Evidence map›Paper›PMID 33615449›Full record

ArticleClinical genetics2021

Influence of molecular classes and growth hormone treatment on growth and dysmorphology in Prader-Willi syndrome: A multicenter study.

Ranim Mahmoud, Anna Leonenko, Merlin G Butler, Pamela Flodman, June-Anne Gold, Jennifer L Miller, Elizabeth Roof, Elisabeth Dykens, Daniel J Driscoll, Virginia Kimonis

Open access · greenAbstract readMulticenter Study
In one paragraph

Article in Clinical genetics, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

8 citing papers in PubMed, 12 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. Genetics of Obesity in Humans: A Clinical Review.International journal of molecular sciences · 2022
    Review
  5. Article
  6. Article
  7. Article
  8. 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

10 authors at 5 institutions in 2 countries.

Ranim MahmoudDepartment of Pediatrics, University of California, Irvine, CA, Children's Hospital of Orange County, Orange, California.
Anna LeonenkoDepartment of Pediatrics, University of California, Irvine, CA, Children's Hospital of Orange County, Orange, California.
Merlin G ButlerDepartments of Psychiatry & Behavioral Sciences and Pediatrics, University of Kansas Medical Center, Kansas City, Kansas, USA.ORCID 0000-0002-2911-0524
Pamela FlodmanDepartment of Pediatrics, University of California, Irvine, CA, Children's Hospital of Orange County, Orange, California.
June-Anne GoldDepartment of Pediatrics, University of California, Irvine, CA, Children's Hospital of Orange County, Orange, California.
Jennifer L MillerDepartment of Pediatrics, University of Florida, College of Medicine, Gainesville, Florida.
Elizabeth RoofVanderbilt Kennedy Center for Research on Human Development, Vanderbilt University, Nashville, Tennessee.
Elisabeth DykensVanderbilt Kennedy Center for Research on Human Development, Vanderbilt University, Nashville, Tennessee.
Daniel J DriscollDepartment of Pediatrics, University of Florida, College of Medicine, Gainesville, Florida.
Virginia KimonisDepartment of Pediatrics, University of California, Irvine, CA, Children's Hospital of Orange County, Orange, California.ORCID 0000-0003-1567-4449
Children's Hospital of Orange County · USUniversity of Florida · USVanderbilt University · USLoma Linda University Medical Center · USUniversity of Kansas Medical Center · US

Funding

University of California Health Participation in the National COVID Cohort Collaborative (N3C)UL1TR001414 · NCATS · UNIVERSITY OF CALIFORNIA-IRVINE · PI COOPER, DAN M, VILAIN, ERIC J. · 2015 to 2023
$35.1M
Institute for Clinical and Translational ScienceUL1TR000153 · NCATS · UNIVERSITY OF CALIFORNIA-IRVINE · PI COOPER, DAN M · 2012 to 2015
$12.1M
NCATS NIH HHS UL1 TR000153NCATS NIH HHS UL1 TR001414
6 · The paper itself

Abstract

Prader-Willi syndrome (PWS) is a complex genetic disorder with three molecular classes but clinical ascertainment is based on distinctive features. The prevalence of dysmorphic features was studied in 355 PWS participants (61% deletion, 36% maternal disomy [UPD], and 3% imprinting defects) from the National Institute of Health PWS Rare Diseases Clinical Research Network. The effect of growth hormone (GH) treatment on growth and dysmorphic features was compared. Among participants, upslanting palpebral fissures were seen in 23%; strabismus in 42%; abnormal dentition in 32%; small hands in 63% and small feet in 70%; hypopigmentation in 30%; striae in 32% and skin picking in 26%. Compared to those with UPD, participants with deletions were found to be heavier (p = 0.002), had smaller head circumference (HC) (p = 0.009), higher incidence of a flat occiput (p = 0.005); low-anterior hairline (p = 0.04); abnormal dentition (p = 0.009); abdominal striae (p = 0.045), nail abnormalities (p = 0.050), and fair-haired (p < 0.001). Participants in both genetic groups receiving GH were taller (p = 0.005), had larger HCs (p = 0.005), and longer hands (p = 0.049). This study suggested that PWS genetic subtypes and GH treatment can influence growth and dysmorphic features that may impact clinical diagnosis of PWS, such as stature, head shape and appearance of the eyes, nose, and genitalia.

Indexed as

AdolescentAdultBody HeightChildChild, PreschoolFemaleGrowth HormoneHumansInfantMaleMiddle AgedPhenotypePrader-Willi SyndromeYoung AdultGrowth Hormonedysmorphologygenetic subtypesgenotype-phenotypegrowthgrowth hormone treatmentPrader-Willi syndrome

Identifiers

PMID33615449
PMCPMC8568051
OpenAlexW3129719203

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.