Database : HANSEN
Search on : PROTROMBINA [Subject descriptor]
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Id:17316
Author:Loizou, S; Singh, S; Wypkema, E; Asherson, R. A
Title:Anticardiolipin, anti-beta(2)-glycoproteiun I and antiprothrombin antibodies in black South African patients with infectious disease ..-
Source:s.l; s.n; 2003. 6 p. ilus, tab.
Abstract:OBJECTIVES: To investigate IgG, IgM, and IgA, antiphospholipid antibodies (aPL), against cardiolipin (aCL), beta(2)-glycoprotein I (anti-beta(2)GPI), and prothrombin (anti-PT), in black South African patients with infectious disease. Unlike patients with systemic lupus erythematosus (SLE) and the antiphospholipid syndrome (APS), raised levels of aPL in infectious diseases are not usually associated with thrombotic complications. PATIENTS AND METHODS: Serum samples from 272 patients with a variety of infectious diseases (100 HIV positive, 112 leprosy, 25 syphilis, 25 malaria, and 10 HCV patients) were studied and compared with autoantibody levels in 100 normal controls. All three aPL were measured using commercial enzyme linked immunosorbent assay (ELISA) kits. RESULTS: Raised levels of all three aPL were found in all patient groups studied: aCL in 7%, anti-beta(2)GPI in 6%, and aPT in 43% of 100 HIV patients, in 29%, 89%, and 21% of 112 patients with leprosy, in 8%, 8%, and 28% of 25 patients with syphilis, in 12%, 8%, and 28% of 25 patients with malaria, and in 20%, 30%, and 30% of 10 HCV patients studied, respectively. CONCLUSIONS: The prevalence of aCL and anti-beta(2)GPI in black South African HIV positive patients, or those with syphilis, malaria, or hepatitis C virus is lower than reported for mixed race or white populations. aPT were the most prevalent aPL detected in these patient groups, except in patients with leprosy, for whom anti-beta(2)GPI was the most prevalent, and where the spectrum of aPL was similar to that seen in patients with SLE and APS. (AU).
Descriptors:Anticorpos Anticardiolipina/BL
Anticorpos Antifosfolipídeos/BL
Síndrome Antifosfolipídica/IM
Auto-Anticorpos/*BL
Estudos de Casos e Controles
Doenças Transmissíveis/*EH/*IM
Glicoproteínas/*IM
Infecções por HIV/IM
Imunoglobulina A/BL
Imunoglobulina G/BL
Imunoglobulina M/BL
Hanseníase/IM
Malaria/IM
Prevalência
Protrombina/*IM
África do Sul
Sífilis/IM
Limits:HUMANO
MASCULINO
FEMININO
ADULTO
MEIA-IDADE
IDOSO
Grupo Ancestral do Continente Africano
Location:BR191.1; 00225/s


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Id:13615
Author:Martinuzzo, M. E; Larrañaga, G. F. de; Forastiero, R. R; Pelegri, Y; Fariña, M. H; Alonso, B. S; Kordich, L. C; Carreras, L. O
Title:Markers of platelet, endothelial cell and blood coagulation activation in leprosy patients with antiphospholipid antibodies ..-
Source:s.l; s.n; 2002. 7 p. tab, graf.
Abstract:OBJECTIVE: To evaluate plasma levels of markers of platelet, endothelial cell and blood coagulation activation in leprosy patients with or without antiphospholipid antibodies (aPL) and to compare them to those found in patients with antiphospholipid syndrome (APS). METHODS: 42 patients with leprosy (35 lepromatous and 7 borderline): 29 aPL(+) and 13 aPL(-), as well as 26 healthy subjects as normal controls (NC) and 79 control aPL patients without leprosy (59 with and 20 without APS) were included in the study. Plasma soluble P and E selectin (sPsel and sEsel), and VCAM-1 (sVCAM-1), prothrombin F1 + 2 fragment (F1 + 2), thrombin-antithrombin complexes (TAT) and D dimer (DD) were measured by ELISA. The protein C pathway was assessed by the ProC global test. RESULTS: Leprosy patients with aPL presented increased median levels of sPsel [ng/ml (82.0 vs 36.0, p smaller 0.001)] and sVCAM-1 [ng/ml (495 vs 335, p smaller 0.001)] compared to NC, as observed in control aPL patients without leprosy. Levels of sPsel in aPL(+) patients with leprosy were significantly higher than in aPL(-) ones (52.5 ng/ml), p = 0.005. However, plasma markers of thrombin generation were increased in control aPL patients without leprosy but not in those with leprosy. ProcC global test was abnormal in 24.1 per cent of leprosy patients with aPL compared to 4.4 per cent of NC (p smaller 0.024), and to 57.2 per cent of control patients with aPL without leprosy (p = 0.005). CONCLUSIONS: We demonstrated that although patients with leprosy present a high prevalence of aPL, and platelet and endothelial cell activation in vivo to the same extent than patients with APS, they do not show a procoagulant state. (AU).
Descriptors:ANTICORPOS ANTIFOSFOLIPIDEOS/*BL
ANTITROMBINA III
MARCADORES BIOLOGICOS/BL
COAGULACAO SANGUINEA/*PH
PLAQUETAS/*PH
MOLECULAS DE ADESAO CELULAR/BL
ENDOTELIO VASCULAR/*PH
ELISA
PRODUTOS DE DEGRADACAO DA FIBRINA E DO FIBRINOGENIO/AN
GLICOPROTEINAS/IM
IMUNOGLOBULINA G/AN
IMUNOGLOBULINA M/AN
HANSENIASE DIMORFA/*BL
HANSENIASE VIRCHOWIANA/*BL
INIBIDOR DE COAGULACAO DO LUPUS/BL
FRAGMENTOS DE PEPTIDEOS/BL
PEPTIDEO HIDROLASES/BL
PROTEINA C/AN
PROTROMBINA
Limits:HUMANO
MASCULINO
FEMININO
ADULTO
MEIA-IDADE
IDOSO
SUPPORT, NON-U.S. GOV'T
ADOLESCENTE
Location:BR191.1; 09034/s


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Id:11567
Author:Larrañaga, G. F. de; Forasteiro, P. R; Martinuzzo, M. E; Carreras, L. O; Tsariktsain, G; Sturno, M. M; Alonso, B. S
Title:High prevalence of antiphospholipid antibodies in leprosy: evaluation of antigen reactivity ..-
Source:s.l; s.n; 2000. 7 p. tab, graf.
Descriptors:ADOLESCENCIA
ANTICORPOS DE ANTICARDIOLIPINA
ANTICORPOS ANTIFOSFOLIPIDIOS
AUTO-ANTICORPOS
ELISA
GLICOPROTEINAS
HANSENIASE
HANSENIASE
PROTROMBINA
IMUNOGLOBULINA G/BL
IMUNOGLOBULINA M/BL
Location:BR191.1; 08403/s



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