[1]
|
(2019) Dilated Cardiomyopathy. Nature Reviews Disease Primers, 5, Article No. 33.
https://doi.org/10.1038/s41572-019-0088-x
|
[2]
|
中华医学会心血管病学分会, 中国心肌炎心肌病协作组. 中国扩张型心肌病诊断和治疗指南[J]. 临床心血管病杂志, 2018, 34(5): 421-434.
|
[3]
|
Lakdawala, N.-K., Winterfield, J.-R. and Funke, B.-H. (2013) Dilated Cardiomyopathy. Circulation: Arrhythmia and Electrophysiology, 6, 228-237. https://doi.org/10.1161/CIRCEP.111.962050
|
[4]
|
Weintraub, R.-G., Semsarian, C. and Macdonald, P. (2017) Di-lated Cardiomyopathy. The Lancet, 390, 400-414.
https://doi.org/10.1016/S0140-6736(16)31713-5
|
[5]
|
Ito, M. and Nomura, S. (2018) Cardiomyopathy with LMNA Mutation. International Heart Journal, 59, 462-464.
https://doi.org/10.1536/ihj.18-214
|
[6]
|
Yamada, T. and Nomura, S. (2021) Recent Findings Related to Cardiomy-opathy and Genetics. International Journal of Molecular Sciences, 22, 12522. https://doi.org/10.3390/ijms222212522
|
[7]
|
McNally, E.-M. and Mestroni, L. (2017) Dilated Cardiomyopathy. Circulation Research, 121, 731-748.
https://doi.org/10.1161/CIRCRESAHA.116.309396
|
[8]
|
Millat, G., Bouvagnet, P., Chevalier, P., et al. (2011) Clinical and Mutational Spectrum in a Cohort of 105 Unrelated Patients with Dilated Cardiomyopathy. European Journal of Medical Genetics, 54, e570-e575.
https://doi.org/10.1016/j.ejmg.2011.07.005
|
[9]
|
Verdonschot, J.A.J., Hazebroek, M.-R., Krapels, I.P.C., et al. (2020) Implications of Genetic Testing in Dilated Cardiomyopathy. Circulation: Genomic and Precision Medicine, 13, 476-487.
https://doi.org/10.1161/CIRCGEN.120.003031
|
[10]
|
Hershberger, R.-E., Hedges, D.-J. and Morales, A. (2013) Dilated Cardiomyopathy: The Complexity of a Diverse Genetic Architecture. Nature Reviews Cardiology, 10, 531-547. https://doi.org/10.1038/nrcardio.2013.105
|
[11]
|
Jordan, E., Peterson, L., Ai, T., et al. (2021) Evidence-Based As-sessment of Genes in Dilated Cardiomyopathy. Circulation, 144, 7-19. https://doi.org/10.1161/CIRCULATIONAHA.120.053033
|
[12]
|
Bang, M.-L., Centner, T., Fornoff, F., et al. (2001) The Complete Gene Sequence of Titin, Expression of an Unusual ≈700-kDa Titin Isoform, and Its Interaction with Ob-scurin Identify a Novel Z-Line to I-Band Linking System. Circulation Research, 89, 1065-1072. https://doi.org/10.1161/hh2301.100981
|
[13]
|
The Organization of Titin Filaments in the Half-Sarcomere Revealed by Monoclonal Antibodies in Immunoelectron Microscopy: A Map of Ten Nonrepetitive Epitopes Starting at the Z Line Extends Close to the M Line.
|
[14]
|
Labeit, S. and Kolmerer, B. (1995) Titins: Giant Proteins in Charge of Muscle Ultra-structure and Elasticity. Science, 270, 293-296. https://doi.org/10.1126/science.270.5234.293
|
[15]
|
Knöll, R., Hoshi-jima, M., Hoffman, H.-M., et al. (2002) The Cardiac Mechanical Stretch Sensor Machinery Involves a Z Disc Complex that Is Defective in a Subset of Human Dilated Cardiomyopathy. Cell, 111, 943-955.
