Mapping a locus for familial thoracic aortic aneurysms and dissections (TAAD2) to 3p24-25.

TitleMapping a locus for familial thoracic aortic aneurysms and dissections (TAAD2) to 3p24-25.
Publication TypeJournal Article
Year of Publication2003
AuthorsHasham, SN, Willing, MC, Guo, D-chuan, Muilenburg, A, He, R, Tran, VT, Scherer, SE, Shete, SS, Milewicz, DM
Date Published2003 Jul 01
KeywordsAdolescent, Adult, Aortic Aneurysm, Thoracic, Aortic Dissection, Calcium-Binding Proteins, Child, Chromosome Mapping, Chromosomes, Human, Pair 3, Comorbidity, DNA Mutational Analysis, Echocardiography, Extracellular Matrix Proteins, Female, Genes, Dominant, Genetic Linkage, Genetic Markers, Genotype, Germany, Haplotypes, Humans, Lod Score, Male, Marfan Syndrome, Middle Aged, Pedigree, Penetrance, Switzerland

BACKGROUND: Familial thoracic aortic aneurysms and dissections (TAAD) occur as part of known syndromes such as Marfan syndrome but can also be inherited in families in an autosomal dominant manner as an isolated condition. Previous studies have mapped genes causing nonsyndromic familial TAAD to 5q13-15 (TAAD1) and 11q23.2-q24 (FAA1). Further genetic heterogeneity for the condition was evident by the presence of TAAD in some families not linked to these known loci.METHODS AND RESULTS: A 4-generation family with dominant mode of inheritance of TAAD was studied. Affected status was determined by dilation of the ascending aorta, surgical repair of an aneurysm or dissection, or death as the result of aortic dissection. None of the family members evaluated met the diagnostic criteria for Marfan syndrome. After exclusion of known loci for familial TAAD, a genome-wide scan was carried out to map the defective gene causing the disease in the family. A locus was mapped to a 25-cM region on 3p24-25 with a maximum multipoint logarithm of the odds score of 4.28.CONCLUSIONS: A third locus for nonsyndromic TAAD was mapped to 3p24-25 and termed the TAAD2 locus. This locus overlaps a previously mapped second locus for Marfan syndrome, termed the MFS2 locus. Future characterization of the TAAD2 gene will determine if TAAD2 is allelic to MFS2. In addition, identification of the TAAD2 gene will improve the presymptomatic diagnosis of individuals with this life-threatening genetic syndrome and provide information concerning the pathogenesis of the disease.

Alternate JournalCirculation
PubMed ID12821554
Grant ListM01RR02558 / RR / NCRR NIH HHS / United States
R01 HL62594 / HL / NHLBI NIH HHS / United States

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