Resting Energy Expenditure in Obese Women with Primary Hypothyroidism and Appropriate Levothyroxine Replacement Therapy

Author:

Muraca Emanuele1ORCID,Ciardullo Stefano12ORCID,Oltolini Alice1,Zerbini Francesca1,Bianconi Eleonora1,Perra Silvia1,Villa Matteo3,Cannistraci Rosa12,Castoldi Giovanna2,Pizzi Pietro4,Manzoni Giuseppina1,Lattuada Guido1,Perseghin Gianluca12ORCID

Affiliation:

1. Department of Medicine and Rehabilitation, Policlinico di Monza, Monza, Italy

2. Department of Medicine and Surgery, Università degli Studi di Milano Bicocca, Monza, Italy

3. Clinical Psychology, Policlinico di Monza, Monza, Italy

4. Centro per lo Studio, la Ricerca e la terapia dell’Obesità, Policlinico di Monza, Monza Italy

Abstract

Abstract Context Growing evidence suggests that appropriate levothyroxine (LT4) replacement therapy may not correct the full set of metabolic defects afflicting individuals with hypothyroidism. Objective To assess whether obese subjects with primary hypothyroidism are characterized by alterations of the resting energy expenditure (REE). Design Retrospective analysis of a set of data about obese women attending the outpatients service of a single obesity center from January 2013 to July 2019. Patients A total of 649 nondiabetic women with body mass index (BMI) > 30 kg/m2 and thyrotropin (TSH) level 0.4–4.0 mU/L were segregated into 2 groups: patients with primary hypothyroidism taking LT4 therapy (n = 85) and patients with normal thyroid function (n = 564). Main outcomes REE and body composition assessed using indirect calorimetry and bioimpedance. Results REE was reduced in women with hypothyroidism in LT4 therapy when compared with controls (28.59 ± 3.26 vs 29.91 ± 3.59 kcal/kg fat-free mass (FFM)/day), including when adjusted for age, BMI, body composition, and level of physical activity (P = 0.008). This metabolic difference was attenuated only when adjustment for homeostatic model assessment of insulin resistance (HOMA-IR) was performed. Conclusions This study demonstrated that obese hypothyroid women in LT4 therapy, with normal serum TSH level compared with euthyroid controls, are characterized by reduced REE, in line with the hypothesis that standard LT4 replacement therapy may not fully correct metabolic alterations related to hypothyroidism. We are not able to exclude that this feature may be influenced by the modulation of insulin sensitivity at the liver site, induced by LT4 oral administration.

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

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