Impact of PSCA Polymorphisms on the Risk of Duodenal Ulcer
Background: While duodenal ulcer (DU) and gastric cancer (GC) are both H. pylori infection-related diseases, individuals with DU are known to have lower risk for GC. Many epidemiological studies have identified the PSCA rs2294008 T-allele as a risk factor of GC, while others have found an associatio...
Main Authors: | , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , |
---|---|
Format: | Article |
Language: | English |
Published: |
Japan Epidemiological Association
2021-01-01
|
Series: | Journal of Epidemiology |
Subjects: | |
Online Access: | https://www.jstage.jst.go.jp/article/jea/31/1/31_JE20190184/_pdf |
id |
doaj-422bf0d7f6d74fc8b8682493bb814618 |
---|---|
record_format |
Article |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Yoshiaki Usui Keitaro Matsuo Isao Oze Tomotaka Ugai Yuriko Koyanagi Yoshinobu Maeda Hidemi Ito Asahi Hishida Kenji Takeuchi Takashi Tamura Mineko Tsukamoto Yuka Kadomatsu Megumi Hara Yuichiro Nishida Ippei Shimoshikiryo Toshiro Takezaki Etsuko Ozaki Daisuke Matsui Isao Watanabe Sadao Suzuki Miki Watanabe Hiroko Nakagawa-Senda Haruo Mikami Yohko Nakamura Kokichi Arisawa Hirokazu Uemura Kiyonori Kuriki Naoyuki Takashima Aya Kadota Hiroaki Ikezaki Masayuki Murata Masahiro Nakatochi Yukihide Momozawa Michiaki Kubo Kenji Wakai |
spellingShingle |
Yoshiaki Usui Keitaro Matsuo Isao Oze Tomotaka Ugai Yuriko Koyanagi Yoshinobu Maeda Hidemi Ito Asahi Hishida Kenji Takeuchi Takashi Tamura Mineko Tsukamoto Yuka Kadomatsu Megumi Hara Yuichiro Nishida Ippei Shimoshikiryo Toshiro Takezaki Etsuko Ozaki Daisuke Matsui Isao Watanabe Sadao Suzuki Miki Watanabe Hiroko Nakagawa-Senda Haruo Mikami Yohko Nakamura Kokichi Arisawa Hirokazu Uemura Kiyonori Kuriki Naoyuki Takashima Aya Kadota Hiroaki Ikezaki Masayuki Murata Masahiro Nakatochi Yukihide Momozawa Michiaki Kubo Kenji Wakai Impact of PSCA Polymorphisms on the Risk of Duodenal Ulcer Journal of Epidemiology psca duodenal ulcer cross-sectional study japan |
author_facet |
Yoshiaki Usui Keitaro Matsuo Isao Oze Tomotaka Ugai Yuriko Koyanagi Yoshinobu Maeda Hidemi Ito Asahi Hishida Kenji Takeuchi Takashi Tamura Mineko Tsukamoto Yuka Kadomatsu Megumi Hara Yuichiro Nishida Ippei Shimoshikiryo Toshiro Takezaki Etsuko Ozaki Daisuke Matsui Isao Watanabe Sadao Suzuki Miki Watanabe Hiroko Nakagawa-Senda Haruo Mikami Yohko Nakamura Kokichi Arisawa Hirokazu Uemura Kiyonori Kuriki Naoyuki Takashima Aya Kadota Hiroaki Ikezaki Masayuki Murata Masahiro Nakatochi Yukihide Momozawa Michiaki Kubo Kenji Wakai |
author_sort |
Yoshiaki Usui |
title |
Impact of PSCA Polymorphisms on the Risk of Duodenal Ulcer |
title_short |
Impact of PSCA Polymorphisms on the Risk of Duodenal Ulcer |
title_full |
Impact of PSCA Polymorphisms on the Risk of Duodenal Ulcer |
title_fullStr |
Impact of PSCA Polymorphisms on the Risk of Duodenal Ulcer |
title_full_unstemmed |
Impact of PSCA Polymorphisms on the Risk of Duodenal Ulcer |
title_sort |
impact of psca polymorphisms on the risk of duodenal ulcer |
publisher |
Japan Epidemiological Association |
series |
Journal of Epidemiology |
issn |
0917-5040 1349-9092 |
publishDate |
2021-01-01 |
description |
Background: While duodenal ulcer (DU) and gastric cancer (GC) are both H. pylori infection-related diseases, individuals with DU are known to have lower risk for GC. Many epidemiological studies have identified the PSCA rs2294008 T-allele as a risk factor of GC, while others have found an association between the rs2294008 C-allele and risk of DU and gastric ulcer (GU). Following these initial reports, however, few studies have since validated these associations. Here, we aimed to validate the association between variations in PSCA and the risk of DU/GU and evaluate its interaction with environmental factors in a Japanese population. Methods: Six PSCA SNPs were genotyped in 584 DU cases, 925 GU cases, and 8,105 controls from the Japan Multi-Institutional Collaborative Cohort (J-MICC). Unconditional logistic regression models were applied to estimate odds ratios (ORs) and 95% confidence intervals (CIs) for the association between the SNPs and risk of DU/GU. Results: PSCA rs2294008 C-allele was associated with per allele OR of 1.34 (95% CI, 1.18–1.51; P = 2.28 × 10−6) for the risk of DU. This association was independent of age, sex, study site, smoking habit, drinking habit, and H. pylori status. On the other hand, we did not observe an association between the risk of GU and PSCA SNPs. Conclusions: Our study confirms an association between the PSCA rs2294008 C-allele and the risk of DU in a Japanese population. |
