The relationship between eating behavior of pediatric obesity and the SNPs of ghrelin gene and ghrelin receptor gene in Japan
Project/Area Number |
24650427
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Research Category |
Grant-in-Aid for Challenging Exploratory Research
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Allocation Type | Multi-year Fund |
Research Field |
Applied health science
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Research Institution | Kyoto Prefectural University of Medicine |
Principal Investigator |
NAKAJIMA Hisakazu 京都府立医科大学, 医学(系)研究科(研究院), 助教 (80363985)
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Research Collaborator |
SUGIMOTO Satoru 京都府立医科大学, 大学院医学研究科, 研修員
KODO Kazuki 京都府立医科大学, 大学院医学研究科
ITOH Ikuyo 京都府立医科大学, 大学院医学研究科
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Project Period (FY) |
2012-04-01 – 2015-03-31
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Project Status |
Completed (Fiscal Year 2014)
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Budget Amount *help |
¥4,030,000 (Direct Cost: ¥3,100,000、Indirect Cost: ¥930,000)
Fiscal Year 2014: ¥650,000 (Direct Cost: ¥500,000、Indirect Cost: ¥150,000)
Fiscal Year 2013: ¥1,040,000 (Direct Cost: ¥800,000、Indirect Cost: ¥240,000)
Fiscal Year 2012: ¥2,340,000 (Direct Cost: ¥1,800,000、Indirect Cost: ¥540,000)
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Keywords | 小児肥満 / グレリン / グレリン受容体 / 遺伝子多型 / 食行動 / グレリンレセプター / エネルギー代謝 / 国際情報交換 |
Outline of Final Research Achievements |
Ghrelin is an important hormone that regulates appetite and eating behavior, and modulates energy metabolism. We performed SNPs analysis of the ghrelin gene (GHRL) and the ghrelin receptor gene (GHSR) and examined its relationship with the childhood obesity in Japan. We recruited and analysed 165 healthy school-aged subjects and 46 obese children from 2010 to 2014. We selected the five SNPs of GHRL: g.-604A>G (rs27647), g.-501C>A (rs26802), g.247C>A(rs696217), g.265A>T (rs4684677), g.62G>T (rs35683), and the three SNPs of GHSR: g.171C>T(rs495225), g.447C>G (rs2232169), g.477G>A (rs572169). The SNPs were genotyped using Taqman SNP Genotyping Assays. The genotype AA of g.-501C>A was associated with the occurrence of pediatric obesity (OR 14.05: 95%Cl 5.76-34.28, p <0.001). We also didn’t identify the relationship between childhood obesity and the 3 SNPs of GHSR. Our study suggested that the GHRL g.-501C>A polymorphism was strongly associated with pediatric obesity in Japan.
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Report
(4 results)
Research Products
(20 results)
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[Presentation] Impaired metabolic compensation in adipose tissues and functional alignment by complemented stem cells in mice with progressive nonalcoholic fatty liver disease2014
Author(s)
Taichiro Nishikawa, Kohichiroh Yasui, Hisakazu Nakajima, Satoru Sugimoto, Ikuyo Itoh, Kazuki Koudou, Tomoki Nakajima, Kanji Yamaguchi, Michihisa Moriguchi, Yosio Sumida, Hironori Mitsuyoshi, Hirohito Minami, Yoshito Itoh
Organizer
The 63th AASLD the liver meeting
Place of Presentation
Boston, USA
Year and Date
2014-11-06 – 2014-11-11
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[Presentation] Miglitol increases energy expenditure by up-regulating uncoupling protein 1(UCP1) of brown adipose tissue (BAT) and reduces obesity in high-fat diet induced obese mice2013
Author(s)
Sigimoto S, Nakajima H, Ito I, Kodo K, Mori J, Matsuo K, Kosaka K, Aoi W, Yoshimoto K, Ikegaya H, Hosoi H
Organizer
第18回アディポサイエンス・シンポジウム
Place of Presentation
豊中市
Related Report
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