Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/48792
Title: Lipid alterations in hereditary peripheral neuropathies: common mechanisms in disease heterogeneity?
Authors: KUIPERS, Koen 
VANHERLE, Sam 
POELMANS, Kirsten 
WOLFS, Esther 
BOGIE, Jeroen 
VANGANSEWINKEL, Tim 
Issue Date: 2026
Publisher: BMC
Source: Molecular neurodegeneration, 21 (1) (Art N° 16)
Abstract: While the impact of lipid alterations on central nervous system disorders is well-studied, increasing evidence indicates that lipids also play an important role in the pathology of hereditary peripheral neuropathies (HPN). It is becoming clear that Schwann cells and neurons in peripheral nerves heavily depend on lipids for membrane interactions, (sub)cellular signalling, and the formation of myelin sheaths. In support of this notion, disturbances in the level and composition of lipid classes, including phospholipids, sphingolipids and cholesterol, perturb normal functioning of peripheral nerves. Intriguingly, lipid disturbances seem to be a common denominator within the heterogeneous group of HPN, with hindrances in cholesterol and sphingolipid metabolism primarily influencing Schwann cell and neuron homeostasis, respectively. In this review, we provide an overview of lipid disturbances in various HPN with the goal of finding main commonalities between the different diseases and to identify potential novel treatment strategies.
Notes: Vangansewinkel, T (corresponding author), Hasselt Univ, Biomed Res Inst, Lab Funct Imaging & Res Stem Cells FIERCELab, Diepenbeek, Belgium.; Vangansewinkel, T (corresponding author), Univ Leuven, KU Leuven, Leuven Brain Inst LBI, Dept Neurosci, Leuven, Belgium.; Vangansewinkel, T (corresponding author), Univ Antwerp, Dept Biomed Sci, Peripheral Neuropathy Res Grp, Antwerp, Belgium.
tim.vangansewinkel@uhasselt.be
Keywords: Peripheral neuropathy;Lipid metabolism;Schwann cells;Neurons;Demyelination;Neurodegeneration
Document URI: http://hdl.handle.net/1942/48792
e-ISSN: 1750-1326
DOI: 10.1186/s13024-026-00932-6
ISI #: 001711880000001
Rights: The Author(s) 2026. Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
Category: A1
Type: Journal Contribution
Appears in Collections:Research publications

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