Pulmonary complications of sickle cell disease
Gregory J Kato Andrew Miller Mark T. Gladwin
American Journal of Respiratory and Critical Care Medicine, 2012
https://doi.org/10.1164/rccm.201111-2082CI
Andrew Miller
Miller Andrew
ORCID: 0000-0001-8474-5090
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Gregory Kato
Kato Gregory / Gregory J. Kato / Gregory Kato, Greg Kato, GJ Kato, G Kato
ORCID: 0000-0003-4465-3217
Email: gregorykatomd@gmail.com
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Elevated Pulse Pressure is Associated with Hemolysis, Proteinuria and Chronic Kidney Disease in Sickle Cell Disease 10.1371/journal.pone.0114309
Reply: Practice Guideline for Pulmonary Hypertension in Sickle Cell: Direct Evidence Needed before Universal Adoption 10.1164/rccm.201404-0733le
RV dysfunction by MRI is associated with elevated transpulmonary gradient and poor prognosis in patients with sickle cell associated pulmonary hypertension 10.1186/1532-429x-15-s1-o43
Critical Reviews: How we treat sickle cell patients with leg ulcers 10.1002/ajh.24134
Gout and sickle cell disease: not all pain is sickle cell pain 10.1111/bjh.13433
Elevated sphingosine-1-phosphate promotes sickling and sickle cell disease progression 10.1172/jci77393
Elevated sphingosine-1-phosphate promotes sickling and sickle cell disease progression 10.1172/jci74604
Strategic plan for pediatric respiratory diseases research: An NHLBI working group report 10.1002/ppul.20973
Topical sodium nitrite for chronic leg ulcers in patients with sickle cell anaemia: a phase 1 dose-finding safety and tolerability trial 10.1016/s2352-3026(14)00019-2
Risk Factors for Death in 632 Patients with Sickle Cell Disease in the United States and United Kingdom 10.1371/journal.pone.0099489
New developments in anti-sickling agents: can drugs directly prevent the polymerization of sickle haemoglobin in vivo ? 10.1111/bjh.14264
Haem augments and iron chelation decreases toll-like receptor 4 mediated inflammation in monocytes from sickle cell patients 10.1111/bjh.14663
Skeletal and myocardial microvascular blood flow in hydroxycarbamide-treated patients with sickle cell disease 10.1111/bjh.14918
Sickle cell vasculopathy: vascular phenotype on fire! 10.1113/JP276705
A Cross-sectional Feasibility Study Testing the Use of Abstract Animations for the Communication and Assessment of Pain (Preprint) 10.2196/preprints.10056
Sickle related events following cardiac catheterisation: risk implication for other invasive procedures 10.1111/bjh.15618
Anakinra, What Is Thy Bidding in Pulmonary Hypertension? 10.1164/rccm.201811-2192ED
Sickle cells and sickle trait in thrombosis 10.1182/blood.2019000694
Cardiac expression of HMOX1 and PGF in sickle cell mice and haem‐treated wild type mice dominates organ expression profiles via Nrf2 ( Nfe2l2 ) 10.1111/bjh.16129
Validation of a composite vascular high‐risk profile for adult patients with sickle cell disease 10.1002/ajh.25624
Abstract Animations for the Communication and Assessment of Pain in Adults: Cross-Sectional Feasibility Study 10.2196/10056
Tricuspid regurgitation velocity and other biomarkers of mortality in children, adolescents and young adults with sickle cell disease in the United States: The PUSH study 10.1002/ajh.25799
Imaging Flow Cytometry and Microfluidic Flow Assays Demonstrate Heterocellular Aggregation Of Immature Sickle Erythrocytes To Neutrophils Via Mac-1/VLA-4 Interactions 10.1182/BLOOD.V122.21.318.318
