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The Persistence of Hypertriglyceridemia and the Risk of Early Onset Colorectal Cancer According to Tumor Subsites: A Nationwide Population-Based Study

Authors
 Young Hoon Chang  ;  Cheol Min Shin  ;  Kyungdo Han  ;  Jin Hyung Jung  ;  Eun Hyo Jin  ;  Joo Hyun Lim  ;  Seung Joo Kang  ;  Yoon Jin Choi  ;  Hyuk Yoon  ;  Young Soo Park  ;  Nayoung Kim  ;  Dong Ho Lee 
Citation
 CANCER RESEARCH AND TREATMENT, Vol.56(3) : 825-837, 2024-07 
Journal Title
CANCER RESEARCH AND TREATMENT
ISSN
 1598-2998 
Issue Date
2024-07
MeSH
Adult ; Age of Onset ; Cohort Studies ; Colorectal Neoplasms* / blood ; Colorectal Neoplasms* / epidemiology ; Colorectal Neoplasms* / etiology ; Female ; Follow-Up Studies ; Humans ; Hypertriglyceridemia* / complications ; Hypertriglyceridemia* / epidemiology ; Incidence ; Male ; Middle Aged ; Republic of Korea / epidemiology ; Risk Factors ; Triglycerides / blood ; Young Adult
Keywords
Colorectal neoplasms ; Hypertriglyceridemia ; Young-adult
Abstract
Purpose: The incidence of early-onset colorectal cancer (EoCRC) is increasing worldwide. The association between hypertriglyceridemia (HTG) and EoCRC risk remains unclear.

Materials and methods: We conducted a nationwide cohort study of 3,340,635 individuals aged 20-49 years who underwent health checkups between 2009 and 2011 under the Korean National Health Insurance Service. HTG was defined as serum triglyceride (TG) level ≥ 150 mg/dL. According to the change in TG status, participants were categorized into persistent normotriglyceridemia (NTG; group 1), NTG to HTG (group 2), HTG to NTG (group 3), and persistent HTG (group 4) groups. The EoCRC incidence was followed up until 2019.

Results: In total, 7,492 EoCRC cases developed after a mean of 6.05 years of follow-up. Group 4 had the highest risk of EoCRC (adjusted hazard ratio [aHR], 1.097; 95% confidence interval [CI], 1.025 to 1.174). While the risk of rectal cancer was significantly increased in groups 3 and 4 (aHR [95% CI], 1.236 [1.076 to 1.419] and 1.175 [1.042-1.325], respectively), no significant risk differences were observed in right colon cancer. In group 4, male sex and diabetes were associated with a further increased risk of EoCRC (aHR [95% CI], 1.149 [1.082 to 1.221] and 1.409 [1.169 to 1.699], respectively). In addition, there was a dose-response relationship between serum TG levels and the risk of EoCRC (p for trends < 0.0001).

Conclusion: Persistent HTG increased the risk of EoCRC, which was significantly higher only for rectal cancer and marginally higher for other colonic subsites.
Files in This Item:
T992024481.pdf Download
DOI
10.4143/crt.2023.753
Appears in Collections:
1. College of Medicine (의과대학) > Dept. of Internal Medicine (내과학교실) > 1. Journal Papers
Yonsei Authors
Choi, Yoon Jin(최윤진)
URI
https://ir.ymlib.yonsei.ac.kr/handle/22282913/202151
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