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1.
Thromb Haemost ; 117(8): 1534-1548, 2017 07 26.
Artigo em Inglês | MEDLINE | ID: mdl-28536718

RESUMO

Von Willebrand disease (VWD), the most common inherited bleeding disorder, is characterised by a variable bleeding tendency, heterogeneous laboratory phenotype and race specific distribution of mutations. The present study aimed to determine the correlation of genotype and phenotype in 200 Chinese individuals from 90 unrelated families with VWD. Next generation sequencing (NGS) of the whole coding VWF, copy number analysis of VWF by CNVplex® technique as well as a comprehensive phenotypic assessment were carried out in all index patients (IPs). We identified putative mutations in all IPs except five mild type 1 (85/90, 94.4 %). In total, 98 different mutations were detected, 62 (63.3 %) of which were reported for the first time (23 missense mutations, 1 regulatory mutation, 12 splice site mutations and 26 null mutations). Mutations p.Ser1506Leu and p.Arg1374His/Cys/Ser were the most frequent mutations in 2A (33 % of cases) and 2M VWD (67 % of cases), respectively. In addition, mutation p.Arg816Trp was detected repeatedly in type 2N patients, while mutation p.Arg854Gln, extremely common in Caucasians, was not found in our cohort. Thirty-three patients had two or more putative mutations. Unlike most cases of type 1 and type 2 VWD, which were transmitted dominantly, we presented seven severe type 1, two type 2A and one type 2M with autosomal recessive inheritance. Here the phenotypic data of patients with novel mutations will certainly contribute to the better understanding of the molecular genetics of VWF-related phenotypes.


Assuntos
Variações do Número de Cópias de DNA , Análise Mutacional de DNA/métodos , Dosagem de Genes , Hemostasia/genética , Sequenciamento de Nucleotídeos em Larga Escala , Reação em Cadeia da Polimerase Multiplex/métodos , Mutação , Doenças de von Willebrand/genética , Fator de von Willebrand/genética , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Povo Asiático/genética , Biomarcadores/sangue , Criança , Pré-Escolar , China , Feminino , Predisposição Genética para Doença , Hereditariedade , Humanos , Lactente , Padrões de Herança , Masculino , Pessoa de Meia-Idade , Taxa de Mutação , Fenótipo , Valor Preditivo dos Testes , Adulto Jovem , Doenças de von Willebrand/sangue , Doenças de von Willebrand/diagnóstico , Doenças de von Willebrand/etnologia
2.
Niger J Clin Pract ; 20(2): 235-238, 2017 02.
Artigo em Inglês | MEDLINE | ID: mdl-28091443

RESUMO

BACKGROUND: Polymorphisms in von Willebrand factor (VWF) gene are an important contributor to the expression of VWF gene and differences in ethnic distribution of these single nucleotide polymorphisms (SNPs) exists. AIMS: Our objective was to molecularly characterize the exon 28 of the VWF gene in the three major ethnic groups of Nigeria. SUBJECTS AND METHODS: We recruited 90 subjects, 45 had a history of bleeding. Questions included those used in the Zimmerman Program for the Molecular and Clinical Biology of von Willebrand disease (VWD), and the bleeding scores were calculated using the Molecular and Clinical Markers for the Diagnosis and Management of type 1 VWD scoring system. Full blood count, coagulation profile, VWF:antigen level and VWF:collagen-binding activities were carried out. Data were analyzed using GraphPad Prism (5.03). GraphPad Software, Inc USA. The BigDye terminator chemistry was used to determine the nucleotide sequences of VWF gene (exon 28). RESULTS: Eight SNPs were identified, rs 216310 (T1547), rs 1800385 (V1565L), rs1800384 (A1515), rs1800383 (D1472H), rs 1800386 (Y1584C), rs 216311 (T1381A), rs 216312 (intronic) and rs 1800381 (P1337). CONCLUSION: The SNPs rs 216311, rs 1800383 and rs 1800386 associated significantly with bleeding in study subjects. rs1800386 occurred in all with bleeding history, no ethnic variations were noted.