Prominent role of platelets in the formation of circulating neutrophil-red cell heterocellular aggregates in sickle cell anemia 10.3324/HAEMATOL.2014.108555
Liver injury is associated with mortality in sickle cell disease 10.1111/APT.13347
Arginine metabolism, pulmonary hypertension, and sickle cell disease - In reply 10.1001/JAMA.294.19.2433-B
Clinical and Genetic Variability of Red Blood Cell Hemolysis in Sickle Cell Anemia 10.1182/BLOOD.V118.21.1077.1077
Genetic Determinants of Hemolysis in Sickle Cell Anemia 10.1182/BLOOD.V120.21.2104.2104
Predictors of Mortality in Children and Adolescents with Sickle Cell Disease: The PUSH Study 10.1182/BLOOD.V118.21.515.515
Amerindian/Asian Ancestry and Mortality Are Associated with Allo-Immunization in Adults with Sickle Cell Disease in a Genome Wide Racial Admixture Study 10.1182/BLOOD.V128.22.3650.3650
A Phase 1, Dose-Escalation Study of Topical Sodium Nitrite in Patients with Sickle Cell Anemia and Leg Ulcers 10.1182/BLOOD.V120.21.86.86
End-Alveolar Carbon Monoxide As a Measure of Erythrocyte Survival and Hemolytic Severity in Sickle Cell Disease 10.1182/BLOOD.V124.21.2696.2696
Effect of Aes-103 Anti-Sickling Agent On Oxygen Affinity and Stability of Red Blood Cells From Patients with Sickle Cell Anemia 10.1182/BLOOD.V120.21.85.85
The Oxidant Response Transcription Factor NRF2 Mediates Heme Activation of Placenta Growth Factor Expression in Erythroid Cells, a Contributor to Pulmonary Hypertension in Sickle Cell Disease 10.1182/BLOOD.V126.23.403.403
Thrombospondin-1 Polymorphisms Are Associated with Chronic Kidney Disease in Sickle Cell Anemia 10.1182/BLOOD.V128.22.2491.2491
Laser Speckle Contrast Imaging Characterizes Delayed Reperfusion After Transient Brachial Artery Occlusion in Patients with Sickle Cell Diseas 10.1182/BLOOD.V120.21.1080.1080
Neutrophil-Platelet Aggregation Enables Vaso-Occlusion in Sickle Cell Disease 10.1182/BLOOD.V128.22.1295.1295
Diastolic dysfunction is an independent risk factor for death in patients with sickle cell disease 10.1182/BLOOD.V106.11.206.206
Amplified expression profiling of platelet transcriptome reveals global activation of arginine metabolic pathways in patients with sickle cell disease 10.1182/BLOOD.V108.11.1536.1536
Placental Growth Factor Is Elevated in Patients with Sickle Cell Disease and Associated with Pulmonary Hypertension, Hemolysis, Inflammation, Iron Overload, and Hepatic Dysfunction 10.1182/BLOOD.V114.22.1531.1531
Hemodynamic Parameters Predict Mortality In Sickle Cell Disease-Related Pulmonary Hypertension 10.1182/BLOOD.V116.21.2668.2668
NT-Pro Brain Natriuretic Peptide Levels and the Risk of Stroke and Death in the Cooperative Study of Sickle Cell Disease 10.1182/BLOOD.V114.22.1541.1541
Blood Flow Is Increased in Wounds and Peri-Wound Area by Laser Speckle Contrast Imaging and Infrared Thermography in Adults with Sickle Cell Leg Ulcers 10.1182/BLOOD.V120.21.1009.1009
Turnover of Heme-Bound Iron Is Associated with Activation of TLR4 and Chemokine Receptor Pathways in the Peripheral Blood Mononuclear Cell Transcriptome in Sickle Cell Anemia 10.1182/BLOOD.V120.21.819.819
Iron Containing Compound Stimulates Expression of Pulmonary Hypertension Promoting Factor PlGF 10.1182/BLOOD.V118.21.900.900
A Cell-Based Adhesion Molecule Bioassay Detects Unexpected Properties of Plasma From Patients with Sickle Cell Disease with Documented Pulmonary Hypertension 10.1182/BLOOD.V118.21.2120.2120
