Evidence map›Paper›PMID 28003098›Full record

ArticleBlood cells, molecules & diseases2018

Validating glycoprotein non-metastatic melanoma B (gpNMB, osteoactivin), a new biomarker of Gaucher disease.

Vagishwari Murugesan, Jun Liu, Ruhua Yang, Haiquin Lin, Andrew Lischuk, Gregory Pastores, Xiaokui Zhang, Wei-Lien Chuang, Pramod K Mistry

Abstract read
In one paragraph

Article in Blood cells, molecules & diseases, 2018. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 42 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
42citing papers in PubMed, 2 pooled it
2.7field-weighted citation impact, top 10% 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

42 citing papers in PubMed, 2 syntheses or guidelines pooled it, 59 citations in OpenAlex.

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  16. GPNMB Biomarker Levels in GBA1 Carriers with Lewy Body Disorders.Movement disorders : official journal of the Movement Disorder Society · 2024
    Article
  17. Glycoprotein Non-Metastatic Protein B (GPNMB): The Missing Link Between Lysosomes and Obesity.Experimental and clinical endocrinology & diabetes : official journal, German Society of Endocrinology [and] German Diabetes Association · 2023
    Review
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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

9 authors at 3 institutions in 2 countries.

Vagishwari MurugesanDepartment of Internal Medicine, Yale University School of Medicine, New Haven, CT, United States.
Jun LiuDepartment of Internal Medicine, Yale University School of Medicine, New Haven, CT, United States.
Ruhua YangDepartment of Internal Medicine, Yale University School of Medicine, New Haven, CT, United States.
Haiquin LinDepartment of Biostatistics, Yale School of Public Health, United States.
Andrew LischukDepartment of Radiology, Yale University School of Medicine, New Haven, CT, United States.
Gregory PastoresDepartment of Metabolic Diseases, Mater Misericordiae University Hospital, Dublin, Ireland.
Xiaokui ZhangSanofi Genzyme, Framingham, MA, United States.
Wei-Lien ChuangSanofi Genzyme, Framingham, MA, United States.
Pramod K MistryDepartment of Internal Medicine & Pediatrics, Yale University School of Medicine, New Haven, CT, United States. Electronic address: pramod.mistry@yale.edu.
Yale University · USSanofi (United States) · USMater Misericordiae University Hospital · IE

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
Yale Liver CenterP30DK034989 · NIDDK · YALE UNIVERSITY · PI YASUKO IWAKIRI · 1986 to 2026
$31.1M
Understanding the skeletal phenotype of Gaucher diseaseR01AR065932 · NIAMS · ICAHN SCHOOL OF MEDICINE AT MOUNT SINAI · PI MISTRY, PRAMOD K, ZAIDI, MONE · 2013 to 2017
$2.6M
NCATS NIH HHS UL1 TR001863NIAMS NIH HHS R01 AR065932NIDDK NIH HHS P30 DK034989
6 · The paper itself

Abstract

In the spleens of Gaucher disease mice and patients, there is a striking elevation of expression of glycoprotein non-Metastatic Melanoma B (gpNMB). We conducted a study in a large cohort of patients with Gaucher disease to assess the utility of serum levels of soluble fragment of gpNMB as a biomarker of disease activity. There was >15-fold elevation of gpNMB in sera of untreated patients with Gaucher disease. gpNMB levels correlated with overall disease severity as well as the severity of individual organ compartments: liver, spleen, bone and hematological disease. Imiglucerase enzyme replacement therapy resulted in significant reduction of gpNMB. Serum levels of gpNMB were highly correlated with accumulation of bioactive lipid substrate of Gaucher disease, glucosylsphingosine as well as established biomarkers, chitotriosidase and chemokine, CCL18. Our results suggest utility of gpNMB as a biomarker of Gaucher disease to monitor individual patients and cohorts of patients for disease progression or response to therapy. Investigation of gpNMB in Gaucher disease pathophysiology is likely to illuminate our understanding disease mechanisms.

Indexed as

AdolescentAdultAgedAnimalsBiomarkersChildChild, PreschoolCohort StudiesDisease ProgressionEnzyme Replacement TherapyFemaleGaucher DiseaseGlucosylceramidaseHexosaminidasesHumansMaleBiomarkerschitotriosidaseGlucosylceramidaseGPNMB protein, humanHexosaminidasesimigluceraseMembrane GlycoproteinsBiomarkerGaucher diseasegpNMBOsteoactivin

Identifiers

PMID28003098
PMCPMC5468511
OpenAlexW2567533903

What OpenQuestion holds

Textmetadata
LicenceTDM
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.