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A common missense variant of monocarboxylate transporter 9 (MCT9/SLC16A9) gene is associated with renal overload gout, but not with all gout susceptibility
Authors:Akiyoshi Nakayama  Hirotaka Matsuo  Takuya Shimizu  Hiraku Ogata  Yuzo Takada  Hiroshi Nakashima  Takahiro Nakamura  Seiko Shimizu  Toshinori Chiba  Masayuki Sakiyama  Chisaki Ushiyama  Tappei Takada  Katsuhisa Inoue  Sayo Kawai  Asahi Hishida  Kenji Wakai  Nobuyuki Hamajima  Kimiyoshi Ichida  Yutaka Sakurai  Yukio Kato  Toru Shimizu  Nariyoshi Shinomiya
Institution:1. Department of Integrative Physiology and Bio-Nano Medicine, National Defense Medical College, 3-2 Namiki, Tokorozawa, Saitama, 359-8513, Japan
2. Medical Group, Headquarters, Iwo-to Air Base Group, Japan Air Self-Defense Force, Ogasawara, Japan
3. Faculty of Pharmacy, Institute of Medical, Pharmaceutical and Health Sciences, Kanazawa University, Kanazawa, Japan
4. Laboratory for Biofunctions, The Central Research Institute, National Defense Medical College, Tokorozawa, Japan
5. Department of Preventive Medicine and Public Health, National Defense Medical College, Tokorozawa, Japan
6. Laboratory for Mathematics, National Defense Medical College, Tokorozawa, Japan
7. Department of Biology, Faculty of Science, Toho University, Funabashi, Japan
8. Department of Pharmacy, Faculty of Medicine, The University of Tokyo Hospital, The University of Tokyo, Tokyo, Japan
9. Department of Biopharmaceutics, School of Pharmacy, Tokyo University of Pharmacy and Life Sciences, Tokyo, Japan
10. Department of Preventive Medicine, Nagoya University Graduate School of Medicine, Nagoya, Japan
11. Department of Healthcare Administration, Nagoya University Graduate School of Medicine, Nagoya, Japan
12. Department of Pathophysiology, Tokyo University of Pharmacy and Life Sciences, Tokyo, Japan
13. Midorigaoka Hospital, Takatsuki, Japan
Abstract:Gout is a common disease caused by hyperuricemia, which shows elevated serum uric acid (SUA) levels. From a viewpoint of urate handling in humans, gout patients can be divided into those with renal overload (ROL) gout with intestinal urate underexcretion, and those with renal underexcretion (RUE) gout. Recent genome-wide association studies (GWAS) revealed an association between SUA and a variant in human monocarboxylate transporter 9 (MCT9/SLC16A9) gene. Although the function of MCT9 remains unclear, urate is mostly excreted via intestine and kidney where MCT9 expression is observed. In this study, we investigated the relationship between a variant of MCT9 and gout in 545 patients and 1,115 healthy volunteers. A missense variant of MCT9 (K258T), rs2242206, significantly increased the risk of ROL gout (p = 0.012), with odds ratio (OR) of 1.28, although it revealed no significant association with all gout cases (p = 0.10), non-ROL gout cases (p = 0.83), and RUE gout cases (p = 0.34). In any case groups and the control group, minor allele frequencies of rs2242206 were >0.40. Therefore, rs2242206 is a common missense variant and is revealed to have an association with ROL gout, indicating that rs2242206 relates to decreased intestinal urate excretion rather than decreased renal urate excretion. Our study provides clues to better understand the pathophysiology of gout as well as the physiological roles of MCT9.
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