Page last updated: 2024-10-18

histamine and HbS Disease

histamine has been researched along with HbS Disease in 7 studies

Research Excerpts

ExcerptRelevanceReference
"Histamine level was elevated in 18% of patients in steady state and in 61% during VOC."1.51Plasma histamine elevation in a large cohort of sickle cell disease patients. ( Allali, S; Arlet, JB; Bachmeyer, C; Brousse, V; Callebert, J; Chalumeau, M; de Montalembert, M; Georgin-Lavialle, S; Grateau, G; Hermine, O; Launay, JM; Lionnet, F; Maciel, TT; Mattioni, S; Stankovic Stojanovic, K, 2019)
"Some sickle cell anemia (SCA) patients suffer significantly worse phenotypes than others."1.40Mast cell activation syndrome as a significant comorbidity in sickle cell disease. ( Afrin, LB, 2014)

Research

Studies (7)

TimeframeStudies, this research(%)All Research%
pre-19902 (28.57)18.7374
1990's1 (14.29)18.2507
2000's2 (28.57)29.6817
2010's2 (28.57)24.3611
2020's0 (0.00)2.80

Authors

AuthorsStudies
Allali, S1
Lionnet, F1
Mattioni, S1
Callebert, J1
Stankovic Stojanovic, K1
Bachmeyer, C1
Arlet, JB1
Brousse, V1
de Montalembert, M1
Chalumeau, M1
Grateau, G1
Maciel, TT1
Launay, JM1
Hermine, O1
Georgin-Lavialle, S1
Afrin, LB1
Wagner, MC1
Eckman, JR1
Wick, TM1
Manodori, AB1
Barabino, GA1
Lubin, BH1
Kuypers, FA1
Enwonwu, CO1
Lu, M1
Ballas, SK1
Mohandas, N1
Clark, MR1
Embury, SH1
Smith, ED1
Marton, LJ1
Shohet, SB1
Wosornu, L1
Konotey-Ahulu, FI1

Clinical Trials (1)

Trial Overview

TrialPhaseEnrollmentStudy TypeStart DateStatus
Sickle Cell Disease (SCD) Biochip': Towards a Simple and Reliable Way to Monitor Sickle Cell Disease[NCT02824471]100 participants (Anticipated)Observational2014-10-31Recruiting
[information is prepared from clinicaltrials.gov, extracted Sep-2024]

Other Studies

7 other studies available for histamine and HbS Disease

ArticleYear
Plasma histamine elevation in a large cohort of sickle cell disease patients.
    British journal of haematology, 2019, Volume: 186, Issue:1

    Topics: Adult; Anemia, Sickle Cell; Child; Cohort Studies; Female; Histamine; Humans; Male; Mast Cells; Pros

2019
Mast cell activation syndrome as a significant comorbidity in sickle cell disease.
    The American journal of the medical sciences, 2014, Volume: 348, Issue:6

    Topics: Adult; Anemia, Sickle Cell; Antisickling Agents; Caseins; Chromogranin A; Cohort Studies; Female; He

2014
Histamine increases sickle erythrocyte adherence to endothelium.
    British journal of haematology, 2006, Volume: 132, Issue:4

    Topics: Analysis of Variance; Anemia, Sickle Cell; Cell Adhesion; Cells, Cultured; Endothelial Cells; Endoth

2006
Adherence of phosphatidylserine-exposing erythrocytes to endothelial matrix thrombospondin.
    Blood, 2000, Feb-15, Volume: 95, Issue:4

    Topics: Anemia, Sickle Cell; Anion Exchange Protein 1, Erythrocyte; Antigens, CD; CD36 Antigens; Cell Adhesi

2000
Elevated plasma histamine in sickle cell anaemia.
    Clinica chimica acta; international journal of clinical chemistry, 1991, Dec-16, Volume: 203, Issue:2-3

    Topics: Adolescent; Adult; Anemia, Sickle Cell; Child; Histamine; Histidine; Humans; Middle Aged

1991
Reduced transglutaminase-catalyzed cross-linking of exogenous amines to membrane proteins in sickle erythrocytes.
    Biochimica et biophysica acta, 1985, Jan-10, Volume: 812, Issue:1

    Topics: Acyltransferases; Anemia, Sickle Cell; Calcimycin; Calcium; Cell Membrane Permeability; Erythrocyte

1985
Gastric acid secretion in sickle-cell anaemia.
    Gut, 1971, Volume: 12, Issue:3

    Topics: Adolescent; Adult; Anemia, Sickle Cell; Body Weight; Child; Digestion; Duodenal Ulcer; Gastric Juice

1971