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Temporal variability of serum miR-191, miR-223, miR-128, and miR-24 in multiple sclerosis: A 4-year follow-up study
被引:3
|作者:
Vistbakka, Julia
[1
]
Sumelahti, Marja-Liisa
[1
]
Lehtimaki, Terho
[3
,4
]
Hagman, Sanna
[1
,2
]
机构:
[1] Tampere Univ, Fac Med & Hlth Technol, Neuroimmunol Res Grp, Tampere, Finland
[2] Tampere Univ Hosp, Res Dev & Innovat Ctr, Tampere, Finland
[3] Tampere Univ, Dept Clin Chem, Fimlab Labs, Tampere 33520, Finland
[4] Tampere Univ, Fac Med & Hlth Technol, Finnish Cardiovasc Res Ctr Tampere, Tampere 33520, Finland
基金:
芬兰科学院;
关键词:
Multiple sclerosis;
Biomarkers;
miRNA;
microRNA;
Follow-up study;
Serum;
EDSS;
MICRORNA EXPRESSION;
BIOMARKERS;
STABILITY;
BLOOD;
D O I:
10.1016/j.jns.2022.120395
中图分类号:
R74 [神经病学与精神病学];
学科分类号:
摘要:
Background: Circulating microRNAs (miRNA) are suggested to be a promising biomarker for multiple sclerosis (MS). Previously, miR-128-3p, miR-24-3p, miR-191-5p and miR-223-3p have been reported to associate with MS pathology. However, their longitudinal changes and association with the disease activity have not been studied.Objectives: To evaluate the serum temporal variability of miR-128-3p, miR-191-5p, miR-24-3p, and miR-223-3p and their association with disability and disease activity in MS.Methods: The expression of four miRNAs in serum was studied in 57 MS patients, 18 clinically isolated syndrome patients, and 32 healthy controls over the four-year follow-up.Results: At the baseline, miR-191-5p was overexpressed in RRMS in comparison to controls, and its levels correlated positively with EDSS and progression index (PI) in RRMS. Increased levels of miR-128-3p were detected in PPMS in comparison to controls, and increased levels correlated with EDSS and PI in RRMS. The expression of miR-24-3p and miR-223-3p did not differ between the subtypes, but miR-223-3p correlated negatively with T1 lesions volumes in SPMS and PPMS. Over the four-years follow-up period, the expression of miR-128-3p and miR-24-3p was stable longitudinally, while temporal changes of miR-191-5p and miR-223-3p were observed in MS. Temporal changes in miR-191-5p were observed to be associated with an increase of EDSS or MRI activity, while the variability of miR-223-3p was associated with relapses.Conclusion: Temporal variability of miR-191-5p and miR-223-3p are associated with changes in disability accumulation and disease activity. While, miR-128-3p was stably expressed and associated with the PPMS subtype and correlated with disability accumulation.
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