지원사업
학술연구/단체지원/교육 등 연구자 활동을 지속하도록 DBpia가 지원하고 있어요.
커뮤니티
연구자들이 자신의 연구와 전문성을 널리 알리고, 새로운 협력의 기회를 만들 수 있는 네트워킹 공간이에요.
논문 기본 정보
- 자료유형
- 학술저널
- 저자정보
- 발행연도
- 2020.7
- 수록면
- 113 - 123 (11page)
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초록· 키워드
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Background: The destruction of circadian rhythms by night shift work affects major circadian genes, which are known to play a role in advancing or killing the cell cycle through tumor suppressor genes. To find out whether night shift work affects the incidence of colorectal cancer, which was found to be associated with long-term night shift work in previous studies, we surveyed effect of night shift work on colorectal polyps that have a higher incidence than colorectal cancer and can progress to colorectal cancer.
Methods: To examine the correlation between rotating night shifts and colorectal polyps, a survey was conducted with 299 men aged 40–60 years from two university hospitals. We examined lifestyle, work history, work patterns, and colonoscopy results. The differences in prevalence among the groups was compared, and prevalence ratio (PR) was calculated via generalized linear modeling.
Results: The prevalence of colorectal polyps in night shift and non-shift workers were 53.0% and 33.5%, respectively. After adjusting for age, smoking status, dietary habits, family history of colorectal cancer, obesity, job type, night shift work (PR: 1.13, 95% CI: 1.02–1.25) was a risk factor of colorectal polyps.
Conclusions: The risk of colorectal polyps was greater in night shift workers than non-shift workers. Also risk of colorectal polyp was higher in older group. Our study investigated colorectal polyp instead of colorectal cancer and lacks information about types and gene mutations of colorectal polyps. Further study is needed to clarify effect of night shift work on development of colorectal cancer.
Methods: To examine the correlation between rotating night shifts and colorectal polyps, a survey was conducted with 299 men aged 40–60 years from two university hospitals. We examined lifestyle, work history, work patterns, and colonoscopy results. The differences in prevalence among the groups was compared, and prevalence ratio (PR) was calculated via generalized linear modeling.
Results: The prevalence of colorectal polyps in night shift and non-shift workers were 53.0% and 33.5%, respectively. After adjusting for age, smoking status, dietary habits, family history of colorectal cancer, obesity, job type, night shift work (PR: 1.13, 95% CI: 1.02–1.25) was a risk factor of colorectal polyps.
Conclusions: The risk of colorectal polyps was greater in night shift workers than non-shift workers. Also risk of colorectal polyp was higher in older group. Our study investigated colorectal polyp instead of colorectal cancer and lacks information about types and gene mutations of colorectal polyps. Further study is needed to clarify effect of night shift work on development of colorectal cancer.
목차
ABSTRACT
METHODS
RESULTS
DISCUSSION
CONCLUSIONS
REFERENCES
참고문헌 (44)
참고문헌 신청
Korea Central Cancer Registry, National Cancer Center / 2020 / Annual report of cancer statistics in Korea in 2017
Ferlay J / Global cancer observatory: cancer today
Schernhammer ES / 2003 / Night-shift work and risk of colorectal cancer in the nurses' health study / J Natl Cancer Inst 95(11):825~828
Papantoniou K / 2018 / Rotating night shift work and colorectal cancer risk in the nurses' health studies / Int J Cancer 143(11):2709~2717
Schernhammer ES / 2004 / Melatonin and cancer risk : does light at night compromise physiologic cancer protection by lowering serum melatonin levels / Br J Cancer 90(5):941~943
Ferlay J / Global cancer observatory: cancer today
Schernhammer ES / 2003 / Night-shift work and risk of colorectal cancer in the nurses' health study / J Natl Cancer Inst 95(11):825~828
Papantoniou K / 2018 / Rotating night shift work and colorectal cancer risk in the nurses' health studies / Int J Cancer 143(11):2709~2717
Schernhammer ES / 2004 / Melatonin and cancer risk : does light at night compromise physiologic cancer protection by lowering serum melatonin levels / Br J Cancer 90(5):941~943
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UCI(KEPA) : I410-ECN-0101-2020-517-001091425