Susceptibility to Colorectal Cancer Based on HSD17B4 rs721673 and rs721675 Polymorphisms and Alcohol Intake among Taiwan Biobank Participants: A Retrospective Case Control Study Using the Nationwide Claims Data

Author:

Lin Tzu-Chiao12,Chuang Min-Hua3,Hsiung Chia-Ni45,Chang Pi-Kai2,Sun Chien-An6ORCID,Yang Tsan7,Chou Yu-Ching38ORCID,Hu Je-Ming128,Hsu Chih-Hsiung39ORCID

Affiliation:

1. School of Medicine, National Defense Medical Center, Taipei 114, Taiwan

2. Division of Colorectal Surgery, Department of Surgery, Tri-Service General Hospital, National Defense Medical Center, Taipei 114, Taiwan

3. School of Public Health, National Defense Medical Center, Taipei 114, Taiwan

4. Institute of Molecular Medicine, National Tsing Hua University, Hsinchu 300, Taiwan

5. Data Science Statistical Cooperation Center, Institute of Statistical Science, Academia Sinica, Taipei 114, Taiwan

6. Department of Public Health, College of Medicine, Fu-Jen Catholic University, New Taipei City 242, Taiwan

7. Department of Health Business Administration, Meiho University, Pingtung County 912, Taiwan

8. Graduate Institute of Medical Sciences, National Defense Medical Center, Taipei 114, Taiwan

9. Health Service and Readiness Section, Armed Forces Taoyuan General Hospital, Taoyuan 325, Taiwan

Abstract

Colorectal cancer (CRC) is a major public health issue, and there are limited studies on the association between 17β-hydroxysteroid dehydrogenase type 4 (HSD17B4) polymorphism and CRC. We used two national databases from Taiwan to examine whether HSD17B4 rs721673, rs721675, and alcohol intake were independently and interactively correlated with CRC development. We linked the Taiwan Biobank (TWB) participants’ health and lifestyle information and genotypic data from 2012 to 2018 to the National Health Insurance Database (NHIRD) to confirm their medical records. We performed a genome-wide association study (GWAS) using data from 145 new incident CRC cases and matched 1316 healthy, non-CRC individuals. We calculated the odds ratios (OR) and 95% confidence intervals (CI) for CRC based on multiple logistic regression analyses. HSD17B4 rs721673 and rs721675 on chromosome 5 were significantly and positively correlated with CRC (rs721673 A > G, aOR = 2.62, p = 2.90 × 10−8; rs721675 A > T, aOR = 2.61, p = 1.01 × 10−6). Within the high-risk genotypes, significantly higher ORs were observed among the alcohol intake group. Our results demonstrated that the rs721673 and rs721675 risk genotypes of HSD17B4 might increase the risk of CRC development in Taiwanese adults, especially those with alcohol consumption habits.

Funder

Tri-Service General Hospital

Publisher

MDPI AG

Subject

Medicine (miscellaneous)

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