DIFFERENCES IN FLOW-MEDIATED DILATATION MEASUREMENTS BETWEEN MULTIPLE SCLEROSIS SUBGROUPS
Öz
OBJECTIVE: We aimed to show the differences in flow-mediated dilatation (FMD) measurements between multiple sclerosis (MS) subgroups and normal control participants.
MATERIAL AND METHODS: There were 96 participants (mean age: 42.7 ± 14.1 years) in this study. We grouped the participants as follows: 47 MS patients (mean age: 40.2 ± 12.2 years) and 49 normal control participants (mean age: 45.22 ± 15.27). The MS patients were subclassified as follows: Group 1 – relapsing-remitting multiple sclerosis (RRMS): 37 patients (mean age: 36.9 ± 11.2); Group 2 – secondary progressive multiple sclerosis (SPMS): 5 patients (mean age: 49.0 ± 6.0); and Group 3 – primary progressive multiple sclerosis (PPMS): 5 patients (mean age: 55.4 ± 10.6 years). We used FMD methods for an indirect evaluation of the brachial artery’s reaction to shear stress and peripheral vasodilatory nitric oxide (NO) production capability.
RESULTS: There were statistically significant differences between the normal control group and the MS subgroups regarding flow-mediated basal, flow-mediated hyperemia, and FMD ratio values (p = 0.001, p = 0.029, and p = 0.020, respectively). No correlation was found between the expanded disability status scale (EDSS) scores and other measurements after statistically controlling for age and gender factors (p > 0.05).
CONCLUSIONS: Our data indicate that FMD measurements decreased more in the MS patients compared to the normal controls. The PPMS group exhibited more severe deterioration with regard to FMD measures than the other groups. FMD ratio values decreased more in the progressive MS groups compared to the normal control and RRMS groups.
Anahtar Kelimeler
Kaynakça
- 1. López-Gambero AJ, Sanjuan C, Serrano-Castro PJ, et al. The Biomedical Uses of Inositols: A Nutraceutical Approach to Metabolic Dysfunction in Aging and Neurodegenerative Diseases. Biomedicines. 2020;8(9):295.
- 2. Lane J, Ng HS, Poyser C, et al. Multiple sclerosis incidence: A systematic review of change over time by geographical region. Mult Scler Relat Disord. 2022;63:103932.
- 3. Correale J, Marrodan M, Ysrraelit MC. Mechanisms of Neurodegeneration and Axonal Dysfunction in Progressive Multiple Sclerosis. Biomedicines. 2019;7(1):14.
- 4. Bennett J, Basivireddy J, Kollar A, et al. Blood-brain barrier disruption and enhanced vascular permeability in the multiplesclerosis model EAE. J Neuroimmunol. 2010;229(1-2):180-91.
- 5. Islam MT. Oxidative stress and mitochondrial dysfunction-linked neurodegenerative disorders. Neurol Res. 2017 ;39(1):73-82.
- 6. Ghafourifar P, Mousavizadeh K, Parihar MS, et al. Mitochondria in multiple sclerosis. Front Biosci. 2008;13:3116- 26.
- 7. Knight JA. Reactive oxygen species and the neurodegenerative disorders. AnnClin Lab Sci. 1997;27(1):11-25.
- 8. Emerit J, Edeas M, Bricaire F. Neurodegenerative diseases and oxidative stress. Biomed Pharmacother. 2004;58(1):39-46.
Ayrıntılar
Birincil Dil
İngilizce
Konular
Kardiyoloji , Nöroloji ve Nöromüsküler Hastalıklar
Bölüm
Araştırma Makalesi
Yazarlar
Çağlar Alp
*
0000-0001-5984-1857
Türkiye
Murat Alpua
0000-0002-0951-5962
Türkiye
Zehra Uyan Ulaş
0000-0003-4240-0937
Türkiye
Yayımlanma Tarihi
12 Ekim 2026
Gönderilme Tarihi
22 Mart 2025
Kabul Tarihi
6 Ocak 2026
Yayımlandığı Sayı
Yıl 2026 Cilt: 27 Sayı: 4
