Key result
Serum endotrophin was an independent predictor of ascending aorta dilatation (OR 0.986, P<0.001), with levels ≤82.38 ng/mL predicting dilatation with 80.3% sensitivity and 78.5% specificity.
Why the study?
Ascending aorta dilatation is related to BAV- and hypertension-associated aortopathy, prompting evaluation of aortic elasticity, deformation via strain imaging, and biomarkers like endotrophin and MMP-2.
Do endotrophin levels and aortic strain parameters correlate with ascending aorta dilatation in patients with BAV- or HTN-associated aortopathy?
Observational (n=86)
Do endotrophin levels and aortic strain parameters correlate with ascending aorta dilatation in patients with BAV- or HTN-associated aortopathy?
Odds Ratio: 0.986
p-value: p=<0.001
Endotrophin levels and aortic strain parameters are significantly impaired in patients with BAV- and HTN-associated aortopathy, suggesting endotrophin could serve as a predictive biomarker for ascending aorta dilatation.
Endotrophin levels were associated with ascending aorta dilatation; leaves open its utility as a biomarker pending prospective validation.
OBJECTIVE: Bicuspid aortic valve (BAV) is the most common congenital heart defect. Ascending aorta dilatation is related to BAV- and hypertension (HTN)-associated aortopathy. The aim of this study was to investigate aortic elasticity, as well as aortic deformation of the ascending aorta, using strain imaging, and to evaluate the possible relationship of biomarkers, such as endotrophin and matrix metalloproteinase-2 (MMP-2), with ascending aorta dilatation in patients with BAV- or HTN-associated aortopathy. PATIENTS AND METHODS: This prospective study included patients with ascending aorta dilatation with BAV (n = 33), or normal tricuspid aortic valve with HTN (n = 33), and 20 control subjects. The mean age of the total patients was 42.76 ± 10.4 years (67% male, 33% female). We calculated aortic elasticity parameters using the relevant formula by M-mode echocardiography and determined layer-specific longitudinal and transverse strains of the proximal aorta by speckle-tracking echocardiography. Blood samples of the participants were drawn for the analysis of endotrophin and MMP-2. RESULTS: Aortic strain and aortic distensibility were significantly decreased, whereas the aortic stiffness index was significantly increased in patient groups with BAV or HTN compared to the control group (p < 0.001). Moreover, longitudinal strain of both the anterior and posterior aortic walls of the proximal aorta were significantly impaired in BAV and HTN patients (p < 0.001). Serum endotrophin levels were significantly reduced in the patient cohort compared to the controls (p = 0.001). Endotrophin was noted to be significantly positively correlated with aortic strain and aortic distensibility (r = 0.37, p = 0.001; r = 0.45, p < 0.001, respectively), whereas inversely associated with aortic stiffness index (r = -0.402, p < 0.001). Furthermore, endotrophin was the single independent predictor of ascending aorta dilatation (OR = 0.986, p < 0.001). A cut-off value of endotrophin ≤ 82.38 ng/mL predicted ascending aorta dilatation with a sensitivity of 80.3% and specificity of 78.5% (p < 0.0001). CONCLUSIONS: The present study showed that aortic deformation parameters and elasticity are impaired in BAV and HTN patients, and strain imaging allows for a good analysis of ascending aorta deformation. Endotrophin could be a predictive biomarker of ascending aorta dilatation in BAV and HTN aortopathy.
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Baykız et al. (2023) conducted an observational in Ascending aorta dilatation associated with bicuspid aortic valve or hypertension (n=86). Serum endotrophin levels was evaluated on Ascending aorta dilatation (OR 0.986, p=<0.001). Serum endotrophin was an independent predictor of ascending aorta dilatation (OR 0.986, P<0.001), with levels ≤82.38 ng/mL predicting dilatation with 80.3% sensitivity and 78.5% specificity.
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