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Trajectories of body mass index amongst children who develop type 2 diabetes as adults

Trajectories of body mass index amongst children who develop type 2 diabetes as adults
Trajectories of body mass index amongst children who develop type 2 diabetes as adults
Design and subjects

A total of 13 345 individuals born in Helsinki, Finland between 1934 and 1944 were included in the study. The participants' growth had been recorded in detail during childhood, and 11.7% (n = 1558) had been diagnosed with T2D. We divided the cohort around the median body mass index (BMI) at 11 years. Body composition and glucose tolerance were assessed in a clinical subsample (n = 2003) in adulthood.

Results

Two pathways of growth were associated with T2D. Both began with low weight and BMI at birth. In one, persistent low BMI through infancy was followed by a rapid increase in BMI in childhood. Amongst individuals with a BMI at 11 years above the median value, the odds ratio for T2D associated with a one z-score increase in BMI between 2 and 11 years was 1.31 (95% confidence interval 1.21–1.42, P < 0.001). In the other pathway, low BMI at birth, accompanied by short length at birth, was followed by low BMI in childhood. Most women who developed diabetes followed this trajectory; they developed T2D at a lower BMI and lower fat percentage than women with a BMI above the median at 11 years of age.

Conclusions

Two pathways of early growth trigger T2D. Low fat deposition leading to thinness at birth and during infancy results in fat acquisition during childhood. Reduced linear growth leading to short length at birth is associated with lower body fat percentage in adulthood but increased risk of developing diabetes.
childhood growth, foetal growth, glucose, obesity, type 2 diabetes
0954-6820
219-226
Eriksson, J.G.
eda300d2-b247-479f-95b9-f12d2c72e92b
Kajantie, E.
d4e32f85-9988-4b83-b353-012210ea0151
Lampl, M.
cb9cb5d9-91a5-4315-952e-f3cd6b724085
Osmond, C.
2677bf85-494f-4a78-adf8-580e1b8acb81
Eriksson, J.G.
eda300d2-b247-479f-95b9-f12d2c72e92b
Kajantie, E.
d4e32f85-9988-4b83-b353-012210ea0151
Lampl, M.
cb9cb5d9-91a5-4315-952e-f3cd6b724085
Osmond, C.
2677bf85-494f-4a78-adf8-580e1b8acb81

Eriksson, J.G., Kajantie, E., Lampl, M. and Osmond, C. (2015) Trajectories of body mass index amongst children who develop type 2 diabetes as adults. Journal of Internal Medicine, 278 (2), 219-226. (doi:10.1111/joim.12354). (PMID:25683182)

Record type: Article

Abstract

Design and subjects

A total of 13 345 individuals born in Helsinki, Finland between 1934 and 1944 were included in the study. The participants' growth had been recorded in detail during childhood, and 11.7% (n = 1558) had been diagnosed with T2D. We divided the cohort around the median body mass index (BMI) at 11 years. Body composition and glucose tolerance were assessed in a clinical subsample (n = 2003) in adulthood.

Results

Two pathways of growth were associated with T2D. Both began with low weight and BMI at birth. In one, persistent low BMI through infancy was followed by a rapid increase in BMI in childhood. Amongst individuals with a BMI at 11 years above the median value, the odds ratio for T2D associated with a one z-score increase in BMI between 2 and 11 years was 1.31 (95% confidence interval 1.21–1.42, P < 0.001). In the other pathway, low BMI at birth, accompanied by short length at birth, was followed by low BMI in childhood. Most women who developed diabetes followed this trajectory; they developed T2D at a lower BMI and lower fat percentage than women with a BMI above the median at 11 years of age.

Conclusions

Two pathways of early growth trigger T2D. Low fat deposition leading to thinness at birth and during infancy results in fat acquisition during childhood. Reduced linear growth leading to short length at birth is associated with lower body fat percentage in adulthood but increased risk of developing diabetes.

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More information

e-pub ahead of print date: 16 March 2015
Published date: August 2015
Keywords: childhood growth, foetal growth, glucose, obesity, type 2 diabetes
Organisations: Faculty of Medicine

Identifiers

Local EPrints ID: 385416
URI: http://eprints.soton.ac.uk/id/eprint/385416
ISSN: 0954-6820
PURE UUID: 2f9c7ac2-72eb-4e21-849f-23655f0baab6
ORCID for C. Osmond: ORCID iD orcid.org/0000-0002-9054-4655

Catalogue record

Date deposited: 19 Jan 2016 15:15
Last modified: 15 Mar 2024 02:50

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Contributors

Author: J.G. Eriksson
Author: E. Kajantie
Author: M. Lampl
Author: C. Osmond ORCID iD

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