Daniel E. Cruz

ORCID: 0000-0002-2576-7051
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About
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Research Areas
  • Metabolomics and Mass Spectrometry Studies
  • Nutritional Studies and Diet
  • Cardiovascular Health and Risk Factors
  • Genetic Associations and Epidemiology
  • Particle physics theoretical and experimental studies
  • Advanced Proteomics Techniques and Applications
  • Diet and metabolism studies
  • Bioinformatics and Genomic Networks
  • Machine Learning in Bioinformatics
  • Click Chemistry and Applications
  • Health disparities and outcomes
  • High-Energy Particle Collisions Research
  • Nutrition, Genetics, and Disease
  • Alcohol Consumption and Health Effects
  • Particle Accelerators and Free-Electron Lasers
  • Soil Geostatistics and Mapping
  • Phagocytosis and Immune Regulation
  • Angiogenesis and VEGF in Cancer
  • Immune cells in cancer
  • Muscle metabolism and nutrition
  • Cardiac Health and Mental Health
  • Reproductive System and Pregnancy
  • Cancer-related gene regulation
  • Superconducting Materials and Applications
  • Liver Disease Diagnosis and Treatment

Beth Israel Deaconess Medical Center
2019-2025

Harvard University
2021-2025

Hadassah Medical Center
2025

Universidade Federal de Viçosa
2024

Boston University
2022-2023

Beth Israel Deaconess Hospital
2020

Johns Hopkins Medicine
2019

Johns Hopkins University
2019

University of California, Los Angeles
1998-2018

Ronald Reagan UCLA Medical Center
2018

High-throughput proteomic profiling using antibody or aptamer-based affinity reagents is used increasingly in human studies. However, direct analyses to address the relative strengths and weaknesses of these platforms are lacking. We assessed findings from SomaScan1.3K ( N = 1301 reagents), SomaScan5K platform 4979 Olink Explore 1472 reagents) techniques 568 adults Jackson Heart Study 219 participants HERITAGE Family across four performance domains: precision, accuracy, analytic breadth,...

10.1126/sciadv.abm5164 article EN cc-by-nc Science Advances 2022-08-19

Background: Heart failure (HF) is a heterogeneous disease characterized by significant metabolic disturbances; however, the breadth of dysfunction before onset overt not well understood. The purpose this study was to determine association circulating metabolites with incident HF uncover novel pathways disease. Methods: We performed targeted plasma metabolomic profiling in deeply phenotyped group Black adults from JHS (Jackson Study; n=2199). related associated established etiological...

10.1161/circheartfailure.120.007275 article EN Circulation Heart Failure 2021-01-01
Usman A. Tahir Daniel H. Katz Julián Ávila-Pacheco Alexander G. Bick Akhil Pampana and 95 more Jeremy Robbins Zhi Yu Zsu‐Zsu Chen Mark D. Benson Daniel E. Cruz Debby Ngo Shuliang Deng Xu Shi Shuning Zheng Aaron S. Eisman Laurie Farrell Michael E. Hall Adolfo Correa Russell P. Tracy Peter Durda Kent D. Taylor Yongmei Liu W. Craig Johnson Xiuqing Guo Jie Yao Yii‐Der Ida Chen Ani Manichaikul Frederick L. Ruberg William S. Blaner Deepti Jain Namiko Abe Gonçalo R. Abecasis François Aguet Christine M. Albert Laura Almasy Álvaro Alonso Seth A. Ament Peter Anderson Pramod Anugu Deborah Applebaum‐Bowden Kristin Ardlie Dan E. Arking Donna K. Arnett Allison E. Ashley‐Koch Stella Aslibekyan Tim Assimes Paul L. Auer Dimitrios Avramopoulos Najib Ayas Adithya Balasubramanian John Barnard Kathleen C. Barnes R. Graham Barr Emily Barron‐Casella Lucas Barwick Terri H. Beaty Gerald J. Beck Diane M. Becker Lewis C. Becker Rebecca Beer Amber L. Beitelshees Emelia J. Benjamin Takis Benos Marcos Bezerra Larry Bielak Joshua C. Bis Thomas W. Blackwell John Blangero Nathan R. Blue Eric Boerwinkle Donald W. Bowden Russell P. Bowler Jennifer A. Brody Ulrich Broeckel Jai Broome Deborah Brown Karen Bunting Esteban G. Burchard Carlos D. Bustamante Erin Buth Brian E. Cade Jonathan Cardwell Vincent J. Carey Julie Carrier April P. Carson Cara L. Carty Richard Casaburi Juan P. Romero James F. Casella Peter J. Castaldi Mark Chaffin Christy Chang Yi–Cheng Chang Daniel I. Chasman Sameer Chavan Bo‐Juen Chen Wei‐Min Chen Michael Cho Seung Hoan Choi Lee‐Ming Chuang

Abstract Integrating genetic information with metabolomics has provided new insights into genes affecting human metabolism. However, gene-metabolite integration been primarily studied in individuals of European Ancestry, limiting the opportunity to leverage genomic diversity for discovery. In addition, these analyses have principally involved known metabolites, majority profiled peaks left unannotated. Here, we perform a whole genome association study 2,291 metabolite (known and unknown...

