# The Role of Lipid Alteration in Multiple Sclerosis

**Authors:** Agnieszka Damiza-Detmer, Małgorzata Pawełczyk, Andrzej Głąbiński

PMC · DOI: 10.3390/ijms27020812 · 2026-01-14

## TL;DR

This paper reviews how lipid changes in the body and brain may contribute to multiple sclerosis, suggesting they could be important for understanding and treating the disease.

## Contribution

The paper highlights new insights into how lipid metabolism in the central nervous system may drive systemic dyslipidemia in MS.

## Key findings

- Lipid abnormalities in MS patients include changes in cholesterol and lipoprotein levels.
- Dyslipidemia in MS may result from CNS cholesterol metabolism disrupted by demyelination.
- Lipid changes correlate with blood-brain barrier dysfunction and CNS inflammation.

## Abstract

Multiple sclerosis (MS) is traditionally recognized as a chronic immune-mediated disorder of the central nervous system (CNS), but increasing evidence suggests that systemic metabolic alterations may also contribute to its pathophysiology. Lipid abnormalities in MS have recently attracted renewed research interest, with studies focusing both on dysregulation of lipid signaling pathways and on alterations in standard lipid profile components, including total cholesterol (TC), low-density lipoprotein (LDL), high-density lipoprotein (HDL), triglycerides (TG), and non-HDL cholesterol. Although disturbances in serum lipid profiles are consistently reported in patients with MS, their origin remains unresolved. Emerging data indicate that dyslipidemia may stem from aberrant cholesterol metabolism within the CNS, secondary to demyelination and myelin sheath destruction, leading to the release of lipid-rich debris and subsequent systemic metabolic imbalance. These lipid changes appear to correlate with blood–brain barrier (BBB) dysfunction, suggesting a link between peripheral lipid metabolism and CNS inflammation. This review summarizes current knowledge on the mechanisms underlying dyslipidemia in MS, its potential impact on disease progression, and its relevance as a possible therapeutic or biomarker target in future translational studies.

## Linked entities

- **Diseases:** Multiple sclerosis (MONDO:0005301)

## Full-text entities

- **Diseases:** demyelination (MESH:D003711), immune-mediated disorder of the central nervous system (MESH:D020274), Lipid abnormalities (MESH:D011017), dyslipidemia (MESH:D050171), inflammation (MESH:D007249), MS (MESH:D009103)
- **Chemicals:** Lipid (MESH:D008055), TC (-), TG (MESH:D014280), cholesterol (MESH:D002784)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

5 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12841116/full.md

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Source: https://tomesphere.com/paper/PMC12841116