Assuntos
Éxons/genética , Hemorragia/genética , Doenças de von Willebrand/etnologia , Fator de von Willebrand/análise , Fator de von Willebrand/genética , Biomarcadores/sangue , Coagulação Sanguínea , Testes de Coagulação Sanguínea , Feminino , Marcadores Genéticos , Predisposição Genética para Doença , Humanos , Masculino , Nigéria , Polimorfismo Genético , Polimorfismo de Nucleotídeo Único , Análise de Sequência , Doenças de von Willebrand/sangue , Doenças de von Willebrand/genética
3.
Ann Thorac Surg ; 103(4): 1239-1244, 2017 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-27717422

RESUMO

BACKGROUND: Supraphysiologic shear stress from continuous-flow left ventricular assist devices (LVADs) accelerates von Willebrand factor (vWF) degradation and predisposes patients to nonsurgical bleeding. It is unknown whether unique design characteristics of LVADs differentially affect vWF degradation. We tested the hypothesis that the centrifugal-flow EVAHEART (Evaheart, Houston, TX) left ventricular assist system (LVAS), which was designed to minimize shear stress (low operational revolutions per minute [rpm], larger flow gaps, low shear stress, flat H-Q curve), reduced vWF degradation versus the axial-flow HeartMate II (Thoratec, Pleasanton, CA) LVAD. METHODS: Whole human blood was obtained from volunteer donors (n = 22). Blood was circulated for 12 hours in mock circulatory loops through a HeartMate II (n = 10; 11,400 rpm, 6.3 ± 0.8 L/min, 76 ± 2 mm Hg) or an EVAHEART LVAS (n = 12; 2,300 rpm, 5.7 ± 0.1 L/min, 80 ± 1 mm Hg). vWF degradation was characterized with electrophoresis and immunoblotting for large vWF multimers and 11 vWF degradation fragments. RESULTS: The HeartMate II eliminated large vWF multimers and significantly (p < 0.05) increased 10 of 11 vWF degradation fragments at 6 and 12 hours. The increase was approximately 2.0-fold at 6 hours and 2.2-fold at 12 hours. In contrast, the EVAHEART LVAS modestly reduced large vWF multimers and significantly increased 5 of 11 and 8 of 11 vWF degradation fragments at 6 and 12 hours, respectively. The increase was approximately 1.5-fold at 6 hours and 1.7-fold at 12 hours. The EVAHEART LVAS caused significantly less degradation (p < 0.01) than the HeartMate II of the 140 kDa vWF fragment (cleavage product of ADAMTS-13, the vWF protease). CONCLUSIONS: The EVAHEART LVAS caused significantly less vWF degradation than the HeartMate II in a mock circulatory loop with whole human blood. LVAD design features may minimize vWF degradation. These data may inform the design and operation of next-generation LVADs to minimize blood trauma.


Assuntos
Desenho de Equipamento/efeitos adversos , Insuficiência Cardíaca/terapia , Coração Auxiliar/efeitos adversos , Doenças de von Willebrand/etnologia , Fator de von Willebrand/metabolismo , Insuficiência Cardíaca/metabolismo , Insuficiência Cardíaca/fisiopatologia , Humanos , Modelos Cardiovasculares
5.
J Thromb Haemost ; 11(2): 261-9, 2013 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-23216583

RESUMO

BACKGROUND: The von Willebrand factor (VWF) gene is highly polymorphic, with variants correlated with VWF antigen levels, adhesion activity, clearance and factor VIII binding. VWF mutations are detected in patients with von Willebrand disease (VWD), whereas polymorphic variants could be associated with thrombosis. However, information on the ethnic diversity of VWF variants and their association with diseases is limited. OBJECTIVES: To characterize novel VWF variants from different ethnicities in the general population. PATIENTS/METHODS: We analyzed samples from 1092 subjects of 14 ethnicities available in the 1000 Genomes database for VWF variants and their potential functional impacts. RESULTS: We identified 2728 SNPs and 91 insertions and deletions that had a high level of ethnic diversity, with Africans having the highest number of variants. The highest level of diversity was found in the D' and D2 domains. Among 94 non-synonymous variants, 31 were predicted to be deleterious, including 19 that were previously associated with VWD. Most of these 'VWD variants' had allele frequencies consistent with disease incidence in European subjects, but some had a significantly higher frequency in other ethnicities. The mutations R2185Q, H817Q and M740I associated with type 1 and type 2N VWD were present in more than 13% of African subjects. CONCLUSIONS: These results highlight the complexity of VWF variations in different ethnic groups and emphasize the importance of interrogating variations on multiple ethnic backgrounds for associations with bleeding and thrombosis.


