Evidence map›Paper›PMID 33411809›Full record

ArticlePloS one2021

Altered acylated ghrelin response to food intake in congenital generalized lipodystrophy.

Camilla O D Araújo, Renan M Montenegro, Amanda P Pedroso, Virgínia O Fernandes, Ana Paula D R Montenegro, Annelise B de Carvalho, Lila M Oyama, Carla S C Maia, Eliane B Ribeiro

Open access · goldAbstract read
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.3field-weighted citation impact, top 45% 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

1 citing paper in PubMed, 4 citations in OpenAlex.

  1. 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

9 authors at 3 institutions in 1 country.

Camilla O D AraújoDepartamento de Fisiologia, Universidade Federal de São Paulo (UNIFESP), Escola Paulista de Medicina, São Paulo, São Paulo, Brazil.
Renan M MontenegroFaculdade de Medicina Universidade Federal do Ceará, Departamento de Medicina Clínica e Departamento de Saúde Comunitária, Brazilian Group for the Study of Inherited and Acquired Lipodystrophies (BRAZLIPO) - Hospital Universitário Walter Cantídio, Fortaleza-Ceará, Brazil.
Amanda P PedrosoDepartamento de Fisiologia, Universidade Federal de São Paulo (UNIFESP), Escola Paulista de Medicina, São Paulo, São Paulo, Brazil.
Virgínia O FernandesFaculdade de Medicina Universidade Federal do Ceará, Departamento de Medicina Clínica e Departamento de Saúde Comunitária, Brazilian Group for the Study of Inherited and Acquired Lipodystrophies (BRAZLIPO) - Hospital Universitário Walter Cantídio, Fortaleza-Ceará, Brazil.
Ana Paula D R MontenegroFaculdade de Medicina Universidade Federal do Ceará, Departamento de Medicina Clínica e Departamento de Saúde Comunitária, Brazilian Group for the Study of Inherited and Acquired Lipodystrophies (BRAZLIPO) - Hospital Universitário Walter Cantídio, Fortaleza-Ceará, Brazil.
Annelise B de CarvalhoFaculdade de Medicina Universidade Federal do Ceará, Departamento de Medicina Clínica e Departamento de Saúde Comunitária, Brazilian Group for the Study of Inherited and Acquired Lipodystrophies (BRAZLIPO) - Hospital Universitário Walter Cantídio, Fortaleza-Ceará, Brazil.
Lila M OyamaDepartamento de Fisiologia, Universidade Federal de São Paulo (UNIFESP), Escola Paulista de Medicina, São Paulo, São Paulo, Brazil.
Carla S C MaiaDepartamento de Nutrição, Universidade Estadual do Ceará (UECE), Campus do Itaperi, Fortaleza, Ceará, Brazil.
Eliane B RibeiroDepartamento de Fisiologia, Universidade Federal de São Paulo (UNIFESP), Escola Paulista de Medicina, São Paulo, São Paulo, Brazil.ORCID 0000-0002-3071-9134
Universidade Federal de São Paulo · BRUniversidade Federal do Ceará · BRUniversidade Estadual do Ceará · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundPatients with congenital generalized lipodystrophy (CGL) have very low levels of leptin and are described as having a voracious appetite. However, a direct comparison between CGL and eutrophic individuals is lacking, regarding both appetite parameters and acylated ghrelin, the hormone form that is active in acute food intake stimulation. The objective of the present study was to address whether and in what extent the subjective appetite parameters and acylated ghrelin response to a meal are affected in CGL individuals, in comparison to eutrophic individuals. Additionally, an obese group was included in the study, to allow the comparison between a leptin-resistant and a leptin-deficient condition on these aspects.

methodsEutrophic controls (EUT, n = 10), obese subjects (OB, n = 10) and CGL (n = 11) were fasted overnight and then received an ad libitum meal. Blood was collected and the visual analogue scale was applied before and 90 minutes after the meal. An additional blood sample was collected at 60 minutes for ghrelin determination.

resultsThe CGL patients showed low fasting levels of leptin and adiponectin, dyslipidemia, and insulin resistance. The caloric intake was similar among the 3 groups. However, both CGL (p = 0.02) and OB (p = 0.04) had shorter satiation times than EUT. The CGL patients also had lower satiety time (p = 0.01) and their sensation of hunger was less attenuated by the meal (p = 0.03). Fasting acylated ghrelin levels were lower in CGL than in EUT (p = 0.003). After the meal, the levels tended to decrease in EUT but not in CGL and OB individuals.

conclusionThe data indicate that, although not hyperphagic, the CGL patients present appetite disturbances in relation to eutrophic individuals. Their low fasting levels of acylated ghrelin and the absence of the physiological drop after meal intake suggest a role of these disturbances in hunger attenuation and satiety but not in acute satiation.

Indexed as

AdiponectinAdolescentAdultEatingFastingFemaleGhrelinHumansLeptinLipodystrophy, Congenital GeneralizedMaleMealsObesityYoung AdultAdiponectinGhrelinLeptin

Identifiers

PMID33411809
PMCPMC7790291
OpenAlexW3120727523

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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.