Publications by authors named "Faraday N"

Introduction: Cardiac function is important to quantify for risk stratification. Although left ventricular ejection fraction (LVEF) is commonly used, and identifies patients with poor systolic function, other easily acquired measures of cardiac function are needed, particularly to stratify patients with relatively preserved LVEF. LV relative wall thickness (RWT) has been associated with adverse clinical outcomes in patients with preserved LVEF, but the clinical relevance of this observation is not known.

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  • Genetic studies have highlighted the need for more diverse research on plasma fibrinogen levels, as previous studies largely focused on Europeans, leading to gaps in understanding and missing heritability.
  • By analyzing data from whole-genome sequencing and genotype data from large cohorts, researchers identified 18 genetic loci related to fibrinogen levels, some of which are more common in African populations and include variants that may impact protein function.
  • The study's findings indicate a connection between fibrinogen levels and various health conditions, emphasizing the importance of whole-genome sequencing in discovering genetic factors in diverse populations and enhancing knowledge about fibrinogen regulation.
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Background: Continuous cardiac output monitoring is not standard practice during cardiac surgery, even though patients are at substantial risk for systemic hypoperfusion. Thus, the frequency of low cardiac output during cardiac surgery is unknown.

Methods: We conducted a prospective cohort study at a tertiary medical center from July 2021 to November 2023.

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  • Inflammation biomarkers offer crucial insights into the inflammatory processes linked to various diseases, and their sequencing can help reveal the genetic makeup of these traits.
  • A study analyzed 21 inflammation biomarkers from around 38,465 individuals, discovering 22 significant associations across 6 inflammatory traits after considering existing findings.
  • The research combined single-variant and rare variant analyses, identifying additional significant associations and highlighting the complexity and diversity of genetic influences on inflammation traits across different ancestries.
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Despite decades of faculty professional development programs created to prepare women for leadership, gender inequities persist in salary, promotion, and leadership roles. Indeed, men still earn more than women, are more likely than women to hold the rank of professor, and hold the vast majority of positions of power in academic medicine. Institutions demonstrate commitment to their faculty's growth by investing resources, including creating faculty development programs.

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  • The study aimed to determine if prior treatment with immune checkpoint inhibitors (ICIs) affects the risk of complications after surgery in cancer patients.
  • It analyzed data from 7,674 cancer patients, finding no significant difference in overall postoperative complications between those exposed to ICIs and those who were not.
  • However, patients exposed to ICIs showed a higher risk for prolonged pressor dependence, suggesting the need for more research on specific complications related to ICI exposure.
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  • * Discovery of 7 new genetic loci associated with FVIII and 1 new locus for VWF, supporting their roles in thrombotic outcomes via Mendelian randomization.
  • * Functional testing revealed that silencing genes like B3GNT2 and CD36 impacted FVIII and VWF release from endothelial cells, indicating their potential regulatory roles.
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Objectives: Patients undergoing cardiac surgery often require blood transfusions, which are associated with increased morbidity and mortality. Patient blood management (PBM) strategies, including acute normovolemic hemodilution (ANH), have been implemented to minimize allogeneic transfusion requirements. Older studies suggested that ANH is associated with reduced transfusions; however, its effectiveness in the modern era of PBM remains unclear.

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  • Inflammation biomarkers play a crucial role in understanding diseases and can reveal insights into genetic traits through whole-genome sequencing studies.
  • A comprehensive analysis of 21 inflammation biomarkers in over 38,000 individuals found 22 significant single-variant associations across six different inflammatory traits, indicating the complexity and diversity of these biomarkers.
  • The study also included rare variant analyses, identifying 19 additional significant associations, which highlights the importance of using multiple analytical approaches to enhance the understanding of inflammation-related traits across different ancestries.
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  • Genetic studies on plasma fibrinogen levels primarily focused on Europeans, revealing numerous associated regions, but there are gaps in understanding due to missing heritability and representation of non-Europeans.
  • The researchers utilized whole genome sequencing (WGS) and array-based genotyping data from large cohorts to identify 18 new genetic loci linked to fibrinogen levels, with some variants more common in African populations.
  • The study highlights the importance of WGS in discovering genetic variations across diverse populations, linking fibrinogen polygenic risk scores to increased risk for thrombotic and inflammatory diseases like gout.
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Background: Increasing clinical demands can adversely impact academic advancement, including the ability to deliver lectures and disseminate scholarly work. The virtual lecture platform became mainstream during the height of the coronavirus-19 pandemic. Lessons learned from this period may offer insight into supporting academic productivity among physicians who must balance multiple demands, including high clinical workloads and family care responsibilities.

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Introduction: Antiplatelet therapy has been associated with fewer exacerbations and reduced respiratory symptoms in chronic obstructive pulmonary disease (COPD). Whether platelet activation is associated with respiratory symptoms in COPD is unknown.

Methods: Former smokers with spirometry-confirmed COPD had urine 11-dehydro-thromboxane B2 (11dTxB2), plasma soluble CD40L (sCD40L), and soluble P-selectin (sP-selectin) repeatedly measured during a 6- to 9-month study period.

