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Longitudinal analysis of risk of non-alcoholic fatty liver disease in adulthood

Cuthbertson, Daniel J.; Brown, Emily; Koskinen, Juha; Magnussen, Costan G.; Hutri‐Kähönen, Nina; Sabin, Matthew; Tossavainen, Päivi; Jokinen, Eero; Laitinen, Tomi; Viikari, Jorma; Raitakari, Olli T.; Juonala, Markus (2019-06-30)

 
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URL:
https://doi.org/10.1111/liv.13993

Cuthbertson, Daniel J.
Brown, Emily
Koskinen, Juha
Magnussen, Costan G.
Hutri‐Kähönen, Nina
Sabin, Matthew
Tossavainen, Päivi
Jokinen, Eero
Laitinen, Tomi
Viikari, Jorma
Raitakari, Olli T.
Juonala, Markus
John Wiley & Sons
30.06.2019

Cuthbertson, DJ, Brown, E, Koskinen, J, et al. Longitudinal analysis of risk of non‐alcoholic fatty liver disease in adulthood. Liver Int. 2019; 39: 1147– 1154. https://doi.org/10.1111/liv.13993

https://rightsstatements.org/vocab/InC/1.0/
© 2018 John Wiley & Sons A/S. This is the peer reviewed version of the following article: Cuthbertson, DJ, Brown, E, Koskinen, J, et al. Longitudinal analysis of risk of non‐alcoholic fatty liver disease in adulthood. Liver Int. 2019; 39: 1147– 1154. https://doi.org/10.1111/liv.13993 , which has been published in final form at https://doi.org/10.1111/liv.13993. This article may be used for non-commercial purposes in accordance with Wiley Terms and Conditions for Self-Archiving.
https://rightsstatements.org/vocab/InC/1.0/
doi:https://doi.org/10.1111/liv.13993
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https://urn.fi/URN:NBN:fi-fe2019070522811
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Abstract

Background & Aims: We aimed to determine how childhood body mass index and metabolic health, along with the change in body mass index between childhood and adulthood, determine the risk of adult non‐alcoholic fatty liver disease.

Methods: Data from 2020 participants aged 3–18 years at baseline, followed up 31 years later, were examined to assess the utility of four childhood metabolic phenotypes (Metabolic Groups I: normal body mass index, no metabolic disturbances; II: normal body mass index, one or more metabolic disturbances; III: overweight/obese, no metabolic disturbances; IV: overweight/obese, one or more metabolic disturbances) and four life‐course adiposity phenotypes (Adiposity Group 1: normal child and adult body mass index; 2, high child, normal adult body mass index; 3, normal child body mass index, high adult body mass index; 4, high child and adult body mass index) in predicting adult non‐alcoholic fatty liver disease.

Results: The risk for adult non‐alcoholic fatty liver disease was similar across all four groups after adjustment for age, sex, lifestyle factors and adult body mass index. Risk of adult non‐alcoholic fatty liver disease was not increased among individuals overweight/obese in childhood but non‐obese in adulthood. In contrast, overweight or obese adults, irrespective of their youth body mass index status, had ~eight‐fold to 10‐fold increased risk (P < 0.001).

Conclusions: Childhood overweight/obesity, not metabolic health, is associated with increased risk for adult non‐alcoholic fatty liver disease. However, the increased risk associated with childhood overweight/obesity can be largely removed by obtaining a normal body mass index by adulthood.

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