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Differential blood-based biomarkers of subcortical and deep brain small vessel disease.

Authors :
Hervella P
Alonso-Alonso ML
Sampedro-Viana A
Rodríguez-Yáñez M
López-Dequidt I
Pumar JM
Ouro A
Romaus-Sanjurjo D
Campos F
Sobrino T
Castillo J
Leira Y
Iglesias-Rey R
Source :
Therapeutic advances in neurological disorders [Ther Adv Neurol Disord] 2024 May 31; Vol. 17, pp. 17562864241243274. Date of Electronic Publication: 2024 May 31 (Print Publication: 2024).
Publication Year :
2024

Abstract

Background: Cerebral small vessel disease is the most common cause of lacunar strokes (LS). Understanding LS pathogenesis is vital for predicting disease severity, prognosis, and developing therapies.<br />Objectives: To research molecular profiles that differentiate LS in deep brain structures from those in subcortical white matter.<br />Design: Prospective case-control study involving 120 patients with imaging-confirmed LS and a 120 control group.<br />Methods: We examined the relationship between Alzheimer's disease biomarkers [amyloid beta (Aβ <subscript>1-40</subscript> , Aβ <subscript>1-42</subscript> )], serum inflammatory marker (interleukin-6, IL-6), and endothelial dysfunction markers [soluble tumor necrosis factor-like weak inducer of apoptosis, and pentraxin-3 (sTWEAK, PTX3)] with respect to LS occurring in deep brain structures and subcortical white matter. In addition, we investigated links between LS, leukoaraiosis presence (white matter hyperintensities, WMHs), and functional outcomes at 3 months. Poor outcome was defined as a modified Rankin scale >2 at 3 months.<br />Results: Significant differences were observed in levels of IL-6, PTX3, and sTWEAK between patients with deep lacunar infarcts and those with recent small subcortical infarcts (20.8 versus 15.6 pg/mL, p  < 0.001; 7221.3 versus 4624.4 pg/mL, p  < 0.0001; 2528.5 versus 1660.5 pg/mL, p  = 0.001). Patients with poor outcomes at 3 months displayed notably higher concentrations of these biomarkers compared to those with good outcomes. By contrast, Aβ <subscript>1-40</subscript> and Aβ <subscript>1-42</subscript> were significantly lower in patients with deep LS ( p  < 0.0001). Aβ <subscript>1-42</subscript> levels were significantly higher in patients with LS in subcortical white matter who had poor outcomes. WMH severity only showed a significant association with deep LS and correlated with sTWEAK ( p  < 0.0001).<br />Conclusion: The pathophysiological mechanisms of lacunar infarcts in deep brain structures seem different from those in the subcortical white matter. As a result, specific therapeutic and preventive strategies should be explored.<br /> (© The Author(s), 2024.)

Details

Language :
English
ISSN :
1756-2856
Volume :
17
Database :
MEDLINE
Journal :
Therapeutic advances in neurological disorders
Publication Type :
Academic Journal
Accession number :
38827243
Full Text :
https://doi.org/10.1177/17562864241243274