Glycoprotein non-metastatic melanoma protein B is a biomarker of inflammation in individuals with Gaucher disease: relationship to clinico-pathological subtypes

Our findings indicate that the association of plasma gpNMB with liver cirrhosis, gammopathy and pulmonary disease in Gaucher disease warrants further investigation. Additionally, plasma gpNMB may serve as a supportive biomarker in the evaluation and clinical monitoring of residual disease activity. However, plasma gpNMB neither differentiated between the neuronopathic subtypes of Gaucher disease nor idiopathic Parkinson's disease.

Authors

Institutions

Publication Details

Journal
Orphanet Journal of Rare Diseases
Published
2025-10-28
DOI
https://doi.org/10.1186/s13023-025-04054-y
Citations
1
Primary Topic
Lysosomal Storage Disorders Research
Type
article
Field-Weighted Citation Impact
1.16

Funders

Controls
|||
ALL TIME
JAN
FEB
MAR
APR
MAY
JUN
JUL
AUG
SEP
OCT
article

Glycoprotein non-metastatic melanoma protein B is a biomarker of inflammation in individuals with Gaucher disease: relationship to clinico-pathological subtypes

Kathy Page, Kerri‐Lee Wallom, Ellen Hertz, Per Svenningsson et al.
1 citations
Orphanet Journal of Rare Diseases
Lysosomal Storage Disorders Research
1.16
article

Glycoprotein non-metastatic melanoma protein B is a biomarker of inflammation in individuals with Gaucher disease: relationship to clinico-pathological subtypes

Kathy Page, Kerri‐Lee Wallom, Ellen Hertz, Per Svenningsson, Chong Yew Tan, Daniëlle te Vruchte, Sebile Kılavuz, Andrea Sturchio, Panagiota Tsitsi, Frances M. Platt, Timothy M. Cox, Aimée Donald, Mattias Andréasson, Simona D’Amore, Ioanna Markak, Ana Catarina Gomes Almeida Augusto Caçote
article en
1 citations

Abstract

Our findings indicate that the association of plasma gpNMB with liver cirrhosis, gammopathy and pulmonary disease in Gaucher disease warrants further investigation. Additionally, plasma gpNMB may serve as a supportive biomarker in the evaluation and clinical monitoring of residual disease activity. However, plasma gpNMB neither differentiated between the neuronopathic subtypes of Gaucher disease nor idiopathic Parkinson's disease.

Orphanet Journal of Rare DiseasesVol. 20(1)
Royal Free London NHS Foundation Trust (GB), University of Cambridge (GB), Manchester Academic Health Science Centre (GB), Karolinska Institutet (SE), University of Manchester (GB), University of Oxford (GB), University of Bari Aldo Moro (IT), Marmara University (TR)
King's College London, Türkiye Bilimsel ve Teknolojik Araştırma Kurumu, Medical Research Council
Openalex Percentile: Top 17%
Lysosomal Storage Disorders Research
1.16
AI Navigator

Ask Laika to Summarize, Analyze, and Connect papers live on the map.

Summarize Papers & Methodologies

Extract key findings, datasets, and comparative methods across publications.

Benchmark Rankings & Visual Analytics

Rank top research institutions, authors, funders, topics, and journals by Field-Weighted Citation Impact (FWCI) and paper volume with instant charts.

Connect Distant Disciplines

Bridge topological clusters on the map to find hidden collaborative intersections.