Multiple mutations in desmosomal proteins encoding genes in arrhythmogenic right ventricular cardiomyopathy/dysplasia

作者：Bauce Barbara; Nava Andrea; Beffagna Giorgia; Basso Cristina; Lorenzon Alessandra; Smaniotto Gessica; De Bortoli Marzia; Rigato Ilaria; Mazzotti Elisa; Steriotis Alexandros; Marra Martina Perazzolo; Towbin Jeffry A; Thiene Gaetano; Danieli Gian Antonio; Rampazzo Alessandra^*

来源：Heart Rhythm, 2010, 7(1): 22-29.

DOI：10.1016/j.hrthm.2009.09.070

• Arrhythmia
• Arrhythmogenic cardiomyopathy
• Sudden death
• Cell adhesion molecules
• Gene mutations
• Compound genotypes

BACKGROUND Arrhythmogenic right ventricular cardiomyopathy/dysplasia (ARVC/D) is a progressive cardiomyopathy showing a wide clinical spectrum in terms of clinical expressions and prognoses.
OBJECTIVE This study sought to estimate the occurrence of compound and double heterozygotes for mutations in desmosomal proteins encoding genes in a cohort of ARVC/D Italian index cases, and to assess the clinical phenotype of mutations carriers.
METHODS Fourty-two consecutive ARVC/D index cases who fulfilled the International Task Force diagnostic criteria were screened for mutations in PKP2, DSP, DSG2, DSC2, and JUP genes by denaturing high-performance liquid chromatography (DHPLC) and direct sequencing.
RESULTS Three probands (7.1%) showing a family history of sudden death carried multiple mutations. Family screening identified an additional 7 multiple-mutation carriers. Among the 7 double heterozygotes for mutations in different genes, 2 were clinically unaffected, 2 were affected, and 3 showed some clinical signs of ARVC/D even if they did not fulfill the diagnostic criteria. Two compound heterozygotes for mutations in the same gene and 1 subject carrying 3 different mutations showed a severe form of the disease with heart failure onset at a young age. Moreover, multiple-mutation carriers showed a higher prevalence of left ventricular involvement (P = .025) than single-mutation carriers.
CONCLUSION Occurrence of compound and double heterozygotes in ARVC/D index cases is particularly relevant to mutation screening strategy and to genetic counseling. Even if multiple-mutation carriers show a wide variability in clinical expression, the extent of the disease is higher compared to that in single-mutation carriers.

• 出版日期2010-1