Abdominal Aortic Aneurysm Research - AAA (Abdominal Aortic Aneurism), Cardiac Disease, Treatment, Symptoms, Surgery

Abdominal Aortic Aneurysm Research Today is a free monthly online journal that collates and summarizes the latest research about Abdominal Aortic Aneurysm, including details on aaa (abdominal aortic aneurism), cardiac disease, treatment, symptoms, surgery.


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Genes involved in the transforming growth factor beta signalling pathway and the risk of intracranial aneurysms.

Ruigrok YM, Tan S, Medic J, Rinkel GJ, Wijmenga C

Department of Neurology, Rudolf Magnus Institute of Neuroscience, University Medical Centre Utrecht, PO Box 85500, 3508 GA Utrecht, The Netherlands. ij.m.ruigrok@umcutrecht.nl

BACKGROUND AND PURPOSE: The 19q13.3 locus for intracranial aneurysms (IA) partly overlaps with the 19q13 locus for abdominal aortic aneurysms (AAA). A common genetic risk factor located in this locus for the two aneurysm types seems plausible. The transforming growth factor beta (TGF-beta) signalling pathway plays a role in aortic aneurysms but may also play a role in aneurysms in general. In the combined region of the 19q13 loci for IA and AAA we identified two candidate genes that are both involved in the TGF-beta signalling pathway: hepsin (HPN) and the latent transforming growth factor beta-binding protein 4 (LTBP4). We hypothesised that single nucleotide polymorphisms (SNP) in the HPN and LTBP4 genes are associated with IA. METHODS: We analyzed all the common variations using tag SNP in the HPN and LTBP4 genes for association with IA in 390 patients and 642 controls in the Dutch population. Six tag SNP in the HPN gene and five tag SNP in the LTBP4 gene were genotyped. RESULTS: No differences in SNP frequency were observed for both the HPN and LTBP4 gene between patients and controls. CONCLUSION: Our findings suggest that variations in or near the HPN and LTBP4 genes do not play a role in the susceptibility to IA in the Dutch population.

Published 19 May 2008 in J Neurol Neurosurg Psychiatry, 79(6): 722-4.
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