, 75019, Paris, France.
Cécile PaganUnité Maladies Héréditaires du Métabolisme, Service de Biochimie et Biologie Moléculaire Grand Est, Centre de Biologie et de Pathologie Est, Hospices Civils de Lyon, 59 boulevard Pinel, 69677, Bron cedex, France.
Magali PettazzoniUnité Maladies Héréditaires du Métabolisme, Service de Biochimie et Biologie Moléculaire Grand Est, Centre de Biologie et de Pathologie Est, Hospices Civils de Lyon, 59 boulevard Pinel, 69677, Bron cedex, France.
Soumeya BekriDepartment of Metabolic Biochemistry, Rouen University Hospital, Rouen, France.
Serge BelliardCentre Mémoire de Ressource et Recherche, CHU Rennes. INSERM U1077, EPHE, Caen, France.
Cyril GoizetCentre de Référence Maladies Rares Neurogénétique, Service de Génétique Médicale, CHU Bordeaux and Laboratoire MRGM, INSERM U1211, Hôpital Pellegrin, Univ. Bordeaux, Bordeaux, France.
David WallonInserm Department of Neurology and CNR-MAJNormandy Center for Genomic and Personalized Medicine, Normandie Univ, UNIROUEN, U1245 and Rouen University Hospital, 76000, Rouen, France.
Foudil LamariDépartement de Biochimie métabolique, UF Biochimie des Maladies neurométaboliques, Hôpital Pitié-Salpêtrière, 47-83 boulevard de l'Hôpital, 75013, Paris, France.
Yann NadjarNeurology Department, Reference Center for Lysosomal Diseases, Neurogenetics and Metabolism Unit, Hôpital Pitié-Salpêtrière, 47-83 boulevard de l'Hôpital, 75013, Paris, France. yann.nadjar@aphp.fr.ORCID http://orcid.org/0000-0003-1466-6957

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Late-onset Niemann-Pick type C (NP-C) is a rare, underdiagnosed lysosomal disease with neurological manifestations. A specific treatment, miglustat, can stabilize the disease if given early. Recently, three plasma screening biomarkers (PSBs) were developed [cholestane3β,5α,6βtriol (C-triol), 7-ketocholesterol (7-KC), and lysosphingomyelin-509 (LSM-509)], allowing a simpler and quite robust screening of patients suitable for genetic testing. The objective of our study was to evaluate practical utility and feasibility of large-scale PSB screening for NP-C in selected adult patients. Patients were prospectively enrolled if they showed, starting from 12 years of age, at least one of the three initial neuro-psychiatric manifestations described in NP-C: (1) gait disorder (cerebellar and/or dystonic); (2) cognitive decline with frontal lobe syndrome; (3) atypical psychosis. PSBs were measured in plasma of all patients and, if positive (LSM-509 and/or C-triol + 7-KC elevated), sequencing of NPC1 and NPC2 genes was performed. A total of 251 patients [136 males, 115 females; median age 42.1 (range 12.2-85.6) years] were screened. Six patients had positive PSBs. Two were confirmed to have NP-C (0.8% diagnostic yield, both with all three PSBs highly increased, especially LSM-509). False-positive rate was 1.2%, which was identical if only considering LSM-509. By contrast, false-positive rates were 8.1% and 5.7% for 7-KC and C-triol, respectively. We showed that selecting patients with neurologic and/or psychiatric symptoms consistent with NP-C for large-scale PSB screening is a simple and valid strategy to identify new adult NP-C patients, and would probably lead to earlier diagnosis and treatment administration if widely applied.

Indexed as

Niemann-Pick Disease, Type CPsychotic DisordersAdolescentAdultAgedAged, 80 and overBiomarkersChildEarly DiagnosisFemaleGenetic TestingHumansMaleMiddle AgedYoung AdultBiomarkersBiomarkersLysosphingomyelin-509Niemann-pick type CScreening

Identifiers

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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.