共 37 条
ADAMTS13 and Von Willebrand factor in patients undergoing hemodialysis
被引:12
作者:

Rios, Danyelle R. A.
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机构:
Univ Fed Minas Gerais, Dept Clin & Toxicol Anal, Fac Pharm, BR-31270901 Belo Horizonte, MG, Brazil Univ Fed Minas Gerais, Dept Clin & Toxicol Anal, Fac Pharm, BR-31270901 Belo Horizonte, MG, Brazil

Carvalho, Maria G.
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机构:
Univ Fed Minas Gerais, Dept Clin & Toxicol Anal, Fac Pharm, BR-31270901 Belo Horizonte, MG, Brazil Univ Fed Minas Gerais, Dept Clin & Toxicol Anal, Fac Pharm, BR-31270901 Belo Horizonte, MG, Brazil

Figueiredo, Roberta C.
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机构:
Univ Fed Minas Gerais, Dept Publ Healthy, Fac Med, BR-31270901 Belo Horizonte, MG, Brazil Univ Fed Minas Gerais, Dept Clin & Toxicol Anal, Fac Pharm, BR-31270901 Belo Horizonte, MG, Brazil

Ferreira, Claudia N.
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机构:
Univ Fed Minas Gerais, Dept Clin & Toxicol Anal, Fac Pharm, BR-31270901 Belo Horizonte, MG, Brazil Univ Fed Minas Gerais, Dept Clin & Toxicol Anal, Fac Pharm, BR-31270901 Belo Horizonte, MG, Brazil

Rodrigues, Valerio L.
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机构:
Inst Mineiro Nefrol, Belo Horizonte, MG, Brazil Univ Fed Minas Gerais, Dept Clin & Toxicol Anal, Fac Pharm, BR-31270901 Belo Horizonte, MG, Brazil

Souza, Regina A.
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机构:
Univ Fed Minas Gerais, Clin Hosp, BR-31270901 Belo Horizonte, MG, Brazil Univ Fed Minas Gerais, Dept Clin & Toxicol Anal, Fac Pharm, BR-31270901 Belo Horizonte, MG, Brazil

Silva, Ana C. Simoes e
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机构:
Univ Fed Minas Gerais, Dept Pediat, Fac Med, BR-31270901 Belo Horizonte, MG, Brazil Univ Fed Minas Gerais, Dept Clin & Toxicol Anal, Fac Pharm, BR-31270901 Belo Horizonte, MG, Brazil

Fernandes, Ana Paula
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机构:
Univ Fed Minas Gerais, Dept Clin & Toxicol Anal, Fac Pharm, BR-31270901 Belo Horizonte, MG, Brazil Univ Fed Minas Gerais, Dept Clin & Toxicol Anal, Fac Pharm, BR-31270901 Belo Horizonte, MG, Brazil

Gomes, Karina B.
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h-index: 0
机构:
Univ Fed Minas Gerais, Dept Clin & Toxicol Anal, Fac Pharm, BR-31270901 Belo Horizonte, MG, Brazil Univ Fed Minas Gerais, Dept Clin & Toxicol Anal, Fac Pharm, BR-31270901 Belo Horizonte, MG, Brazil

Dusse, Luci M. S.
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h-index: 0
机构:
Univ Fed Minas Gerais, Dept Clin & Toxicol Anal, Fac Pharm, BR-31270901 Belo Horizonte, MG, Brazil Univ Fed Minas Gerais, Dept Clin & Toxicol Anal, Fac Pharm, BR-31270901 Belo Horizonte, MG, Brazil
机构:
[1] Univ Fed Minas Gerais, Dept Clin & Toxicol Anal, Fac Pharm, BR-31270901 Belo Horizonte, MG, Brazil
[2] Univ Fed Minas Gerais, Dept Publ Healthy, Fac Med, BR-31270901 Belo Horizonte, MG, Brazil
[3] Inst Mineiro Nefrol, Belo Horizonte, MG, Brazil
[4] Univ Fed Minas Gerais, Clin Hosp, BR-31270901 Belo Horizonte, MG, Brazil
[5] Univ Fed Minas Gerais, Dept Pediat, Fac Med, BR-31270901 Belo Horizonte, MG, Brazil
关键词:
Hemodialysis;
ADAMTS13;
VWF;
Vascular access thrombosis;
FACTOR-CLEAVING PROTEASE;
THROMBOTIC THROMBOCYTOPENIC PURPURA;
ENDOTHELIAL-CELLS;
LIVER;
PLATELETS;
PLASMA;
MEMBER;
D O I:
10.1007/s11239-012-0682-1
中图分类号:
R5 [内科学];
学科分类号:
1002 ;
100201 ;
摘要:
Hemodialysis (HD) is associated with increasing thrombotic trend. Vascular access thrombosis (VAT) increases morbidity in HD patients. The aim of this study was to evaluate ADAMTS13 and VWF plasma levels from patients undergoing HD as putative biomarkers of the hypercoagulability state, as well the association between these markers and VAT occurrence. This study included 195 patients on HD for more than 6 months. HD patients were allocated into two groups according to the occurrence or not of previous episode of VAT; HD with VAT (N = 46) and HD without VAT (N = 149). ADAMTS13 and VWF were performed by ELISA. There was no significant difference between HD patients with and without VAT for ADAMTS13 and VWF levels. However, VWF levels were higher (P < 0.001) and ADAMTS13 were lower (P < 0.001) in HD patients, comparing to the control group composed by healthy subjects without kidney disease, age and sex-matched (N = 80). Taken together our data suggest a potential role of the kidneys function compromised on ADAMTS13 synthesis or metabolism, regardless other known sources of ADAMTS13. The imbalance between ADAMTS13 and VWF levels does not explain the development of VAT in HD patients by itself, although it should contribute for the hypercoagulability state. Therefore, additional studies to identify other risk factors are warranted and essential for better management of HD patients.
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页码:73 / 78
页数:6
相关论文
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机构: Univ Michigan, Med Ctr, Howard Hughes Med Inst, Dept Internal Med, Ann Arbor, MI 48109 USA

Stark, KR
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Gruppo, R
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机构: Univ Michigan, Med Ctr, Howard Hughes Med Inst, Dept Internal Med, Ann Arbor, MI 48109 USA

Sarode, R
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机构: Univ Michigan, Med Ctr, Howard Hughes Med Inst, Dept Internal Med, Ann Arbor, MI 48109 USA

Shurin, SB
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Chandrasekaran, V
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机构: Univ Michigan, Med Ctr, Howard Hughes Med Inst, Dept Internal Med, Ann Arbor, MI 48109 USA

Stabler, SP
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Sabio, H
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Bouhassira, EE
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Upshaw, JD
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Ginsburg, D
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Univ Michigan, Med Ctr, Howard Hughes Med Inst, Dept Internal Med, Ann Arbor, MI 48109 USA Univ Michigan, Med Ctr, Howard Hughes Med Inst, Dept Internal Med, Ann Arbor, MI 48109 USA

Tsai, HM
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