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Influence of Lifestyles on Polyp Burden and Cancer Development in Hereditary Colorectal Cancer Syndromes
DC Field | Value | Language |
---|---|---|
dc.contributor.author | 김태일 | - |
dc.contributor.author | 박수정 | - |
dc.contributor.author | 박재준 | - |
dc.contributor.author | 박지수 | - |
dc.contributor.author | 박지혜 | - |
dc.contributor.author | 천재희 | - |
dc.contributor.author | 현혜경 | - |
dc.date.accessioned | 2025-06-27T02:42:37Z | - |
dc.date.available | 2025-06-27T02:42:37Z | - |
dc.date.issued | 2025-02 | - |
dc.identifier.issn | 0815-9319 | - |
dc.identifier.uri | https://ir.ymlib.yonsei.ac.kr/handle/22282913/206034 | - |
dc.description.abstract | Background: Whether the progression of precursor lesions or the occurrence of cancer is influenced by lifestyle factors in carriers of genetic mutations has not been fully investigated, especially in Asian patients of hereditary colorectal cancer (CRC) syndrome. Methods: Patients at a high risk of hereditary CRC were included. For polyposis CRC syndromes, colorectal polyp burden was measured using at least 60 images per colonoscopy in each patient and classified into five stages using the International Society for Gastrointestinal Hereditary Tumours staging system according to the polyp number and size. Increase in tumor burden stage for polyposis CRC syndrome and the occurrence of CRC or any cancer for Lynch syndrome were analyzed according to lifestyle factors. Results: Ninety-six patients with suspected hereditary polyposis CRC syndrome and 106 patients with Lynch syndrome were recruited. For polyposis CRC syndromes, multivariate analysis showed that exposure to smoking and > 100 polyps independently predicted a high risk of increased polyp burden (p = 0.008 and p = 0.012, respectively). Significant genetic mutations or phenotype of polyposis syndromes were significantly associated with an increased polyp burden. For Lynch syndrome, smokers showed to be diagnosed with CRC in younger age than never-smokers (42.2 years vs. 49.0 years; p = 0.021), and heavy drinkers had high risk for occurrence of CRC (HR, 2.381, 95% CI, 1.338-4.236; p = 0.003) and any cancer (HR, 2.254; 95% CI, 1.334-3.806; p = 0.002). Conclusions: The lifestyle factors (smoking and alcohol consumption) were associated with increasing precursor lesions and occurrence of cancer in patients with hereditary CRC syndrome. Lifestyle modifications may reduce the risk of hereditary CRC in carriers. | - |
dc.description.statementOfResponsibility | restriction | - |
dc.language | English | - |
dc.publisher | Blackwell Scientific Publications | - |
dc.relation.isPartOf | JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY | - |
dc.rights | CC BY-NC-ND 2.0 KR | - |
dc.subject.MESH | Adenomatous Polyposis Coli* / genetics | - |
dc.subject.MESH | Adenomatous Polyposis Coli* / pathology | - |
dc.subject.MESH | Adult | - |
dc.subject.MESH | Age Factors | - |
dc.subject.MESH | Aged | - |
dc.subject.MESH | Alcohol Drinking / adverse effects | - |
dc.subject.MESH | Colonic Polyps* / pathology | - |
dc.subject.MESH | Colonoscopy | - |
dc.subject.MESH | Colorectal Neoplasms* / etiology | - |
dc.subject.MESH | Colorectal Neoplasms* / pathology | - |
dc.subject.MESH | Colorectal Neoplasms, Hereditary Nonpolyposis* / etiology | - |
dc.subject.MESH | Colorectal Neoplasms, Hereditary Nonpolyposis* / genetics | - |
dc.subject.MESH | Colorectal Neoplasms, Hereditary Nonpolyposis* / pathology | - |
dc.subject.MESH | Female | - |
dc.subject.MESH | Humans | - |
dc.subject.MESH | Life Style* | - |
dc.subject.MESH | Male | - |
dc.subject.MESH | Middle Aged | - |
dc.subject.MESH | Mutation | - |
dc.subject.MESH | Risk Factors | - |
dc.subject.MESH | Smoking / adverse effects | - |
dc.subject.MESH | Tumor Burden* | - |
dc.title | Influence of Lifestyles on Polyp Burden and Cancer Development in Hereditary Colorectal Cancer Syndromes | - |
dc.type | Article | - |
dc.contributor.college | College of Medicine (의과대학) | - |
dc.contributor.department | Dept. of Internal Medicine (내과학교실) | - |
dc.contributor.googleauthor | Hye Kyung Hyun | - |
dc.contributor.googleauthor | Ji Soo Park | - |
dc.contributor.googleauthor | Jihye Park | - |
dc.contributor.googleauthor | Soo Jung Park | - |
dc.contributor.googleauthor | Jae Jun Park | - |
dc.contributor.googleauthor | Jae Hee Cheon | - |
dc.contributor.googleauthor | Tae Il Kim | - |
dc.identifier.doi | 10.1111/jgh.16833 | - |
dc.contributor.localId | A01079 | - |
dc.contributor.localId | A01539 | - |
dc.contributor.localId | A01636 | - |
dc.contributor.localId | A01686 | - |
dc.contributor.localId | A04575 | - |
dc.contributor.localId | A04030 | - |
dc.contributor.localId | A06135 | - |
dc.relation.journalcode | J01417 | - |
dc.identifier.eissn | 1440-1746 | - |
dc.identifier.pmid | 39582265 | - |
dc.identifier.url | https://onlinelibrary.wiley.com/doi/10.1111/jgh.16833 | - |
dc.subject.keyword | Lynch syndrome | - |
dc.subject.keyword | hereditary colorectal cancer syndrome | - |
dc.subject.keyword | lifestyle | - |
dc.subject.keyword | polyp burden | - |
dc.subject.keyword | polyposis | - |
dc.contributor.alternativeName | Kim, Tae Il | - |
dc.contributor.affiliatedAuthor | 김태일 | - |
dc.contributor.affiliatedAuthor | 박수정 | - |
dc.contributor.affiliatedAuthor | 박재준 | - |
dc.contributor.affiliatedAuthor | 박지수 | - |
dc.contributor.affiliatedAuthor | 박지혜 | - |
dc.contributor.affiliatedAuthor | 천재희 | - |
dc.contributor.affiliatedAuthor | 현혜경 | - |
dc.citation.volume | 40 | - |
dc.citation.number | 2 | - |
dc.citation.startPage | 433 | - |
dc.citation.endPage | 445 | - |
dc.identifier.bibliographicCitation | JOURNAL OF GASTROENTEROLOGY AND HEPATOLOGY, Vol.40(2) : 433-445, 2025-02 | - |
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