학술논문

Leptin receptor expression in blood mononuclear cells of lactating women is associated with infant body weight: Potential role as a molecular biomarker.
Document Type
Article
Source
Pediatric Obesity. Nov2023, Vol. 18 Issue 11, p1-11. 11p.
Subject
*BIOMARKERS
*LACTATION
*MOTHERS
*CYTOKINES
*MONONUCLEAR leukocytes
*BODY weight
*SKINFOLD thickness
*CONFIDENCE intervals
*LEPTIN
*CHILDHOOD obesity
*BREAST milk
*CELL receptors
*INSULIN
*GENE expression
*RISK assessment
*CELLULAR signal transduction
*RESEARCH funding
*PUERPERIUM
*DESCRIPTIVE statistics
*BODY mass index
*ADIPOSE tissues
*ARM circumference
*DISEASE risk factors
*BLOOD
*CHILDREN
Language
ISSN
2047-6302
Abstract
Summary: Background: Molecular biomarkers of maternal leptin resistance associated with infant weight are needed. Objectives: To evaluate gene expression of leptin receptor (LEPR), suppressor of cytokine signalling 3 (SOCS3) and insulin receptor in peripheral blood mononuclear cells (PBMCs) of lactating women and their relationship with infant body weight and adiposity. Methods: At day 10 postpartum, maternal gene expression in PBMCs as well as leptin and insulin concentrations in plasma and milk were assessed (n = 68). Infant weight and BMI z‐scores, skinfolds and arm circumference were obtained at 10 days and/or at 3 months old. Results: In mothers with pre‐pregnancy overweight or obesity (OW/OB), LEPR expression was reduced (p = 0.013) whereas plasma and milk leptin and milk insulin concentrations were elevated. LEPR expression was positively related with infant weight z‐score (Beta (95% CI): 0.40 (0.17, 0.63), p = 0.001) but not with leptin concentrations. SOCS3 expression was positively related with infant weight z‐score (Beta (95% CI): 0.28 (0.04, 0.51), p = 0.024) and arm circumference (Beta (95% CI): 0.57 (0.32, 0.82), p < 0.001). Relationships remained significant after adjusting for maternal and infant confounders. Conclusions: LEPR and SOCS3 gene expression in PBMCs are novel maternal molecular biomarkers that reflect leptin resistance and are associated with infant body weight and adiposity. [ABSTRACT FROM AUTHOR]