Assuntos
Etnicidade/genética , Projeto Genoma Humano , Mutação , Polimorfismo de Nucleotídeo Único , Doenças de von Willebrand/genética , Fator de von Willebrand/genética , Negro ou Afro-Americano/genética , Povo Asiático/genética , População Negra/genética , Análise Mutacional de DNA , Bases de Dados Genéticas , Frequência do Gene , Predisposição Genética para Doença , Hemostasia/genética , Humanos , Incidência , Fenótipo , População Branca/genética , Doenças de von Willebrand/sangue , Doenças de von Willebrand/etnologia , Fator de von Willebrand/metabolismo
6.
Blood ; 119(9): 2135-40, 2012 Mar 01.
Artigo em Inglês | MEDLINE | ID: mdl-22197721

RESUMO

Diagnosis and classification of VWD is aided by molecular analysis of the VWF gene. Because VWF polymorphisms have not been fully characterized, we performed VWF laboratory testing and gene sequencing of 184 healthy controls with a negative bleeding history. The controls included 66 (35.9%) African Americans (AAs). We identified 21 new sequence variations, 13 (62%) of which occurred exclusively in AAs and 2 (G967D, T2666M) that were found in 10%-15% of the AA samples, suggesting they are polymorphisms. We identified 14 sequence variations reported previously as VWF mutations, the majority of which were type 1 mutations. These controls had VWF Ag levels within the normal range, suggesting that these sequence variations might not always reduce plasma VWF levels. Eleven mutations were found in AAs, and the frequency of M740I, H817Q, and R2185Q was 15%-18%. Ten AA controls had the 2N mutation H817Q; 1 was homozygous. The average factor VIII level in this group was 99 IU/dL, suggesting that this variation may confer little or no clinical symptoms. This study emphasizes the importance of sequencing healthy controls to understand ethnic-specific sequence variations so that asymptomatic sequence variations are not misidentified as mutations in other ethnic or racial groups.


Assuntos
Negro ou Afro-Americano/genética , Variação Genética , Mutação , Doenças de von Willebrand/etnologia , Doenças de von Willebrand/genética , Fator de von Willebrand/genética , Substituição de Aminoácidos , Éxons , Ordem dos Genes , Humanos , Fator de von Willebrand/metabolismo
7.
Blood ; 114(5): 1091-8, 2009 Jul 30.
Artigo em Inglês | MEDLINE | ID: mdl-19372260

RESUMO

Direct sequencing of VWF genomic DNA in 21 patients with type 3 von Willebrand disease (VWD) failed to reveal a causative homozygous or compound heterozygous VWF genotype in 5 cases. Subsequent analysis of VWF mRNA led to the discovery of a deletion (c.221-977_532 + 7059del [p.Asp75_Gly178del]) of VWF in 7 of 12 white type 3 VWD patients from 6 unrelated families. This deletion of VWF exons 4 and 5 was absent in 9 patients of Asian origin. We developed a genomic DNA-based assay for the deletion, which also revealed its presence in 2 of 34 type 1 VWD families, segregating with VWD in an autosomal dominant fashion. The deletion was associated with a specific VWF haplotype, indicating a possible founder origin. Expression studies indicated markedly decreased secretion and defective multimerization of the mutant VWF protein. Further studies have found the mutation in additional type 1 VWD patients and in a family expressing both type 3 and type 1 VWD. The c.221-977_532 + 7059del mutation represents a previously unreported cause of both types 1 and 3 VWD. Screening for this mutation in other type 1 and type 3 VWD patient populations is required to elucidate further its overall contribution to VWD arising from quantitative deficiencies of VWF.


