» Articles » PMID: 36562851

Adipokines in Multiple Sclerosis Patients Are Related to Clinical and Radiological Measures

Overview
Journal J Neurol
Specialty Neurology
Date 2022 Dec 23
PMID 36562851
Authors
Affiliations
Soon will be listed here.
Abstract

Background: An imbalance of adipokines, hormones secreted by white adipose tissue, is suggested to play a role in the immunopathology of multiple sclerosis (MS). In people with MS (PwMS) of the same age, we aimed to determine whether the adipokines adiponectin, leptin, and resistin are associated with MS disease severity. Furthermore, we aimed to investigate whether these adipokines mediate the association between body mass index (BMI) and MS disease severity.

Methods: Adiponectin, resistin, and leptin were determined in serum using ELISA. 288 PwMS and 125 healthy controls (HC) were included from the Project Y cohort, a population-based cross-sectional study of people with MS born in the Netherlands in 1966, and age and sex-matched HC. Adipokine levels and BMI were related to demographic, clinical and disability measures, and MRI-based brain volumes.

Results: Adiponectin levels were 1.2 fold higher in PwMS vs. HC, especially in secondary progressive MS. Furthermore, we found a sex-specific increase in adiponectin levels in primary progressive (PP) male patients compared to male controls. Leptin and resistin levels did not differ between PwMS and HC, however, leptin levels were associated with higher disability (EDSS) and resistin strongly related to brain volumes in progressive patients, especially in several grey matter regions in PPMS. Importantly, correction for BMI did not significantly change the results.

Conclusion: In PwMS of the same age, we found associations between adipokines (adiponectin, leptin, and resistin) and a range of clinical and radiological metrics. These associations were independent of BMI, indicating distinct mechanisms.

Citing Articles

Vascular risk factors are associated with grey matter atrophy in secondary progressive multiple sclerosis.

John N, Li Y, De Angelis F, Stutters J, Prados F, Doshi A Eur J Neurol. 2024; 32(1):e16586.

PMID: 39691073 PMC: 11653023. DOI: 10.1111/ene.16586.


Impact of Lifestyle Interventions on Multiple Sclerosis: Focus on Adipose Tissue.

Mallardo M, Mazzeo F, Lus G, Signoriello E, Daniele A, Nigro E Nutrients. 2024; 16(18).

PMID: 39339700 PMC: 11434938. DOI: 10.3390/nu16183100.


Oral Contraceptives Interact with Adiposity-Associated Markers in Patients with Multiple Sclerosis.

Ferret-Sena V, Ramos C, Cascais M, Capela C, Sena A J Clin Med. 2024; 13(2).

PMID: 38256598 PMC: 10816152. DOI: 10.3390/jcm13020464.

References
1.
Frommer K, Zimmermann B, Meier F, Schroder D, Heil M, Schaffler A . Adiponectin-mediated changes in effector cells involved in the pathophysiology of rheumatoid arthritis. Arthritis Rheum. 2010; 62(10):2886-99. DOI: 10.1002/art.27616. View

2.
Chatzantoni K, Papathanassopoulos P, Gourzoulidou E, Mouzaki A . Leptin and its soluble receptor in plasma of patients suffering from remitting-relapsing multiple sclerosis (MS) In vitro effects of leptin on type-1 and type-2 cytokine secretion by peripheral blood mononuclear cells, T-cells and monocytes of MS.... J Autoimmun. 2004; 23(2):169-77. DOI: 10.1016/j.jaut.2004.05.007. View

3.
Coban A, DUzel B, Tuzun E, Tamam Y . Investigation of the prognostic value of adipokines in multiple sclerosis. Mult Scler Relat Disord. 2017; 15:11-14. DOI: 10.1016/j.msard.2017.04.006. View

4.
Dashti M, Alroughani R, Jacob S, Al-Temaimi R . Leptin rs7799039 polymorphism is associated with multiple sclerosis risk in Kuwait. Mult Scler Relat Disord. 2019; 36:101409. DOI: 10.1016/j.msard.2019.101409. View

5.
De Stefano N, Stromillo M, Giorgio A, Bartolozzi M, Battaglini M, Baldini M . Establishing pathological cut-offs of brain atrophy rates in multiple sclerosis. J Neurol Neurosurg Psychiatry. 2015; 87(1):93-9. PMC: 4717444. DOI: 10.1136/jnnp-2014-309903. View