• 文献检索
  • 文档翻译
  • 深度研究
  • 学术资讯
  • Suppr Zotero 插件Zotero 插件
  • 邀请有礼
  • 套餐&价格
  • 历史记录
应用&插件
Suppr Zotero 插件Zotero 插件浏览器插件Mac 客户端Windows 客户端微信小程序
定价
高级版会员购买积分包购买API积分包
服务
文献检索文档翻译深度研究API 文档MCP 服务
关于我们
关于 Suppr公司介绍联系我们用户协议隐私条款
关注我们

Suppr 超能文献

核心技术专利:CN118964589B侵权必究
粤ICP备2023148730 号-1Suppr @ 2026

文献检索

告别复杂PubMed语法,用中文像聊天一样搜索,搜遍4000万医学文献。AI智能推荐,让科研检索更轻松。

立即免费搜索

文件翻译

保留排版,准确专业,支持PDF/Word/PPT等文件格式,支持 12+语言互译。

免费翻译文档

深度研究

AI帮你快速写综述,25分钟生成高质量综述,智能提取关键信息,辅助科研写作。

立即免费体验

台湾静脉血栓形成倾向的中国患者中抗凝血酶III、蛋白C和蛋白S缺乏症的高患病率,但无因子V莱顿突变。

High prevalence of antithrombin III, protein C and protein S deficiency, but no factor V Leiden mutation in venous thrombophilic Chinese patients in Taiwan.

作者信息

Shen M C, Lin J S, Tsay W

机构信息

Department of Internal Medicine, National Taiwan University Hospital, Taipei, Republic of China.

出版信息

Thromb Res. 1997 Aug 15;87(4):377-85. doi: 10.1016/s0049-3848(97)00141-2.

DOI:10.1016/s0049-3848(97)00141-2
PMID:9271815
Abstract

We studied the prevalence of antithrombin III (AT III), protein C (PC) and protein S (PS) deficiencies and factor V Leiden mutation in thrombophilia in Taiwan. Eighty-five consecutive and unrelated patients with otherwise unexplained venous thrombophilia were studied. Both antigen and activity of inhibitors were determined using commercial kits (Stago), activated PC sensitivity ratio (APC SR) by Coatest (Chromogenix), and factor V mutation by polymerase chain reaction with sequence specific primer. Of 85 patients, 41 were male, 44 female, and mean age 49.4 years (17-82 years). None had factor V mutation, or APC SR of less than 2; 50 (58.8%) showed a deficiency of inhibitor proteins; 34 (68.0%) were hereditary, 16 (32.0%) non-hereditary; 3 had an AT III deficiency, 16 a PC deficiency, 28 a PS deficiency, and 3 a combined deficiency. Thirty-five were non-deficient without a known cause. The average age at the first thrombotic episode was 48.5 years (13-81 years). Thrombosis occurred spontaneously in 39 (78.0%) of 50 deficient patients. In conclusion, a relatively higher prevalence of AT III, PC and PS deficiency (59%), but no factor V Leiden mutation, was found in venous thrombophilic Chinese patients in Taiwan compared to that in western countries. Screening for inhibitor protein deficiency in Chinese thrombophilic patients is highly recommended.

摘要

我们研究了台湾地区血栓形成倾向中抗凝血酶III(AT III)、蛋白C(PC)和蛋白S(PS)缺乏症以及因子V莱顿突变的患病率。对85例连续且无亲缘关系的不明原因静脉血栓形成倾向患者进行了研究。使用商用试剂盒(Stago)测定抑制剂的抗原和活性,通过Coatest(Chromogenix)测定活化蛋白C敏感率(APC SR),并通过聚合酶链反应与序列特异性引物检测因子V突变。85例患者中,男性41例,女性44例,平均年龄49.4岁(17 - 82岁)。无人有因子V突变或APC SR小于2;50例(58.8%)表现出抑制剂蛋白缺乏;34例(68.0%)为遗传性,16例(32.0%)为非遗传性;3例有AT III缺乏,16例有PC缺乏,28例有PS缺乏,3例有联合缺乏。35例无已知原因的非缺乏患者。首次血栓形成发作的平均年龄为48.5岁(13 - 81岁)。50例缺乏患者中有39例(78.0%)血栓形成是自发的。总之,与西方国家相比,台湾地区静脉血栓形成倾向的中国患者中AT III、PC和PS缺乏症的患病率相对较高(59%),但无因子V莱顿突变。强烈建议对中国血栓形成倾向患者进行抑制剂蛋白缺乏的筛查。

