Level of kisspeptin-10 in patients with multiple sclerosis and the association between third ventricle diameter size and vitamin D level.
Akdag. T T; Uca. A U AU; Altas. M M; Odabas. F O FO; Aktas. F F
Key Findings
- Serum kisspeptin-10 was significantly lower in MS patients (2.3 ng/mL) than in healthy controls (9.3 ng/mL).
- Kisspeptin-10 showed good diagnostic performance for MS (AUC = 0.881, cut‑off 2.47 ng/mL, 80% sensitivity, 73% specificity).
- Lower kisspeptin-10 levels were negatively correlated with third ventricle diameter and vitamin D levels, but not with other clinical scores like EDSS.
Practical Outcomes
- For biohackers and self‑experimenters, this study doesn’t provide a new supplement or protocol to try. It suggests kisspeptin-10 might be a useful blood marker for MS diagnosis, but there’s no evidence it can be safely altered to improve health or longevity. Until more research clarifies its role, measuring or supplementing kisspeptin-10 isn’t a practical strategy.
Summary
Researchers measured a small protein called kisspeptin-10 in the blood of people with relapsing‑remitting multiple sclerosis (MS) and healthy volunteers. They found that MS patients had much lower levels of this protein, and the level could somewhat distinguish patients from healthy people. The study also noticed that lower kisspeptin-10 was linked to larger brain ventricle size and lower vitamin D, but it didn’t relate to most other disease measures.
Abstract
Multiple sclerosis (MS) is a chronic and progressive neurological disease affecting the central nervous system (CNS). Some studies report an association between MS pathogenesis and cytokines. Here, we aimed to determine and evaluate serum kisspeptin-10 level in MS patients and its related clinic parameters. A total of 92 participants, 46 patients with relapsing-remitting MS (mean age, 38.92 ± 14.76; 22 men and 24 women) and 46 healthy controls (mean age, 37.04 ± 15.49; 22 men and 24 women) were enrolled in the study. All MS patients were neurologically examined, and magnetic resonance imaging (MRI) was performed. Clinical data (neuropathic pain, expanded disability status scale (EDSS) score, etc.) and the patients' demographic characteristics were recorded. The serum level of kisspeptin-10 was analyzed by enzyme-linked immunosorbent assay (ELISA) method. The level of kisspeptin-10 was measured as 2.305 ± 2.781 ng/mL in MS patients and 9.342 ± 9.483 ng/mL in controls. MS patients had significantly lower kisspeptin-10 levels than controls (P = 0.000). Kisspeptin-10 has the highest diagnostic value [Area under curve (AUC) = 0.881, 95% confidence interval (CI), 0.812-0.950] as cut-off value (2.470), sensitivity (80.40%) and specificity (72.87%) in the MS group. Furthermore, the kisspeptin-10 level was negatively correlated with third ventricle diameter (TVD) (P = 0.048) and vitamin D concentration (P = 0.004). No significant difference was determined between kisspeptin-10 and other clinical parameters. As a potential prognostic biomarker, serum kisspeptin-10 level was significantly lower in patients with MS than in those without. Moreover, we observed negative correlations between vitamin D, TVD size, and kisspeptin-10. We think comprehensive studies are needed to verify and elucidate this issue.
Study Information
pubmed
2021
2021-06-16T00:00:00.000Z
10.1556/2060.2021.00179
2