24 results match your criteria: "The University of Maryland-Institute for Health Computing[Affiliation]"
Am J Med
December 2024
The Department of Medicine, University of Maryland School of Medicine, the University of Maryland-Institute for Health Computing, Bethesda, MD, USA. Electronic address:
Eur Respir J
November 2024
Division of Pulmonology, Department of Internal Medicine, Medical University of Graz, Graz, Austria.
Background: Exercise pulmonary hypertension (exercise PH) was defined by a mean pulmonary arterial pressure (mPAP)/cardiac output (CO) slope >3 mmHg·L·min between rest and exercise in the 2022 ESC/ERS PH guidelines. However, large, multi-center studies on the prognostic relevance of exercise hemodynamics and its added value to resting hemodynamics are missing.
Patients And Methods: The PEX-NET (Pulmonary Hemodynamics during Exercise Network) registry enrolled patients who underwent clinically indicated right heart catheterizations both at rest and ergometer exercise from 23 PH-centers worldwide.
Heart Fail Clin
January 2025
Department of Medicine, University of Maryland School of Medicine, 6116 Executive Boulevard, North Bethesda, MD 20852, USA; The University of Maryland-Institute for Health Computing, Baltimore, MD, USA.
The invasive cardiopulmonary exercise test (iCPET) provides a comprehensive, simultaneous evaluation of an individual's cardiovascular, respiratory, and metabolic response to exercise. The test is uniquely suited for the evaluation of exercise intolerance, as well as the deep phenotyping of disease states including pulmonary arterial hypertension and post-coronavirus disease symptomatology. Despite an expanding list of clinical and research applications, both the complexity of the test and a lack of familiarity with how the test is performed have been barriers to the widespread use of iCPET.
View Article and Find Full Text PDFJ Card Fail
September 2024
Division of Cardiology, Department of Medicine, Medical University of South Carolina, Charleston, South Carolina.
Eur Respir J
October 2024
Division of Cardiology, Department of Medicine, Medical University of South Carolina, Charleston, SC, USA.
Left heart disease (LHD) is the most common cause of pulmonary hypertension (PH), which may be classified further as isolated post-capillary (ipcPH) or combined post- and pre-capillary PH (cpcPH). The 7th World Symposium on Pulmonary Hypertension PH-LHD task force reviewed newly reported randomised clinical trials and contemplated novel opportunities for improving outcome. Results from major randomised clinical trials reinforced prior recommendations against the use of pulmonary arterial hypertension therapy in PH-LHD outside of clinical trials, and suggested possible harm.
View Article and Find Full Text PDFEur Heart J
September 2024
Department of Medicine, University of Maryland School of Medicine, Baltimore, MD, USA.
Cell
September 2024
Department of Genetics, Ecology and Evolution, Biological Sciences Institute, Universidade Federal de Minas Gerais, Belo Horizonte, Brazil; Emerge, Emerging Diseases and Climate Change Research Unit, School of Public Health and Administration, Universidad Peruana Cayetano Heredia, Lima, Peru. Electronic address:
More globally diverse perspectives are needed in genomic studies and precision medicine practices on non-Europeans. Here, we illustrate this by discussing the distribution of clinically actionable genetic variants involved in drug response in Andean highlanders and Amazonians, considering their environment, history, genetic structure, and historical biases in the perception of biological diversity of Native Americans.
View Article and Find Full Text PDFEur Respir J
July 2024
Department of Medicine, University of Maryland School of Medicine, Baltimore, MD, USA
Stat Med
September 2024
Maryland Psychiatric Research Center, Department of Psychiatry, University of Maryland School of Medicine, Baltimore, Maryland, USA.
The joint analysis of imaging-genetics data facilitates the systematic investigation of genetic effects on brain structures and functions with spatial specificity. We focus on voxel-wise genome-wide association analysis, which may involve trillions of single nucleotide polymorphism (SNP)-voxel pairs. We attempt to identify underlying organized association patterns of SNP-voxel pairs and understand the polygenic and pleiotropic networks on brain imaging traits.
View Article and Find Full Text PDFNat Rev Nephrol
November 2024
Division of Cardiovascular Medicine, University of Maryland School of Medicine, Baltimore, MD, USA.
Pulmonary hypertension (PH) is common in patients with chronic kidney disease (CKD) or kidney failure, with an estimated prevalence of up to 78% in those referred for right-heart catheterization. PH is independently associated with adverse outcomes in CKD, raising the possibility that early detection and appropriate management of PH might improve outcomes in at-risk patients. Among patients with PH, the prevalence of CKD stages 3 and 4 is estimated to be as high as 36%, and CKD is also independently associated with adverse outcomes.
View Article and Find Full Text PDFBrief Bioinform
May 2024
Maryland Psychiatric Research Center, School of Medicine, University of Maryland, Baltimore, MD 21201, United States.