10.1038/s41467-022-32275-3 article EN cc-by Nature Communications 2022-08-22
Daniel H. Katz Usman A. Tahir Alexander G. Bick Akhil Pampana Debby Ngo and 95 more Mark D. Benson Zhi Yu Jeremy Robbins Zsu‐Zsu Chen Daniel E. Cruz Shuliang Deng Laurie Farrell Sumita Sinha Alec A. Schmaier Dongxiao Shen Yan Gao Michael E. Hall Adolfo Correa Russell P. Tracy Peter Durda Kent D. Taylor Yongmei Liu W. Craig Johnson Xiuqing Guo Jie Yao Yii‐Der Ida Chen Ani Manichaikul Deepti Jain Claude Bouchard Mark A. Sarzynski Stephen S. Rich Jerome I. Rotter Thomas J. Wang James G. Wilson Pradeep Natarajan Robert E. Gerszten Namiko Abe Gonçalo R. Abecasis François Aguet Christine M. Albert Laura Almasy Álvaro Alonso Seth A. Ament Peter Anderson Pramod Anugu Deborah Applebaum‐Bowden Kristin Ardlie Dan E. Arking Donna K. Arnett Allison E. Ashley‐Koch Stella Aslibekyan Tim Assimes Paul L. Auer Dimitrios Avramopoulos Najib Ayas Adithya Balasubramanian John Barnard Kathleen C. Barnes R. Graham Barr Emily Barron‐Casella Lucas Barwick Terri Beaty Gerald J. Beck Diane M. Becker Lewis C. Becker Rebecca Beer Amber L. Beitelshees Emelia J. Benjamin Takis Benos Marcos Bezerra Larry Bielak Joshua Bis Thomas W. Blackwell John Blangero Eric Boerwinkle Donald W. Bowden Russell Bowler Jennifer A. Brody Ulrich Broeckel Jai Broome Deborah Brown Karen Bunting Esteban Burchard Carlos Bustamante Erin Buth Brian E. Cade Jonathan Cardwell Vincent J. Carey Julie Carrier April P. Carson Cara L. Carty Richard Casaburi Juan P. Romero James F. Casella Peter J. Castaldi Mark Chaffin Christy Chang Yi–Cheng Chang Daniel I. Chasman Sameer Chavan

Plasma proteins are critical mediators of cardiovascular processes and the targets many drugs. Previous efforts to characterize genetic architecture plasma proteome have been limited by a focus on individuals European descent leveraged genotyping arrays imputation. Here we describe whole genome sequence analysis in with greater African ancestry, increasing our power identify novel determinants.

10.1161/circulationaha.121.055117 article EN Circulation 2021-11-24

Measures from affinity-proteomics platforms often correlate poorly, challenging interpretation of protein associations with genetic variants (pQTL) and phenotypes. Here, we examined 2,157 proteins measured on both SomaScan 7k Olink Explore 3072 across 1,930 participants similarity to European, African, East Asian, Admixed American ancestry references. Inter-platform correlation coefficients for these followed a bimodal distribution (median r=0.30). Protein measures were associated (pQTLs),...

10.21203/rs.3.rs-5968391/v1 preprint EN cc-by Research Square (Research Square) 2025-02-13

Metabolic responses to exercise training are variable. Metabolite profiling may aid in the clinical assessment of an individual's responsiveness interventions.To investigate association between a novel circulating biomarker hepatic fat, dimethylguanidino valeric acid (DMGV), and metabolic health traits before after 20 weeks endurance training.This study involved cross-sectional longitudinal analyses Health, Risk Factors, Exercise Training, Genetics (HERITAGE) Family Study, 20-week,...

10.1001/jamacardio.2019.1573 article EN JAMA Cardiology 2019-06-05

<h3>Importance</h3> African American individuals have disproportionate rates of coronary heart disease (CHD) but lower levels artery calcium (CAC), a marker subclinical CHD, than non-Hispanic White individuals. may distinct metabolite profiles associated with incident CHD risk compared individuals, and examination these differences could highlight important processes that differ between them. <h3>Objectives</h3> To identify novel biomarkers CAC among to replicate findings in multiethnic...

10.1001/jamacardio.2021.4925 article EN JAMA Cardiology 2021-12-01

Racial differences in metabolomic profiles may reflect underlying social determinants of health by self-reported race and be related to racial disparities coronary heart disease (CHD) among women the United States. However, magnitude between Black White States has not been well-described. It also remains unknown whether such are CHD risk. Plasma were analyzed using liquid chromatography-tandem mass spectrometry WHI-OS (Women's Health Initiative-Observational Study; 138 696 women), WHI-HT...

10.1161/circresaha.121.320134 article EN cc-by-nc-nd Circulation Research 2022-09-02

The endothelium plays a critical role in promoting inflammation cardiovascular disease and other chronic inflammatory conditions, many small-molecule screens have sought to identify agents that prevent endothelial cell activation. Conversely, an augmented immune response can be protective against microbial pathogens cancer immunotherapy. Yet, induce activation not been reported. In this regard, bioassay was developed identifies activated by its capacity trigger macrophage protein 1 beta from...

