Evidence map›Paper›PMID 34177811›Full record

SynthesisFrontiers in endocrinology2021

Two Cases With an Early Presented Proopiomelanocortin Deficiency-A Long-Term Follow-Up and Systematic Literature Review.

Nadan Gregoric, Urh Groselj, Natasa Bratina, Marusa Debeljak, Mojca Zerjav Tansek, Jasna Suput Omladic, Jernej Kovac, Tadej Battelino, Primoz Kotnik, Magdalena Avbelj Stefanija

Open access · goldAbstract readCase ReportsSystematic Review
In one paragraph

Synthesis in Frontiers in endocrinology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
2.9field-weighted citation impact, top 9% 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

16 citing papers in PubMed, 1 synthesis or guideline pooled it, 37 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. The Genetic Blueprint of Obesity: From Pathogenesis to Novel Therapies.Obesity reviews : an official journal of the International Association for the Study of Obesity · 2025
    Review
  4. Review
  5. Article
  6. Article
  7. Review
  8. Article
  9. A comprehensive review of genetic causes of obesity.World journal of pediatrics : WJP · 2024
    Review
  10. Article
  11. Review
  12. Review
  13. Review
  14. Article
  15. Genetics of Obesity in Humans: A Clinical Review.International journal of molecular sciences · 2022
    Review
  16. Obesity and Hyperphagia With Increased Defective ACTH: A Novel POMC Variant.The Journal of clinical endocrinology and metabolism · 2022
    Article
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

10 authors at 2 institutions in 1 country.

Nadan GregoricDepartment for Endocrinology, Diabetes and Metabolic Diseases, Division of Internal Medicine, University Medical Centre Ljubljana, Ljubljana, Slovenia.
Urh GroseljFaculty of Medicine, University of Ljubljana, Ljubljana, Slovenia.
Natasa BratinaFaculty of Medicine, University of Ljubljana, Ljubljana, Slovenia.
Marusa DebeljakFaculty of Medicine, University of Ljubljana, Ljubljana, Slovenia.
Mojca Zerjav TansekFaculty of Medicine, University of Ljubljana, Ljubljana, Slovenia.
Jasna Suput OmladicFaculty of Medicine, University of Ljubljana, Ljubljana, Slovenia.
Jernej KovacClinical Institute for Special Laboratory Diagnostics, University Children's Hospital, University Medical Centre Ljubljana, Ljubljana, Slovenia.
Tadej BattelinoFaculty of Medicine, University of Ljubljana, Ljubljana, Slovenia.
Primoz KotnikFaculty of Medicine, University of Ljubljana, Ljubljana, Slovenia.
Magdalena Avbelj StefanijaFaculty of Medicine, University of Ljubljana, Ljubljana, Slovenia.
Ljubljana University Medical Centre · SIUniversity of Ljubljana · SI

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Proopiomelanocortin (POMC) deficiency is an extremely rare inherited autosomal recessive disorder characterized by severe obesity, adrenal insufficiency, skin hypopigmentation, and red hair. It is caused by pathogenic variants in the

Indexed as

Adrenal InsufficiencyAdultChild, PreschoolDiabetes Mellitus, Type 1FemaleHumansMaleObesityPro-OpiomelanocortinSkin PigmentationPro-Opiomelanocortinadrenal insufficiencyobesityPOMC deficiencyproopiomelanocortinsetmelanotidesystematic reviewtype 1 diabetes

Identifiers

PMID34177811
PMCPMC8220084
OpenAlexW3171650278

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.