期刊
JOURNAL OF THE AMERICAN HEART ASSOCIATION
卷 4, 期 11, 页码 -出版社
WILEY
DOI: 10.1161/JAHA.115.002645
关键词
cardiomyopathy; cardiovascular genetics; dilated cardiomyopathy; heart failure; missense variants
资金
- National Institutes of Health [UL1 RR025780, UL1 TR001082 N01-HV-48194, R01 HL69071, R01 116906]
- Leducq Foundation [14-CVD 03]
- Fondazione CRTrieste
- Fondazione GENERALI
- [K23 JL067915]
- [R01HL109209]
- [3R01HL109209-01A1S]
- [3R01HL109209-01A1S1]
- [HL062881]
Background-The titin gene (TTN) encodes the largest human protein, which plays a central role in sarcomere organization and passive myocyte stiffness. TTN truncating mutations cause dilated cardiomyopathy (DCM); however, the role of TTN missense variants in DCM has been difficult to elucidate because of the presence of background TTN variation. Methods and Results-A cohort of 147 DCM index subjects underwent DNA sequencing for 313 TTN exons covering the N2B and N2BA cardiac isoforms of TTN. Of the 348 missense variants, we identified 44 severe rare variants by using a bioinformatic filtering process in 37 probands. Of these, 5 probands were double heterozygotes (additional variant in another DCM gene) and 7 were compound heterozygotes (2 TTN severe variants). Segregation analysis allowed the classification of the severe variants into 5 likely (cosegregating), 5 unlikely (noncosegregating), and 34 possibly (where family structure precluded segregation analysis) disease-causing variants. Patients with DCM carrying likely or possibly pathogenic TTN severe variants did not show a different outcome compared with unlikely and noncarriers of a severe TTN variant. However, the likely and possibly disease-causing variants were overrepresented in the C-zone of the A-band region of the sarcomere. Conclusions-TTN missense variants are common and present a challenge for bioinformatic classification, especially when informative families are not available. Although DCM patients carrying bioinformatically severe TTN variants do not appear to have a worse clinical course than noncarriers, the nonrandom distribution of likely and possibly disease-causing variants suggests a potential biological role for some TTN missense variants.
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