- Opurum H. C. and Austin. A. Ajah
- DOI: 10.5281/zenodo.19916681
- SSR Journal of Medical Sciences (SSRJMS)
Background: Early-life nutritional imbalance
is increasingly recognized as a key determinant of long-term cardiometabolic
health. Both undernutrition and overnutrition during critical developmental
periods can induce persistent alterations in growth, adiposity, endocrine
regulation, and organ function, predisposing individuals to metabolic disorders
later in life.
Objective: This study evaluated the long-term
metabolic consequences of early-life nutritional imbalance in Wistar rats by
comparing growth patterns, organ morphometry, metabolic biomarkers, and
cardiometabolic risk indices following underfeeding and overfeeding.
Methods: A controlled experimental study
was conducted using male Wistar rats randomly assigned to three groups:
underfed, normal-fed, and overfed. Somatic growth parameters (weight, height,
length, and circumference gain) were monitored. After the experimental period,
major organs were harvested for morphometric analysis. Serum biochemical
markers including liver and renal function indices, glucose, lipid profile,
inflammatory markers, and oxidative stress indicators were measured.
Cardiometabolic risk indices such as the atherogenic index of plasma, Castelli
risk indices, and TG/HDL ratio were calculated. Data were analyzed using
one-way ANOVA and multiple regression.
Results: Overfeeding significantly
increased weight gain and promoted multi-organ hypertrophy, particularly in the
liver, heart, spleen, kidneys, and brain, whereas underfeeding restricted
somatic growth and reduced organ weights. Underfed animals exhibited lower
glucose, triglycerides, cholesterol, inflammatory markers, and oxidative
stress, alongside higher HDL and antioxidant activity. Regression analyses
revealed that organ morphometry strongly predicted lipid-related cardiometabolic
indices.
Conclusion: Early-life nutritional imbalance significantly alters growth, organ development, and cardiometabolic risk profiles. Organ morphometric changes appear closely linked to metabolic regulation and may serve as potential indicators of cardiometabolic risk.

