Evidence map›Paper›PMID 25355237›Full record

ArticleAmerican journal of medical genetics. Part A2015

Hyperghrelinemia in Prader-Willi syndrome begins in early infancy long before the onset of hyperphagia.

Frederick A Kweh, Jennifer L Miller, Carlos R Sulsona, Clive Wasserfall, Mark Atkinson, Jonathan J Shuster, Anthony P Goldstone, Daniel J Driscoll

Abstract read
In one paragraph

Article in American journal of medical genetics. Part A, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 36 papers.

0numbers the graph read from it
0cells of the map it votes in
36citing papers in PubMed
5.6field-weighted citation impact, top 4% 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

36 citing papers in PubMed, 67 citations in OpenAlex.

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  12. Prader-Willi syndrome: an update on obesity and endocrine problems.Annals of pediatric endocrinology & metabolism · 2021
    Article
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  14. Review
  15. Article
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  19. An overview of ghrelinExpert opinion on therapeutic patents · 2020
    Review
  20. 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

8 authors at 4 institutions in 2 countries.

Frederick A KwehDepartment of Pediatrics, College of Medicine, University of Florida, Gainesville, Florida.
Jennifer L Miller
Carlos R Sulsona
Clive Wasserfall
Mark Atkinson
Jonathan J Shuster
Anthony P Goldstone
Daniel J Driscoll
University of Florida · USEpigenetix (United States) · USFlorida Department of Health · USImperial College London · GB

Funding

Using social networks to map and evaluate team science across CTSA hubsUL1TR001427 · NCATS · UNIVERSITY OF FLORIDA · PI MITCHELL, DUANE A. · 2015 to 2024
$37.2M
Training and Career Development ComponentU54HD061222 · NICHD · UNIVERSITY OF ALABAMA AT BIRMINGHAM · PI PERCY, ALAN KENNETH · 2009 to 2019
$12.4M
UF Clinical and Translational Science AwardUL1TR000064 · NCATS · UNIVERSITY OF FLORIDA · PI NELSON, DAVID R · 2012 to 2014
$12.2M
RARE DISEASE CRC FOR NEW THERAPIES AND NEW DIAGNOSTICSU54RR019478 · NCRR · BAYLOR COLLEGE OF MEDICINE · PI BEAUDET, ARTHUR L. · 2003 to 2008
$7.3M
Neuroanatomic Studies in Prader-Willi Syndrome and Early-onset ObesityK23DK081203 · NIDDK · UNIVERSITY OF FLORIDA · PI MILLER, JENNIFER L · 2008 to 2012
$852k
RESEARCH IN PRADER-WILLI SYNDROME AND OBESITYK24HD001361 · NICHD · UNIVERSITY OF FLORIDA · PI DRISCOLL, DANIEL J · 2000 to 2004
$533k
NCATS NIH HHS UL1 TR000064NCATS NIH HHS UL1 TR001427NCRR NIH HHS RR019478NCRR NIH HHS U54 RR019478NICHD NIH HHS K24 HD001361NICHD NIH HHS U54 HD061222NIDDK NIH HHS 1K23 DK081203NIDDK NIH HHS K23 DK081203
6 · The paper itself

Abstract

Circulating total ghrelin levels are elevated in older children and adults with Prader-Willi syndrome (PWS). However, the presence or absence of hyperghrelinemia in young children with PWS remains controversial. We hypothesized that a more robust way to analyze appetite-regulating hormones in PWS would be by nutritional phases rather than age alone. Our objectives were to compare total serum ghrelin levels in children with PWS by nutritional phase as well as to compare total ghrelin levels in PWS (5 weeks to 21 years of age) to normal weight controls and individuals with early-onset morbid obesity (EMO) without PWS. Fasting serum total ghrelin levels were measured in 60 subjects with PWS, 39 subjects with EMO of unknown etiology, and in 95 normal non-obese sibling controls of PWS or EMO subjects (SibC) in this 12 year longitudinal study. Within PWS, total ghrelin levels were significantly (P < 0.001) higher in earlier nutritional phases: phase 1a (7,906  ±  5,887); 1b (5,057 ± 2,624); 2a (2,905 ± 1,521); 2b (2,615 ± 1,370) and 3 (2,423 ± 1,350). Young infants with PWS also had significantly (P = 0.009) higher total ghrelin levels than did the sibling controls. Nutritional phase is an important independent prognostic factor of total ghrelin levels in individuals with PWS. Circulating ghrelin levels are elevated in young children with PWS long before the onset of hyperphagia, especially during the early phase of poor appetite and feeding. Therefore, it seems unlikely that high ghrelin levels are directly responsible for the switch to the hyperphagic nutritional phases in PWS.

Indexed as

Age DistributionChildChild, PreschoolFastingFemaleGhrelinHumansHyperphagiaInfantInsulin ResistanceMaleObesity, MorbidPrader-Willi SyndromeSiblingsYoung AdultGhrelinghrelinhyperghrelinemiahyperphagianutritional phaseobesityPrader-Willi

Identifiers

PMID25355237
PMCPMC4391201
OpenAlexW2004090718

What OpenQuestion holds

Textmetadata
LicenceTDM
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.