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Leptin and adiponectin concentrations in infants with low birth weight: relationship with maternal health and
Juliana Fernandez Santana-Meneses1, Fabíola I Suano-Souza1,2, Maria do Carmo Franco1
1Universidade Federal de São Paulo, Escola Paulista de Medicina, Pediatrics Department, São Paulo, São Paulo, Brazil.
Insights
Low birth weight (LBW) infants show early changes in leptin and adiponectin, influenced by maternal nutrition and infant growth. These hormonal shifts may increase their risk of developing chronic non-communicable diseases later in life.
Area of Science:
- Pediatrics
- Endocrinology
- Public Health
Background:
- Infant health significantly impacts long-term risk for chronic non-communicable diseases (NCDs).
- Leptin and adiponectin play crucial roles in metabolic regulation.
- Understanding hormonal profiles in low birth weight (LBW) infants is vital for early intervention.
Purpose of the Study:
- To determine leptin and adiponectin concentrations in LBW infants.
- To explore associations between these hormones and maternal nutritional status, gestational age adequacy, postnatal weight gain, and current diet.
- To identify early risk factors for NCDs in LBW infants.
Main Methods:
- Cross-sectional study of 54 LBW infants aged 9-12 months.
- Collected data on maternal background, pre-pregnancy nutrition, infant anthropometry (birth and current), nutritional recovery, dietary intake, and blood leptin/adiponectin levels.
- Analyzed associations using statistical methods, considering factors like small for gestational age (SGA) status and pre-gestational BMI.
Main Results:
- LBW infants exhibited altered leptin and adiponectin concentrations.
- Small for gestational age (SGA) infants showed faster weight recovery, higher leptin levels, and increased leptin/adiponectin ratios.
- Higher maternal pre-gestational BMI modified the relationship between weight-for-age z-score (WAZ) and leptin levels in LBW infants.
Conclusions:
- LBW infants experience early hormonal changes (leptin, adiponectin) influenced by maternal, intrauterine, and postnatal factors.
- These early metabolic alterations may predispose LBW infants to an increased risk of NCDs.
- Maternal pre-gestational BMI is a significant factor in modulating hormonal profiles in LBW infants.
Abstract:
Health in pregnancy and infancy can affect the risk of chronic non-communicable diseases. We aimed to describe leptin and adiponectin concentrations in low birth weight (LBW) infants and identify possible associations with maternal nutritional status, adequacy for gestational age, nutritional recovery, and current dietary intake. A cross-sectional study with LBW infants (9-12 months) including maternal background and pre-pregnancy nutritional condition was performed. From the Infants: anthropometry at birth and current was expressed as z-score (weight: WAZ, length, head circumference), nutritional recovery, dietary intake, leptin, and adiponectin blood concentrations. The mean age of the 54 infants was 10.0 ± 1.5 months, 32 (59.3%) were female, 36 (66.7%) preterm, 23 (42.6%) small for gestational age (SGA), and 25 pregnancies (46.3%) were twin. Almost all (98%) of the infants intake energy and protein above the recommendation, and 47 (87.6%) consumed ultra-processed foods. At the time of the assessment, 8 (14.8%) were overweight and 4 (7.4%) had short stature. SGA infants showed faster weight recovery (WAZ 1.54; 95% CI 1.17, 1.91; p = 0.001), higher leptin's concentration (3.0 ng/ml (1.7, 3.0) versus 1.6 ng/ml (0.9, 2.6); p = 0.032)), and leptin/adiponectin ratio (0.13 ± 0.08 versus 0.07 ± 0.07; p = 0.018). The pre-gestational BMI was a modifier of the effect of WAZ on leptin levels (p = 0.027) in LBW infants. Higher pre-gestational BMI increased the effect of WAZ variation (birth and current) on leptin levels. Concluding, LBW infants showed early changes in leptin and adiponectin concentrations, influenced by maternal (pre-gestational BMI), intrauterine (gestational age adequacy - SGA), and postnatal weight gain. This combination of factors may increase the risk of NCD for this group of children.
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