Category Ranking

98%

Total Visits

921

Avg Visit Duration

2 minutes

Citations

20

Article Abstract

Background Epidemiologic studies have identified risk factors associated with pulmonary hypertension and right heart failure, but causative drivers of pulmonary hypertension and right heart adaptation are not well known. We sought to leverage unbiased genetic approaches to determine clinical conditions that share genetic architecture with pulmonary pressure and right ventricular dysfunction. Methods and Results We leveraged Vanderbilt University's deidentified electronic health records and DNA biobank to identify 14 861 subjects of European ancestry who underwent at least 1 echocardiogram with available estimates of pulmonary pressure and right ventricular function. Analyses of the study were performed between 2020 and 2022. The final analytical sample included 14 861 participants (mean [SD] age, 63 [15] years and mean [SD] body mass index, 29 [7] kg/m). An unbiased phenome-wide association study identified diabetes as the most statistically significant clinical , () code associated with polygenic risk for increased pulmonary pressure. We validated this finding further by finding significant associations between genetic risk for diabetes and a related condition, obesity, with pulmonary pressure estimate. We then used 2-sample univariable Mendelian randomization and multivariable Mendelian randomization to show that diabetes, but not obesity, was independently associated with genetic risk for increased pulmonary pressure and decreased right ventricle load stress. Conclusions Our findings show that genetic risk for diabetes is the only significant independent causative driver of genetic risk for increased pulmonary pressure and decreased right ventricle load stress. These findings suggest that therapies targeting genetic risk for diabetes may also potentially be beneficial in treating pulmonary hypertension and right heart dysfunction.

Download full-text PDF

Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10492967PMC
http://dx.doi.org/10.1161/JAHA.122.029190DOI Listing

Publication Analysis

Top Keywords

pulmonary pressure
28
genetic risk
20
pulmonary hypertension
12
hypertension heart
12
risk increased
12
increased pulmonary
12
risk diabetes
12
pulmonary
9
risk
8
pressure ventricular
8

Similar Publications

Association of Ventilatory Ratio with Acute Cor Pulmonale and Mortality in COVID-19 ARDS: A Cohort Study.

J Intensive Care Med

September 2025

Departamento de Medicina Intensiva, Facultad de Medicina, Pontificia Universidad Católica de Chile, Santiago, Chile.

PurposeAn elevated ventilatory ratio (VR) and acute cor pulmonale (ACP) are associated with mortality in ARDS patients. The primary aim of this study was to assess the association between VR and ACP in patients with COVID-19-related ARDS (C-ARDS). The secondary objectives were to analyze the association between VR and ICU mortality, describe VR temporal behavior in survivors and non-survivors, and evaluate the association between VR and pulmonary embolism.

View Article and Find Full Text PDF

Accurate modeling of lung parenchymal biomechanics is critical for understanding respiratory function and improving diagnoses. Traditional hyperelastic models capture tissue deformation but miss essential physiological interactions. This study evaluates an experimentally informed poroelastic model (Birzle's formulation) against hyperelastic-only models within a finite element framework.

View Article and Find Full Text PDF

The lung undergoes continuous remodeling throughout normal development and aging, including changes to alveolar and capillary structure and function. While histological methods allow for static analysis of these age-related changes, characterizing the changes that occur in response to mechanical stimuli remains difficult, particularly over a dynamic, physiologically relevant range in a functioning lung. Alveolar and capillary distension - the change in diameter of alveoli and capillaries, respectively, in response to pressure changes - is one such process, where dynamically controlling and monitoring the diameter of the same capillary or alveolus is essential to inferring its mechanical properties.

View Article and Find Full Text PDF

Introduction: The goal of perioperative management in reactive airway disease (RAD) patients is to ensure optimal airway stability, maintain adequate oxygenation, and reduce the need for mechanical ventilation while minimizing airway irritation and inflammation. Due to the airway hyperresponsiveness and increased risk of respiratory complications in RAD patients, non-opioid adjuncts that provide both bronchodilation and analgesia are preferred. Lignocaine and magnesium sulfate (MgSO₄) have emerged as effective agents in this context.

View Article and Find Full Text PDF

Aim: Positive expiratory pressure devices are frequently used for airway clearance in children with cystic fibrosis and tracheobronchomalacia. This study aimed to establish if electrical impedance tomography is a feasible measure to titrate pressures in non-sedated children.

Method: Ten children with cystic fibrosis and tracheobronchomalacia performed airway clearance using positive pressure devices whilst monitored with electrical impedance tomography.

View Article and Find Full Text PDF