https://doi.org/10.1016/S0092-8674(02)01226-6
|
[16]
|
Roberts, A.-M., Ware, J.-S., Herman, D.-S., et al. (2015) Integrated Allelic, Transcriptional, and Phenomic Dissection of the Cardiac Effects of Titin Truncations in Health and Disease. Science Translational Medicine, 7, 270r-276r.
|
[17]
|
Fatkin, D. and Huttner, I.-G. (2017) Titin-Truncating Muta-tions in Dilated Cardiomyopathy. Current Opinion in Cardiology, 32, 232-238. https://doi.org/10.1097/HCO.0000000000000382
|
[18]
|
Franaszczyk, M., Chmielewski, P., Truszkowska, G., et al. (2017) Titin Truncating Variants in Dilated Cardiomyopathy—Prevalence and Genotype-Phenotype Correlations. PLOS ONE, 12, e169007.
https://doi.org/10.1371/journal.pone.0169007
|
[19]
|
Bione, S., Small, K., Aksmanovic, V.-M., et al. (1995) Identifi-cation of New Mutations in the Emery-Dreifuss Muscular Dystrophy Gene and Evidence for Genetic Heterogeneity of the Disease. Human Molecular Genetics, 4, 1859-1863.
https://doi.org/10.1093/hmg/4.10.1859
|
[20]
|
Lu, J.-T., Muchir, A., Nagy, P.-L., et al. (2011) Cardiomyopathy: Cell Biology and Genetics Meet Clinical Medicine. Disease Models & Mechanisms, 4, 562-568. https://doi.org/10.1242/dmm.006346
|
[21]
|
Captur, G., Arbustini, E., Bonne, G., et al. (2018) Lamin and the Heart. Heart, 104, 468-479.
https://doi.org/10.1136/heartjnl-2017-312338
|
[22]
|
Kumar, S., Baldinger, S.-H., Gandjbakhch, E., et al. (2016) Long-Term Arrhythmic and Nonarrhythmic Outcomes of Lamin A/C Mutation Carriers. Journal of the American College of Cardiology, 68, 2299-2307.
https://doi.org/10.1016/j.jacc.2016.08.058
|
[23]
|
Peters, S., Kumar, S., Elliott, P., et al. (2019) Arrhythmic Geno-types in Familial Dilated Cardiomyopathy: Implications for Genetic Testing and Clinical Management. Heart, Lung and Circulation, 28, 31-38.
https://doi.org/10.1016/j.hlc.2018.09.010
|
[24]
|
Donnaloja, F., Carnevali, F., Jacchetti, E., et al. (2020) Lamin A/C Mechanotransduction in Laminopathies. Cells, 9, 1306. https://doi.org/10.3390/cells9051306
|
[25]
|
Malashicheva, A. and Perepelina, K. (2021) Diversity of Nuclear Lamin A/C Action as a Key to Tissue-Specific Regulation of Cellular Identity in Health and Disease. Frontiers in Cell and Developmental Biology, 9, Article ID: 761469.
