Increased liver fat associates with severe metabolic perturbations in low birth weight men

Author:

Brøns Charlotte12ORCID,Thuesen Anne Cathrine Baun123,Elingaard-Larsen Line Ohrt1,Justesen Louise1,Jensen Rasmus Tanderup23,Henriksen Nicolai Stevns2,Juel Helene Bæk3,Størling Joachim14,Ried-Larsen Mathias5,Sparks Lauren M6,van Hall Gerrit7,Danielsen Else Rubæk8,Hansen Torben3,Vaag Allan14

Affiliation:

1. Steno Diabetes Center Copenhagen, Herlev, Denmark

2. Department of Endocrinology, Rigshospitalet, Copenhagen, Denmark

3. Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark

4. Department of Biomedical Sciences, University of Copenhagen, Copenhagen, Denmark

5. Centre for Physical Activity Research (CFAS), Rigshospitalet, Copenhagen, Denmark

6. Translational Research Institute, Advent Health, Orlando, Florida, USA

7. Clinical Metabolomics Core Facility, Rigshospitalet, Copenhagen, Denmark

8. Department of Radiology, Rigshospitalet, Copenhagen, Denmark

Abstract

Objective Ectopic liver fat deposition, resulting from impaired subcutaneous adipose tissue expandability, may represent an age-dependent key feature linking low birth weight (LBW) with increased risk of type 2 diabetes (T2D). We examined whether presumably healthy early middle-aged, non-obese LBW subjects exhibit increased liver fat content, whether increased liver fat in LBW is associated with the severity of dysmetabolic traits and finally whether such associations may be confounded by genetic factors. Methods Using 1H magnetic resonance spectroscopy, we measured hepatic fat content in 26 early middle-aged, non-obese LBW and 22 BMI-matched normal birth weight (NBW) males. Endogenous glucose production was measured by stable isotopes, and a range of plasma adipokine and gut hormone analytes were measured by multiplex ELISA. Genetic risk scores were calculated from genome-wide association study (GWAS) data for birth weight, height, T2D, plasma cholesterol and risk genotypes for non-alcoholic fatty liver disease (NAFLD). Results The LBW subjects had significantly increased hepatic fat content compared with NBW controls (P= 0.014), and 20% of LBW vs no controls had overt NAFLD. LBW subjects with NAFLD displayed widespread metabolic changes compared with NBW and LBW individuals without NAFLD, including hepatic insulin resistance, plasma adipokine and gut hormone perturbations as well as dyslipidemia. As an exception, plasma adiponectin levels were lower in LBW subjects both with and without NAFLD as compared to NBW controls. Genetic risk for selected differential traits did not differ between groups. Conclusion Increased liver fat content including overt NAFLD may be on the critical path linking LBW with increased risk of developing T2D in a non-genetic manner.

Publisher

Oxford University Press (OUP)

Subject

Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism

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