Digestive and Liver Disease
Volume 44, Issue 3 , Pages 201-205, March 2012

Association of SLCO1B1*1b with peptic ulcer amongst Japanese patients taking low-dose aspirin

  • Akiko Shiotani

      Affiliations

    • Department of Internal Medicine, Kawasaki Medical School, Okayama, Japan
    • Corresponding Author InformationCorresponding author at: 577 Matsushima Kurashiki City, Okayama Prefecture 701-0192, Japan. Tel.: +81 86 462 1111; fax: +81 86 464 1195.
  • ,
  • Takahisa Murao

      Affiliations

    • Department of Internal Medicine, Kawasaki Medical School, Okayama, Japan
  • ,
  • Takashi Sakakibara

      Affiliations

    • Department of Gastroenterology, Sakakibara Heart Institute of Okayama, Okayama, Japan
  • ,
  • Ken-ichi Tarumi

      Affiliations

    • Department of Internal Medicine, Kawasaki Medical School, Okayama, Japan
  • ,
  • Noriaki Manabe

      Affiliations

    • Department of Internal Medicine, Kawasaki Medical School, Okayama, Japan
  • ,
  • Tomoari Kamada

      Affiliations

    • Department of Internal Medicine, Kawasaki Medical School, Okayama, Japan
  • ,
  • Hiroaki Kusunoki

      Affiliations

    • Department of Internal Medicine, Kawasaki Medical School, Okayama, Japan
  • ,
  • Ken Haruma

      Affiliations

    • Department of Internal Medicine, Kawasaki Medical School, Okayama, Japan

Received 3 June 2011; accepted 7 October 2011. published online 16 November 2011.

Abstract 

Background

In the recent case–control study, we showed an inverse association between peptic ulcer and angiotensin type 1 receptor (AT1R) blockers (ARBs) or HMG-Co A reductase inhibitors (statins). The aim was to evaluate whether the genotypes of uptake and efflux transporters of ARBs and statins relate to the presence of peptic ulcer and/or ulcer bleeding associated with aspirin use.

Methods

Patients taking 100mg of enteric-coated aspirin for cardiovascular diseases who also participated in endoscopic surveillance were studied. SLCO1B, ABCC2, ABCG2, and MDR1 genotypes were determined by PCR or PCR-RFLP.

Results

492 patients enrolled including 78 with peptic ulcer. The frequencies of the SLCO1B1 521TT genotype were significantly higher in the ulcer group (p=0.006) compared to the controls. After adjustment for significant factors, the SLCO1B1 *1b haplotype was significantly associated with peptic ulcer (OR, 3.64; 95% CI, 1.81–7.29).

Conclusions

SLCO1B1*1b haplotype may identify patients at increased risk for aspirin-induced peptic ulcer.

Keywords: Angiotensin type 1 receptor blockers, Clinical pharmacology, HMG-Co A reductase inhibitors

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PII: S1590-8658(11)00383-5

doi:10.1016/j.dld.2011.10.005

Digestive and Liver Disease
Volume 44, Issue 3 , Pages 201-205, March 2012