Measurement of immunofunctional leptin to detect and monitor patients with functional leptin deficiency

Author:

Wabitsch Martin1,Pridzun Lutz2,Ranke Michael3,von Schnurbein Julia1,Moss Anja1,Brandt Stephanie1,Kohlsdorf Katja1,Moepps Barbara4,Schaab Michael5,Funcke Jan-Bernd1,Gierschik Peter4,Fischer-Posovszky Pamela1,Flehmig Bertram2,Kratzsch Jürgen5

Affiliation:

1. 1Division of Pediatric Endocrinology and DiabetesDepartment of Pediatrics and Adolescent Medicine, University Medical Center Ulm, Ulm, Germany

2. 2Mediagnost GmbHReutlingen, Germany

3. 3Division of Pediatric Endocrinology and DiabetesDepartment of Pediatrics and Adolescent Medicine, University of Tübingen, Tübingen, Germany

4. 4Institute of Pharmacology and ToxicologyUniversity Medical Center Ulm, Ulm, Germany

5. 5Institute of Laboratory MedicineClinical Chemistry and Molecular Diagnostics, University of Leipzig, Leipzig, Germany

Abstract

Context and aims Functional leptin deficiency is characterized by high levels of circulating immunoreactive leptin (irLep), but a reduced bioactivity of the hormone due to defective receptor binding. As a result of the fact that affected patients can be successfully treated with metreleptin, it was aimed to develop and validate a diagnostic tool to detect functional leptin deficiency. Methods An immunoassay capable of recognizing the functionally relevant receptor-binding complex with leptin was developed (bioLep). The analytical quality of bioLep was validated and compared to a conventional assay for immune-reactive leptin (irLep). Its clinical relevance was evaluated in a cohort of lean and obese children and adults as well as in children diagnosed with functional leptin deficiency and their parents. Results In the clinical cohort, a bioLep/irLep ratio of 1.07 (range: 0.80–1.41) was observed. Serum of patients with non-functional leptin due to homozygous amino acid exchanges (D100Y or N103K) revealed high irLep but non-detectable bioLep levels. Upon treatment of these patients with metreleptin, irLep levels decreased, whereas levels of bioLep increased continuously. In patient relatives with heterozygous amino acid exchanges, a bioLep/irLep ratio of 0.52 (range: 0.48–0.55) being distinct from normal was observed. Conclusions The new bioLep assay is able to diagnose impaired leptin bioactivity in severely obese patients with a homozygous gene defect and in heterozygous carriers of such mutations. The assay serves as a diagnostic tool to monitor leptin bioactivity during treatment of these patients.

Publisher

Bioscientifica

Subject

Endocrinology,General Medicine,Endocrinology, Diabetes and Metabolism

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