Authors
Shaynah Wanga, Stijntje Hibender, Yanto Ridwan, Cindy van Roomen, Mariska Vos, Ingeborg Van Der Made, Nicole van Vliet, Romy Franken, Luigi AMJG van Riel, Maarten Groenink, Aeilko H Zwinderman, Barbara JM Mulder, Carlie JM de Vries, Jeroen Essers, Vivian De Waard
Publication date
2017/11
Journal
The Journal of pathology
Volume
243
Issue
3
Pages
294-306
Publisher
John Wiley & Sons, Ltd
Description
Marfan syndrome (MFS) is a connective tissue disorder in which aortic rupture is the major cause of death. MFS patients with an aortic diameter below the advised limit for prophylactic surgery (<5 cm) may unexpectedly experience an aortic dissection or rupture, despite yearly monitoring. Hence, there is a clear need for improved prognostic markers to predict such aortic events. We hypothesize that elastin fragments play a causal role in aortic calcification in MFS, and that microcalcification serves as a marker for aortic disease severity. To address this hypothesis, we analysed MFS patient and mouse aortas. MFS patient aortic tissue showed enhanced microcalcification in areas with extensive elastic lamina fragmentation in the media. A causal relationship between medial injury and microcalcification was revealed by studies in vascular smooth muscle cells (SMCs); elastin peptides were shown to increase the …
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