Body composition in adults born preterm with very low birth weight.


Journal

Pediatric research
ISSN: 1530-0447
Titre abrégé: Pediatr Res
Pays: United States
ID NLM: 0100714

Informations de publication

Date de publication:
16 Nov 2023
Historique:
received: 16 08 2023
accepted: 26 10 2023
revised: 17 10 2023
medline: 17 11 2023
pubmed: 17 11 2023
entrez: 17 11 2023
Statut: aheadofprint

Résumé

Studies on body composition in preterm very low birth weight (VLBW < 1500 g) survivors are inconsistent and trajectories later in life unknown. We assessed body composition and its change from young to mid-adulthood in VLBW adults. We studied 137 VLBW adults and 158 term-born controls from two birth cohorts in Finland and Norway at mean age 36 years. Body composition was assessed by 8-polar bioelectrical impedance. We compared results with dual-energy x-ray absorptiometry measurements at 24 years. In mid-adulthood, VLBW women and men were shorter than controls. Fat percentage (mean difference in women 1.1%; 95% CI, -1.5% to 3.5%, men 0.8%; -2.0% to 3.6%) and BMI were similar. VLBW women had 2.9 (0.9 to 4.8) kg and VLBW men 5.3 (2.7 to 8.1) kg lower lean body mass than controls, mostly attributable to shorter height. Between young and mid-adulthood, both groups gained fat and lean body mass (p for interaction VLBW x age>0.3). Compared with term-born controls, VLBW adults had similar body fat percentage but lower lean body mass, largely explained by their shorter height. This could contribute to lower insulin sensitivity and muscular fitness previously found in VLBW survivors and predispose to functional limitations with increasing age. In mid-adulthood, individuals born preterm with very low birth weight had similar body fat percentage but lower lean body mass than those born at term. This was largely explained by their shorter height. First study to report longitudinal assessments of body size and composition from young to mid-adulthood in very low birth weight adults. Lower lean body mass in very low birth weight adults could contribute to lower insulin sensitivity and muscular fitness and lead to earlier functional limitations with increasing age.

Sections du résumé

BACKGROUND BACKGROUND
Studies on body composition in preterm very low birth weight (VLBW < 1500 g) survivors are inconsistent and trajectories later in life unknown. We assessed body composition and its change from young to mid-adulthood in VLBW adults.
METHODS METHODS
We studied 137 VLBW adults and 158 term-born controls from two birth cohorts in Finland and Norway at mean age 36 years. Body composition was assessed by 8-polar bioelectrical impedance. We compared results with dual-energy x-ray absorptiometry measurements at 24 years.
RESULTS RESULTS
In mid-adulthood, VLBW women and men were shorter than controls. Fat percentage (mean difference in women 1.1%; 95% CI, -1.5% to 3.5%, men 0.8%; -2.0% to 3.6%) and BMI were similar. VLBW women had 2.9 (0.9 to 4.8) kg and VLBW men 5.3 (2.7 to 8.1) kg lower lean body mass than controls, mostly attributable to shorter height. Between young and mid-adulthood, both groups gained fat and lean body mass (p for interaction VLBW x age>0.3).
CONCLUSION CONCLUSIONS
Compared with term-born controls, VLBW adults had similar body fat percentage but lower lean body mass, largely explained by their shorter height. This could contribute to lower insulin sensitivity and muscular fitness previously found in VLBW survivors and predispose to functional limitations with increasing age.
IMPACT CONCLUSIONS
In mid-adulthood, individuals born preterm with very low birth weight had similar body fat percentage but lower lean body mass than those born at term. This was largely explained by their shorter height. First study to report longitudinal assessments of body size and composition from young to mid-adulthood in very low birth weight adults. Lower lean body mass in very low birth weight adults could contribute to lower insulin sensitivity and muscular fitness and lead to earlier functional limitations with increasing age.

Identifiants

pubmed: 37973945
doi: 10.1038/s41390-023-02896-5
pii: 10.1038/s41390-023-02896-5
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© 2023. The Author(s).

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Auteurs

Laura Jussinniemi (L)

Clinical Medicine Research Unit, Oulu University Hospital and University of Oulu, Oulu, Finland. laura.jussinniemi@oulu.fi.
Public Health Unit, Finnish Institute for Health and Welfare, Helsinki, Finland. laura.jussinniemi@oulu.fi.

Maarit K Kulmala (MK)

Public Health Unit, Finnish Institute for Health and Welfare, Helsinki, Finland.
Helsinki University Eye and Ear Hospital, Helsinki, Finland.

Kristina A D Aakvik (KAD)

Department of Clinical and Molecular Medicine, Norwegian University of Science and Technology, Trondheim, Norway.

Silje D Benum (SD)

Department of Clinical and Molecular Medicine, Norwegian University of Science and Technology, Trondheim, Norway.

Anna P M Jørgensen (APM)

Department of Neuromedicine and Movement Science, Norwegian University of Science and Technology, Trondheim, Norway.

Chandima N D Balasuriya (CND)

Department of Endocrinology, St. Olavs Hospital, Trondheim University Hospital, Trondheim, Norway.

Astrid K Stunes (AK)

Department of Clinical and Molecular Medicine, Norwegian University of Science and Technology, Trondheim, Norway.
Center for Oral Health Services and Research, Mid-Norway (TkMidt), Trondheim, Norway.

Unni Syversen (U)

Department of Clinical and Molecular Medicine, Norwegian University of Science and Technology, Trondheim, Norway.
Department of Endocrinology, St. Olavs Hospital, Trondheim University Hospital, Trondheim, Norway.

Marit S Indredavik (MS)

Department of Clinical and Molecular Medicine, Norwegian University of Science and Technology, Trondheim, Norway.

Sture Andersson (S)

Children's Hospital, Pediatric Research Center, University of Helsinki, Helsinki, Finland.
Helsinki University Hospital, Helsinki, Finland.

Petteri Hovi (P)

Public Health Unit, Finnish Institute for Health and Welfare, Helsinki, Finland.
Children's Hospital, Pediatric Research Center, University of Helsinki, Helsinki, Finland.
Helsinki University Hospital, Helsinki, Finland.

Kari Anne I Evensen (KAI)

Department of Clinical and Molecular Medicine, Norwegian University of Science and Technology, Trondheim, Norway.
Department of Rehabilitation Science and Health Technology, Oslo Metropolitan University, Oslo, Norway.
Children's Clinic, St. Olavs Hospital, Trondheim University Hospital, Trondheim, Norway.

Eero Kajantie (E)

Clinical Medicine Research Unit, Oulu University Hospital and University of Oulu, Oulu, Finland.
Public Health Unit, Finnish Institute for Health and Welfare, Helsinki, Finland.
Department of Clinical and Molecular Medicine, Norwegian University of Science and Technology, Trondheim, Norway.

Classifications MeSH