Title | Cancer Survivorship and Subclinical Myocardial Damage. |
Publication Type | Journal Article |
Year of Publication | 2019 |
Authors | Florido R, Lee AK, McEvoy JW, Hoogeveen RC, Koton S, Vitolins MZ, Shenoy C, Russell SD, Blumenthal RS, Ndumele CE, Ballantyne CM, Joshu CE, Platz EA |
Secondary Authors | Selvin E |
Journal | Am J Epidemiol |
Volume | 188 |
Issue | 12 |
Pagination | 2188-2195 |
Date Published | 2019 12 31 |
ISSN | 1476-6256 |
Keywords | Aged, Aged, 80 and over, Biomarkers, Cancer Survivors, Cardiomyopathies, Cohort Studies, Female, Humans, Male, Troponin T |
Abstract | Cancer survivors might have an excess risk of cardiovascular disease (CVD) resulting from toxicities of cancer therapies and a high burden of CVD risk factors. We sought to evaluate the association of cancer survivorship with subclinical myocardial damage, as assessed by elevated high-sensitivity cardiac troponin T (hs-cTnT) test results. We included 3,512 participants of the Atherosclerosis Risk in Communities Study who attended visit 5 (2011-2013) and were free of CVD (coronary heart disease, heart failure, or stroke). We used multivariate logistic regression to evaluate the cross-sectional associations of survivorship from any, non-sex-related, and sex-related cancers (e.g., breast, prostate) with elevated hs-cTnT (≥14 ng/L). Of 3,512 participants (mean age, 76 years; 62% women; 21% black), 19% were cancer survivors. Cancer survivors had significantly higher odds of elevated hs-cTnT (OR = 1.26, 95% CI: 1.03, 1.53). Results were similar for survivors of non-sex-related and colorectal cancers, but there was no association between survivorship from breast and prostate cancers and elevated hs-cTnT. Results were similar after additional adjustments for CVD risk factors. Survivors of some cancers might be more likely to have elevated hs-cTnT than persons without prior cancer. The excess burden of subclinical myocardial damage in this population might not be fully explained by traditional CVD risk factors. |
DOI | 10.1093/aje/kwz088 |
Alternate Journal | Am J Epidemiol |
PubMed ID | 30927355 |
PubMed Central ID | PMC7212406 |
Grant List | K23 HL122447 / HL / NHLBI NIH HHS / United States P30 CA006973 / CA / NCI NIH HHS / United States R01 DK089174 / DK / NIDDK NIH HHS / United States T32 HL007024 / HL / NHLBI NIH HHS / United States HHSN268201700002C / HL / NHLBI NIH HHS / United States HHSN268201700001I / HL / NHLBI NIH HHS / United States HHSN268201700004C / HL / NHLBI NIH HHS / United States HHSN268201700003I / HL / NHLBI NIH HHS / United States K24 DK106414 / DK / NIDDK NIH HHS / United States HHSN268201700004I / HL / NHLBI NIH HHS / United States HHSN268201700005C / HL / NHLBI NIH HHS / United States HHSN268201700001C / HL / NHLBI NIH HHS / United States HHSN268201700003C / HL / NHLBI NIH HHS / United States HHSN268201700002I / HL / NHLBI NIH HHS / United States HHSN268201700005I / HL / NHLBI NIH HHS / United States R01 HL146907 / HL / NHLBI NIH HHS / United States U01 CA164975 / CA / NCI NIH HHS / United States R01 HL134320 / HL / NHLBI NIH HHS / United States |