Evidence map›Paper›PMID 27240401›Full record

ArticleNutrients2016

Complementary Effects of Genetic Variations in LEPR on Body Composition and Soluble Leptin Receptor Concentration after 3-Month Lifestyle Intervention in Prepubertal Obese Children.

Joanna Gajewska, Alina Kuryłowicz, Ewa Mierzejewska, Jadwiga Ambroszkiewicz, Magdalena Chełchowska, Halina Weker, Monika Puzianowska-Kuźnicka

Open access · goldAbstract read
In one paragraph

Article in Nutrients, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
6citing papers in PubMed, 2 pooled it
1.2field-weighted citation impact, top 24% 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

6 citing papers in PubMed, 2 syntheses or guidelines pooled it, 16 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Article
  5. Article
  6. 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

7 authors at 2 institutions in 1 country.

Joanna GajewskaScreening Department, Institute of Mother and Child, Kasprzaka 17a, Warsaw 01-211, Poland. joanna.gajewska@imid.med.pl.
Alina KuryłowiczDepartment of Human Epigenetics, Mossakowski Medical Research Center, Polish Academy of Sciences, Warsaw 02-106, Poland. kurylowiczala@gazeta.pl.
Ewa MierzejewskaDepartment of Epidemiology and Biostatistics, Institute of Mother and Child, Warsaw 01-211, Poland. ewa.mierzejewska@imid.med.pl.
Jadwiga AmbroszkiewiczScreening Department, Institute of Mother and Child, Kasprzaka 17a, Warsaw 01-211, Poland. jagoda.ambroszkiewicz@imid.med.pl.
Magdalena ChełchowskaScreening Department, Institute of Mother and Child, Kasprzaka 17a, Warsaw 01-211, Poland. magdalena.chelchowska@imid.med.pl.
Halina WekerDepartment of Nutrition, Institute of Mother and Child, Warsaw 01-211, Poland. halina.weker@imid.med.pl.
Monika Puzianowska-KuźnickaDepartment of Human Epigenetics, Mossakowski Medical Research Center, Polish Academy of Sciences, Warsaw 02-106, Poland. mpuzianowska@wum.edu.pl.
Mossakowski Medical Research Institute, Polish Academy of Sciences · PLPostgraduate School of Molecular Medicine · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

In obese individuals, weight loss might be affected by variants of the adipokine-encoding genes. We verified whether selected functional single nucleotide polymorphisms in LEP, LEPR and ADIPOQ are associated with changes in serum levels of the respective adipokines and weight loss in 100 prepubertal obese (SDS-BMI > 2) Caucasian children undergoing lifestyle intervention. Frequencies of the -2548G > A LEP, Q223R LEPR, K656N LEPR, -11377C > G and -11426A > G ADIPOQ polymorphisms were analyzed by restriction fragment length polymorphism. Serum adipokine and soluble leptin receptor (sOB-R) concentrations were measured using the ELISA method. Among the analyzed polymorphisms, only LEPR polymorphisms were associated with changes of SDS-BMI or sOB-R concentrations in children after therapy. Carriers of the wild-type K665N and at least one minor Q223R allele had the greatest likelihood of losing weight (OR = 5.09, p = 0.006), an increase in sOB-R (ptrend = 0.022) and decrease in SDS-BMI correlated with the decrease of fat mass (p < 0.001). In contrast, carrying of the wild-type Q223R and at least one minor K665N allele were associated with a decrease in sOB-R concentrations and a decrease in SDS-BMI correlated with a decrease in fat-free mass (p = 0.002). We suggest that the combination of different LEPR variants, not a single variant, might determine predisposition to weight loss in the prepubertal period.

Indexed as

AdiposityDiet, HealthyDiet, ReducingHealthy LifestylePolymorphism, Single NucleotideAdiponectinAllelesBody Mass IndexChildChild, PreschoolCombined Modality TherapyExerciseFemaleGenetic Association StudiesHeterozygoteHumansAdiponectinADIPOQ protein, humanLEPR protein, humanLeptinReceptors, Leptinadipokinesleptin receptorpolymorphismsprepubertal periodweight loss

Identifiers

PMID27240401
PMCPMC4924169
OpenAlexW2396339121

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.