Evidence map›Paper›PMID 28504003›Full record

ArticleJournal of the renin-angiotensin-aldosterone system : JRAAS

Different metabolic responses induced by long-term interdisciplinary therapy in obese adolescents related to ACE I/D polymorphism.

Sandro S Almeida, Flavia C Corgosinho, Carlos En Amorim, Marcos F Gregnani, Raquel Ms Campos, Deborah Cl Masquio, Priscila L Sanches, Aline P Ganen, João B Pesquero, Ana R Dâmaso and 3 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of the renin-angiotensin-aldosterone system : JRAAS. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed, 1 pooled it
0.6field-weighted citation impact, top 31% 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

3 citing papers in PubMed, 1 synthesis or guideline pooled it, 8 citations in OpenAlex.

  1. Pooled it
  2. Article
  3. 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

13 authors at 1 institution in 1 country.

Sandro S Almeida1 Department of Biophysics, Federal University of São Paulo, Brazil.
Flavia C Corgosinho2 Post-Graduate Program of Nutrition, Federal University of São Paulo, Brazil.
Carlos En Amorim1 Department of Biophysics, Federal University of São Paulo, Brazil.
Marcos F Gregnani1 Department of Biophysics, Federal University of São Paulo, Brazil.
Raquel Ms Campos2 Post-Graduate Program of Nutrition, Federal University of São Paulo, Brazil.
Deborah Cl Masquio2 Post-Graduate Program of Nutrition, Federal University of São Paulo, Brazil.
Priscila L Sanches2 Post-Graduate Program of Nutrition, Federal University of São Paulo, Brazil.
Aline P Ganen2 Post-Graduate Program of Nutrition, Federal University of São Paulo, Brazil.
João B Pesquero1 Department of Biophysics, Federal University of São Paulo, Brazil.
Ana R Dâmaso2 Post-Graduate Program of Nutrition, Federal University of São Paulo, Brazil.
Marco T Mello2 Post-Graduate Program of Nutrition, Federal University of São Paulo, Brazil.
Sergio Tufik3 Department of Psychobiology, Federal University of São Paulo, Brazil.
Ronaldo C Araújo1 Department of Biophysics, Federal University of São Paulo, Brazil.
Universidade Federal de São Paulo · BR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionThe main purpose of the present study was to investigate whether I/D polymorphism of the ACE gene might affect metabolic changes related to the metabolic syndrome through a long-term interdisciplinary therapy in obese adolescents.

methodsIn total, 125 obese adolescents who entered the interdisciplinary obesity programme were assigned to the following two subgroups: metabolic syndrome or non-metabolic syndrome. They were evaluated at baseline and after 1 year. Genomic DNA was extracted from circulating leukocytes.

resultsSubjects with the II genotype in the non-metabolic syndrome group were only to increase their fat-free mass after therapy. Regarding lipid profile, subjects with ID and DD genotypes from both groups reduced their low-density lipoprotein cholesterol levels significantly. The metabolic parameters from the ID and DD genotypes of the non-metabolic syndrome group showed a significantly improved insulin response.

conclusionIn the present study, we showed that the ACE polymorphism was able to influence the fat-free mass in the I-carry allele in the non-metabolic syndrome group positively. In addition, the I-carry allele was able to improve the insulin resistance of the metabolic syndrome group significantly. These results suggest that the ACE I/D genotypes can influence, in different ways, the specific parameters of metabolism among obese adolescents submitted for long-term interdisciplinary therapy.

Indexed as

Patient Care TeamPolymorphism, GeneticAdolescentFemaleGene FrequencyGenetic Predisposition to DiseaseGenotypeHomeostasisHumansINDEL MutationInsulinMaleModels, BiologicalObesityPeptidyl-Dipeptidase ARisk FactorsACE protein, humanInsulinPeptidyl-Dipeptidase Aangiotensin-converting enzymeInterdisciplinary therapymetabolic syndromeobesitypolymorphism

Identifiers

PMID28504003
PMCPMC5843858
OpenAlexW2616761094

What OpenQuestion holds

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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.