期刊论文详细信息
JACC-CARDIOVASCULAR IMAGING 卷:8
Assessment of the Radiation Effects of Cardiac CT Angiography Using Protein and Genetic Biomarkers
Article
Nguyen, Patricia K.1,2,3  Lee, Won Hee1,3  Li, Yong Fuga4  Hong, Wan Xing1,3  Hu, Shijun1,3  Chan, Charles5  Liang, Grace1  Nguyen, Ivy1  Ong, Sang-Ging1,3  Churko, Jared1,3  Wang, Jia6  Altman, Russ B.4  Fleischmann, Dominik1,7  Wu, Joseph C.1,3,7 
[1] Stanford Univ, Stanford Cardiovasc Inst, Sch Med, Stanford, CA 94305 USA
[2] Vet Adm Palo Alto, Palo Alto, CA USA
[3] Stanford Univ, Dept Med, Div Cardiol, Sch Med, Stanford, CA 94305 USA
[4] Stanford Univ, Dept Genet, Sch Med, Stanford, CA 94305 USA
[5] Stanford Univ, Dept Surg, Sch Med, Stanford, CA 94305 USA
[6] Stanford Univ, Environm Hlth & Safety, Sch Med, Stanford, CA 94305 USA
[7] Stanford Univ, Dept Radiol, Sch Med, Stanford, CA 94305 USA
关键词: CT/MRI;    gene expression;    gene regulation;    imaging;   
DOI  :  10.1016/j.jcmg.2015.04.016
来源: Elsevier
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【 摘 要 】

OBJECTIVES The purpose of this study was to evaluate whether radiation exposure from cardiac computed tomographic angiography (CIA) is associated with deoxyribonucleic acid (DNA) damage and whether damage leads to programmed cell death and activation of genes involved in apoptosis and DNA repair. BACKGROUND Exposure to radiation from medical imaging has become a public health concern, but whether it causes significant cell damage remains unclear. METHODS We conducted a prospective cohort study in 67 patients undergoing cardiac CIA between January 2012 and December 2013 in 2 U.S. medical centers. Median blood radiation exposure was estimated using phantom dosimetry. Biomarkers of DNA damage and apoptosis were measured by flow cytometry, whole genome sequencing, and single cell polymerase chain reaction. RESULTS The median dose length product was 1,535.3 mGy.cm (969.7 to 2,674.0 mGy.cm). The median radiation dose to the blood was 29.8 mSv (18.8 to 48.8 mSv). Median DNA damage increased 3.39% (1.29% to 8.04%, p < 0.0001) and median apoptosis increased 3.1-fold (interquartile range [IQR]: 1.4- to 5.1-fold, p < 0.0001) post-radiation. Whole genome sequencing revealed changes in the expression of 39 transcription factors involved in the regulation of apoptosis, cell cycle, and DNA repair. Genes involved in mediating apoptosis and DNA repair were significantly changed post-radiation, including DDB2 (1.9-fold [IQR: 1.5- to 3.0-fold], p < 0.001), XRCC4 (3.0-fold [IQR: 1.1- to 5.4-fold], p = 0.005), and BAX (1.6-fold [IQR: 0.9- to 2.6-fold], p < 0.001). Exposure to radiation was associated with DNA damage (odds ratio [OR]: 1.8 [1.2 to 2.6], p = 0.003). DNA damage was associated with apoptosis (OR: 1.9 [1.2 to 5.1], p < 0.0001) and gene activation (OR: 2.8 [1.2 to 6.2], p = 0.002). CONCLUSIONS Patients exposed to >7.5 mSv of radiation from cardiac CIA had evidence of DNA damage, which was associated with programmed cell death and activation of genes involved in apoptosis and DNA repair. (C) 2015 by the American College of Cardiology Foundation.

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