Topical Sodium Nitrite Is Effective In Reducing Leg Ulcer-Associated Pain In Patients With Sickle Cell Disease 10.1182/BLOOD.V122.21.2236.2236
The Anti-Sickling Agent Aes-103 Decreases Sickle Erythrocyte Fragility, Hypoxia-Induced Sickling and Hemolysis In Vitro 10.1182/BLOOD.V122.21.940.940
Serum Transferrin: An Independent Predictor of Mortality in Sickle Cell Anemia 10.1182/BLOOD.V118.21.2126.2126
Cardiopulmonary Functional Status in Children with SCD at Baseline: Pulse Pressure As a Biomarker of Early Compromise 10.1182/BLOOD.V124.21.2663.2663
Evaluation of Exercise Capacity In Children with SCD by Six Minute Walk Test 10.1182/BLOOD.V116.21.2664.2664
Increased Transpulmonary Gradient Predicts Functional Class, Mortality, and RV Dysfunction by MRI in Patients with Sickle Cell Associated Pulmonary Hypertension 10.1182/BLOOD.V120.21.89.89
[Correction] Corticosteroids for acute chest syndrome in children with sickle cell disease: Variation in use and association with length of stay and readmission (vol 85, pg 24, 2010) 10.1002/AJH.21708
NT-Probnp as a Marker of Cardiopulmonary Compromise and Exercise Limitation In Adults with Sickle Cell Anemia In the Walk-PHaSST Study 10.1182/BLOOD.V116.21.1639.1639
Chronic Pain Is An Independent Predictor of Lower 6 Minute Walk Distance In Patients with Sickle Cell Disease: Results From Walk-PHaSST Study 10.1182/BLOOD.V116.21.2658.2658
Predictors of Six-Minute Walk Distance In Adults with Sickle Cell Anemia In the Walk-PHaSST Study 10.1182/BLOOD.V116.21.947.947
Non-Cardiopulmonary Factors Affecting the Six-Minute Walk Distance in Patients with Sickle Cell Disease: Results From the Walk-PHaSST Study 10.1182/BLOOD.V118.21.1074.1074
AN AMINO-TERMINAL C-MYC DOMAIN REQUIRED FOR NEOPLASTIC TRANSFORMATION ACTIVATES TRANSCRIPTION 10.1128/MCB.10.11.5914
INTRACELLULAR LEUCINE ZIPPER INTERACTIONS SUGGEST C-MYC HETERO-OLIGOMERIZATION 10.1128/MCB.11.2.954
ACTIVATION DOMAINS OF L-MYC AND C-MYC DETERMINE THEIR TRANSFORMING POTENCIES IN RAT EMBRYO CELLS 10.1128/MCB.12.7.3130
DISCRIMINATION BETWEEN RELATED DNA SITES BY A SINGLE AMINO-ACID RESIDUE OF MYC-RELATED BASIC HELIX LOOP HELIX PROTEINS 10.1073/PNAS.89.2.599
Stimulation of Nitric Oxide Synthase Activity By Plasma Apolipoproteins: a Biomarker of Endothelial Function in Adults with Sickle Cell Disease 10.1182/BLOOD.V124.21.4015.4015
Pulmonary hypertension in adults and children with sickle cell disease in Nigeria: Prevalence, clinical characteristics and role of endemic tropical infections 10.1182/BLOOD.V110.11.80.80
Prospective evaluation of the prevalence of elevated tricuspid regurgitant jet velocity and associated clinical and echocardiographic factors in children and adolescents with sickle cell disease 10.1182/BLOOD.V110.11.3388.3388
Association of Hemolysis with Clinical Manifestations of Sickle Cell Disease 10.1182/BLOOD.V112.11.2482.2482
Lower Ferritin Concentrations Are Associated with Decreased Hemolysis in Sickle Cell Disease Children without Iron Overload 10.1037/H0092264
Longitudinal Change in Pulmonary Function in Children with Sickle Cell Disease and Associated Factors 10.1164/AJRCCM-CONFERENCE.2010.181.1_MEETINGABSTRACTS.A6732
Plasma Level of NT-Pro-BNP In Children with Sickle Cell Disease Is Associated with Degree of Anemia and Left Ventricular Measures: The PUSH Study 10.1182/BLOOD.V116.21.948.948
Integration of Genomic and Genetic Approaches Highlight a Novel Validated Gene Signature for Pulmonary Hypertension Associated with Sickle Cell Disease 10.1182/BLOOD.V118.21.511.511
