Related Experiment Video
Updated: Jun 14, 2026

Isolation and Differentiation of Primary White and Brown Preadipocytes from Newborn Mice
Published on: January 25, 2021
Infants With Low Birth Weight Have Larger Adipocytes During Early Childhood
Tetsuro Murakawa1, Yuya Nakano1, Akio Ebata1
1Department of Pediatrics, Showa Medical University, Tokyo, Japan.
Insights
Infants with low birth weight (LBW) have larger adipocytes in early childhood, a potential precursor to insulin resistance. This finding highlights the importance of monitoring LBW infants for metabolic health risks.
Area of Science:
- Metabolic health
- Pediatric endocrinology
- Adipose tissue biology
Background:
- Infants with low birth weight (LBW) face an elevated risk of developing insulin resistance later in life.
- Adipocyte size is a key indicator of metabolic function and can be influenced by early-life factors.
Purpose of the Study:
- To compare adipocyte size in early childhood between infants born with low birth weight and those born appropriate for gestational age at full-term.
- To investigate the relationship between birth weight and adipocyte characteristics in young children.
Main Methods:
- A cross-sectional study involving 92 children (0.8-5.2 years old) undergoing surgery.
- Intraoperative adipose tissue samples were collected and analyzed for mean adipocyte diameter using osmic acid fixation and separation techniques.
Main Results:
- Despite similar body mass index (BMI), the low-birth-weight group exhibited significantly larger mean adipocyte diameters (87.0 μm) compared to the appropriate-for-gestational-age group (74.7 μm).
- Low birth weight and higher BMI at surgery were identified as significant predictors of larger adipocyte size (p < 0.001).
- No association was found between mean adipocyte diameter and key hematological parameters like insulin, adiponectin, or leptin levels.
Conclusions:
- Early childhood is characterized by larger adipocytes in infants born with low birth weight compared to their full-term, appropriate-for-gestational-age peers.
- These findings suggest a potential link between low birth weight, adipocyte morphology, and future metabolic disturbances, warranting further investigation into insulin resistance development.
Background:
Infants with low birth weight are at increased risk of developing insulin resistance later in life.
Objectives:
To evaluate differences in adipocyte size during early childhood between infants with low birth weight and infants born appropriate for gestational age at full-term.
Methods:
This cross-sectional study included 92 children (77 infants born appropriate for gestational age at full-term and 15 with low birth weight), aged 0.8-5.2 years, scheduled for surgery. Adipose tissue samples were obtained intraoperatively, fixed in osmic acid, and assessed for mean adipocyte diameter after adipocyte separation.
Results:
Despite a similar body mass index, the low-birth-weight group had larger mean adipocyte diameters during early childhood than the term appropriate-for-gestational-age group (87.0 μm vs. 74.7 μm). Multiple regression analysis revealed that low birth weight and higher body mass index at surgery were significant determinants of larger mean adipocyte diameter (p < 0.001). Mean adipocyte diameter was not associated with haematological parameters, including insulin, adiponectin, and leptin levels.
Conclusion:
During early childhood, infants with low birth weight had larger adipocytes than infants born appropriate for gestational age at term. Further studies are required to determine whether this observation is associated with insulin resistance development later in life.
Related Concept Videos
Obesity
Signs of Puberty
Hypodermis
Anatomy of the Intestines
Small Intestines
The small intestine is an ~7 meter-long tube with an inner diameter of just 2.5 cm. Since most nutrients are absorbed here, the inner lining of the small...
Development of Immunocompetence
The initial cells that migrate from the fetal thymus settle within the skin and epithelial tissues lining the mouth, digestive tract, and in females, the uterus and vagina. These cells, including skin-based dendritic cells, serve as antigen-presenting cells, playing a key role in T cell activation.
Subsequent T...

