Cited by 171Pulmonary Hypertension Research and TreatmentsCardiovascular Function and Risk FactorsHeart Failure Treatment and Management

Association of the metabolic syndrome with pulmonary venous hypertension

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Robbins, Ivan M., Newman, John H., Johnson, Roger F., Hemnes, Anna R., Fremont, Richard D., Piana, Robert N., Zhao, David X., Byrne, Daniel W.·2009·Chest

Abstract

Background Pulmonary venous hypertension (PVH) is a well-described cause of pulmonary hypertension (PH) in patients with left heart disease associated with elevated left heart filling pressure. PVH results from a number of processes, including left-sided valvular disease, constrictive pericardial disease, restrictive cardiomyopathies, and left ventricular (LV) systolic dysfunction. PVH in patients with normal LV systolic function, commonly referred to as diastolic dysfunction, is not well characterized. We observed that many patients with PH due to PVH have obesity, hypertension, diabetes mellitus, and hypercholesterolemia, which are clinical features of the metabolic syndrome (MS), a previously identified cause for systemic vascular disease.Methods We evaluated 122 consecutive patients referred for diagnosis and treatment of PH and compared the prevalence of features of the MS between patients with PVH and those with pulmonary arterial hypertension (PAH). We also compared clinical and hemodynamic characteristics between these two groups.Results Compared to patients with PAH, patients with PVH had a higher frequency of hypertension, obesity, diabetes mellitus, and hyperlipidemia. Two or more features of the MS were found in 16 of 17 patients with PVH (94.1%) compared with 34.3% of patients with PAH (p < 0.001; odds ratio, 30.7; 95% confidence interval, 3.6 to 260.0). PH was substantial, but less severe overall, in patients with PVH compared to those with PAH (mean pulmonary artery pressure, 45 +/- 17 mm Hg [range, 26 to 71 mm Hg] vs 53 +/- 10 [range, 33 to 72 mm Hg], respectively [p = 0.041]; and pulmonary vascular resistance, 4.4 +/- 2.9 units [range, 1.2 to 10.8 units] vs 10.8 +/- 4.7 units [range, 4.8 to 21.9 units], respectively [p < 0.001]).Conclusion PVH is highly associated with the MS. Our results suggest that the MS may predispose patients to develop pulmonary vascular disease.

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  1. Humbert M, Sitbon O, Simonneau G. Treatment of pulmo- nary arterial hypertension. N Engl J Med 2004; 351:1425- 1436

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Authors
Robbins, I. M., Newman, J. H., Johnson, R. F., Hemnes, A. R., Fremont, R. D., Piana, R. N., Zhao, D. X., & Byrne, D. W.
Affiliations
Vanderbilt University (US)
Corresponding author
Robbins, Ivan M.
Venue
Chest
Publisher
Elsevier BV
Published
2009-07
Volume
136
Issue
1
Pages
31-36
ISSN
0012-3692 (ISSN-L)
OpenAlex
W2135935974
Cited by
171
References
26
Citations by year
2026: 3 · 2025: 5 · 2024: 4 · 2023: 5 · 2022: 7 · 2021: 9 · 2020: 8 · 2019: 8 · 2018: 11 · 2017: 10 · 2016: 16 · 2015: 18 · 2014: 11 · 2013: 12 · 2012: 14
FWCI
12.35
Type
journal article
Language
en
Open access
Locations
  • CHEST Journal (publishedVersion)
  • PubMed Central (publishedVersion)
  • PubMed (publishedVersion)
Funders
  • U.S. Public Health Service (P01 072058)
  • National Heart, Lung, and Blood Institute (F32HL082132)
  • National Center for Research Resources (M01RR000095, MO1-RR-00095)
Topics
  • Health Sciences › Medicine › Pulmonary and Respiratory Medicine › Pulmonary Hypertension Research and Treatments
  • Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiovascular Function and Risk Factors
  • Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Heart Failure Treatment and Management
Keywords
pulmonary venous hypertension, metabolic syndrome, pulmonary arterial hypertension, left heart disease, obesity, hypertension, diabetes mellitus, hyperlipidemia, pulmonary vascular resistance, diastolic dysfunction, pulmonary hypertension etiology
MeSH terms
Adult, Aged, Diastole, Female, Humans, Hypertension, Pulmonary, Male, Middle Aged, Pulmonary Artery, Pulmonary Veins, Retrospective Studies, Venous Pressure, Cohort Studies, Prevalence, Ventricular Dysfunction, Left, Metabolic Syndrome

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