Genome-wide scan for serum ghrelin detects linkage on chromosome 1p36 in Hispanic children: Results from the Viva La Familia study

V. Saroja Voruganti, Harald H.H. Göring, Vincent P. Diego, Guowen Cai, Nitesh R. Mehta, Karin Haack, Shelley A. Cole, Nancy F. Butte, Anthony G. Comuzzie

Research output: Contribution to journalArticlepeer-review

16 Scopus citations

Abstract

This study was conducted to investigate genetic influence on serum ghrelin and its relationship with adiposity-related phenotypes in Hispanic children (n = 1030) from the Viva La Familia study (VFS). Anthropometric measurements and levels of serum ghrelin were estimated and genetic analyses conducted according to standard procedures. Mean age, body mass index (BMI), and serum ghrelin were 11 ± 0.13 y, 25 ± 0.24 kg/m and 38 ± 0.5 ng/mL, respectively. Significant heritabilities (p < 0.001) were obtained for BMI, weight, fat mass, percent fat, waist circumference, waist-to-height ratio, and ghrelin. Bivariate analyses of ghrelin with adiposity traits showed significant negative genetic correlations (p < 0.0001) with weight, BMI, fat mass, percent fat, waist circumference, and waist-to-height ratio. A genome-wide scan for ghrelin detected significant linkage on chromosome 1p36.2 between STR markers D1S2697 and D1S199 (LOD = 3.2). The same region on chromosome 1 was the site of linkage for insulin (LOD = 3.3), insulinlike growth factor binding protein 1 (IGFBP1) (LOD = 3.4), homeostatic model assessment method (HOMA) (LOD = 2.9), and C-peptide (LOD = 2.0). Several family-based studies have reported linkages for obesity-related phenotypes in the region of 1p36. These results indicate the importance of this region in relation to adiposity in children from the VFS.

Original languageEnglish (US)
Pages (from-to)445-450
Number of pages6
JournalPediatric Research
Volume62
Issue number4
DOIs
StatePublished - Oct 2007
Externally publishedYes

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health

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