10.1073/pnas.1015254108 article EN Proceedings of the National Academy of Sciences 2011-03-07

The differentiation of intestinal intraepithelial lymphocytes (IEL) remains controversial, which may be due in part to the phenotypic complexity these T cells. We have investigated here development IEL mice on recombination activating gene (RAG)-2−/− background express a cell antigen receptor (TCR) transgene specific for an H-Y peptide presented by Db (H-Y/Db × RAG-2− mice). In contrast thymus, small intestine female H-Y/Db is severely deficient number IEL; TCR transgene+ CD8αα and CD8αβ are...

10.1084/jem.188.2.255 article EN The Journal of Experimental Medicine 1998-07-20

Brief Summary COVID-19 is one of the most consequential pandemics in last century, yet biological mechanisms that confer disease risk are incompletely understood. Further, heterogeneity outcomes influenced by race, though relative contributions structural/social and genetic factors remain unclear. 1,2 Very recent unpublished work has identified two loci greater for respiratory failure COVID-19: ABO locus 3p21.31 locus. 3 To understand how these might whether this differs we utilized...

10.1101/2020.06.09.20125690 preprint EN medRxiv (Cold Spring Harbor Laboratory) 2020-06-11

Background: Increased left ventricular (LV) mass is associated with adverse cardiovascular events including heart failure (HF). Both increased LV and HF disproportionately affect Black individuals. To understand the underlying mechanisms, we undertook a proteomic screen in cohort compared findings to results from White cohort. Methods: We measured 1305 plasma proteins using SomaScan platform 1772 participants (mean age, 56 years; 62% women) JHS (Jackson Heart Study) assessed by 2-dimensional...

10.1161/circgen.120.003191 article EN Circulation Genomic and Precision Medicine 2021-05-21

Nontargeted metabolomics methods have increased potential to identify new disease biomarkers, but assessments of the additive information provided in large human cohorts by these less biased techniques are limited. To diversify our knowledge diabetes-associated metabolites, we leveraged a method that measures 305 targeted or “known” and 2,342 nontargeted “unknown” compounds fasting plasma samples from 2,750 participants (315 incident cases) Jackson Heart Study (JHS)—a community cohort...

10.2337/db22-0033 article EN Diabetes 2022-08-23

BACKGROUNDMost GWAS of plasma proteomics have focused on White individuals European ancestry, limiting biological insight from other ancestry-enriched protein quantitative loci (pQTL).METHODSWe conducted a discovery approximately 3,000 proteins measured by the antibody-based Olink platform in 1,054 Black adults Jackson Heart Study (JHS) and validated our findings Multi-Ethnic Atherosclerosis (MESA). The genetic architecture identified pQTLs was further explored through fine mapping admixture...

10.1172/jci181802 article EN cc-by Journal of Clinical Investigation 2024-09-24

Scope New biomarkers are needed that representative of dietary intake. Methods and Results We assess metabolites associated with Southern patterns in 1401 Jackson Heart Study participants. Three empirically derived using principal component analysis: meat fast food, fish vegetables, starchy foods. randomly select two subsets the study population: two‐third sample for discovery ( n = 934) one‐third replication 467). Among 327 analyzed, 14 significantly food pattern, four vegetables none foods...

10.1002/mnfr.202000796 article EN Molecular Nutrition & Food Research 2021-02-25

Abstract Severe heart failure is increasingly being managed by cardiac transplantation, and in some cases mechanical support devices serve as destination therapies. Left ventricular assist (LVADs) were approved for therapy end stage patients before the more advanced total artificial modality became available. One common complication of device placement acute kidney injury. Historically, with have had to inpatient hemodialysis until combined transplant. Though, units started accepting LVAD...

10.1111/hdi.12631 article EN Hemodialysis International 2018-01-23

N-acyl amino acids are a large family of circulating lipid metabolites that modulate energy expenditure and fat mass in rodents. However, little is known about the regulation potential cardiometabolic functions humans. Here, we analyze phenotype associations genetic four plasma N-fatty acyl (N-oleoyl-leucine, N-oleoyl-phenylalanine, N-oleoyl-serine, N-oleoyl-glycine) 2,351 individuals from Jackson Heart Study. N-oleoyl-leucine N-oleoyl-phenylalanine were positively associated with traits...

10.1101/2023.03.09.531581 preprint EN bioRxiv (Cold Spring Harbor Laboratory) 2023-03-09

N-acyl amino acids are a large family of circulating lipid metabolites that modulate energy expenditure and fat mass in rodents. However, little is known about the regulation potential cardiometabolic functions humans. Here, we analyze phenotype associations genomic four plasma (N-oleoyl-leucine, N-oleoyl-phenylalanine, N-oleoyl-serine, N-oleoyl-glycine) 2351 individuals from Jackson Heart Study. We find levels specific associated with disease endpoints independent free acid patterns...

10.1016/j.jbc.2023.104764 article EN cc-by Journal of Biological Chemistry 2023-04-28
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