Assuntos
Deleção de Sequência , Doenças de von Willebrand/genética , Fator de von Willebrand/genética , Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Povo Asiático/genética , Inglaterra/epidemiologia , Éxons/genética , Feminino , Efeito Fundador , Genes Dominantes , Genótipo , Haplótipos/genética , Humanos , Masculino , Pessoa de Meia-Idade , Proteínas Recombinantes de Fusão/biossíntese , Análise de Sequência de DNA , População Branca/genética , Adulto Jovem , Doenças de von Willebrand/classificação , Doenças de von Willebrand/etnologia , Fator de von Willebrand/biossíntese , Fator de von Willebrand/química , Fator de von Willebrand/metabolismo
8.
Br J Haematol ; 130(5): 752-8, 2005 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-16115133

RESUMO

von Willebrand disease (VWD), the most common inherited bleeding disorder, is very heterogeneous, both in its phenotype and genotype. One particular molecular mechanism of VWD is due to recombination events between the true gene and its pseudogene on chromosome 22. We assessed the frequency and extension of such events in 50 multi-ethnic index patients with severe VWD type 3 and in five index patients with VWD type 2M Vicenza. One additional unclassified patient had been diagnosed with possible VWD in Russia solely on a clinical basis. Gene conversions, previously thought to be rare events, were identified in >10% of our study population: in six multi-ethnic patients with severe VWD type 3, in one patient with VWD type 2M Vicenza and the Russian patient was finally diagnosed with VWD type 2B New York/Malmoe. Our results suggest a significant contribution of this particular molecular mechanism to the manifestation of VWD. The location of the gene conversions, their extension and their occurrence as homozygous, compound heterozygous or heterozygous mutations determines the resulting phenotype.


Assuntos
Conversão Gênica , Mutação de Sentido Incorreto , Doenças de von Willebrand/classificação , Fator de von Willebrand/genética , Células Cultivadas , Análise Mutacional de DNA , Etnicidade , Alemanha , Grécia , Haplótipos , Humanos , Índia , Fenótipo , Agregação Plaquetária , Ristocetina/farmacologia , Federação Russa , Doenças de von Willebrand/etnologia , Doenças de von Willebrand/genética
10.
Clin Lab Haematol ; 25(4): 247-9, 2003 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-12890164

RESUMO

The amount and function of von Willebrand factor (VWF), measured against a panel of laboratory tests, is the normal basis for the diagnosis of von Willebrand's disease (VWD). The normal range for each test is usually obtained by assaying samples from a cross section of the local population or from a manufacturer's kit insert. While collecting normal controls for another study, population from Durban in South Africa, with its distinct ethnic mix of Africans, Indians and Caucasians were also studied. Previously, Indians from their subcontinent have not been looked at separately and compared with Africans and Caucasians. It is confirmed in a previous study (Miller, Dilley, Richardson, Craig, Evatt. (2001) American Journal of Hematology 67, 125) that African Americans had significantly higher VWF:Ag and FVIII levels when compared with Caucasians. In addition, it was found that there was a significant difference in VWF:Ag levels between Indians and Africans, and between Caucasians and Africans, whereas no significant difference between Indians and Caucasians. Africans, Indians and Caucasians with blood group O showed significantly lower VWF:Ag and FVIII than the other ABO blood groups. Normal ranges of VWF for different blood groups are well established and this information should be utilized while considering a diagnosis of VWD. It is proposed here that the influence of racial origin should also be considered in the clinical and laboratory evaluation of VWD.


