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DOI 10.1371/journal.pone.0062330

Медицинская библиотека · PloS one · 2013

TLR-4 and VEGF polymorphisms in chronic periaortitis.

Atzeni Fabiola, Boiardi Luigi, Vaglio Augusto, Nicoli Davide, Farnetti Enrico, Palmisano Alessandra, Pipitone Nicolò, Martorana Davide, Moroni Gabriella, Longhi Selena, Bonatti Francesco, Buzio Carlo, Salvarani Carlo

СтатьяПоддержка исследования: вне правительства СШАПеревод пока не подготовлен

Аннотация

OBJECTIVE

Chronic periaortitis (CP) is a rare disease that is characterised by fibro-inflammatory tissue surrounding the abdominal aorta and has both non-aneurysmal (idiopathic retroperitoneal fibrosis [IRF]) and aneurysmal forms (inflammatory abdominal aortic aneurysm [IAAA]). We investigated whether toll-like receptor 4 (TLR-4) and vascular endothelial growth factor (VEGF) polymorphisms were associated with susceptibility to, and the clinical features of CP.

METHODS

One hundred and two CP patients and 200 healthy controls were molecularly genotyped for TLR-4 gene polymorphism (+896 A/G) (rs4986790), VEGF mutations +936 C/T (rs3025039) and -634 C/G (rs2010963), and an 18 base pair (bp) insertion/deletion (I/D) polymorphism at -2549 of the VEGF promoter region. The patients were grouped on the basis of the type of CP (IRF or IAAA), and the presence or absence of established atherosclerotic disease (ischemic heart disease, cerebrovascular disease, and peripheral arterial disease).

RESULTS

There were no significant differences in the distribution of the studied polymorphisms between the patients and controls. However, carriage of the +936 T allele was significantly more frequent in the patients with IRF than in those with IAAA (26.5% vs 5.3%; p = 0.046; OR 6.49 [95% CI 0.82-51.54]). There were significantly more carriers of the I allele among the patients with ureteral obstruction (83.8% vs 58.8%; p = 0.006; OR 3.63 [95% CI 1.42-9.28]) and those who received conservative treatment (48.5% vs 23.5%; p = 0.015; OR 3.06 [95% CI 1.22-7.721]) than among those without, and II homozygosity was significantly more frequent in the patients with deep vein thrombosis than in those without (30.4% vs 11.7%, p = 0.031; OR 3.31 [95% CI 1.07-10.21]).

CONCLUSION

The VEGF +936 C/T polymorphism may be associated with an increased risk of developing the non-aneurysmal IRF form of CP. Carriers of the I allele and II homozygosity are respectively at increased risk of developing ureteral obstruction and deep vein thrombosis.

Для цитирования: Atzeni Fabiola, Boiardi Luigi, Vaglio Augusto, Nicoli Davide, Farnetti Enrico, Palmisano Alessandra, Pipitone Nicolò, Martorana Davide, Moroni Gabriella, Longhi Selena, Bonatti Francesco, Buzio Carlo, Salvarani Carlo. TLR-4 and VEGF polymorphisms in chronic periaortitis.. PloS one. 2013. DOI: 10.1371/journal.pone.0062330.

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