New candidate blood biomarkers potentially associated with white matter hyperintensities progression

• Published in: Scientific reports Vol. 11; no. 1; pp. 14324 - 10
• Main Authors: Jiménez-Balado, Joan, Pizarro, Jesús, Riba-Llena, Iolanda, Penalba, Anna, Faura, Júlia, Palà, Elena, Montaner, Joan, Hernández-Guillamon, Mar, Delgado, Pilar
• Format: Journal Article
• Language: English
• Published: London Nature Publishing Group UK 12.07.2021; Nature Publishing Group; Nature Portfolio
• Subjects: 631/378; 631/378/1341; 631/378/2607; Biomarkers; Blood; c-Met protein; Ceramidase; Gelatinase B; Hepatocyte growth factor; Humanities and Social Sciences; Hypertension; Magnetic resonance imaging; Matrix metalloproteinase; Metalloproteinase; multidisciplinary; Replication; Science; Science (multidisciplinary); Substantia alba
• ISSN: 2045-2322; 2045-2322
• DOI: 10.1038/s41598-021-93498-w

We aimed to discover blood biomarkers associated with longitudinal changes in white matter hyperintensities (WMH). This study was divided into a discovery phase and a replication phase. Subjects in both studies were patients with hypertension, aged 50–70, who underwent two magnetic resonance imaging (MRI) sessions and blood extractions over a 4-year follow-up period. In the discovery phase, we screened 1305 proteins in 12 subjects with WMH progression and in 12 matched control subjects. We found that 41 proteins were differentially expressed: 13 were upregulated and 28 were downregulated. We subsequently selected three biomarkers for replication in baseline and follow-up samples in 80 subjects with WMH progression and in 80 control subjects. The selected protein candidates for the replication were MMP9 (matrix metalloproteinase-9), which was higher in cases, MET (hepatocyte growth factor receptor) and ASAH2 (neutral ceramidase), which were both lower in cases of WMH progression. Baseline biomarker concentrations did not predict WMH progression. In contrast, patients with WMH progression presented a steeper decline in MET over time. Furthermore, cases showed higher MMP9 and lower ASAH2 levels than controls at the follow-up. These results indicate that MMP9, MET, and ASAH2 are potentially associated with the progression of WMH, and could therefore be interesting candidates to validate in future studies.