Assuntos
Etnicidade/genética , Grupos Raciais/genética , Doenças de von Willebrand/etnologia , Fator de von Willebrand/análise , Sistema ABO de Grupos Sanguíneos/análise , Sistema ABO de Grupos Sanguíneos/genética , África/etnologia , População Negra/genética , Europa (Continente)/etnologia , Feminino , Variação Genética , Humanos , Índia/etnologia , Masculino , Valores de Referência , África do Sul , População Branca/genética , Doenças de von Willebrand/sangue , Doenças de von Willebrand/diagnóstico , Doenças de von Willebrand/genética , Fator de von Willebrand/genética
11.
Blood Cells Mol Dis ; 30(3): 264-70, 2003.
Artigo em Inglês | MEDLINE | ID: mdl-12737944

RESUMO

Type 3 von Willebrand disease (VWD) is characterized by unmeasurable von Willebrand factor (VWF) levels in plasma and platelets and severe hemorrhagic symptoms. We have characterized at the molecular level a group of 40 patients (12 Italians, 14 Iranians, and 14 Indians) to evaluate genetic heterogeneity among these populations. Some of these patients have been previously investigated by us (mutations shown in italics); they are included in this study to provide a more comprehensive pattern of gene defects in type 3 VWD. Patients' DNA were first tested for more frequently reported mutations, then screened by single-strand conformation polymorphism and direct sequence analysis. Fifty gene defects were identified, of which 45 are novel. As expected most of these defects caused null alleles, 17 being nonsense mutations (Q218X, W222X, R365X, R373X, Y610X, W642X, E644X, Q706X, Q1311X, S1338X, Q1346X, Y1542X, R1659X, E1981X, E2129X, R2434X, and Q2544X), 12 small deletions (191delG, 276delT, 788del24, 2016del4, 2157delA, 2269delCT, 2435delC, 4092delAC, 6182delT, 7294delGT, 7683delT, and 8241del9), 4 small insertions (4414insC, 7130insC, 7137insT, and 7674insC), 8 possible splice site mutations (1110(-1)G-->A, 1946(-4)C-->T, 3108(+5)G-->A, 3379(+1)G-->A, 5053(+1)G-->A, 5170(+10)C-->T, 6977(-1)G-->C, and 7729(+7)C-->T), 8 candidate missense mutations (D47H, S85P, D141N, D141Y, C275S, C1071F, C2174G, and C2804Y), and 1 large gene deletion (exons 23-52). Only 2 of these patients have developed alloantibodies against VWF. This study extend our previous finding that mutations responsible for type 3 VWD are scattered throughout the entire VWF gene and that there is no founder effect in these three populations studied.


Assuntos
Mutação/genética , Doenças de von Willebrand/etnologia , Códon sem Sentido , Análise Mutacional de DNA , Efeito Fundador , Humanos , Índia , Irã (Geográfico) , Isoanticorpos/sangue , Itália , Epidemiologia Molecular , Mutação de Sentido Incorreto , Sítios de Splice de RNA/genética , Deleção de Sequência , Doenças de von Willebrand/epidemiologia
12.
Am J Hematol ; 67(2): 125-9, 2001 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-11343385

RESUMO

Diagnosis of von Willebrand disease (vWD) is based on a panel of laboratory tests that measure the amount and function of von Willebrand factor (vWF). In population studies, vWF is higher in African Americans than Caucasians. Bleeding time, factor VIII activity (FVIII), vWF antigen (vWF:Ag), "vWF activity" ELISA (vWF:Act), ristocetin cofactor (vWF:RCof), and ristocetin-induced platelet aggregation (RIPA) were measured on 123 women with menorrhagia and 123 randomly selected control women; 70 cases and 76 controls were African American. Among controls, African Americans had significantly higher levels of vWF:Ag (mean 120 vs. 102 U/dl, P = 0.017). Among all subjects, African Americans had higher levels of vWF:Ag (mean 123 vs. 103, P = 0.001), vWF:Act (mean 101 vs. 89, P = 0.006), and FVIII (mean 118 vs. 104, P = 0.008). VWF:RCof did not differ between races (93 vs. 94 U/dl). RIPA was reduced in African Americans (P < 0.0001). In both races, women with type O blood differed significantly from those with other ABO types in vWF:Ag, vWF:Act, FVIII, and vWF:RCof. Based on criteria of two or more tests below race- and ABO-specific reference ranges, 6.5% of menorrhagia cases and 0.8% of controls were classified as having vWD, or its phenocopy. Among Caucasians, no controls and 7 cases (15.6%) were classified as affected, and in African Americans, 1 control (1.3%) and 1 case (1.4%) were so classified. Racial differences in vWF further complicate the issues surrounding diagnosis of vWD. The finding of increased vWF:Ag not accompanied by increased vWF:RCof has implications for understanding the structure-function relationships of vWF. Published 2001 Wiley-Liss, Inc.