topic |
psca duodenal ulcer cross-sectional study japan |
url |
https://www.jstage.jst.go.jp/article/jea/31/1/31_JE20190184/_pdf |
work_keys_str_mv |
AT yoshiakiusui impactofpscapolymorphismsontheriskofduodenalulcer AT keitaromatsuo impactofpscapolymorphismsontheriskofduodenalulcer AT isaooze impactofpscapolymorphismsontheriskofduodenalulcer AT tomotakaugai impactofpscapolymorphismsontheriskofduodenalulcer AT yurikokoyanagi impactofpscapolymorphismsontheriskofduodenalulcer AT yoshinobumaeda impactofpscapolymorphismsontheriskofduodenalulcer AT hidemiito impactofpscapolymorphismsontheriskofduodenalulcer AT asahihishida impactofpscapolymorphismsontheriskofduodenalulcer AT kenjitakeuchi impactofpscapolymorphismsontheriskofduodenalulcer AT takashitamura impactofpscapolymorphismsontheriskofduodenalulcer AT minekotsukamoto impactofpscapolymorphismsontheriskofduodenalulcer AT yukakadomatsu impactofpscapolymorphismsontheriskofduodenalulcer AT megumihara impactofpscapolymorphismsontheriskofduodenalulcer AT yuichironishida impactofpscapolymorphismsontheriskofduodenalulcer AT ippeishimoshikiryo impactofpscapolymorphismsontheriskofduodenalulcer AT toshirotakezaki impactofpscapolymorphismsontheriskofduodenalulcer AT etsukoozaki impactofpscapolymorphismsontheriskofduodenalulcer AT daisukematsui impactofpscapolymorphismsontheriskofduodenalulcer AT isaowatanabe impactofpscapolymorphismsontheriskofduodenalulcer AT sadaosuzuki impactofpscapolymorphismsontheriskofduodenalulcer AT mikiwatanabe impactofpscapolymorphismsontheriskofduodenalulcer AT hirokonakagawasenda impactofpscapolymorphismsontheriskofduodenalulcer AT haruomikami impactofpscapolymorphismsontheriskofduodenalulcer AT yohkonakamura impactofpscapolymorphismsontheriskofduodenalulcer AT kokichiarisawa impactofpscapolymorphismsontheriskofduodenalulcer AT hirokazuuemura impactofpscapolymorphismsontheriskofduodenalulcer AT kiyonorikuriki impactofpscapolymorphismsontheriskofduodenalulcer AT naoyukitakashima impactofpscapolymorphismsontheriskofduodenalulcer AT ayakadota impactofpscapolymorphismsontheriskofduodenalulcer AT hiroakiikezaki impactofpscapolymorphismsontheriskofduodenalulcer AT masayukimurata impactofpscapolymorphismsontheriskofduodenalulcer AT masahironakatochi impactofpscapolymorphismsontheriskofduodenalulcer AT yukihidemomozawa impactofpscapolymorphismsontheriskofduodenalulcer AT michiakikubo impactofpscapolymorphismsontheriskofduodenalulcer AT kenjiwakai impactofpscapolymorphismsontheriskofduodenalulcer |
_version_ |
1724348529721212928 |
spelling |
doaj-422bf0d7f6d74fc8b8682493bb8146182021-01-05T06:31:04ZengJapan Epidemiological AssociationJournal of Epidemiology0917-50401349-90922021-01-01311122010.2188/jea.JE20190184Impact of PSCA Polymorphisms on the Risk of Duodenal UlcerYoshiaki Usui0Keitaro Matsuo1Isao Oze2Tomotaka Ugai3Yuriko Koyanagi4Yoshinobu Maeda5Hidemi Ito6Asahi Hishida7Kenji Takeuchi8Takashi Tamura9Mineko Tsukamoto10Yuka Kadomatsu11Megumi Hara12Yuichiro Nishida13Ippei Shimoshikiryo14Toshiro Takezaki15Etsuko Ozaki16Daisuke Matsui17Isao Watanabe18Sadao Suzuki19Miki Watanabe20Hiroko Nakagawa-Senda21Haruo Mikami22Yohko Nakamura23Kokichi Arisawa24Hirokazu Uemura25Kiyonori Kuriki26Naoyuki Takashima27Aya Kadota28Hiroaki Ikezaki29Masayuki Murata30Masahiro Nakatochi31Yukihide Momozawa32Michiaki Kubo33Kenji Wakai34Division of Cancer Information and Control, Department of Preventive Medicine, Aichi Cancer Center, Nagoya, JapanDivision of Cancer Epidemiology and Prevention, Department of Preventive Medicine, Aichi Cancer Center, Nagoya, JapanDivision of Cancer Epidemiology and Prevention, Department of Preventive Medicine, Aichi Cancer Center, Nagoya, JapanDivision of Cancer Epidemiology and Prevention, Department of Preventive Medicine, Aichi Cancer Center, Nagoya, JapanDivision of Cancer Information and Control, Department of Preventive Medicine, Aichi Cancer Center, Nagoya, JapanDepartment of Hematology and Oncology, Okayama University Graduate School of Medicine, Dentistry and Pharmaceuticals Sciences, Okayama, JapanDivision of