Original Article
International Journal of Obesity (2007) 31, 820–828. doi:10.1038/sj.ijo.0803470; published online 24 October 2006
Depot-specific messenger RNA expression of 11
-hydroxysteroid dehydrogenase type 1 and leptin in adipose tissue of children and adults
X Li1,2, S Lindquist1, R Chen2, T Myrnäs3, G Angsten4, T Olsson5 and O Hernell1
- 1Department of Clinical Sciences, Pediatrics, Umeå University, Umeå, Sweden
- 2Children's Research Institute of Nanjing Medical University, Nanjing, China
- 3Department of Surgical and Perioperative Sciences, Surgery, Umeå University, Umeå, Sweden
- 4Department of Pediatric Surgery, University Children's Hospital, Uppsala, Sweden
- 5Department of Public Health and Clinical Medicine, Medicine, Umeå University, Umeå, Sweden
Correspondence: Dr X Li, Department of Clinical Sciences, Pediatrics, Umeå University, Umeå SE-901 85, Sweden. E-mail: xiaonan.li@pediatri.umu.se
Received 29 June 2005; Revised 5 July 2006; Accepted 21 July 2006; Published online 24 October 2006.
Abstract
Objective:
To compare expression of messenger RNA (mRNA) coding for the cortisol regenerating enzyme 11
-hydroxysteroid dehydrogenase type 1 (11
-HSD1), and the adipocytokines leptin and resistin in paired biopsies of subcutaneous adipose tissue (SC) and omental adipose tissue (OM) from children.
Design:
Paired biopsies (SC and OM) were obtained from 54 children (age 0.17–16 years, body mass index (BMI) 12.5–28.3 kg/m2, BMI standard deviation score (SDS) -2.5–4.5) and 16 adults (age 27–79 years, BMI 19–46 kg/m2) undergoing open abdominal surgery. mRNA levels of 11
-HSD1, leptin and resistin were measured using quantitative real-time polymerase chain reaction (PCR).
Results:
11
-HSD1 mRNA level was higher in OM than in SC (P<0.05), whereas leptin mRNA was higher in SC than in OM (P<0.001). There was no difference in the resistin mRNA level between SC and OM. These results were consistent in children and adults. In children, 11
-HSD1 mRNA in SC was positively associated with BMI SDS (P<0.05), whereas in OM it was positively associated with age (P<0.05). The association between 11
-HSD1 expression and age remained significant after adjustment for BMI SDS and gender. Leptin mRNA was positively associated with BMI SDS (SC: P<0.001, OM: P<0.001) but not with age in children. In multiple regression analyses, including anthropometric variables and age, BMI SDS was independently associated with mRNA levels of 11
-HSD1 (P<0.05) and leptin (P<0.001) in SC. When normal weight and overweight children were analyzed separately, 11
-HSD1 mRNA levels were positively associated with leptin in OM in the overweight group (P<0.05).
Conclusion:
There are depot-specific differences in mRNA levels of 11
-HSD1 and leptin in children and adults. The positive association of 11
-HSD1 mRNA in OM with age may reflect a causal role in visceral fat accumulation during growth. Increasing 11
-HSD1 and leptin mRNA in SC with increasing BMI SDS could suggest that the risk of metabolic consequences of obesity may be established early in life.
Keywords:
depot-specific genes, adipose tissue, anthropometrics, childhood
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