Assessment of Serum Apelin Levels in Girls with Anorexia Nervosa

Author:

Ziora Katarzyna1,Oświęcimska Joanna1,Świętochowska Elżbieta2,Ziora Dariusz3,Ostrowska Zofia2,Stojewska Małgorzata1,Klimacka-Nawrot Ewa4,Dyduch Antoni1,Błońska-Fajfrowska Barbara4

Affiliation:

1. Department of Pediatrics in Zabrze (K.Z., J.O., M.S., A.D.), Medical University of Silesia in Katowice, 41-800 Zabrze, Poland

2. Department of Biochemistry in Zabrze (E.S., Z.O.), Medical University of Silesia in Katowice, 41-808 Zabrze, Poland

3. Department of Pneumonology and Tuberculosis in Zabrze (D.Z.), Medical University of Silesia in Katowice, 41-800 Zabrze, Poland

4. Department of Basic Biomedical Science in Sosnowiec (E.K.-N., B.B.-F.), Medical University of Silesia in Katowice, 41-200 Sosnowiec, Poland

Abstract

Abstract Context: Pilot studies in rats have suggested that apelin (APE) is involved in the control of appetite and food intake. APE is secreted in the organs involved in the control of hunger and satiety: the stomach, hypothalamus, and fat tissue. Anorexia nervosa (AN) is an eating disorder that represents a good biological model of chronic fat tissue atrophy in humans. To date, there are no reports of APE expression in the fat tissue and its circulating concentrations in patients with AN. Objective: Our objective was to assess serum APE concentrations in girls with AN. Design, Participants, and Setting: APE-36 and APE-12 serum concentrations were evaluated in 87 Polish girls with restrictive AN, in 61 healthy (H) controls, 17 girls with no otherwise specified eating disorders (NOS), and 30 girls with simple obesity (OB). Results: Mean serum APE-36 and APE-12 concentrations in patients with AN and NOS were significantly lower than in the H and OB groups. However, no differences between AN, H, and NOS groups were observed when APE concentrations were calculated per body mass index (BMI). In participants with normal BMI, serum APE-36 (r = 0.35) and APE-12 (r = 0.37) concentrations correlated positively with BMI. Conclusions: We conclude that compared with H controls, serum APE-36 and APE-12 concentrations decreased as a result of fat tissue depletion in patients with AN. Conversely, obese adolescents had elevated APE-36 and APE-12 due to excessive fat mass as well as increased APE production in adipose tissue.

Publisher

The Endocrine Society

Subject

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

Reference37 articles.

1. Isolation and characterization of a novel endogenous peptide ligand for the human APJ receptor;Tatemoto;Biochem Biophys Res Commun,1998

2. Emerging roles of apelin in biology and medicine;Kleinz;Pharmacol Ther,2005

3. Apelin and visfatin: unique “beneficial” adipokines upregulated in obesity;Bełtowski;Med Sci Monit,2006

4. The novel peptide apelin lowers blood pressure via a nitric oxide-dependent mechanism;Tatemoto;Regul Pept,2001

5. Apelin, a newly identified adipokine up-regulated by insulin and obesity;Boucher;Endocrinology,2005

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