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Genetics of Pulmonary Pressure and Right Ventricle Stress Identify Diabetes As a Causal Risk Factor

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Date 2023 Jul 31
PMID 37522172
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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.

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References
1.
Li J, Szczerbinski L, Dawed A, Kaur V, Todd J, Pearson E . A Polygenic Score for Type 2 Diabetes Risk Is Associated With Both the Acute and Sustained Response to Sulfonylureas. Diabetes. 2020; 70(1):293-300. PMC: 7881853. DOI: 10.2337/db20-0530. View

2.
Pugh M, Robbins I, Rice T, West J, Newman J, Hemnes A . Unrecognized glucose intolerance is common in pulmonary arterial hypertension. J Heart Lung Transplant. 2011; 30(8):904-11. PMC: 3129440. DOI: 10.1016/j.healun.2011.02.016. View

3.
Hemnes A, Luther J, Rhodes C, Burgess J, Carlson J, Fan R . Human PAH is characterized by a pattern of lipid-related insulin resistance. JCI Insight. 2019; 4(1). PMC: 6485674. DOI: 10.1172/jci.insight.123611. View

4.
Chen X, Austin E, Talati M, Fessel J, Farber-Eger E, Brittain E . Oestrogen inhibition reverses pulmonary arterial hypertension and associated metabolic defects. Eur Respir J. 2017; 50(2). PMC: 6532788. DOI: 10.1183/13993003.02337-2016. View

5.
Mahajan A, Taliun D, Thurner M, Robertson N, Torres J, Rayner N . Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps. Nat Genet. 2018; 50(11):1505-1513. PMC: 6287706. DOI: 10.1038/s41588-018-0241-6. View