Evidence map›Paper›PMID 35445532›Full record

ArticleDiabetes, obesity & metabolism2022

Therapeutic indications and metabolic effects of metreleptin in patients with lipodystrophy syndromes: Real-life experience from a national reference network.

Héléna Mosbah, Marie-Christine Vantyghem, Estelle Nobécourt, Fabrizio Andreelli, Francoise Archambeaud, Elise Bismuth, Claire Briet, Maryse Cartigny, Benjamin Chevalier, Bruno Donadille and 18 more

Open access · hybridAbstract read
In one paragraph

Article in Diabetes, obesity & metabolism, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 21 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
21citing papers in PubMed, 1 pooled it
3.2field-weighted citation impact, top 7% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

21 citing papers in PubMed, 1 synthesis or guideline pooled it, 38 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. Observational
  4. Evaluating the therapeutic impact of tirzepatide in people with partial lipodystrophy.The Journal of clinical endocrinology and metabolism · 2026
    Observational
  5. Article
  6. Review
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Article
  13. Lipodystrophic Laminopathies: From Dunnigan Disease to Progeroid Syndromes.International journal of molecular sciences · 2024
    Review
  14. Article
  15. Article
  16. Article
  17. Article
  18. Review
  19. Observational
  20. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

28 authors at 14 institutions in 1 country.