相似文献

1
High prevalence of antithrombin III, protein C and protein S deficiency, but no factor V Leiden mutation in venous thrombophilic Chinese patients in Taiwan.台湾静脉血栓形成倾向的中国患者中抗凝血酶III、蛋白C和蛋白S缺乏症的高患病率,但无因子V莱顿突变。
Thromb Res. 1997 Aug 15;87(4):377-85. doi: 10.1016/s0049-3848(97)00141-2.
2
[A study on the deficiency of anticoagulant proteins in Chinese patients with deep venous thrombosis].[中国深静脉血栓形成患者抗凝蛋白缺乏的研究]
Zhonghua Nei Ke Za Zhi. 2000 Nov;39(11):746-8.
3
Different risks of thrombosis in four coagulation defects associated with inherited thrombophilia: a study of 150 families.与遗传性易栓症相关的四种凝血缺陷中不同的血栓形成风险:一项对150个家庭的研究
Blood. 1998 Oct 1;92(7):2353-8.
4
Incidence of thrombophilia detected in southern Taiwanese patients with venous thrombosis.在台湾南部静脉血栓形成患者中检测到的血栓形成倾向发生率。
Ann Hematol. 2003 Feb;82(2):114-117. doi: 10.1007/s00277-002-0603-z. Epub 2003 Jan 30.
5
Protein C and protein S deficiencies are the most important risk factors associated with thrombosis in Chinese venous thrombophilic patients in Taiwan.
Thromb Res. 2000 Sep 1;99(5):447-52. doi: 10.1016/s0049-3848(00)00265-6.
6
[Hereditary deficiency of antithrombin III, protein C, protein S and factor XII in 121 patients with venous or arterial thrombosis].121例静脉或动脉血栓形成患者的抗凝血酶III、蛋白C、蛋白S和因子XII遗传性缺乏症
Srp Arh Celok Lek. 1999 Jan-Feb;127(1-2):21-7.
7
Hereditary deficiencies of antithrombin III, protein S, and the protein C pathway in Jordanian thrombosis patients.约旦血栓形成患者中抗凝血酶III、蛋白S及蛋白C途径的遗传性缺陷
Clin Lab Sci. 2002 Fall;15(4):196-9.
8
Thrombophilia among Chinese women with venous thromboembolism during pregnancy.中国妊娠期静脉血栓栓塞妇女中的血栓形成倾向。
Gynecol Obstet Invest. 2012;73(3):183-8. doi: 10.1159/000331648. Epub 2012 Mar 6.
9
Hereditary thrombophilia in elite athletes.精英运动员中的遗传性血栓形成倾向
Med Sci Sports Exerc. 2002 Feb;34(2):218-21. doi: 10.1097/00005768-200202000-00006.
10
Thrombotic risk in hereditary antithrombin III, protein C, or protein S deficiency. A cooperative, retrospective study. Gesellschaft fur Thrombose- und Hamostaseforschung (GTH) Study Group on Natural Inhibitors.遗传性抗凝血酶III、蛋白C或蛋白S缺乏症的血栓形成风险。一项合作性回顾性研究。血栓与止血研究协会(GTH)天然抑制剂研究组。
Arterioscler Thromb Vasc Biol. 1996 Jun;16(6):742-8. doi: 10.1161/01.atv.16.6.742.

引用本文的文献

1
Validation for the function of protein C in mouse models.验证蛋白 C 在小鼠模型中的功能。
PeerJ. 2024 Apr 24;12:e17261. doi: 10.7717/peerj.17261. eCollection 2024.
2
Hereditary protein C deficiency with portal vein thrombosis in a Chinese male: A case report.一名中国男性患遗传性蛋白C缺乏症伴门静脉血栓形成:病例报告
Exp Ther Med. 2022 Nov 8;24(6):751. doi: 10.3892/etm.2022.11688. eCollection 2022 Dec.
3
To Test or Not to Test: Thrombophilia in Venous Thromboembolisms.检测还是不检测:静脉血栓栓塞症中的易栓症
Acta Cardiol Sin. 2021 Mar;37(2):211-212. doi: 10.6515/ACS.202103_37(2).20210118A.
4
Association between congenital thrombophilia and outcomes in pulmonary embolism patients.先天性血栓形成倾向与肺栓塞患者预后之间的关联。
Blood Adv. 2020 Dec 8;4(23):5958-5965. doi: 10.1182/bloodadvances.2020002955.
5
Genotypic and phenotypic character of Chinese neonates with congenital protein C deficiency: a case report and literature review.中国先天性蛋白C缺乏症新生儿的基因型和表型特征:病例报告及文献复习
Thromb J. 2019 Oct 2;17:19. doi: 10.1186/s12959-019-0208-6. eCollection 2019.
6
Successful medical management of acute mesenteric ischemia due to superior mesenteric and portal vein thrombosis in a 27-year-old man with protein S deficiency: a case report.一名27岁蛋白S缺乏男性因肠系膜上静脉和门静脉血栓形成导致急性肠系膜缺血的成功药物治疗:病例报告
J Med Case Rep. 2017 Nov 9;11(1):315. doi: 10.1186/s13256-017-1463-4.
7
The prevalence and clinical manifestation of hereditary thrombophilia in Korean patients with unprovoked venous thromboembolisms.遗传性血栓形成倾向在韩国无诱因静脉血栓栓塞症患者中的流行率和临床表现。
PLoS One. 2017 Oct 17;12(10):e0185785. doi: 10.1371/journal.pone.0185785. eCollection 2017.
8
Low-molecular-weight-heparin can benefit women with recurrent pregnancy loss and sole protein S deficiency: a historical control cohort study from Taiwan.低分子量肝素对复发性流产且单纯蛋白S缺乏的女性有益:一项来自台湾的历史性对照队列研究。
Thromb J. 2016 Oct 28;14:44. doi: 10.1186/s12959-016-0118-9. eCollection 2016.
9
Diagnosis and Treatment of Lower Extremity Deep Vein Thrombosis: Korean Practice Guidelines.下肢深静脉血栓形成的诊断与治疗:韩国实践指南
Vasc Specialist Int. 2016 Sep;32(3):77-104. doi: 10.5758/vsi.2016.32.3.77. Epub 2016 Sep 30.
10
Familial Budd-Chiari Syndrome in China: A Systematic Review of the Literature.中国的家族性布加综合征:文献系统评价
ISRN Hepatol. 2013 Feb 28;2013:763508. doi: 10.1155/2013/763508. eCollection 2013.