Cancer Information and Control, Department of Preventive Medicine, Aichi Cancer Center, Nagoya, JapanDepartment of Preventive Medicine, Nagoya University Graduate School of Medicine, Nagoya, JapanDepartment of Preventive Medicine, Nagoya University Graduate School of Medicine, Nagoya, JapanDepartment of Preventive Medicine, Nagoya University Graduate School of Medicine, Nagoya, JapanDepartment of Preventive Medicine, Nagoya University Graduate School of Medicine, Nagoya, JapanDepartment of Preventive Medicine, Nagoya University Graduate School of Medicine, Nagoya, JapanDepartment of Preventive Medicine, Faculty of Medicine, Saga University, Saga, JapanDepartment of Preventive Medicine, Faculty of Medicine, Saga University, Saga, JapanDepartment of International Island and Community Medicine, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, JapanDepartment of International Island and Community Medicine, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima, JapanDepartment of Epidemiology for Community Health and Medicine Kyoto Prefectural University of Medicine, Kyoto, JapanDepartment of Epidemiology for Community Health and Medicine Kyoto Prefectural University of Medicine, Kyoto, JapanDepartment of Epidemiology for Community Health and Medicine Kyoto Prefectural University of Medicine, Kyoto, JapanDepartment of Public Health, Nagoya City University Graduate School of Medical Sciences, Nagoya, JapanDepartment of Public Health, Nagoya City University Graduate School of Medical Sciences, Nagoya, JapanDepartment of Public Health, Nagoya City University Graduate School of Medical Sciences, Nagoya, JapanCancer Prevention Center, Chiba Cancer Center Research Institute, Chiba, JapanCancer Prevention Center, Chiba Cancer Center Research Institute, Chiba, JapanDepartment of Preventive Medicine, Institute of Biomedical Sciences, Tokushima University Graduate School, Tokushima, JapanDepartment of Preventive Medicine, Institute of Biomedical Sciences, Tokushima University Graduate School, Tokushima, JapanLaboratory of Public Health, University of Shizuoka, Shizuoka, JapanDepartment of Public Health, Faculty of Medicine, Kindai University, Osaka, JapanDepartment of Public Health, Shiga University of Medical Science, Otsu, JapanDepartment of General Internal Medicine, Kyushu University Hospital, Fukuoka, JapanDepartment of General Internal Medicine, Kyushu University Hospital, Fukuoka, JapanDepartment of Nursing, Nagoya University Graduate School of Medicine, Nagoya, JapanLaboratory for Genotyping Development, RIKEN Center for Integrative Medical Sciences, Yokohama, JapanLaboratory for Genotyping Development, RIKEN Center for Integrative Medical Sciences, Yokohama, JapanDepartment of Preventive Medicine, Nagoya University Graduate School of Medicine, Nagoya, JapanBackground: While duodenal ulcer (DU) and gastric cancer (GC) are both H. pylori infection-related diseases, individuals with DU are known to have lower risk for GC. Many epidemiological studies have identified the PSCA rs2294008 T-allele as a risk factor of GC, while others have found an association between the rs2294008 C-allele and risk of DU and gastric ulcer (GU). Following these initial reports, however, few studies have since validated these associations. Here, we aimed to validate the association between variations in PSCA and the risk of DU/GU and evaluate its interaction with environmental factors in a Japanese population. Methods: Six PSCA SNPs were genotyped in 584 DU cases, 925 GU cases, and 8,105 controls from the Japan Multi-Institutional Collaborative Cohort (J-MICC). Unconditional logistic regression models were applied to estimate odds ratios (ORs) and 95% confidence intervals (CIs) for the association between the SNPs and risk of DU/GU. Results: PSCA rs2294008 C-allele was associated with per allele OR of 1.34 (95% CI, 1.18–1.51; P = 2.28 × 10−6) for the risk of DU. This association was independent of age, sex, study site, smoking habit, drinking habit, and H. pylori status. On the other hand, we did not observe an association between the risk of GU and PSCA SNPs. Conclusions: Our study confirms an association between the PSCA rs2294008 C-allele and the risk of DU in a Japanese population.https://www.jstage.jst.go.jp/article/jea/31/1/31_JE20190184/_pdfpscaduodenal ulcercross-sectional studyjapan |