Longitudinal changes in high molecular weight serum adiponectin levels in healthy infants

Satoshi Hibino1, Kazuo Itabashi, Yuya Nakano

  • 1Department of Pediatrics, Showa University School of Medicine, Tokyo 142-8666, Japan.

Pediatric Research
|December 19, 2008
PubMed

Insights

High molecular weight adiponectin (HMW-ad) levels in infants decrease significantly by 12 months. Cord blood HMW-ad levels predict infant levels, suggesting prenatal regulation.

Area of Science:

  • Pediatrics
  • Endocrinology
  • Metabolic Health

Background:

  • Adiponectin, particularly high molecular weight adiponectin (HMW-ad), plays a crucial role in metabolic regulation.
  • Understanding the factors influencing HMW-ad levels in early life is essential for predicting long-term metabolic health.
  • Longitudinal data on HMW-ad during infancy is limited.

Purpose of the Study:

  • To investigate the longitudinal changes in serum HMW-ad levels from birth to 12 months of age in healthy infants.
  • To identify factors associated with HMW-ad levels during the first year of life.

Main Methods:

  • A longitudinal study measuring total adiponectin, HMW-ad, and leptin in 56 healthy infants from birth to 12 months.
  • Serum samples were collected at birth, 6 months, and 12 months.
  • Multiple regression analysis was used to determine predictive factors for HMW-ad levels.

Main Results:

  • Serum HMW-ad levels showed a strong positive correlation with total adiponectin levels (R2 = 0.93).
  • HMW-ad levels at 12 months (7.7 ± 0.5 μg/mL) were significantly lower than at birth (13.7 ± 0.9 μg/mL) and 6 months (13.3 ± 0.8 μg/mL).
  • Multiple regression analysis indicated that only cord blood HMW-ad levels significantly predicted HMW-ad levels at 12 months (β = 0.680).

Conclusions:

  • Postnatal HMW-ad production during infancy may be regulated prenatally.
  • Cord blood HMW-ad levels are a key determinant of HMW-ad levels in the first year of life.
  • Further research is needed to explore the role of cord blood HMW-ad in metabolic syndrome development.