The role of human leukocyte antigen genes in the formation of abdominal aortic aneurysms

被引:14
作者
Badger, Stephen A. [1 ]
Soong, Chee V.
O'Donnell, Mark E.
Middleton, Derek
机构
[1] Belfast City Hosp, Vasc & Endovasc Surg Ctr, Belfast BT9 7AB, Antrim, North Ireland
[2] Belfast City Hosp, Histocompatabil & Immunogenet Lab, Belfast BT9 7AB, Antrim, North Ireland
关键词
D O I
10.1016/j.jvs.2006.09.067
中图分类号
R61 [外科手术学];
学科分类号
摘要
Background. Increasing evidence suggests an autoimmune component to abdominal aortic aneurysm (AAA) formation. This study was conducted to determine if a difference exists in human leukocyte antigen (HLA) allele distribution between patients with AAA and population controls, and between patients with small and large AAA. Methods. Patients with known AAA attending the vascular unit were consented for recruitment. HLA-A, HLA-B and HLA-DR was determined by polymerase chain reaction and sequence-specific oligonucleotide probes. The distribution of these alleles in the Northern Ireland general population was obtained from the histocompatability and inummogenetics database. The chi(2) test was used for statistical analysis with Bonferroni correction. Results. A total of 241 AAA patients were recruited, with a wide range of aneurysm size. In class 1, the most frequent allele families were HLA-A*02 and *01 and HLA-B*07, *08, and *44. In class 11, HLA-DRB1*03, *04, *07, and *15 were the most frequent. HLA-A*11 was lower in AAA cases (10.4% vs 15.0%; P =.08), whereas HLA-13*08 was lower in the controls (29.8% vs 36.5%; P =.05) and HLA-DRBI* 11 was lower in cases (4.2% vs 8.1%; P =.05). After Bonferroni correction, however, the proportion of allele families was not significantly different in AAA patients compared with the proportion seenin controls. HLA-DRB1*11 and *14hadalowerprevalencein largeAAAs (0.9%vs 6.7% [P=.05]; 0.0% vs 5.9% [P =.03]). HLA-A*68 was also lower in large AAA (1.9% vs 11.9%; P =.0075). After Bonferroni correction, however, no difference was demonstrated between small and large aneurysms. Conclusion: This study provides more definitive results on this important subject and has failed to demonstrate the risk association between AAA and these alleles as reported by others. Therefore, the role of these particular genes and the autoinumme component in AAA etiology does not appear to be as crucial as previously proposed.
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页码:475 / 480
页数:6
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