Key result
Elevated aortic wall shear stress in patients with bicuspid aortic valve-associated aortopathy was associated with significantly increased aortic wall cell death compared to normal shear stress regions (13.74% vs 7.98%, p=0.0027).
Why the study?
The study sought to identify aorta-specific differentially methylated regions detectable in plasma cell-free DNA from patients with bicuspid aortic valve-associated aortopathy.
Does aorta-specific cell-free DNA correlate with aortic wall cell death and wall shear stress in patients with bicuspid aortic valve-associated aortopathy?
Observational (n=33)
Yes
Does aorta-specific cell-free DNA correlate with aortic wall cell death and wall shear stress in patients with bicuspid aortic valve-associated aortopathy?
Aorta-specific cell-free DNA methylation patterns correlate with aortic wall cell death in BAV-associated aortopathy, offering a potential non-invasive biomarker for disease severity that is independent of aortic diameter.
Answers are grounded in this paper and cite their sources.
Hypothesis-generating for shear stress in bicuspid aortopathy progression; prospective validation required before clinical consideration.
Objective In a proof-of-concept study we sought to identify aorta-specific differentially methylated regions (DMRs) detectable in plasma cell-free DNA (cfDNA) obtained from patients with bicuspid aortic valve (BAV)-associated aortopathy. Methods We used bioinformatics and publicly-available human methylomes to identify aorta-specific DMRs. We used data from 4D-flow cardiac magnetic resonance imaging to identify regions of elevated aortic wall shear stress (WSS) in patients with BAV-associated aortopathy undergoing surgery and correlated WSS regions with aortic tissue cell death assessed using TUNEL staining. Cell-free DNA was isolated from patient plasma and levels of candidate DMRs were correlated with aortic diameter and aortic wall cell death. Results Aortic wall cell death was not associated with maximal aortic diameter but was significantly associated with elevated WSS. We identified 24 candidate aorta-specific DMRs and selected 4 for further study. A DMR on chromosome 11 showed acceptable specificity for the aorta and correlated significantly with aortic wall cell death. Plasma levels of total and aorta-specific cfDNA did not correlate with aortic diameter. Conclusions Elevated WSS created by abnormal flow hemodynamics is associated with increased aortic wall cell death which supports the use of aorta-specific cfDNA as a potential tool to identify aortopathy and stratify patient risk.
No takes yet. Share an insight, caveat, or question.
Maredia et al. (2020) conducted an observational in Bicuspid aortic valve-associated aortopathy (n=33). Elevated aortic wall shear stress vs. Normal aortic wall shear stress was evaluated on Aortic wall cell death (percent colocalization of TUNEL and DAPI staining) (p=0.0027). Elevated aortic wall shear stress in patients with bicuspid aortic valve-associated aortopathy was associated with significantly increased aortic wall cell death compared to normal shear stress regions (13.74% vs 7.98%, p=0.0027).
Synapse has enriched 8 closely related papers on similar clinical questions. Consider them for comparative context: