Abstract
BACKGROUND: The GH secretagogue receptor type 1a gene (GHSR) encodes the cognate receptor of ghrelin, a gut hormone that regulates food intake and pituitary GH secretion. Previous studies in U.S. families and a German population suggested GHSR to be a candidate quantitative locus for association with human obesity and growth.
AIM: The aim of the study was to test common genetic variation in GHSR for association with body size in children and adults.
METHODS: Sequencing was performed to systematically identify novel single nucleotide polymorphisms (SNPs) in GHSR. A set of three haplotype-tagging SNPs that captured all the genetic variation in GHSR was identified. These three haplotype-tagging SNPs were then genotyped in three large population-based U.K. cohort studies (two adult and one childhood cohort) comprising 5807 adults and 843 children.
RESULTS: No significant genotype or haplotype associations were found with adult or childhood height, weight, or body mass index.
CONCLUSION: Common variation in GHSR is not associated with body size in U.K. adults or children.
Original language | English |
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Pages (from-to) | 4158-4161 |
Number of pages | 4 |
Journal | Journal of Clinical Endocrinology and Metabolism |
Volume | 93 |
Issue number | 10 |
DOIs | |
Publication status | Published - Oct 2008 |
Keywords
- Adult
- Aged
- Body Size/genetics
- Child
- Child, Preschool
- Cohort Studies
- DNA Mutational Analysis
- Female
- Gene Frequency
- Genotype
- Humans
- Infant
- Linkage Disequilibrium
- Male
- Middle Aged
- Polymorphism, Single Nucleotide
- Receptors, Ghrelin/genetics
- United Kingdom