https://doi.org/10.3389/fcell.2021.761469
|
[26]
|
Martino, F., Perestrelo, A.-R., Vinarský, V., et al. (2018) Cellular Mechanotransduction: From Tension to Function. Frontiers in Physiology, 9, 824. https://doi.org/10.3389/fphys.2018.00824
|
[27]
|
Melcer, S. and Meshorer, E. (2010) The Silence of the LADs: Dy-namic Genome-Lamina Interactions during ESC Differentiation. Cell Stem Cell, 6, 495-497. https://doi.org/10.1016/j.stem.2010.05.006
|
[28]
|
Parker, F., Baboolal, T.-G. and Peckham, M. (2020) Actin Muta-tions and Their Role in Disease. International Journal of Molecular Sciences, 21, 3371. https://doi.org/10.3390/ijms21093371
|
[29]
|
Olson, T.-M., Michels, V.-V., Thibodeau, S.-N., et al. (1998) Actin Mutations in Dilated Cardiomyopathy, a Heritable Form of Heart Failure. Science, 280, 750-752. https://doi.org/10.1126/science.280.5364.750
|
[30]
|
Kaski, J.-P., Syrris, P., Burch, M., et al. (2008) Idiopathic Re-strictive Cardiomyopathy in Children Is Caused by Mutations in Cardiac Sarcomere Protein Genes. Heart, 94, 1478-1484. https://doi.org/10.1136/hrt.2007.134684
|
[31]
|
Ito, K., Patel, P.-N., Gorham, J.-M., et al. (2017) Identification of Pathogenic Gene Mutations in LMNA and MYBPC3 That Alter RNA Splicing. Proceedings of the National Academy of Sciences, 114, 7689-7694.
https://doi.org/10.1073/pnas.1707741114
|
[32]
|
Stelzer, J.-E., Dunning, S.-B. and Moss, R.-L. (2006) Ablation of Cardiac Myosin-Binding Protein-C Accelerates Stretch Activation in Murine Skinned Myocardium. Circulation Research, 98, 1212-1218.
https://doi.org/10.1161/01.RES.0000219863.94390.ce
|
[33]
|
Pohlmann, L., Kroger, I., Vignier, N., et al. (2007) Cardiac Myosin-Binding Protein C Is Required for Complete Relaxation in Intact Myocytes. Circulation Research, 101, 928-938. https://doi.org/10.1161/CIRCRESAHA.107.158774
|
[34]
|
Jaenicke, T., Diederich, K.-W., Haas, W., et al. (1990) The Complete Sequence of the Human β-Myosin Heavy Chain Gene and a Comparative Analysis of Its Product. Genomics, 8, 194-206.
https://doi.org/10.1016/0888-7543(90)90272-V
|
[35]
|
Rani, D.-S., Vijaya, K.-A., Nallari, P., et al. (2022) Novel Mutations in Beta-MYH7 Gene in Indian Patients with Dilated Cardiomyopathy. CJC Open, 4, 1-11. https://doi.org/10.1016/j.cjco.2021.07.020
|
[36]
|
Lillioja, S., Mott, D.-M., Spraul, M., et al. (1993) Insulin Re-sistance and Insulin Secretory Dysfunction as Precursors of Non-Insulin-Dependent Diabetes Mellitus. Prospective Studies of Pima Indians. The New England Journal of Medicine, 329, 1988-1992. https://doi.org/10.1056/NEJM199312303292703
|
[37]
|
Farza, H., Townsend, P.-J., Carrier, L., et al. (1998) Ge-nomic Organisation, Alternative Splicing and Polymorphisms of the Human Cardiac Troponin T Gene. Journal of Mo-lecular and Cellular Cardiology, 30, 1247-1253.
https://doi.org/10.1006/jmcc.1998.0698
|
[38]
|
Jáchymová, M., Muravská, A., Paleček, T., et al. (2012) Genetic Var-iation Screening of TNNT2 Gene in a Cohort of Patients with Hypertrophic and Dilated Cardiomyopathy. Physiological Research, 61, 169-175.
https://doi.org/10.33549/physiolres.932157
|
[39]
|
Seidman, J.-G. and Christine, S. (2001) The Genetic Basis for Cardiomyopathy: From Mutation Identification to Mechanistic Paradigms. Cell, 104, 557-567. https://doi.org/10.1016/S0092-8674(01)00242-2
|
[40]
|
Lapidos, K.-A., Kakkar, R. and McNally, E.-M. (2004) The Dystrophin Glycoprotein Complex. Circulation Research, 94, 1023-1031. https://doi.org/10.1161/01.RES.0000126574.61061.25
|
[41]
|
Yoshida, T., Pan, Y., Hanada, H., et al. (1998) Bidi-rectional Signaling between Sarcoglycans and the Integrin Adhesion System in Cultured L6 Myocytes. The Journal of Biological Chemistry, 273, 1583-1590.
