Inverse associations of cord blood mitochondrial DNA copy number with childhood adiposity

Author:

Reddam Aalekhya1ORCID,Bloomquist Tessa R.1,Covell Lindsey T.1,Hu Heng1,Oberfield Sharon E.2,Gallagher Dympna3ORCID,Miller Rachel L.4,Goldsmith Jeff5,Rundle Andrew G.6,Baccarelli Andrea A.1,Herbstman Julie B.1,Kupsco Allison1

Affiliation:

1. Department of Environmental Health Sciences, Mailman School of Public Health Columbia University New York New York USA

2. Department of Pediatrics, New York‐Presbyterian Hospital Columbia University Medical Center New York New York USA

3. Nutrition Obesity Research Center Columbia University Medical Center New York New York USA

4. Division of Clinical Immunology, Department of Medicine Icahn School of Medicine at Mount Sinai New York New York USA

5. Department of Biostatistics, Mailman School of Public Health Columbia University New York New York USA

6. Department of Epidemiology, Mailman School of Public Health Columbia University New York New York USA

Abstract

AbstractObjectiveThe objective of this study was to examine associations between umbilical cord mitochondrial DNA copy number (mtDNAcn) and adiposity across childhood.MethodsIn a prospective birth cohort of Dominican and African American children from New York City, New York (1998–2006), mtDNAcn was measured in cord blood. Children (N = 336) were evaluated for their height, weight, and bioimpedance at age 5, 7, 9, and 11 years. We used linear mixed‐effects models to assess associations of mtDNAcn tertiles in cord blood with child BMI, BMI z scores, fat mass index, and body fat percentage. Latent class growth models and interactions between mtDNAcn and child age or child age2 were used to assess associations between age and adiposity trajectories.ResultsBMI was, on average, 1.5 kg/m2 higher (95% CI: 0.58, 2.5) in individuals with mtDNAcn in the low‐ compared with the middle‐mtDNAcn tertile. Results were similar for BMI z score, fat mass index, and body fat percentage. Moreover, children in the low‐mtDNAcn group had increased odds of being in an “increasing” or “high‐stable” adiposity class.ConclusionsLower mtDNAcn at birth may predict greater childhood adiposity, highlighting the potential key role of perinatal mitochondrial function in adiposity during development.

Funder

National Institute of Environmental Health Sciences

Publisher

Wiley

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