Assuntos
População Negra , Doenças de von Willebrand/diagnóstico , Doenças de von Willebrand/etnologia , Fator de von Willebrand/metabolismo , Sistema ABO de Grupos Sanguíneos , População Negra/genética , Estudos de Casos e Controles , Fator VIII/metabolismo , Feminino , Humanos , Menorragia , Agregação Plaquetária/efeitos dos fármacos , Ristocetina/farmacologia , População Branca/genética , Doenças de von Willebrand/sangue
13.
Thromb Haemost ; 79(4): 709-17, 1998 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-9569178

RESUMO

The genetic defects causing recessive type 1 and type 3 von Willebrand disease (VWD) in eight families from the northern part of Italy have been investigated. Mutations were identified in 14 of the 16 disease-associated von Willebrand factor (VWF) genes. Only one mutation, a stop codon in exon 45, was previously reported. Several new mutations were identified: one cytosine insertion in exon 42, one guanine deletion in exon 28, one probably complete VWF gene deletion, one substitution in the 3' splice site of intron 13, one possible gene conversion, and three candidate missense mutations. One missense mutation, the substitution of a cysteine in exon 42, was identified in all type 3 VWD patients that were previously characterized as a subgroup with significant increase of factor VIII procoagulant activity after desmopressin infusion. This paper demonstrates again that the molecular defects of quantitative VWD are diverse and located throughout the entire VWF gene.


Assuntos
Doenças de von Willebrand/genética , Fator de von Willebrand/genética , Análise Mutacional de DNA , Éxons/genética , Feminino , Conversão Gênica , Genes Recessivos , Haplótipos/genética , Humanos , Itália/epidemiologia , Masculino , Linhagem , Fenótipo , Mutação Puntual , Prevalência , Splicing de RNA , Deleção de Sequência , Doenças de von Willebrand/classificação , Doenças de von Willebrand/etnologia
14.
Genomics ; 21(1): 188-93, 1994 May 01.
Artigo em Inglês | MEDLINE | ID: mdl-8088787

RESUMO

Twenty-four patients with von Willebrand disease type III were screened for mutations in the von Willebrand factor (VWF) gene using the PCR technique, followed by direct sequencing. More than 250 kb of genomic DNA were sequenced, including the promoter and coding regions (52 exons) of the VWF gene from 24 patients. In addition to the previously reported mutations of a single cytosine deletion in exon 18 and the nonsense mutations in exons 28, 32, and 45, nine new mutations were detected: two nonsense mutations in exons 15 and 16, one allele with a thymidine insertion in exon 14, one allele with a cytosine insertion in exon 28, one 20-bp deletion in exon 15, one mutation in the donor splice site of exon 43, and three missense mutations in exons 28, 49, and 51. Forty-two mutant chromosomes were identified (42/48); 11 probands are homozygous for the mutations, and 8 are compound heterozygous. In addition, a new subfamily of the Alu sequence in the promoter region and 10 new polymorphisms were identified.


