Genetic Studies of Hypertrophic Cardiomyopathy in Singaporeans Identify Variants in TNNI3 and TNNT2 That Are Common in Chinese Patients

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Pua, Chee Jian ^{[1, 2]} ; Tham, Nevin ^[2] ; Chin, Calvin W. L. ^{[2, 3]} ; Walsh, Roddy ^[4] ; Khor, Chiea Chuen ^[5] ; Toepfer, Christopher N. ^{[6, 7]} ; Repetti, Giuliana G. ^[6] ; Garfinkel, Amanda C. ^[6] ; Ewoldt, Jourdan F. ^[8] ; Cloonan, Paige ^[8] ; Chen, Christopher S. ^[8] ; Lim, Shi Qi ^[2] ; Cai, Jiashen ^[3] ; Loo, Li Yang ^[1] ; Kong, Siew Ching ^[2] ; Chiang, Charleston W. K. ^{[9, 10]} ; Whiffin, Nicola ^{[11, 12]} ; de Marvao, Antonio ^{[11, 12]} ; Lio, Pei Min ^[2] ; Hii, An An ^[2] ; Yang, Cheng Xi ^[2] ; Le, Thu Thao ^[2] ; Bylstra, Yasmin ^[13] ; Lim, Weng Khong ^[13] ; Teo, Jing Xian ^[13] ; Padilha, Kallyandra ^{[6, 14]} ; Silva, Gabriela V. ^{[6, 14]} ; Pan, Bangfen ^[15] ; Govind, Risha ^{[11, 12]} ; Buchan, Rachel J. ^{[11, 12]} ; Barton, Paul J. R. ^{[11, 12]} ; Tan, Patrick ^{[5, 13]} ; Foo, Roger ^{[5, 15]} ; Yip, James W. L. ^[16] ; Wong, Raymond C. C. ^[16] ; Chan, Wan Xian ^[16] ; Pereira, Alexandre C. ^{[6, 14]} ; Tang, Hak Chiaw ^[2] ; Jamuar, Saumya Shekhar ^{[17, 3, 13, 18]} ; Ware, James S. ^{[11, 12]} ; Seidman, Jonathan G. ^[6] ; Seidman, Christine E. ^{[6, 19]} ; Cook, Stuart A. ^{[11, 2, 3, 12]}

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^[1] Natl Univ Singapore, Yong Loo Lin Sch Med, Singapore - Singapore

^[2] Natl Heart Ctr Singapore, Singapore - Singapore

^[3] Duke Natl Univ Singapore, Med Sch, Singapore - Singapore

^[4] Univ Amsterdam, Amsterdam UMC, Amsterdam Cardiovasc Sci, Dept Clin & Expt Cardiol, Heart Ctr, Amsterdam - Netherlands

^[5] Genome Inst Singapore, Singapore - Singapore

^[6] Harvard Med Sch, Dept Genet, Boston, MA 02115 - USA

^[7] Univ Oxford, Radcliffe Dept Med, Oxford - England

^[8] Boston Univ, Dept Biomed Engn, Boston, MA 02215 - USA

^[9] Univ Calif Los Angeles, Ctr Neurobehav Genet, Los Angeles, CA - USA

^[10] Univ Southern Calif, Ctr Genet Epidemiol, Los Angeles, CA 90007 - USA

^[11] Imperial Coll London, Natl Heart & Lung Inst, London - England

^[12] Royal Brompton Hosp, Cardiovasc Res Ctr, London - England

^[13] SingHlth Duke NUS Precis Med Inst, Singapore - Singapore

^[14] Univ Sao Paulo, Med Sch, Heart Inst Incor, Lab Genet & Mol Cardiol, Sao Paulo - Brazil

^[15] Natl Univ Hlth Syst, Cardiovasc Res Inst, Singapore - Singapore

^[16] Natl Univ Heart Ctr, Cardiol Dept, Singapore - Singapore

^[17] KK Womens & Childrens Hosp, Singapore - Singapore

^[18] SingHlth Duke NUS Genom Med Ctr, Singapore - Singapore

^[19] Brigham & Womens Hosp, Howard Hughes Med Inst, Cardiovasc Div, Boston, MA 02115 - USA

• Tipo de documento: Artigo Científico
• Fonte: CIRCULATION-GENOMIC AND PRECISION MEDICINE; v. 13, n. 5, p. 424-434, OCT 2020.
• Citações Web of Science: 1

Resumo

Background: To assess the genetic architecture of hypertrophic cardiomyopathy (HCM) in patients of predominantly Chinese ancestry. Methods: We sequenced HCM disease genes in Singaporean patients (n=224) and Singaporean controls (n=3634), compared findings with additional populations and White HCM cohorts (n=6179), and performed in vitro functional studies. Results: Singaporean HCM patients had significantly fewer confidently interpreted HCM disease variants (pathogenic/likely pathogenic: 18%, P<0.0001) but an excess of variants of uncertain significance (24%, P<0.0001), as compared to Whites (pathogenic/likely pathogenic: 31%, excess of variants of uncertain significance: 7%). Two missense variants in thin filament encoding genes were commonly seen in Singaporean HCM (TNNI3:p.R79C, disease allele frequency {[}AF]=0.018; TNNT2:p.R286H, disease AF=0.022) and are enriched in Singaporean HCM when compared with Asian controls (TNNI3:p.R79C, Singaporean controls AF=0.0055, P=0.0057, genome aggregation database-East Asian AF=0.0062, P=0.0086; TNNT2:p.R286H, Singaporean controls AF=0.0017, P<0.0001, genome aggregation database-East Asian AF=0.0009, P<0.0001). Both these variants have conflicting annotations in ClinVar and are of low penetrance (TNNI3:p.R79C, 0.7%; TNNT2:p.R286H, 2.7%) but are predicted to be deleterious by computational tools. In population controls, TNNI3:p.R79C carriers had significantly thicker left ventricular walls compared with noncarriers while its etiological fraction is limited (0.70 {[}95% CI, 0.35-0.86]) and thus TNNI3:p.R79C is considered variant of uncertain significance. Mutant TNNT2:p.R286H iPSC-CMs (induced pluripotent stem cells derived cardiomyocytes) show hypercontractility, increased metabolic requirements, and cellular hypertrophy and the etiological fraction (0.93 {[}95% CI, 0.83-0.97]) support the likely pathogenicity of TNNT2:p.R286H. Conclusions: As compared with Whites, Chinese HCM patients commonly have low penetrance risk alleles in TNNT2 or TNNI3 but exhibit few clinically actionable HCM variants overall. This highlights the need for greater study of HCM genetics in non-White populations. (AU)

• Processo FAPESP: 19/11821-1 - Construção de uma biblioteca de phage display de epítopos de Trypanosoma cruzi para identificação de um perfil de anticorpos em cardiomiopatia chagásica crônica
• Beneficiário: Gabriela Venturini da Silva
• Modalidade de apoio: Bolsas no Exterior - Estágio de Pesquisa - Pós-Doutorado