Publication

High yield of LMNA mutations in patients with dilated cardiomyopathy and/or conduction disease referred to cardiogenetics outpatient clinics

van Tintelen, J. P., Hofstra, R. M. W., Katerberg, H., Rossenbacker, T., Wiesfeld, A. C. P., Sarvaas, G. J. D. M., Wilde, A. A. M., van Langen, I. M., Nannenberg, E. A., van der Kooi, A. J., Kraak, M., van Gelder, I. C., van Veldhuisen, D. J., Vos, Y. & van den Berg, M. P., Dec-2007, In : American Heart Journal. 154, 6, p. 1130-1139 10 p., ARTN 1130-9.

Research output: Contribution to journalArticleAcademicpeer-review

Background Among the most frequently encountered mutations in dilated cardiomyopathy (DCM) are those in the lamin A/C (LMNA) gene. Our goal was to analyze the LMNA gene in patients with DCM and/or conduction disease referred to the cardiogenetics outpatient clinic and to evaluate the prevalence of LMNA mutations and their clinical expression.

Methods and Results The LMNA gene was screened in 61 index patients. Eleven mutations (including 6 novel) were identified, mainly in the subgroup of familial DCM with cardiac conduction disease (3/10 index patients) and in patients with DCM and Emery-Dreifuss, Limb-Girdle, or unclassified forms of muscular dystrophy (7/8 index patients). In addition, a mutation was identified in 1 of 4 families with only cardiac conduction disease. We did not identify any large deletions or duplications.Genotype-phenotype relationships revealed a high rate of sudden death and cardiac transplants in carriers of the p.N 195K mutation. Our study confirmed that the p.R225X mutation leads to cardiac conduction disease with late or no development of DCM, underscoring the importance of this mutation in putative familial "lone conduction disease." Nearly one third of LMNA mutation carriers had experienced a thromboembolic event.

Conclusions This study highlights the role of LMNA mutations in DCM and related disorders. A severe phenotype in p.N 195K mutation carriers and preferential cardiac conduction disease in p.R225X carriers was encountered. Because of the clinical variability, including the development of associated symptoms in time, LMNA screening should be considered in patients with DCM or familial lone conduction disease.

Original languageEnglish
Article numberARTN 1130-9
Pages (from-to)1130-1139
Number of pages10
JournalAmerican Heart Journal
Volume154
Issue number6
Publication statusPublished - Dec-2007

    Keywords

  • LAMIN-A/C GENE, DREIFUSS MUSCULAR-DYSTROPHY, SYSTEM DISEASE, MISSENSE MUTATIONS, NATURAL-HISTORY, SUDDEN-DEATH, IDENTIFICATION, PHENOTYPE, FAMILIES, SPECTRUM

ID: 4650178