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The genetics of Henoch–Schönlein purpura: a systematic review and meta-analysis

Overview of attention for article published in Rheumatology International, January 2013
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Title
The genetics of Henoch–Schönlein purpura: a systematic review and meta-analysis
Published in
Rheumatology International, January 2013
DOI 10.1007/s00296-012-2661-4
Pubmed ID
Authors

Xuelian He, Chunhua Yu, Peiwei Zhao, Yan Ding, Xiaohui Liang, Yulan Zhao, Xin Yue, Yanxiang Wu, Wei Yin

Abstract

Henoch-Schönlein purpura (HSP) is the most common form of systemic vasculitis of unknown etiology. This study aimed at reviewing published studies investigating the association of genetic polymorphisms with HSP and its severity. We systematically reviewed all published data on genetic risk factors for HSP by searching MEDLINE. We also performed a meta-analysis of association studies of HLA-DRB1-01, 07, and 11, angiotensin I-converting enzyme (ACE) insertion/deletion (I/D) polymorphism. We identified 45 studies investigating polymorphisms in 39 genes in association with HSP and/or its severity. Most of these genes are involved in immunological and/or inflammatory responses or vasomotor regulation. Most results were negative. The most convincing finding is the association of HLA-DRB1 01, 07, and 11 with HSP susceptibility. The overall odds ratios (ORs) for the three loci were significant for HSP: HLA-DRB1 01 (OR = 1.805, 95 % CI 1.259-2.588, p = 0.0012); HLA-DRB1 07 (OR = 0.671, 95 % CI 0.469-0.961, p = 0.058); HLA-DRB1 11 (OR = 2.001, 95 % CI 1.50-2.67, p = 0.027). Genetic regulation of endothelial function, such as polymorphisms in genes coding rennin-angiotensin system (RAS) components, endothelial nitric oxide synthases, Inter-Cellular Adhesion Molecule 1, and vascular endothelial growth factor, could also confer effect on HSP. In addition, MEFV, whose mutations cause familial Mediterranean fever, could be an important candidate gene for HSP. Further large studies are required to investigate the association between genetic polymorphisms and HSP. Alternative approaches, such as genome-wide association study, are necessary to help to identify genetic risks for HSP.

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Mendeley readers

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Geographical breakdown

Country Count As %
Unknown 46 100%

Demographic breakdown

Readers by professional status Count As %
Student > Master 10 22%
Student > Bachelor 8 17%
Researcher 5 11%
Student > Ph. D. Student 5 11%
Student > Doctoral Student 4 9%
Other 8 17%
Unknown 6 13%
Readers by discipline Count As %
Medicine and Dentistry 23 50%
Agricultural and Biological Sciences 5 11%
Biochemistry, Genetics and Molecular Biology 3 7%
Nursing and Health Professions 2 4%
Immunology and Microbiology 2 4%
Other 2 4%
Unknown 9 20%
Attention Score in Context

Attention Score in Context

This research output has an Altmetric Attention Score of 1. This is our high-level measure of the quality and quantity of online attention that it has received. This Attention Score, as well as the ranking and number of research outputs shown below, was calculated when the research output was last mentioned on 18 January 2013.
All research outputs
#20,178,948
of 22,693,205 outputs
Outputs from Rheumatology International
#1,965
of 2,172 outputs
Outputs of similar age
#251,886
of 284,627 outputs
Outputs of similar age from Rheumatology International
#42
of 47 outputs
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