Motivation: The advent of multimodal omics data has provided an unprecedented opportunity to systematically investigate underlying biological mechanisms from distinct yet complementary angles. However, the joint analysis of multi-omics data remains challenging because it requires modeling interactions between multiple sets of high-throughput variables. Furthermore, these interaction patterns may vary across different clinical groups, reflecting disease-related biological processes.
View Article and Find Full Text PDFA blood test identifying patients at increased risk of pulmonary hypertension (PH) could streamline the investigative pathway. The prospective, multicenter CIPHER study aimed to develop a microRNA-based signature for detecting PH in breathless patients and enrolled adults with a high suspicion of PH who had undergone right heart catheterization (RHC). The CIPHER-MRI study was added to assess the performance of this CIPHER signature in a population with low probability of having PH who underwent cardiac magnetic resonance imaging (cMRI) instead of RHC.
View Article and Find Full Text PDFERJ Open Res
May 2024
VA Boston Healthcare System, Boston, MA, USA.
Background: Clinical trials repurposing pulmonary arterial hypertension (PAH) therapies to patients with lung disease- or hypoxia-pulmonary hypertension (PH) (classified as World Health Organization Group 3 PH) have failed to show a consistent benefit. However, Group 3 PH clinical heterogeneity suggests robust phenotyping may inform detection of treatment-responsive subgroups. We hypothesised that cluster analysis would identify subphenotypes with differential responses to oral PAH therapy.
View Article and Find Full Text PDFAnn Am Thorac Soc
August 2024
Division of Cardiovascular Medicine, University of Maryland School of Medicine, Baltimore, Maryland; and.
The definition of pulmonary hypertension (PH) has been revised recently, with the mean pulmonary artery pressure (mPAP) threshold (assessed by right heart catheterization) reduced from ⩾25 mm Hg to >20 mm Hg. This change reflects the mPAP upper limit of normal and a lower limit that is independently associated with adverse outcomes. To improve the specificity of diagnosing pathogenic increases in mPAP, however, a diagnosis of precapillary PH now also includes pulmonary vascular resistance >2.
View Article and Find Full Text PDFInfect Control Hosp Epidemiol
April 2024
Department of Epidemiology and Public Health, The University of Maryland School of Medicine, Baltimore, MD, USA.
Unlabelled: Identifying long-term care facility (LTCF)-exposed inpatients is important for infection control research and practice, but ascertaining LTCF exposure is challenging. Across a large validation study, electronic health record data fields identified 76% of LTCF-exposed patients compared to manual chart review.
Objective: Residence or recent stay in a long-term care facility (LTCF) is an important risk factor for antibiotic-resistant bacterial colonization.
J Am Heart Assoc
April 2024
Veterans Affairs Boston Healthcare System Boston MA.
Background: Portopulmonary hypertension (PoPH), associated with increased mortality, can limit treatment options for liver diseases. Data on the continuum of clinical risk related to cardiopulmonary hemodynamics in PoPH are lacking.
Methods And Results: As part of the United States national Veterans Affairs Clinical Assessment, Reporting, and Tracking database, we performed a retrospective cohort study of adults with cirrhosis undergoing right heart catheterization between October 1, 2017, and September 30, 2022.
JAMA
February 2024
Department of Epidemiology and Public Health, The University of Maryland School of Medicine, Baltimore.
CHEST Pulm
December 2023
Division of Pulmonary and Critical Care (A. J. S.), Beth Israel Deaconess Medical Center, the Division of Pulmonary and Critical Care (E. M. H., A. B. W., G. R. W., and F. N. R.), Department of Radiology (P. N., J. C. R., and R. S. J. E.), and the Division of Cardiovascular Medicine (J. A. L.), Brigham and Women's Hospital, Harvard Medical School; and the Department of Medicine (B. A. M.), University of Maryland School of Medicine, and the University of Maryland-Institute for Health Computing (B. A. M.), Bethesda, MD.
JACC Basic Transl Sci
October 2023
Department of Medicine, University of Maryland School of Medicine, Baltimore, Maryland, USA.
Circulation
October 2023
Harvard Medical School, Boston, MA (J.M.K., R.M.S., B.A.M.).
N Engl J Med
August 2023
From the Department of Epidemiology and Public Health, University of Maryland School of Medicine (K.E.G., D.J.M.), and the VA Maryland Healthcare System (D.J.M.) - both in Baltimore; the University of Maryland Institute for Health Computing, Bethesda (K.E.G.); and the Department of Medicine, Beth Israel Deaconess Medical Center, Boston (A.M.R.).
Am J Respir Crit Care Med
September 2023
Division of Cardiovascular Medicine, Brigham and Women's Hospital, and Harvard Medical School, Boston, Massachusetts.
Background: Pulmonary hypertension (PH) poses a significant health threat with high morbidity and mortality, necessitating improved diagnostic tools for enhanced management. Current biomarkers for PH lack functionality and comprehensive diagnostic and prognostic capabilities. Therefore, there is a critical need to develop biomarkers that address these gaps in PH diagnostics and prognosis.
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