Mr. Takiguchi : Do adult patients and pediatric patients differ with regard to radiation exposure risks in CT examinations?
Prof. Awai : It is very difficult to perform epidemiological studies on radiation exposure. For example, to investigate the effects of a 50-mGy dose, it would be necessary to conduct a long-term follow-up study with a population of approximately 80,000 people. And for a 25-mGy dose, a population study of approximately 320,000 people would be needed.7) For this reason, it is almost impossible to find any report on this topic. However, in 2012, the world was stunned when the results of a study involving a 23-year follow-up of approximately 180,000 pediatric and young adult cases were presented.8) The study showed that the risk of developing leukemia or brain tumors was slightly increased in pediatric patients who underwent CT scanning. The study was critically analyzed and carefully reviewed from various standpoints, including the validity of subject selection in the study as well as the interpretation of the data. The repeat analysis of the data still supported the findings of that study.9) Although the validity of the study has been analyzed in many subsequent studies, with some supporting the findings and others not supporting the findings, a large number of recent analyses appear to validate the study findings. To my knowledge, there have not been such epidemiological studies involving adults since.
Mr. Takiguchi : Lately, DNA damage associated with radiation exposure has been the focus of such studies.
Prof. Awai : In cooperation with Professor Satoshi Tashiro at the Research Institute for Radiation Biology and Medicine of Hiroshima University, we are currently conducting a study to investigate damage to lymphocytes by obtaining data before and after CT scanning. Radiation exposure has a variety of effects on DNA. The most severe effect is a double-stranded DNA break. When a double-stranded DNA break occurs, a histone protein called γH2AX is released, so we employed γH2AX as a biomarker for assessing DNA damage. The results of an in-vitro study showed that some DNA damage induced by CT scanning is repaired within a few days.10) However, during the repair process, errors such as gene translocations or the formation of dicentric chromosomes may occur. The accumulation of such errors due to multiple damage-inducing events may lead to the development of cancer.
Mr. Takiguchi : Does the degree of damage correspond to the intensity of radiation?
Prof. Awai : The findings of the in-vitro study showed a direct relationship between the exposure dose in CT scanning and the amount of γH2AX released.10) Therefore, our research team decided to investigate the differences in the rates of double-stranded DNA breaks and chromosomal abnormalities between low-dose scanning and standard-dose scanning. This study included patients who were referred to the department of thoracic surgery at our hospital and gave informed consent to participate. The patients were divided into two groups, and CT scanning was performed. The results for low-dose CT did not show any effects on the DNA, but the results for standard-dose CT showed that the rates of double-stranded DNA breaks and chromosomal abnormalities were increased.11) The median exposure dose for low-dose CT was 1.5 mSv, while that for standard-dose CT was 5.0 mSv. This suggests that the effects of radiation on DNA and chromosomes would be minimized if the exposure dose for standard-dose CT could be reduced to 1.5 mSv. Therefore, in the future, we look forward to CT systems being developed that can provide high-precision images at an exposure dose as low as 1.5 mSv.
Mr. Takiguchi : We still have a long way to go before we can perform all CT examinations at an exposure dose of 1.5 mSv, but this information provides us with a clear development goal.