Assuntos
Doenças de von Willebrand/genética , Fator de von Willebrand/genética , Alelos , Sequência de Bases , Análise Mutacional de DNA , Éxons , Finlândia , Frequência do Gene , Genes , Genótipo , Humanos , Dados de Sequência Molecular , Reação em Cadeia da Polimerase , Polimorfismo Genético , Regiões Promotoras Genéticas , Sequências Repetitivas de Ácido Nucleico , Deleção de Sequência , Suécia , Doenças de von Willebrand/classificação , Doenças de von Willebrand/etnologia
15.
J Pediatr ; 123(6): 893-8, 1993 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-8229521

RESUMO

OBJECTIVE: Von Willebrand disease (vWD) was thought to be a rare disorder until a recent survey reported a prevalence of 0.8% in an ethnically homogenous community in northern Italy. The purpose of this study was to determine the prevalence of vWD in an ethnically heterogenous population. METHODS: Von Willebrand factor (vWF) was measured by the ristocetin cofactor method in 600 healthy children, aged 2 to 18 years, seen for routine school physical examinations in a three-state region. Personal and family bleeding symptoms were determined by questionnaire. The diagnosis of vWD required a personal history of bleeding symptoms, an abnormal vWF activity concentration, and a family history of at least one immediate family member with bleeding symptoms. RESULTS: A total of 315 subjects were white, 212 were black, 16 were Hispanic, 10 were from other groups, and 47 were biracial. Eight subjects (four black, four white) met the criteria for vWD, for a prevalence of 1.3%. Seven subjects with vWD had blood group O (mean vWF = 32 U/dl; range, 10 to 42 U/dl), and one had blood group A (vWF = 41 U/dl). Children who had blood group O had significantly (p < 0.001) lower vWF activities (median, 83 U/dl, range, 43 to 162 U/dl) than those from non-O blood groups (median, 98 U/dl; range, 51 to 190 U/dl). There were no significant differences in vWF activity by ethnicity. The vWF activity was significantly (p < 0.02) greater for boys than girls in both blood groups. CONCLUSION: Von Willebrand disease is the most common congenital hemostatic disorder; its high prevalence is not limited to one ethnic group.


Assuntos
Doenças de von Willebrand/epidemiologia , Adolescente , Antígenos de Grupos Sanguíneos , Criança , Pré-Escolar , Feminino , Humanos , Masculino , Prevalência , Grupos Raciais , Fatores Sexuais , Estados Unidos/epidemiologia , Doenças de von Willebrand/etnologia
16.
Am J Clin Pathol ; 93(3): 395-9, 1990 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-2106777

RESUMO

The authors have identified six Southeast Asian patients ranging in age from 14 to 21 years with hemoglobin E-beta(0) thalassemia and a coagulopathy involving von Willebrand factor (vWF). These patients had normal or only slightly decreased plasma clotting factor levels. The activated partial thromboplastin time was prolonged in four of the patients. The abnormal feature common to all patients was a qualitative loss of high molecular weight multimers of vWF by crossed immunoelectrophoresis (vWF:CIE). Plasma vWF antigen concentration (vWF:Ag) and ristocetin cofactor activity (vWF:RCo) also were decreased and bleeding time prolonged in three patients. Epistaxis was present in two. No family history of increased bleeding tendency was present in any patient. Coagulation parameters and vWF:CIE were normal in two first-degree relatives without this hemoglobinopathy. vWF abnormalities and clinical manifestations were greatest in those patients with the most severe anemia and hepatosplenomegaly. These six patients appear to have an acquired abnormality of vWF, although they lack the clinical characteristics of acquired von Willebrand disease. While the etiology of this abnormality is unclear, the authors speculate that proteolysis of vWF secondary to extramedullary hematopoiesis or loss through high cardiac output shear stress in these anemic patients may be involved.


Assuntos
Antígenos/análise , Hemoglobina E/análise , Hemoglobinas Anormais/análise , Talassemia/sangue , Adolescente , Adulto , Tempo de Sangramento , Testes de Coagulação Sanguínea/métodos , Fator VIII/análise , Feminino , Humanos , Imunoeletroforese/métodos , Laos/etnologia , Masculino , Minnesota , Peso Molecular , Ristocetina/sangue , Talassemia/etnologia , Talassemia/genética , Talassemia/fisiopatologia , Doenças de von Willebrand/sangue , Doenças de von Willebrand/etnologia , Doenças de von Willebrand/genética , Doenças de von Willebrand/fisiopatologia , Fator de von Willebrand/imunologia
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