NEFA Dynamics in Adults With Severe Obesity and Insulin Resistance: No Coupling to the rs9939609 FTO Risk Allele

Author:

Mostad Ingrid Løvold12ORCID,Grill Valdemar2ORCID

Affiliation:

1. Department of Clinical Nutrition and Speech-Language Therapy, Clinic of Rehabilitation, St. Olavs hospital—Trondheim University Hospital , NO 7006 Trondheim , Norway

2. Department of Clinical and Molecular Medicine, Faculty of Medicine and Health Sciences, Norwegian University of Science and Technology , NO 7491 Trondheim , Norway

Abstract

Abstract Context The FTO gene is highly expressed in adipose tissues; however, whether nonesterified fatty acids (NEFA) dynamics are impacted by FTO has not been rigorously tested for in a uniformly obese study population comprising both sexes. Objective To test for associations of the rs9939609 FTO risk allele with NEFA suppression. Methods We investigated 97 subjects with severe obesity but without diabetes, having genotype TT (n = 32), AT (n = 31), or AA (n = 34) in a cross-sectional observation study. NEFA suppression was assessed from a low-dose hyperinsulinemic euglycemic clamp with glucose-tracer as well as from the response to a standardized meal. Insulin sensitivity was assessed by hepatic and total insulin sensitivity measurements in the clamp and by the Matsuda index during the meal. Variables of possible importance for NEFA dynamics were primarily assessed by linear regression. Results No genotype associations with fasting or suppressed NEFA were found, whether in the clamp or meal situation (P > .7 for all comparisons). Independent of genotype, higher fasting concentrations of NEFA and larger NEFA suppression were found in female compared with male subjects. Fasting NEFA or degree of suppression were not associated with total fat mass or body mass index. The respiratory quotient was negatively associated with NEFA suppression. Conclusion In a gender-mixed adult population of obese individuals, an FTO obesity-risk allele did not affect fasting NEFA nor suppression thereof. These negative results on NEFA dynamics appear strengthened by the documentation of gender influence and associations with parameters reflective of insulin resistance.

Funder

Liaison Committee

Central Norway Regional Health Authority

Norwegian University of Science and Technology

Joint Research Committee

St. Olavs Hospital

Faculty of Medicine and Health Sciences

NTNU

Publisher

The Endocrine Society

Subject

Endocrinology, Diabetes and Metabolism

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