Evaluation Of Sildenafil Therapy For Patients With Sickle Cell Disease And Increased Tricuspid Regurgitant Velocity: Preliminary Results Of The Walk-PHaSST Trial 10.1164/AJRCCM-CONFERENCE.2010.181.1_MEETINGABSTRACTS.A2514
Iron, Expression of the Pattern Recognition Receptor-Inflammasome System, and Early Death in Adults with Sickle Cell Disease 10.1182/BLOOD.V124.21.2702.2702
Association of FOXO3A Polymorphisms with Hematocrit, LDH and Longevity in Patients with Sickle Cell Anemia from CSSCD, Walk-Phasst, and PUSH Clinical Trials 10.1182/BLOOD.V126.23.2176.2176
Detection of the mRNA transcription level of several genes of the HIF and NO metabolic pathways in PBMCs of sickle cell disease patients using quantitative RT-PCR assay 10.1182/BLOOD.V110.11.844.844
Iron, Inflammation, and Early Death in Adults With Sickle Cell Disease 10.1161/CIRCRESAHA.116.304577
Response to: Early regression of cervical lesions in HIV-seropositive women receiving highly active antiretroviral therapy - Reply 10.1097/00002030-199906180-00028
MAX - FUNCTIONAL DOMAINS AND INTERACTION WITH C-MYC 10.1101/GAD.6.1.81
Abnormal Methacholine Challenge Associated With Pulmonary Arterial Hypertension In Adults With Sickle Cell Disease 10.1164/AJRCCM-CONFERENCE.2011.183.1_MEETINGABSTRACTS.A2013
Genetic Polymorphisms in NEDD4L Are Associated with Pulmonary Hypertension of Sickle Cell Anemia 10.1182/BLOOD.V114.22.2562.2562
Risk Factors for Echocardiography-Determined Cardiopulmonary Abnormalities In Sickle Cell Anemia In the Walk-PHaSST Study 10.1182/BLOOD.V116.21.260.260
The Defective Arginine-Nitric Oxide Pathway in Sickle Cell Disease 10.1016/B978-0-12-804273-1.00026-0
Imaging flow cytometry documents incomplete resistance of human sickle F-cells to ex vivo hypoxia-induced sickling 10.1182/BLOOD-2014-03-559054
Intravascular hemolysis and the pathophysiology of sickle cell disease 10.1172/JCI89741
Sickle cell disease 10.1038/NRDP.2018.10
Study Of Clinical Characteristics Of Sickle Cell Disease Patients Developing Cor-Pulmonale During Acute Hospitalization 10.1164/AJRCCM-CONFERENCE.2011.183.1_MEETINGABSTRACTS.A5945
Corrigendum 10.1111/BJH.12783
The Impact of Cognitive Function on Adherence to Hydroxyurea Therapy in Patients with Sickle Cell Disease 10.1182/BLOOD.V128.22.2493.2493
An Elevated Tricuspid Regurgitant Jet Velocity In Sickle Cell Disease Is Associated With Polymorphisms In Genes Impacting Innate Immunity 10.1164/AJRCCM-CONFERENCE.2012.185.1_MEETINGABSTRACTS.A6519
Prostacyclin-analog therapy in sickle cell pulmonary hypertension 10.3324/HAEMATOL.2015.131227
Microvascular oxygen consumption during sickle cell pain crisis 10.1182/BLOOD-2013-11-533406
Quantification of Anti-Sickling Effect of Aes-103 in Sickle Cell Disease Using an in Vitro Microfluidic Assay 10.1182/BLOOD.V124.21.2699.2699
Pulmonary Function In Adults With Sickle Cell Related Pulmonary Hypertension 10.1164/AJRCCM-CONFERENCE.2011.183.1_MEETINGABSTRACTS.A1932
Thrombospondin-1 gene polymorphism is associated with estimated pulmonary artery pressure in patients with sickle cell anemia 10.1002/AJH.24635
Platelet Nucleation on Arrested Neutrophils Drives Vaso-Occlusion in Sickle Cell Disease 10.1182/BLOOD.V126.23.414.414
Health Care Utilization for Painful Events Is Associated with Early Mortality in a Contemporary Population of Adults with Sickle Cell Anemia 10.1182/BLOOD.V118.21.2115.2115
Imaging Flow Cytometry Documents Incomplete Resistance Of F-Cells To Hypoxia-Induced Sickling In Blood Samples From Patients With Sickle Cell Anemia 10.1182/BLOOD.V122.21.183.183
