Abstract | PURPOSE: METHODS: Clinical data from 60 cases with MYLK pathogenic variants were analyzed (five null and two missense variants), and the effect of missense variants on kinase activity was assessed. RESULTS: Twenty-three individuals (39%) experienced an aortic event (defined as aneurysm repair or dissection); the majority of these events (87%) were aortic dissections. Aortic diameters were minimally enlarged at the time of dissection in many cases. Time-to-aortic-event curves showed that missense pathogenic variant (PV) carriers have earlier-onset aortic events than null PV carriers. An MYLK missense variant segregated with aortic disease over five generations but decreases MYLK kinase acitivity marginally. Functional Assays fail to identify all pathogenic variants in MYLK. CONCLUSION: These data further define the aortic phenotype associated with MYLK pathogenic variants. Given minimal aortic enlargement before dissection, an alternative approach to guide the timing of aortic repair is proposed based on the probability of a dissection at a given age.
|
Authors | Stephanie E Wallace, Ellen S Regalado, Limin Gong, Alexandra L Janda, Dong-Chuan Guo, Claudio F Russo, Richard J Kulmacz, Nadine Hanna, Guillaume Jondeau, Catherine Boileau, Pauline Arnaud, Kwanghyuk Lee, Suzanne M Leal, Matias Hannuksela, Bo Carlberg, Tami Johnston, Christian Antolik, Ellen M Hostetler, Roberto Colombo, Dianna M Milewicz |
Journal | Genetics in medicine : official journal of the American College of Medical Genetics
(Genet Med)
Vol. 21
Issue 1
Pg. 144-151
(01 2019)
ISSN: 1530-0366 [Electronic] United States |
PMID | 29925964
(Publication Type: Journal Article, Research Support, N.I.H., Extramural, Research Support, Non-U.S. Gov't)
|
Chemical References |
- Calcium-Binding Proteins
- MYLK protein, human
- Myosin-Light-Chain Kinase
|
Topics |
- Adult
- Aged
- Aortic Dissection
- Aorta
(pathology, surgery)
- Aortic Diseases
(genetics, pathology, surgery)
- Calcium-Binding Proteins
(genetics)
- Female
- Genetic Testing
- Heterozygote
- High-Throughput Nucleotide Sequencing
- Humans
- Male
- Middle Aged
- Myosin-Light-Chain Kinase
(genetics)
- Pedigree
- Pregnancy
|