Recurrent and founder mutations in the Netherlands: cardiac Troponin I (TNNI3) gene mutations as a cause of severe forms of hypertrophic and restrictive cardiomyopathy

A van den Wijngaard; P Volders; J P Van Tintelen; J D H Jongbloed; M P van den Berg; R H Lekanne Deprez; M M A M Mannens; N Hofmann; M Slegtenhorst; D Dooijes; M Michels; Y Arens; R Jongbloed; B J M Smeets

doi:10.1007/s12471-011-0135-z

Recurrent and founder mutations in the Netherlands: cardiac Troponin I (TNNI3) gene mutations as a cause of severe forms of hypertrophic and restrictive cardiomyopathy

Neth Heart J. 2011 Aug;19(7-8):344-51. doi: 10.1007/s12471-011-0135-z.

Authors

A van den Wijngaard¹, P Volders, J P Van Tintelen, J D H Jongbloed, M P van den Berg, R H Lekanne Deprez, M M A M Mannens, N Hofmann, M Slegtenhorst, D Dooijes, M Michels, Y Arens, R Jongbloed, B J M Smeets

Affiliation

¹ Department of Clinical Genetics, Maastricht University Medical Center, Maastricht, the Netherlands, [email protected].

Abstract

Background: About 2-7% of familial cardiomyopathy cases are caused by a mutation in the gene encoding cardiac troponin I (TNNI3). The related clinical phenotype is usually severe with early onset. Here we report on all currently known mutations in the Dutch population and compared these with those described in literature.

Methods: TheTNNI3 gene was screened for mutations in all coding exons and flanking intronic sequences in a large cohort of cardiomyopathy patients. All Dutch index cases carrying a TNNI3 mutation that are described in this study underwent extensive cardiological evaluation and were listed by their postal codes.

Results: In 30 families, 14 different mutations were identified. Three TNNI3 mutations were found relatively frequently in both familial and non-familial cases of hypertrophic cardiomyopathy (HCM) or restrictive cardiomyopathy (RCM). Haplotype analysis showed that p.Arg145Trp and p.Ser166Phe are founder mutations in the Netherlands, while p.Glu209Ala is not. The majority of Dutch TNNI3 mutations were associated with a HCM phenotype. Mean age at diagnosis was 36.5 years. Mutations causing RCM occurred less frequently, but were identified in very young children with a poor prognosis.

Conclusion: In line with previously published data, we found TNNI3 mutations to be rare and associated with early onset and severe clinical presentation.