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Cord Blood Adipokines and Lipids and Adolescent Nonalcoholic Fatty Liver Disease
Joy Simpson1, Andrew D Smith1, Abigail Fraser1
1School of Medicine (J.S., S.M.N.), University of Glasgow, Glasgow G31 2ER, United Kingdom; Medical Research Council Integrative Epidemiology Unit (A.D.S., A.F., D.A.L.), School of Social and Community Medicine (A.D.S., A.F., D.A.L.), University of Bristol, Bristol BS13NY United Kingdom; Institute of Cardiovascular and Metabolic Medicine (N.S., R.S.L.), British Heart Foundation Glasgow Cardiovascular Research Centre, Glasgow G61 1QH, United Kingdom; and University Hospitals Bristol National Health Service Foundation Trust (M.C.), Bristol BS1 3NY, United Kingdom.
Insights
Infant adiposity markers like birth weight were not linked to adolescent nonalcoholic fatty liver disease (NAFLD). Greater birth weight was associated with larger liver volume in adolescence, but not NAFLD risk.
Area of Science:
- Pediatric Health
- Metabolic Disorders
- Liver Disease
Background:
- Maternal adiposity during pregnancy is linked to offspring adiposity and metabolic issues, including nonalcoholic fatty liver disease (NAFLD).
- The precise roles of in-utero environment versus later-life factors in this association remain unclear.
Purpose of the Study:
- To investigate the association between infant adiposity markers and markers of NAFLD in adolescence.
- To determine if birth weight, umbilical cord blood leptin, adiponectin, and lipids predict adolescent NAFLD.
Main Methods:
- A UK prospective birth cohort study followed 1037 participants for 17 years.
- Liver function tests and ultrasound-assessed liver fat, volume, and sheer velocity were measured at age 17.
Main Results:
- Birth weight, cord blood leptin, and adiponectin showed no association with NAFLD diagnosis.
- Birth weight was linked to increased liver volume, and cord high-density lipoprotein-cholesterol to higher alanine aminotransferase, mediated by offspring adiposity.
Conclusions:
- Infant fat mass and birth size measurements provided little evidence of association with adolescent NAFLD markers.
- The link between birth weight and liver volume may reflect organ size tracking rather than NAFLD risk.
Context:
Maternal adiposity in pregnancy is associated with offspring adiposity and metabolic dysfunction postnatally, including greater risk of nonalcoholic fatty liver disease (NAFLD). Recent genetic analyses suggest a causal effect of greater maternal body mass index on offspring birth weight and ponderal index, but the relative roles of the environment in utero or later in life remains unclear.
Objective:
We sought to determine whether markers of infant adiposity (birth weight, umbilical cord blood leptin, adiponectin, and lipids) were associated with markers of NAFLD in adolescence.
Design, Setting, And Participants:
This was a UK prospective birth cohort with 17 years of follow-up with liver function tests (aspartate aminotransferase, alanine aminotransferase, gamma-glutamyltransferase) (n = 1037 participants), and ultrasound scan assessed liver fat, volume, and sheer velocity at age 17 (n = 541 participants). Missing covariate data were imputed.
Main Outcomes:
Ultrasound and biochemical measures of NAFLD were measured.
Results:
Birth weight, cord blood leptin, and adiponectin were not associated with a diagnosis of NAFLD. In adjusted analyses, 2 of 42 associations attained conventional 5% levels of significance. Birth weight was positively associated with liver volume (1.0% greater per 100 g [95% confidence interval 0.5%-2.0%]). Cord high-density lipoprotein-cholesterol was positively associated with alanine aminotransferase (11.6% higher per 1 mmol/L [95% confidence interval 0.3, 23.4]); however, this association was primarily mediated via offspring adiposity.
Conclusions:
In this extensive analysis, we found little evidence measurements of infant fat mass and birth size were related to adolescent markers of NAFLD. The association between birth weight and adolescent liver volume may indicate the contribution of greater organ size to birth weight and tracking of organ size.
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