4.4 Article

Genome-wide association study suggested copy number variation may be associated with body mass index in the Chinese population

Journal

JOURNAL OF HUMAN GENETICS
Volume 54, Issue 4, Pages 199-202

Publisher

NATURE PUBLISHING GROUP
DOI: 10.1038/jhg.2009.10

Keywords

10q11.22; BMI; copy number variation (CNV); PPYR1

Funding

  1. National Natural Science Foundation of China [30230210, 30771222, 30731160618]
  2. Xi'an Jiaotong University
  3. Ministry of Education of China
  4. Huo Ying Dong Education Foundation, Hunan Province
  5. Hunan Normal University. HWD
  6. Dickson/ Missouri endowment from University of Missouri Kansas City
  7. NIH [R01 AR050496, R21 AG027110, R01 AG026564, P50 AR055081, R21 AA015973]

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Obesity is a major public health problem characterized with high body mass index (BMI). Copy number variations (CNVs) have been identified to be associated with complex human diseases. The effect of CNVs on obesity is unknown. In this study, we explored the association of CNVs with BMI in 597 Chinese Han subjects using Affymetrix GeneChip Human Mapping 500K Array Set. We found that one CNV at 10q11.22 (from 46.36Mb to 46.56 Mb) was associated with BMI (the raw P=0.011). The CNV contributed 1.6% of BMI variation, and it covered one important obesity gene-pancreatic polypeptide receptor 1(PPYR1). It was reported that PPYR1 was a key regulator of energy homeostasis. Our findings suggested that CNV might be potentially important for the BMI variation. In addition, our study suggested that CNV might be used as a genetic marker to locate genes associated with BMI in Chinese population. Journal of Human Genetics (2009) 54, 199-202; doi: 10.1038/jhg.2009.10; published online 20 February 2009

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