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(1) Importance: Abnormal left ventricular (LV) diastolic function, with or without a diagnosis of heart failure, is a common finding that can be easily diagnosed by intra-operative transesophageal echocardiography (TEE). The association of diastolic function with duration of hospital stay after coronary artery bypass (CAB) is unknown. (2) Objective: To determine if selected TEE parameters of diastolic dysfunction are associated with length of hospital stay after coronary artery bypass surgery (CAB).

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Hyperinflammation triggered by SARS-CoV-2 is a major cause of disease severity, with activated macrophages implicated in this response. OP-101, a hydroxyl-polyamidoamine dendrimer--acetylcysteine conjugate that specifically targets activated macrophages, improves outcomes in preclinical models of systemic inflammation and neuroinflammation. In this multicenter, randomized, double-blind, placebo-controlled, adaptive phase 2a trial, we evaluated safety and preliminary efficacy of OP-101 in patients with severe COVID-19.

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Background: Acute kidney injury (AKI) after major noncardiac surgery is commonly attributed to cardiovascular dysfunction. Identifying novel associations between preoperative cardiovascular markers and kidney injury may guide risk stratification and perioperative intervention. Increased left ventricular relative wall thickness (RWT), routinely measured on echocardiography, is associated with myocardial dysfunction and long-term risk of heart failure in patients with preserved left ventricular ejection fraction (LVEF); however, its relationship to postoperative complications has not been studied.

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Genome-wide association studies (GWAS) have successfully identified thousands of single nucleotide polymorphisms (SNPs) associated with complex traits; however, the identified SNPs account for a fraction of trait heritability, and identifying the functional elements through which genetic variants exert their effects remains a challenge. Recent evidence suggests that SNPs associated with complex traits are more likely to be expression quantitative trait loci (eQTL). Thus, incorporating eQTL information can potentially improve power to detect causal variants missed by traditional GWAS approaches.

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  • A large-scale GWAS was conducted on leukocyte traits using data from 61,802 individuals of diverse backgrounds, focusing on over 109 million genetic variants.
  • The study identified 7 associations related to leukocyte counts, including a significant variant on chromosome X linked to lower eosinophil counts and variants prevalent in African Americans associated with monocyte and lymphocyte counts.
  • Findings suggest that the discovered eosinophil-lowering variant may reduce the risk of allergic diseases, indicating the importance of diverse samples in uncovering genetic associations often overlooked in studies focusing on European ancestry.
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Platelets play a key role in thrombosis and hemostasis. Platelet count (PLT) and mean platelet volume (MPV) are highly heritable quantitative traits, with hundreds of genetic signals previously identified, mostly in European ancestry populations. We here utilize whole genome sequencing (WGS) from NHLBI's Trans-Omics for Precision Medicine initiative (TOPMed) in a large multi-ethnic sample to further explore common and rare variation contributing to PLT (n = 61 200) and MPV (n = 23 485).

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Physiological data, such as heart rate and blood pressure, are critical to clinical decision-making in the intensive care unit (ICU). Vital signs data, which are available from electronic health records, can be used to diagnose and predict important clinical outcomes; While there have been some reports on the data quality of nurse-verified vital sign data, little has been reported on the data quality of higher frequency time-series vital signs acquired in ICUs, that would enable such predictive modeling. In this study, we assessed the data quality issues, defined as the completeness, accuracy, and timeliness, of minute-by-minute time series vital signs data within the MIMIC-III data set, captured from 16009 patient-ICU stays and corresponding to 9410 unique adult patients.

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  • Platelet aggregation at sites of vascular injury is a key factor in causing heart attacks and strokes.
  • Researchers identified 16 genetic loci related to platelet aggregation through whole genome sequencing of nearly 3,900 participants.
  • Notable findings include the RGS18 locus associated with G-protein signaling in platelets, and the SVEP1 gene linked to coronary artery disease, highlighting the role of genetics in cardiovascular disease risk and the importance of rare variants in understanding complex health conditions.
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Importance: The association of the nasal microbiome with outcomes in surgical patients is poorly understood.

Objective: To characterize the composition of nasal microbiota in patients undergoing clean elective surgical procedures and to examine the association between characteristics of preoperative nasal microbiota and occurrence of postoperative infection.

Design, Setting, And Participants: Using a nested matched case-control design, 53 individuals who developed postoperative infection were matched (approximately 3:1 by age, sex, and surgical procedure) with 144 individuals who were not infected (ie, the control group).

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  • Whole-genome sequencing (WGS) was used to analyze genetic variants associated with seven red blood cell (RBC) traits in a diverse group of 62,653 participants, revealing 14 novel variant-RBC trait associations.
  • Many of these associations, particularly those linked to genes like RPN1 and PIEZO1, were found to be rare and more common in non-European ancestry populations.
  • The study underscores the potential of WGS and gene editing techniques to enhance understanding of genetic factors influencing RBC traits and hereditary disorders.
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  • - Researchers aimed to create a detailed dataset of genes and proteins in megakaryocytes (MKs) derived from induced pluripotent stem cells (iPSCs) to better understand their biology.
  • - They successfully derived MKs from iPSCs taken from individuals of diverse backgrounds and confirmed that these cells expressed known markers important for platelet function, although expression levels varied by individual.
  • - Findings revealed that certain genes and proteins linked to platelet function were associated with higher MK marker expression, with differences noted based on sex and race, suggesting that individual-specific factors influence MK differentiation from iPSCs.
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