Small-for-gestational-age and predictors of HOMA indices, leptin and adiponectin in infancy

Rong Huang1,2, Hua He3,4, Anne Monique Nuyt2

  • 1Lunenfeld-Tanenbaum Research Institute, Department of Obstetrics and Gynecology, Mount Sinai Hospital, Faculty of Medicine, Institute of Health Policy, Management and Evaluation, Dalla Lana School of Public Health, University of Toronto, Toronto, Ontario, Canada.

Insights

Infants born small-for-gestational-age (SGA) show normal metabolic health biomarkers at age two. However, SGA infants may have a dysfunctional adiposity-adiponectin feedback loop, indicated by a BMI-adiponectin association.

Area of Science:

  • Pediatric Endocrinology
  • Metabolic Health
  • Fetal Growth Research

Background:

  • Small-for-gestational-age (SGA) is an indicator of impaired fetal growth.
  • Metabolic health in infancy is crucial for long-term well-being.
  • Understanding factors influencing infant metabolic health is essential.

Purpose of the Study:

  • To determine if small-for-gestational-age (SGA) impacts metabolic health biomarkers in infancy.
  • To identify predictors of metabolic health in SGA infants.
  • To explore insulin resistance, beta-cell function, leptin, and adiponectin levels in SGA infants.

Main Methods:

  • A nested matched (1:2) prospective observational study.
  • Compared 65 SGA infants with 130 optimal-for-gestational-age (OGA) control infants.
  • Assessed homeostasis model assessment of insulin resistance (HOMA-IR), beta-cell function (HOMA-β), leptin, and adiponectin at age 2 years.

Main Results:

  • No significant differences in HOMA-IR, HOMA-β, leptin, or adiponectin between SGA and OGA infants.
  • Female sex and accelerated length growth were linked to higher HOMA-IR.
  • Caucasian ethnicity and decelerated weight growth were linked to lower HOMA-IR.
  • A positive association between BMI and adiponectin was observed in SGA infants.

Conclusions:

  • Infants born SGA exhibit normal insulin resistance, secretion, leptin, and adiponectin levels at age two.
  • A novel finding suggests a potentially dysfunctional adiposity-adiponectin feedback loop in SGA infants.
  • This dysfunction may relate to altered adiposity regulation during infancy in SGA individuals.
Abstract