Plasma Thrombospondin 1 Is Increased and Associated with Markers of Vasculopathy In Sickle Cell Disease 10.1182/BLOOD.V116.21.946.946
Cellular normoxic biophysical markers of hydroxyurea treatment in sickle cell disease 10.1073/PNAS.1610435113
Elevated transpulmonary gradient and cardiac magnetic resonance-derived right ventricular remodeling predict poor outcomes in sickle cell disease 10.3324/HAEMATOL.2015.125229
Heme-bound iron activates placenta growth factor in erythroid cells via erythroid Kruppel-like factor 10.1182/BLOOD-2013-11-539718
Lung vaso-occlusion in sickle cell disease mediated by arteriolar neutrophil-platelet microemboli 10.1172/JCI.INSIGHT.89761
Placenta Growth Factor Is Regulated By Heme-Bound Iron Via Erythroid Kruppel-Like Factor In Erythroid Cells and Is Linked To Iron Status In Vivo In Sickle Cell Disease and Hereditary Hemochromatosis 10.1182/BLOOD.V122.21.432.432
Vascular complications after splenectomy for hematologic disorders 10.1182/BLOOD-2009-10-251439
Novel Small Molecule Therapeutics for Sickle Cell Disease: Nitric Oxide, Carbon Monoxide, Nitrite, and Apolipoprotein A-I 10.1182/ASHEDUCATION-2008.1.186
Pulmonary Complications of Sickle Cell Disease 10.1164/RCCM.201111-2082CI
Childhood Hodgkin and Non-Hodgkin Lymphomas 10.1542/PIR.12-6-171
Sickle particulars of microparticles 10.1182/blood.2020006303
Serum albumin is independently associated with higher mortality in adult sickle cell patients: Results of three independent cohorts 10.1371/journal.pone.0237543
Heme Induces IL-6 and Cardiac Hypertrophy Genes Transcripts in Sickle Cell Mice 10.3389/FIMMU.2020.01910
Nrf2 deficiency in mice attenuates erythropoietic stress-related macrophage hypercellularity 10.1016/J.EXPHEM.2020.02.005
A PROSPECTIVE PHASE II, OPEN-LABEL, SINGLE-ARM, MULTICENTER STUDY TO ASSESS THE EFFICACY AND SAFETY OF SEG101 (CRIZANLIZUMAB) IN SICKLE CELL DISEASE PATIENTS WITH PRIAPISM (SPARTAN) 10.1016/J.JSXM.2019.11.092
Platelet Extracellular Vesicles Drive Inflammasome-IL-1 beta-Dependent Lung Injury in Sickle Cell Disease 10.1164/RCCM.201807-1370OC
End points for sickle cell disease clinical trials: renal and cardiopulmonary, cure, and low-resource settings 10.1182/BLOODADVANCES.2019000883
Free heme regulates placenta growth factor through NRF2-antioxidant response signaling 10.1016/J.FREERADBIOMED.2019.08.009
Identifying Clinical and Research Priorities in Sickle Cell Lung Disease An Official American Thoracic Society Workshop Report 10.1513/ANNALSATS.201906-433ST
Health-related quality of life in sickle cell disease REPLY 10.1038/S41572-019-0080-5
THE RELATIONSHIP BETWEEN OXYCODONE AND QTC INTERVAL IN SICKLE CELL DISEASE 10.1136/JIM-2018-000974.610
Clinical and Laboratory Predictors of 30-Day Hospital Readmission Risk in Adult Patients with Sickle Cell Disease 10.1182/BLOOD-2018-99-115248
Sleep phenotype in the Townes mouse model of sickle cell disease 10.1007/S11325-018-1711-X
Heterogeneity in Multi-Organ Expression of HO-1 and P1GF in Sickle Mice Mimic Exposure of Non-Sickle Mice to Extracellular Heme Via Nrf2-Dependent Pathways 10.1182/BLOOD-2018-99-113451
Clinical Outcomes Associated With Sickle Cell Trait A Systematic Review 10.7326/M18-1161
Exercise training: a prescription for sickle-cell disease? 10.1016/S2352-3026(18)30178-9
Assessment of Iron Overload Impact on QTc Interval in Patients with Sickle Cell Disease 10.1182/BLOOD-2018-99-115125
