A novel locus for dilated cardiomyopathy, diffuse myocardial fibrosis, and sudden death on chromosome 10q25-26
Patrick T Ellinor, Sabine Sasse-Klaassen, Susanne Probst, Brenda Gerull, Jordan T Shin, Andrea Toeppel, Arnd Heuser, Beate Michely, Danita M Yoerger, Bong-Seok Song, Bernhard Pilz, Gregor Krings, Bruce Coplin, Peter E Lange, G William Dec, Hans Christian Hennies, Ludwig Thierfelder, Calum A MacRae, Patrick T Ellinor, Sabine Sasse-Klaassen, Susanne Probst, Brenda Gerull, Jordan T Shin, Andrea Toeppel, Arnd Heuser, Beate Michely, Danita M Yoerger, Bong-Seok Song, Bernhard Pilz, Gregor Krings, Bruce Coplin, Peter E Lange, G William Dec, Hans Christian Hennies, Ludwig Thierfelder, Calum A MacRae
Abstract
Objectives: We sought to identify the genetic locus for an inherited form of dilated cardiomyopathy (DCM) that is characterized by diffuse myocardial fibrosis and sudden death.
Background: Genetic studies have mapped multiple loci for DCM, which is a major cause of nonischemic heart failure; however, the genes responsible for the majority of cases have yet to be identified.
Methods: Sixty-six family members were evaluated by 12-lead electrocardiogram (ECG), echocardiogram, and laboratory studies. Individuals with echocardiographically documented DCM were defined as affected. Subjects were considered unaffected if they were older than 20 years of age, had a normal ECG and echocardiogram, no personal history of heart failure, and had no affected offspring. Genotyping was performed using polymorphic markers.
Results: Genome-wide linkage analysis identified a novel locus for this inherited phenotype on chromosome 10q25.3-q26.13. Peak two-point logarithm of the odds scores >3.0 were obtained independently with each family using the markers D10S1773 and D10S1483, respectively. Haplotype analyses defined a critical interval of 14.0 centiMorgans between D10S1237 and D10S1723, corresponding to a physical distance of 9.5 megabases. Multipoint linkage analyses confirmed this interval and generated a peak logarithm of the odds score of 8.2 indicating odds of >100,000,000:1 in favor of this interval as the location of the gene defect responsible for DCM in these families.
Conclusions: We have mapped a novel locus for cardiomyopathy, diffuse myocardial fibrosis, and sudden death to chromosome 10q25-q26. The identification of the causative gene in this interval will be an important step in understanding the fundamental mechanisms of heart failure and sudden death.
Source: PubMed