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本文引用的文献

1
Significance of valine/leucine247 polymorphism of beta2-glycoprotein I in antiphospholipid syndrome: increased reactivity of anti-beta2-glycoprotein I autoantibodies to the valine247 beta2-glycoprotein I variant.β2-糖蛋白I缬氨酸/亮氨酸247多态性在抗磷脂综合征中的意义:抗β2-糖蛋白I自身抗体对缬氨酸247β2-糖蛋白I变体的反应性增加。
Arthritis Rheum. 2005 Jan;52(1):212-8. doi: 10.1002/art.20741.
2
Association of HLA-DM polymorphism with the production of antiphospholipid antibodies.HLA - DM基因多态性与抗磷脂抗体产生的关联
Ann Rheum Dis. 2004 Dec;63(12):1645-8. doi: 10.1136/ard.2003.015552.
3
Genetics of antiphospholipid syndrome.抗磷脂综合征的遗传学
Curr Rheumatol Rep. 2004 Dec;6(6):458-62. doi: 10.1007/s11926-004-0025-0.
4
Systemic lupus erythematosus in Tunisia: demographic and clinical analysis of 100 patients.突尼斯的系统性红斑狼疮:100例患者的人口统计学和临床分析
Lupus. 2004;13(3):204-11. doi: 10.1191/0961203303lu530xx.
5
Is HLA class II susceptibility to primary antiphospholipid syndrome different from susceptibility to secondary antiphospholipid syndrome?人类白细胞抗原II类分子对原发性抗磷脂综合征的易感性与对继发性抗磷脂综合征的易感性是否不同?
Lupus. 2004;13(2):125-31. doi: 10.1191/0961203304lu520oa.
6
HLA class II alleles and genetic predisposition to the antiphospholipid syndrome.人类白细胞抗原II类等位基因与抗磷脂综合征的遗传易感性
Autoimmun Rev. 2003 Oct;2(6):387-94. doi: 10.1016/s1568-9972(03)00068-5.
7
HLA-DPB1 alleles association of anticardiolipin and anti-beta2GPI antibodies in a large series of European patients with systemic lupus erythematosus.一大组欧洲系统性红斑狼疮患者中抗心磷脂抗体和抗β2糖蛋白I抗体与HLA - DPB1等位基因的关联
Lupus. 2003;12(7):560-3. doi: 10.1191/0961203303lu402oa.
8
High prevalence of prothrombin G20210A mutation among patients with deep venous thrombosis in Lebanon.黎巴嫩深静脉血栓形成患者中凝血酶原G20210A突变的高流行率。
Thromb Haemost. 2003 May;89(5):945-6.
9
Lack of association of beta2-glycoprotein I polymorphisms Val247Leu and Trp316Ser with antiphospholipid antibodies in patients with thrombosis and pregnancy complications.
Br J Haematol. 2003 Mar;120(6):1066-72. doi: 10.1046/j.1365-2141.2003.04187.x.
10
Valine/valine genotype at position 247 of the beta2-glycoprotein I gene in Mexican patients with primary antiphospholipid syndrome: association with anti-beta2-glycoprotein I antibodies.墨西哥原发性抗磷脂综合征患者β2-糖蛋白I基因第247位缬氨酸/缬氨酸基因型:与抗β2-糖蛋白I抗体的关联
Arthritis Rheum. 2003 Feb;48(2):471-4. doi: 10.1002/art.10771.

抗磷脂(休斯)综合征的种族和地理差异。

Ethnic and geographical variation in antiphospholipid (Hughes) syndrome.

作者信息

Uthman I, Khamashta M

机构信息

American University of Beirut, Medical Centre, PO Box 113-6044, Beirut, Lebanon.

出版信息

Ann Rheum Dis. 2005 Dec;64(12):1671-6. doi: 10.1136/ard.2005.038448. Epub 2005 May 26.

DOI:10.1136/ard.2005.038448
PMID:15919676
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1755326/
Abstract

Investigation of the clinical epidemiology of the antiphospholipid syndrome (APS) is in its early stages. During the past 20 years, studies of antiphospholipid antibodies (aPL) and APS have been made in many countries and ethno-geographical groups. aPL appear to occur in all populations studied, with some variations noted in their frequency and in the clinical complications. Environmental and genetic factors contribute to ethnic variation and susceptibility to APS and thus inter-ethnic differences in disease patterns may be due to environmental or genetic factors, or both.

摘要

抗磷脂综合征(APS)的临床流行病学研究尚处于早期阶段。在过去20年里,许多国家和不同种族地理群体都开展了抗磷脂抗体(aPL)和APS的研究。在所有研究的人群中似乎都存在aPL,但其频率和临床并发症存在一些差异。环境和遗传因素导致了种族差异以及对APS的易感性,因此疾病模式的种族间差异可能是由环境因素或遗传因素,或两者共同作用所致。