https://doi.org/10.1074/jbc.273.3.1583
|
[42]
|
Yoshida, M., Hama, H., Ishikawa-Sakurai, M., et al. (2000) Biochem-ical Evidence for Association of Dystrobrevin with the Sarcoglycan-Sarcospan Complex as a Basis for Understanding Sarcoglycanopathy. Human Molecular Genetics, 9, 1033-1040. https://doi.org/10.1093/hmg/9.7.1033
|
[43]
|
Zatz, M., de Paula Flavia, S.A., et al. (2003) The 10 Autosomal Recessive Limb-Girdle Muscular Dystrophies. Neuromuscular Disorders, 13, 532-544. https://doi.org/10.1016/S0960-8966(03)00100-7
|
[44]
|
Sandonà, D. and Betto, R. (2009) Sarcoglycanopathies: Molecular Pathogenesis and Therapeutic Prospects. Expert Reviews in Molecular Medicine, 11, e28. https://doi.org/10.1017/S1462399409001203
|
[45]
|
Rkk Inen, S.K., Miettinen, R., Tuomainen, P., et al. (2003) A Novel Mutation, Arg71Thr, in the δ-Sarcoglycan Gene Is Associated with Dilated Cardiomyopathy. Journal of Molecu-lar Medicine, 81, 795-800.
https://doi.org/10.1007/s00109-003-0480-5
|
[46]
|
Politano, L., Nigro, V., Passamano, L., et al. (2001) Evaluation of Cardiac and Respiratory Involvement in Sarcoglycanopathies. Neuromuscular Disorders, 11, 178-185. https://doi.org/10.1016/S0960-8966(00)00174-7
|
[47]
|
扬翼, 谢利剑, 肖婷婷, 等. 限制型心肌病患儿致病基因检测1例报告[J]. 临床儿科杂志, 2021, 39(1): 65-68, 73.
|
[48]
|
Murphy, R.-T., Mogensen, J., Shaw, A., et al. (2004) Novel Mutation in Cardiac Troponin I in Recessive Idiopathic Dilated Cardiomyopathy. The Lancet, 363, 371-372. https://doi.org/10.1016/S0140-6736(04)15468-8
|
[49]
|
Sheng, J.-J. and Jin, J.-P. (2016) TNNI1, TNNI2 and TNNI3: Evolution, Regulation, and Protein Structure-Function Relationships. Gene, 576, 385-394. https://doi.org/10.1016/j.gene.2015.10.052
|
[50]
|
Govindaraj, P., Rani, B., Sundaravadivel, P., et al. (2019) Mito-chondrial Genome Variations in Idiopathic Dilated Cardiomyopathy. Mitochondrion, 48, 51-59. https://doi.org/10.1016/j.mito.2019.03.003
|
[51]
|
Hoffman, E.-P., Brown, R.H. and Kunkel, L.-M. (1987) Dystro-phin: The Protein Product of the Duchenne Muscular Dystrophy Locus. Cell, 51, 919-928. https://doi.org/10.1016/0092-8674(87)90579-4
|
[52]
|
Kamdar, F. and Garry, D.-J. (2016) Dystrophin-Deficient Cardiomyopathy. Journal of the American College of Cardiology, 67, 2533-2546. https://doi.org/10.1016/j.jacc.2016.02.081
|
[53]
|
Towbin, J.-A., Hejtmancik, J.-F., Brink, P., et al. (1993) X-Linked Dilated Cardiomyopathy. Molecular Genetic Evidence of Linkage to the Duchenne Muscular Dystrophy (Dystrophin) Gene at the Xp21 Locus. Circulation, 87, 1854-1865.
https://doi.org/10.1161/01.CIR.87.6.1854
|