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Abstract 4136316: BMP10 as novel marker for right atrial dilatation and pressure in precapillary pulmonary hypertension
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Introduction:
Precapillary pulmonary hypertension (precPH) leads to increased right atrial (RA) stretch and pressure. The right atrium is the major source of bone morphogenetic protein 10 (BMP10) in adults.
Aim:
This study aims to investigate BMP10 in relation to RA dilatation and pressure overload.
Methods:
We studied
BMP10
mRNA in fresh RA tissue of N=5 Chronic Thromboembolic Pulmonary Hypertension (CTEPH) patients and N=9 controls and protein expression in paraffin-embedded RA tissue of N=4 Pulmonary Arterial Hypertension (PAH) patients and N=6 controls. We prospectively included 48 precPH patients (N=22 idiopathic PAH, N=14 hereditary PAH and N=12 CTEPH, and N=16 controls. To study BMP10-induced transcriptional activity, we assayed serum samples in human microvascular endothelial cells (HMEC) with a BMP-responsive transcriptional luciferase assay. BMP10 activity was calculated by subtracting BMP activity after incubation with antibodies for Alk1Fc and bone morphogenetic protein 9 (BMP9). We assessed correlations between BMP10 activity and RA dilatation (RA max volume>79 ml/m
2
for male or >69 ml/m
2
for female) and right ventricular (RV) dilatation (RV end-diastolic volume>108 ml/m
2
for male and >96 ml/m
2
for female). In a cohort of CTEPH patients that underwent pulmonary endarterectomy (PEA) we assessed the effect of pressure unloading on BMP10 activity. Normality of data was checked and statistical differences between groups were tested using an independent sample t-test or Wilcoxon rank-sum test.
Results:
BMP10
mRNA, protein and downstream activity were higher in the precPH RA tissue (Figure 1A-F). High systemic BMP10 activity was associated with RA dilatation and high RA pressure, but not RV dilatation in precPH (Figure 2A-C). Finally, pressure unloading after PEA in CTEPH patients results in a reduction in BMP10 activity (figure 2D).
Conclusions:
Local RA BMP10 expression and activity is increased in precPH. Increased systemic BMP10 activity was related to RA dilatation and pressure. Pressure unloading of the right heart leads to a reduction of systemic BMP10 activity. Future studies are needed to determine whether increased BMP10 release is an adaptative mechanism or can be used as therapeutic target.
Ovid Technologies (Wolters Kluwer Health)
Title: Abstract 4136316: BMP10 as novel marker for right atrial dilatation and pressure in precapillary pulmonary hypertension
Description:
Introduction:
Precapillary pulmonary hypertension (precPH) leads to increased right atrial (RA) stretch and pressure.
The right atrium is the major source of bone morphogenetic protein 10 (BMP10) in adults.
Aim:
This study aims to investigate BMP10 in relation to RA dilatation and pressure overload.
Methods:
We studied
BMP10
mRNA in fresh RA tissue of N=5 Chronic Thromboembolic Pulmonary Hypertension (CTEPH) patients and N=9 controls and protein expression in paraffin-embedded RA tissue of N=4 Pulmonary Arterial Hypertension (PAH) patients and N=6 controls.
We prospectively included 48 precPH patients (N=22 idiopathic PAH, N=14 hereditary PAH and N=12 CTEPH, and N=16 controls.
To study BMP10-induced transcriptional activity, we assayed serum samples in human microvascular endothelial cells (HMEC) with a BMP-responsive transcriptional luciferase assay.
BMP10 activity was calculated by subtracting BMP activity after incubation with antibodies for Alk1Fc and bone morphogenetic protein 9 (BMP9).
We assessed correlations between BMP10 activity and RA dilatation (RA max volume>79 ml/m
2
for male or >69 ml/m
2
for female) and right ventricular (RV) dilatation (RV end-diastolic volume>108 ml/m
2
for male and >96 ml/m
2
for female).
In a cohort of CTEPH patients that underwent pulmonary endarterectomy (PEA) we assessed the effect of pressure unloading on BMP10 activity.
Normality of data was checked and statistical differences between groups were tested using an independent sample t-test or Wilcoxon rank-sum test.
Results:
BMP10
mRNA, protein and downstream activity were higher in the precPH RA tissue (Figure 1A-F).
High systemic BMP10 activity was associated with RA dilatation and high RA pressure, but not RV dilatation in precPH (Figure 2A-C).
Finally, pressure unloading after PEA in CTEPH patients results in a reduction in BMP10 activity (figure 2D).
Conclusions:
Local RA BMP10 expression and activity is increased in precPH.
Increased systemic BMP10 activity was related to RA dilatation and pressure.
Pressure unloading of the right heart leads to a reduction of systemic BMP10 activity.
Future studies are needed to determine whether increased BMP10 release is an adaptative mechanism or can be used as therapeutic target.
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