Héléna MosbahEndocrinology Department, Assistance Publique-Hôpitaux de Paris (AP-HP), Saint-Antoine University Hospital, National Reference Centre for Rare Diseases of Insulin Secretion and Insulin Sensitivity (PRISIS), Paris, France.
Marie-Christine VantyghemDepartment of Endocrinology, Diabetology and Metabolism, Lille University Hospital; University of Lille, INSERM U1190, European Genomic Institute for Diabetes, Lille, France.
Estelle NobécourtDepartment of Endocrinology, Diabetology and Metabolism, La Réunion University Hospital, Saint Pierre de la Réunion, France.
Fabrizio AndreelliAP-HP, Pitié-Salpêtrière University Hospital, Department of Diabetology; Sorbonne University, INSERM, Nutrition and Obesity: systemic approaches « NutriOmics », Paris, France.
Francoise ArchambeaudDepartment of Endocrinology, Diabetology and Metabolism, Dupuytren University Hospital, Limoges, France.
Elise BismuthAP-HP, Robert-Debré University Hospital, Department of Paediatric Endocrinology, Diabetology and Metabolism, University of Paris, Paris, France.
Claire BrietDepartment of Endocrinology, Diabetology and Metabolism, Angers University Hospital, Laboratory MITOVASC, UMR CNRS 6015, INSERM 1083, Angers, France.
Maryse CartignyReference Centre for Rare Diseases of Genital Development DEVGEN, Endocrinology Unit, Diabetology and Paediatric Gynecology Department, Lille University Hospital, Lille, France.
Benjamin ChevalierDepartment of Endocrinology, Diabetology and Metabolism, Lille University Hospital; University of Lille, INSERM U1190, European Genomic Institute for Diabetes, Lille, France.
Bruno DonadilleEndocrinology Department, Assistance Publique-Hôpitaux de Paris (AP-HP), Saint-Antoine University Hospital, National Reference Centre for Rare Diseases of Insulin Secretion and Insulin Sensitivity (PRISIS), Paris, France.
Anne DaguenelDepartment of Pharmacy, AP-HP, Saint-Antoine University Hospital, Paris, France.
Mathilde FichetDepartment of Endocrinology, Diabetology and Metabolism, Rennes University Hospital, Rennes, France.
Jean-François GautierDepartment of Endocrinology, Diabetology and Metabolism, AP-HP, Lariboisière University Hospital, Paris, France.
Sonja JanmaatEndocrinology Department, Assistance Publique-Hôpitaux de Paris (AP-HP), Saint-Antoine University Hospital, National Reference Centre for Rare Diseases of Insulin Secretion and Insulin Sensitivity (PRISIS), Paris, France.
Isabelle JéruEndocrinology Department, Assistance Publique-Hôpitaux de Paris (AP-HP), Saint-Antoine University Hospital, National Reference Centre for Rare Diseases of Insulin Secretion and Insulin Sensitivity (PRISIS), Paris, France.
Carole LegagneurDepartment of Paediatric Endocrinology, Diabetology and Metabolism, University Hospital Brabois-Vandoeuvre lès Nancy, Vandoeuvre lès Nancy, France.
Lysiane LeguierDepartment of Endocrinology, Diabetology and Metabolism, Lille University Hospital; University of Lille, INSERM U1190, European Genomic Institute for Diabetes, Lille, France.
Julie MaitreDepartment of Paediatrics and Endocrinology, Diabetology and Metabolism, Orléans Hospital, Orléans, France.
Elise MongeoisDepartment of Paediatrics and Endocrinology, Diabetology and Metabolism, Orléans Hospital, Orléans, France.
Christine PoitouNutrition Department, Sorbonne University/INSERM, Research Unit: Nutrition and Obesity; Systemic Approaches (NutriOmics), AP-HP, Pitié-Salpêtrière University Hospital, Reference Centre for Rare Diseases PRADORT (PRADer-Willi Syndrome and other Rare Obesities with Eating Disorders), Paris, France.
Eric RenardDepartment of Endocrinology, Diabetes and Nutrition, Montpellier University Hospital; Clinical Investigation Centre INSERM1411; Institute of Functional Genomics, CNRS, INSERM, University of Montpellier, Montpellier, France.ORCID 0000-0002-3407-7263
Yves ReznikDepartment of Endocrinology, Diabetology and Metabolism, Côte de Nacre University Hospital, Caen, France.ORCID 0000-0002-6267-8058
Anne SpiteriDepartment of Endocrinology, Diabetology and Metabolism, Grenoble University Hospital, Grenoble, France.
Florence TravertDepartment of Diabetology and Metabolism, AP-HP, Bichat University Hospital, Paris, France.
Bruno VergèsDepartment of Endocrinology, Diabetology and Metabolism, Bocage University Hospital, Dijon, France.
Jamila ZammouriSorbonne University, Inserm UMR_S 938, Saint-Antoine Research Centre, Cardiometabolism and Nutrition University Hospital Institute (ICAN), Paris, France.
Corinne VigourouxEndocrinology Department, Assistance Publique-Hôpitaux de Paris (AP-HP), Saint-Antoine University Hospital, National Reference Centre for Rare Diseases of Insulin Secretion and Insulin Sensitivity (PRISIS), Paris, France.ORCID 0000-0002-8181-4721
Camille VatierEndocrinology Department, Assistance Publique-Hôpitaux de Paris (AP-HP), Saint-Antoine University Hospital, National Reference Centre for Rare Diseases of Insulin Secretion and Insulin Sensitivity (PRISIS), Paris, France.
Inserm · FRCentre hospitalier universitaire d'Orléans · FRCentre National de la Recherche Scientifique · FRAssistance Publique – Hôpitaux de Paris · FRCentre Hospitalier Universitaire de Grenoble · FRCentre Hospitalier Universitaire de La Réunion · FRHôpital Dupuytren · FRHôpital Lariboisière · FRMaison des Sciences sociales et des Humanités de Dijon · FRSorbonne Université · FRUniversité de Caen Normandie · FRUniversité de Lille · FRUniversité Paris Cité · FRUniversité Rennes 2 · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

aimTo describe baseline characteristics and follow-up data in patients with lipodystrophy syndromes treated with metreleptin in a national reference network, in a real-life setting. PATIENTS AND

methodsClinical and metabolic data from patients receiving metreleptin in France were retrospectively collected, at baseline, at 1 year and at the latest follow-up during treatment.

resultsForty-seven patients with lipodystrophy including generalized lipodystrophy (GLD; n = 28) and partial lipodystrophy (PLD; n = 19) received metreleptin over the last decade. At baseline, the median (interquartile range [IQR]) patient age was 29.3 (16.6-47.6) years, body mass index was 23.8 (21.2-25.7) kg/m

conclusionsIn this real-life setting study, metabolic outcomes are improved by metreleptin therapy in patients with GLD. The therapeutic indication for metreleptin needs to be clarified in patients with PLD.

Indexed as

LipodystrophyLipodystrophy, Congenital GeneralizedAdolescentAdultHumansLeptinMiddle AgedRetrospective StudiesSyndromeYoung AdultLeptinmetreleptin

Identifiers

PMID35445532
PMCPMC9541305
OpenAlexW4224236828

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.