Breast Cancer Clinical Trial of Chemotherapy and Trastuzumab: Potential Tool to Identify Cardiac Modifying Variants of Dilated Cardiomyopathy

• Published in: Journal of cardiovascular development and disease Vol. 4; no. 2; p. 6
• Main Authors: Serie, Daniel J, Crook, Julia E, Necela, Brian M, Axenfeld, Bianca C, Dockter, Travis J, Colon-Otero, Gerardo, Perez, Edith A, Thompson, E Aubrey, Norton, Nadine
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI 04.05.2017; MDPI AG
• Subjects: breast cancer; dilated cardiomyopathy; doxorubicin; GWAS; LVEF; modifying variants; OBSCN; trastuzumab; trastuzumab; GWAS; OBSCN; LVEF; breast cancer; doxorubicin; modifying variants; dilated cardiomyopathy
• ISSN: 2308-3425; 2308-3425
• DOI: 10.3390/jcdd4020006

Doxorubicin and the ERBB2 targeted therapy, trastuzumab, are routinely used in the treatment of HER2+ breast cancer. In mouse models, doxorubicin is known to cause cardiomyopathy and conditional cardiac knock out of Erbb2 results in dilated cardiomyopathy and increased sensitivity to doxorubicin-induced cell death. In humans, these drugs also result in cardiac phenotypes, but severity and reversibility is highly variable. We examined the association of decline in left ventricular ejection fraction (LVEF) at 15,204 single nucleotide polymorphisms (SNPs) spanning 72 cardiomyopathy genes, in 800 breast cancer patients who received doxorubicin and trastuzumab. For 7033 common SNPs (minor allele frequency (MAF) > 0.01) we performed single marker linear regression. For all SNPs, we performed gene-based testing with SNP-set (Sequence) Kernel Association Tests: SKAT, SKAT-O and SKAT-common/rare under rare variant non-burden; rare variant optimized burden and non-burden tests; and a combination of rare and common variants respectively. Single marker analyses identified seven missense variants in ( = 0.0045-0.0009, MAF = 0.18-0.50) and two in (both = 0.04, MAF = 0.22). Gene-based rare variant analyses, SKAT and SKAT-O, performed very similarly ( , , , , , and , = 0.042-0.006). Gene-based tests of rare/common variants were significant at the nominal 5% level for as well as , , , , and ( = 0.044-0.008). Our results suggest that rare and common variants in , as well as in other genes, could have modifying effects in cardiomyopathy.