Lower leptin level at discharge in acute anorexia nervosa is associated with early weight-loss.

anorexia nervosa ghrelin inpatients leptin neuropeptides obestatin outcome risk factor

Journal

European eating disorders review : the journal of the Eating Disorders Association
ISSN: 1099-0968
Titre abrégé: Eur Eat Disord Rev
Pays: England
ID NLM: 9436977

Informations de publication

Date de publication:
07 2021
Historique:
revised: 16 02 2021
received: 18 06 2020
accepted: 14 03 2021
pubmed: 22 4 2021
medline: 29 3 2022
entrez: 21 4 2021
Statut: ppublish

Résumé

Predictive values of acute phase metabolic abnormalities of anorexia nervosa (AN) have seldom been studied. As early postrestoration weight loss is associated with poor outcome, discharge biologic parameters were assessed to detect an association with 2-month follow-up weight loss as a proxy to poor outcome. Fasting plasma levels of leptin, acyl-ghrelin, obestatin, PYY, oxytocin and BDNF were measured in 26 inpatients, at inclusion, at discharge and 2 months later. A body mass index less than 18 2-month postdischarge was considered a poor outcome. Nineteen patients (73%) had a fair outcome and seven (27%) had a poor one with a mean loss of 0.69 versus 4.54 kg, respectively. Only discharge leptin levels were significantly higher in fair versus poor outcome patients (14.1 vs. 7.0 ng/ml, p = 0.006). The logistic regression model using discharge leptin, acyl-ghrelin, obestatin, oxytocin, PYY and BDNF levels as predictors of outcome disclosed a nearly significant effect of leptin (p < 0.10). Receiver operating characteristic analysis showed 11.9 ng/ml was the best value of threshold. Neither clinical variables differed according to outcome. Leptin level may be a biomarker of early weight relapse after acute inpatient treatment of AN. Its clinical usefulness in monitoring care in AN should further be determined.

Identifiants

pubmed: 33880836
doi: 10.1002/erv.2830
doi:

Substances chimiques

Leptin 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

634-644

Informations de copyright

© 2021 Eating Disorders Association and John Wiley & Sons Ltd.

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Auteurs

Roland Dardennes (R)

Faculté de Médecine, Université de Paris Descartes, Paris, France.
Institute of Psychiatry and Neuroscience of Paris (IPNP), Université de Paris, INSERM UMR-S 1266, Paris, France.
Clinique des Maladies Mentales et de l'encéphale, Hospital Sainte-Anne, Paris, France.

Virginie Tolle (V)

Institute of Psychiatry and Neuroscience of Paris (IPNP), Université de Paris, INSERM UMR-S 1266, Paris, France.

Guillaume Lavoisy (G)

Faculté de Médecine, Université de Paris Descartes, Paris, France.
Institute of Psychiatry and Neuroscience of Paris (IPNP), Université de Paris, INSERM UMR-S 1266, Paris, France.
Clinique des Maladies Mentales et de l'encéphale, Hospital Sainte-Anne, Paris, France.

Dominique Grouselle (D)

Institute of Psychiatry and Neuroscience of Paris (IPNP), Université de Paris, INSERM UMR-S 1266, Paris, France.

Nebal Alanbar (N)

Faculté de Médecine, Université de Paris Descartes, Paris, France.

Philibert Duriez (P)

Faculté de Médecine, Université de Paris Descartes, Paris, France.
Institute of Psychiatry and Neuroscience of Paris (IPNP), Université de Paris, INSERM UMR-S 1266, Paris, France.
Clinique des Maladies Mentales et de l'encéphale, Hospital Sainte-Anne, Paris, France.

Philip Gorwood (P)

Faculté de Médecine, Université de Paris Descartes, Paris, France.
Institute of Psychiatry and Neuroscience of Paris (IPNP), Université de Paris, INSERM UMR-S 1266, Paris, France.
Clinique des Maladies Mentales et de l'encéphale, Hospital Sainte-Anne, Paris, France.

Nicolas Ramoz (N)

Institute of Psychiatry and Neuroscience of Paris (IPNP), Université de Paris, INSERM UMR-S 1266, Paris, France.

Jacques Epelbaum (J)

Institute of Psychiatry and Neuroscience of Paris (IPNP), Université de Paris, INSERM UMR-S 1266, Paris, France.

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