Common Variants Near Melanocortin 4 Receptor Are Associated with General and Visceral Adiposity in European- and African-American Youth

Gaifen Liu, Haidong Zhu, Vasiliki Lagou, Bernard Gutin, Paule Barbeau, Frank A. Treiber, Yanbin Dong, Harold Snieder

Research output: Contribution to journalArticle

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Abstract

Objective: Recent genome-wide association studies found common variants near the melanocortin 4 receptor gene associated with obesity. This study aimed to assess the influence of the identified single nucleotide polymorphisms rs17782313 and rs17700633 on general and visceral adiposity in European- and African-American youth. Study design: In 1890 youth (49.1% European-American, 45.6% male, mean age 16.7 years), we examined the associations of the rs17782313 and rs17700633 with anthropometry, percent body fat, visceral adipose tissue, and subcutaneous abdominal adipose tissue. Interaction of the single nucleotide polymorphisms with ethnicity or sex was investigated and haplotype analyses conducted. Results: Rs17782313 was significantly associated with weight (P = .02) and waist circumference (P = .03) in all subjects and with body mass index (P = .002) in females. In females rs17700633 was significantly associated with percent body fat (P = .001), visceral adipose tissue (P < .001), and subcutaneous abdominal adipose tissue (P < .001). Rs17700633 was significantly associated with fasting insulin and homeostasis model assessment, but the significance attenuated after adjustment for percent body fat. These findings were confirmed by haplotype analysis. No significant interactions of the variants with ethnicity were found for any of these phenotypes. Conclusions: The relatively large effect of these common variants near melanocortin 4 receptor on general and visceral adiposity in childhood, especially in girls, could prove helpful in elucidating the molecular mechanisms underlying the development of obesity in early life.

Original languageEnglish (US)
JournalJournal of Pediatrics
Volume156
Issue number4
DOIs
StatePublished - Jan 1 2010

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Receptor, Melanocortin, Type 4
Adiposity
Abdominal Subcutaneous Fat
African Americans
Adipose Tissue
Intra-Abdominal Fat
Haplotypes
Single Nucleotide Polymorphism
Obesity
Anthropometry
Genome-Wide Association Study
Waist Circumference
Fasting
Body Mass Index
Homeostasis
Insulin
Phenotype
Weights and Measures
Genes

ASJC Scopus subject areas

  • Pediatrics, Perinatology, and Child Health

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Common Variants Near Melanocortin 4 Receptor Are Associated with General and Visceral Adiposity in European- and African-American Youth. / Liu, Gaifen; Zhu, Haidong; Lagou, Vasiliki; Gutin, Bernard; Barbeau, Paule; Treiber, Frank A.; Dong, Yanbin; Snieder, Harold.

In: Journal of Pediatrics, Vol. 156, No. 4, 01.01.2010.

Research output: Contribution to journalArticle

Liu, Gaifen ; Zhu, Haidong ; Lagou, Vasiliki ; Gutin, Bernard ; Barbeau, Paule ; Treiber, Frank A. ; Dong, Yanbin ; Snieder, Harold. / Common Variants Near Melanocortin 4 Receptor Are Associated with General and Visceral Adiposity in European- and African-American Youth. In: Journal of Pediatrics. 2010 ; Vol. 156, No. 4.
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abstract = "Objective: Recent genome-wide association studies found common variants near the melanocortin 4 receptor gene associated with obesity. This study aimed to assess the influence of the identified single nucleotide polymorphisms rs17782313 and rs17700633 on general and visceral adiposity in European- and African-American youth. Study design: In 1890 youth (49.1{\%} European-American, 45.6{\%} male, mean age 16.7 years), we examined the associations of the rs17782313 and rs17700633 with anthropometry, percent body fat, visceral adipose tissue, and subcutaneous abdominal adipose tissue. Interaction of the single nucleotide polymorphisms with ethnicity or sex was investigated and haplotype analyses conducted. Results: Rs17782313 was significantly associated with weight (P = .02) and waist circumference (P = .03) in all subjects and with body mass index (P = .002) in females. In females rs17700633 was significantly associated with percent body fat (P = .001), visceral adipose tissue (P < .001), and subcutaneous abdominal adipose tissue (P < .001). Rs17700633 was significantly associated with fasting insulin and homeostasis model assessment, but the significance attenuated after adjustment for percent body fat. These findings were confirmed by haplotype analysis. No significant interactions of the variants with ethnicity were found for any of these phenotypes. Conclusions: The relatively large effect of these common variants near melanocortin 4 receptor on general and visceral adiposity in childhood, especially in girls, could prove helpful in elucidating the molecular mechanisms underlying the development of obesity in early life.",
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