Published November 22, 2021 | Version v1
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Posterior cervical brown fat and CXCL14 levels in the first year of life: sex differences and association with adiposity

  • 1. University of Barcelona

Description

Context: Brown adipose tissue (BAT) is particularly abundant in neonates but its association with measures of adiposity and metabolic health in early infancy is poorly delineated. Besides sustaining non-shivering thermogenesis, BAT secretes brown adipokines that act on systemic metabolism. The chemokine CXCL14 has been identified as a brown adipokine in experimental studies.

Objective: To determine the relationships among BAT activity, adiposity and circulating CXCL14 levels in the first year of life in girls and boys.

Design, setting and participants: Indices of fat accretion, circulating endocrine-metabolic parameters and serum CXCL14 levels were assessed longitudinally in a cohort of infants at birth and at 4 and 12 months. BAT activity was estimated using infrared thermography only at age 12 months.

Main outcome measures: Weight and length Z-scores, total and abdominal fat content (by DXA), BAT activity at the posterior-cervical and supraclavicular regions, serum levels of glucose, insulin, insulin-like growth factor-I, high-molecular-weight adiponectin and CXCL14; CXCL14 transcript levels in neonatal BAT and liver.

Results: Posterior-cervical BAT was more active in girls than in boys (p=0.02). BAT activity was negatively associated with adiposity parameters only in girls. CXCL14 levels were higher in girls than in boys at age 12 months and correlated positively with the area of active posterior-cervical BAT in girls. Neonatal BAT showed high CXCL14 gene expression levels.

Conclusions: BAT activity and the levels of CXCL14 -a potential surrogate of BAT activity- are sex-specific in the first year of life. BAT activity associates negatively with indices of adiposity only in girls.

Notes

Funding provided by: Sant Joan de Déu Research Institute*
Crossref Funder Registry ID:
Award Number: BR201601

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Additional details

Related works

Is cited by
10.1210/clinem/dgab761 (DOI)
Is source of
10.5281/zenodo.5714390 (DOI)