Brief topical sodium nitrite and its impact on the quality of life in patients with sickle leg ulcers 10.1097/MD.0000000000012614
Simultaneous polymerization and adhesion under hypoxia in sickle cell disease 10.1073/PNAS.1807405115
Cellular Biophysical Markers of Hydroxyurea Treatment in Sickle Cell Disease 10.1117/12.2273139
Structural and Functional Insight of Sphingosine 1-Phosphate-Mediated Pathogenic Metabolic Reprogramming in Sickle Cell Disease 10.1182/BLOOD.V128.22.2474.2474
Thrombospondin-1 Gene Polymorphism Is Associated with Estimated Pulmonary Artery Pressure in Patients with Sickle Cell Anemia 10.1182/BLOOD.V126.23.970.970
Elevated Pulse Pressure Is Associated with Hemolysis, Proteinuria and Chronic Kidney Disease in Sickle Cell Disease 10.1182/BLOOD.V124.21.2711.2711
Serum B12 Levels In Children with Sickle Cell Disease Are Lower Than In Healthy Control Subjects 10.1182/BLOOD.V116.21.1647.1647
Human genetic diseases of proteolysis 10.1002/(SICI)1098-1004(1999)13:2<87::AID-HUMU1>3.3.CO;2-B
Identifying adolescent and young adult patients with sickle cell disease at highest risk of death 10.1002/ajh.26035
Impaired Bile Secretion Promotes Hepatobiliary Injury in Sickle Cell Disease 10.1002/HEP.31239
Kynurenine-derived Electrophiles: Potential Adaptive Mediators in Sickle Cell Disease 10.1016/J.FREERADBIOMED.2020.10.103
TheCYB5R3 (c)(.350C>G)andG6PDA alleles modify severity of anemia in malaria and sickle cell disease 10.1002/AJH.25941
A Prospective Phase II, Open-Label, Single-Arm, Multicenter Study to Assess the Efficacy and Safety of SEG101 (Crizanlizumab) in Sickle Cell Disease Patients with Priapism (SPARTAN) 10.1182/BLOOD-2019-125790
Sickle Cell Disease Promotes Dysregulation of Hepatic Iron Homeostasis By Regulating Hepcidin Expression 10.1182/BLOOD-2019-131921
Nrf2 Null Mice Are Deficient in CD169(+) Macrophages, Associated with Impaired Erythroid Response and Delayed Recovery from Acute Blood Loss 10.1182/BLOOD-2019-127295
A Phase II Trial of Topical Sodium Nitrite in Patients with Sickle Cell Disease and Leg Ulcers 10.1182/BLOOD-2019-124440
Lactate Dehydrogenase to Carboxyhemoglobin Ratio As a Biomarker of Heme Release to Heme Processing Is Associated with Higher Tricuspid Regurgitant Jet Velocity and Early Death in Sickle Cell Disease 10.1182/BLOOD-2019-124048
Macrophage Hypercellularity Accompanies Erythroid Hyperplasia in Sickle Cell Mice and during Recovery from Blood Loss in Wild Type Mice 10.1182/BLOOD-2019-127224
Impaired Bile Secretion Promotes Chronic Liver Injury in Sickle Cell Disease 10.1182/BLOOD-2019-131915
360 degrees View of a Day Hospital Program Performing Exchange Transfusion and Outpatient Pain Management on Adults with Sickle Cell Disease 10.1182/BLOOD-2019-122397
Lactate dehydrogenase to carboxyhemoglobin ratio as a biomarker of heme release to heme processing is associated with higher tricuspid regurgitant jet velocity and early death in sickle cell disease 10.1002/ajh.26243
Gene therapy as the new frontier for Sickle Cell Disease. 10.2174/0929867328666210527092456
Effect of Poloxamer 188 vs Placebo on Painful Vaso-Occlusive Episodes in Children and Adults With Sickle Cell Disease: A Randomized Clinical Trial. 10.1001/jama.2021.3414
The Worst Things in Life are Free: The Role of Free Heme in Sickle Cell Disease. 10.3389/fimmu.2020.561917
Summary of the Sussex-Huawei locomotion-transportation recognition challenge
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