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Lamin A/C-Related Cardiac Disease Late Onset With a Variable and Mild Phenotype in a Large Cohort of Patients With the Lamin A/C p.(Arg331Gln) Founder Mutation
- Source :
- Circulation. Cardiovascular Genetics, 10, 4, pp. UNSP e001631-UNSP e001631, Circulation-Cardiovascular Genetics, 10(4):001631. LIPPINCOTT WILLIAMS & WILKINS, Circulation-Cardiovascular genetics, 10(4). Lippincott Williams and Wilkins, Circulation. Cardiovascular Genetics, 10, UNSP e001631-UNSP e001631, Circulation : Cardiovascular Genetics, 10(4):001631. LIPPINCOTT WILLIAMS & WILKINS, Circulation-cardiovascular genetics, 10(4):e001631. Lippincott Williams and Wilkins, Hoorntje, E T, Bollen, I A, Barge-Schaapveld, D Q, van Tienen, F H J, te Meerman, G J, Jansweijer, J A, van Essen, A J, Volders, P G, Constantinescu, A A, van den Akker, P C, van Spaendonck-Zwarts, K Y, Oldenburg, R A, Marcelis, C L, van der Smagt, J J, Hennekam, E A, Vink, A, Bootsma, M, Aten, E, Wilde, A A M, van den Wijngaard, A, Broers, J L, Jongbloed, J D, van der Velden, J, van den Berg, M P & van Tintelen, J P 2017, ' Lamin A/C-Related Cardiac Disease Late Onset With a Variable and Mild Phenotype in a Large Cohort of Patients With the Lamin A/C p.(Arg331Gln) Founder Mutation ', Circulation-cardiovascular genetics, vol. 10, no. 4, e001631 . https://doi.org/10.1161/CIRCGENETICS.116.001631, Circulation. Cardiovascular genetics, 10(4):e001631. Lippincott Williams and Wilkins, Circulation: Cardiovascular Genetics, 10(4), Circulation-cardiovascular genetics, 10(4):UNSP e001631. Lippincott Williams & Wilkins
- Publication Year :
- 2017
-
Abstract
- Background— Interpretation of missense variants can be especially difficult when the variant is also found in control populations. This is what we encountered for the LMNA c.992G>A (p.(Arg331Gln)) variant. Therefore, to evaluate the effect of this variant, we combined an evaluation of clinical data with functional experiments and morphological studies. Methods and Results— Clinical data of 23 probands and 35 family members carrying this variant were retrospectively collected. A time-to-event analysis was performed to compare the course of the disease with carriers of other LMNA mutations. Myocardial biopsies were studied with electron microscopy and by measuring force development of the sarcomeres. Morphology of the nuclear envelope was assessed with immunofluorescence on cultured fibroblasts. The phenotype in probands and family members was characterized by atrioventricular conduction disturbances (61% and 44%, respectively), supraventricular arrhythmias (69% and 52%, respectively), and dilated cardiomyopathy (74% and 14%, respectively). LMNA p.(Arg331Gln) carriers had a significantly better outcome regarding the composite end point (malignant ventricular arrhythmias, end-stage heart failure, or death) compared with carriers of other pathogenic LMNA mutations. A shared haplotype of 1 Mb around LMNA suggested a common founder. The combined logarithm of the odds score was 3.46. Force development in membrane-permeabilized cardiomyocytes was reduced because of decreased myofibril density. Structural nuclear LMNA -associated envelope abnormalities, that is, blebs, were confirmed by electron microscopy and immunofluorescence microscopy. Conclusions— Clinical, morphological, functional, haplotype, and segregation data all indicate that LMNA p.(Arg331Gln) is a pathogenic founder mutation with a phenotype reminiscent of other LMNA mutations but with a more benign course.
- Subjects :
- RIGHT-VENTRICULAR CARDIOMYOPATHY
MISSENSE MUTATIONS
0301 basic medicine
Pathology
medicine.medical_specialty
congenital, hereditary, and neonatal diseases and abnormalities
lipodystrophy
cardiomyopathy, dilated
Cardiomyopathy
030204 cardiovascular system & hematology
Gene mutation
Biology
Sudden death
survival
324 UNRELATED PATIENTS
LMNA
03 medical and health sciences
SUDDEN-DEATH
0302 clinical medicine
ATRIOVENTRICULAR-BLOCK
Idiopathic dilated cardiomyopathy
atrioventricular block
Genetics
medicine
Journal Article
Missense mutation
atrial fibrillation
SCN5A
Genetics (clinical)
integumentary system
Haplotype
medicine.disease
HIGH-RISK
030104 developmental biology
IDIOPATHIC DILATED CARDIOMYOPATHY
Cardiology and Cardiovascular Medicine
LMNA CAUSES
cardiomyopathy
dilated
GENE-MUTATIONS
Lamin
Rare cancers Radboud Institute for Health Sciences [Radboudumc 9]
Subjects
Details
- Language :
- English
- ISSN :
- 1942325X and 19423268
- Volume :
- 10
- Issue :
- 4
- Database :
- OpenAIRE
- Journal :
- Circulation-cardiovascular genetics
- Accession number :
- edsair.doi.dedup.....1f58eef0be6d324744d52cdf66058e46
- Full Text :
- https://doi.org/10.1161/circgenetics.116.001631