Key result
Natalizumab and fingolimod in RRMS linked to elevated apelin and ghrelin respectively versus healthy controls.
Why the study?
Peptide hormones may influence the pathogenesis of multiple sclerosis by affecting inflammatory processes and metabolic dysregulation, but their role in treated RRMS patients is unclear.
Do serum levels of apelin and ghrelin differ between RRMS patients treated with natalizumab or fingolimod and healthy controls?
Cross-Sectional (n=87)
Yes
Do serum levels of apelin and ghrelin differ between RRMS patients treated with natalizumab or fingolimod and healthy controls?
Absolute Event Rate: 4559.82% vs 1045.67%
p-value: p=0.0063
Serum apelin and ghrelin levels differ between RRMS patients on immunomodulatory therapy and healthy controls, suggesting a link between treatment, metabolism, and peptide hormones in MS.
Introduction: Multiple sclerosis (MS) is an autoimmune disorder with a complex and multifactorial etiology. Increasing evidence suggests that peptide hormones may significantly influence the pathogenesis of MS by affecting inflammatory processes and metabolic dysregulation. The aim of the study was to evaluate the levels of apelin and ghrelin, which are two peptide hormones, in patients with relapsing-remitting MS (RRMS) receiving natalizumab and fingolimod compared to healthy controls. Methods: We enrolled forty-nine patients with RRMS and thirty-eight healthy individuals. The participants were divided into three groups i.e., natalizumab-treated patients, fingolimod-treated patients, and healthy controls. We assessed the serum levels of apelin and ghrelin. Statistical analysis was performed using STATISTICA 12. In both groups, correlations between the duration of the disease and treatment, BMI and hormone concentrations were evaluated. Results: analysis revealed that all women treated with natalizumab and fingolimod had higher apelin levels than healthy women (p=0.025). In the group of women with MS, ghrelin levels increased with disease duration (p=0.045, R = 0.357). Additionally, apelin levels correlated positively with BMI in the fingolimod-treated group (p=0.001, R = 0.694). Conclusion: The study demonstrates differences in serum apelin and ghrelin levels between RRMS patients treated with natalizumab or fingolimod and healthy controls, suggesting a potential association between immunomodulatory treatment, metabolic factors, and peptide hormone regulation in multiple sclerosis.
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Adamczyk et al. (2026) conducted a cross-sectional in Relapsing-remitting multiple sclerosis (n=87). Natalizumab and Fingolimod vs. Healthy controls was evaluated on Serum apelin concentration (p=0.0063). Natalizumab-treated RRMS patients had significantly higher serum apelin levels (p=0.0063), and fingolimod-treated patients had higher ghrelin levels (p=0.0035) compared to healthy controls.
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