Evidence map›Paper›PMID 24283216›Full record

Trial reportBMC pediatrics2013

Association analyses for dopamine receptor gene polymorphisms and weight status in a longitudinal analysis in obese children before and after lifestyle intervention.

Christian L Roth, Anke Hinney, Ellen A Schur, Clinton T Elfers, Thomas Reinehr

Registry-linked trialOpen access · goldAbstract readClinical TrialComparative Study
In one paragraph

Trial report in BMC pediatrics, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT00435734 (Evaluation of the Intervention Program "Obeldicks" for Obese Children and Adolescents), which is not on this map. Cited by 18 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 3 pooled it
4.6field-weighted citation impact, top 6% 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.

NCT00435734 active not recruitingnot on this map

Evaluation of the Intervention Program "Obeldicks" for Obese Children and Adolescents

TypeobservationalSponsorUniversity of Witten/HerdeckeRan1999 to 2030Enrolled4,000ConditionsObesityArmsobesity intervention
3 · Its place in the literature

Who cites it

18 citing papers in PubMed, 3 syntheses or guidelines pooled it, 40 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. Pooled it
  4. [Influence of rs2587552 polymorphism ofBeijing da xue xue bao. Yi xue ban = Journal of Peking University. Health sciences · 2023
    Trial
  5. Review
  6. High Fat Diet Increases [Neurochemical research · 2022
    Article
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
  12. DRD2: Bridging the Genome and Ingestive Behavior.Trends in cognitive sciences · 2017
    Review
  13. Article
  14. Article
  15. Article
  16. Review
  17. Article
  18. 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

5 authors at 5 institutions in 2 countries.

Christian L RothDepartment of Pediatrics, University of Washington, Seattle Children's Research Institute, 1900 Ninth Ave, Seattle, WA 98101, USA. christian.roth@seattlechildrens.org.
Anke Hinney
Ellen A Schur
Clinton T Elfers
Thomas Reinehr
Boston Children's Hospital · USEssen University Hospital · DESeattle Children's Hospital · USSeattle University · USUniversity of Washington · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundDopamine receptors are involved in midbrain reward circuit activation. Polymorphisms in two dopamine receptor genes, DRD2 and DRD4, have been associated with altered perception of food reward and weight gain. The objective of this study was to determine whether the same risk alleles were associated with overweight/obesity and with lower reduction of overweight after a 1-year lifestyle intervention.

methodsIn a longitudinal study the association of polymorphisms in DRD2 (rs18000497, risk allele: T, formerly A1 allele at the TaqI A1 polymorphism) and DRD4 (variable number of tandem repeats (VNTR); 48 bp repeat in exon III; risk alleles: 7 repeats or longer: 7R+) was tested on weight loss success following a 1-year lifestyle childhood obesity intervention (OBELDICKS). An additional exploratory cross-sectional case-control study was performed to compare the same DRD polymorphisms in these overweight/obese children and adolescents versus lean adult controls. Subjects were 423 obese and 28 overweight children participating in lifestyle intervention (203 males), age median 12.0 (interquartile range 10.0-13.7) years, body mass index - standard deviation score (BMI-SDS) 2.4 ± 0.5; 583 lean adults (232 males); age median 25.3 (interquartile range 22.5-26.8) years, BMI 19.1 ± 1.9 kg/m2. BMI, BMI-SDS and skinfold thickness measures were assessed at baseline and after 1 year; genotyping was performed for DRD2 risk variant rs1800497 and DRD4 exon III VNTR.

resultsThe DRD2 genotype had a nominal effect on success in the weight loss intervention. The weakest BMI-SDS reduction was in children homozygous for two rs1800497 T-alleles (n = 11) compared to the combined group with zero (n = 308) or one (n = 132) rs1800497 T-allele (-0.08 ± 0.36 vs. -0.28 ± 0.34; p < 0.05). There was no association between the DRD4 VNTR alleles and genotypes and success in the weight loss intervention. No associations of the risk alleles of the DRD2 and DRD4 polymorphisms and obesity were observed in the cross-sectional part of the study.

conclusionsWe did not find association between polymorphisms in DRD2 and DRD4 genes and weight status. However, obese carriers of two DRD2 rs1800497 T-alleles may be at risk for weak responses to lifestyle interventions aimed at weight reduction.

trial registrationObesity intervention program "Obeldicks" is registered at clinicaltrials.gov (NCT00435734).

Indexed as

Polymorphism, GeneticAdolescentAdultAllelesBody Mass IndexCase-Control StudiesChildFemaleGenotypeHumansLongitudinal StudiesMaleMinisatellite RepeatsObesityOverweightPolymorphism, Single NucleotideReceptors, Dopamine D2Receptors, Dopamine D4

Identifiers

PMID24283216
PMCPMC4219494
OpenAlexW2048386457

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

Registered trials

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.