Evidence map›Paper›PMID 35329900›Full record

ArticleJournal of clinical medicine2022

High Prevalence of Scoliosis in a Large Cohort of Patients with Prader-Willi Syndrome.

Antonino Crinò, Michela Armando, Marco Crostelli, Osvaldo Mazza, Dario Bruzzese, Alessio Convertino, Danilo Fintini, Sarah Bocchini, Sara Ciccone, Alessandro Sartorio and 1 more

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
3.4field-weighted citation impact, top 7% 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

13 citing papers in PubMed, 18 citations in OpenAlex.

  1. Article
  2. Review
  3. Article
  4. Article
  5. Article
  6. Article
  7. Scoliosis and rare diseases: our experience with the Prader-Willi syndrome.European spine journal : official publication of the European Spine Society, the European Spinal Deformity Society, and the European Section of the Cervical Spine Research Society · 2024
    Article
  8. Article
  9. Article
  10. Review
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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

11 authors at 3 institutions in 1 country.

Antonino CrinòReference Center for Prader-Willi Syndrome, Bambino Gesù Children's Hospital, Research Institute, Palidoro, 00050 Rome, Italy.ORCID 0000-0003-3548-7114
Michela ArmandoPaediatric Neurorehabilitation Unit, Bambino Gesù Children's Hospital, Research Institute, Palidoro, 00050 Rome, Italy.
Marco CrostelliSpine Surgery Unit, Bambino Gesù Children's Hospital, Research Institute, 00165 Rome, Italy.
Osvaldo MazzaSpine Surgery Unit, Bambino Gesù Children's Hospital, Research Institute, 00165 Rome, Italy.ORCID 0000-0002-1850-2864
Dario BruzzeseDepartment of Public Health, University of Naples "Federico II", 80131 Naples, Italy.ORCID 0000-0001-9911-4646
Alessio ConvertinoReference Center for Prader-Willi Syndrome, Bambino Gesù Children's Hospital, Research Institute, Palidoro, 00050 Rome, Italy.
Danilo FintiniReference Center for Prader-Willi Syndrome, Bambino Gesù Children's Hospital, Research Institute, Palidoro, 00050 Rome, Italy.
Sarah BocchiniReference Center for Prader-Willi Syndrome, Bambino Gesù Children's Hospital, Research Institute, Palidoro, 00050 Rome, Italy.
Sara CicconeReference Center for Prader-Willi Syndrome, Bambino Gesù Children's Hospital, Research Institute, Palidoro, 00050 Rome, Italy.ORCID 0000-0002-2881-6672
Alessandro SartorioDivision of Auxology, Istituto Auxologico Italiano, IRCCS, 28824 Piancavallo, Italy.ORCID 0000-0002-9620-4133
Graziano GrugniDivision of Auxology, Istituto Auxologico Italiano, IRCCS, 28824 Piancavallo, Italy.ORCID 0000-0003-4708-2544
Bambino Gesù Children's Hospital · ITIRCCS Istituto Auxologico Italiano · ITUniversity of Naples Federico II · IT

Funding

partially supported by Progetti di Ricerca Corrente, Istituto Auxologico Italiano, IRCCS, Milan, Italy (ref. no. 01C406; acronym: SCOLADUPWS). partially supported by Progetti di Ricerca Corrente, Istituto Auxologico Italiano, IRCCS, Milan, Italy (ref. no. 01C406; acronym: SCOLADUPWS).
6 · The paper itself

Abstract

The characteristics of scoliosis were investigated in a large cohort of children and adults with Prader-Willi syndrome (PWS), analysing the role of age, gender, puberty, body mass index (BMI), genotype and growth hormone therapy (GHT) on its onset and severity. A retrospective cross-sectional study was performed in 180 patients with genetically confirmed PWS (96 females), aged 17.6 ± 12 years. Eighty-five subjects (47%) were obese. One hundred and fifty subjects (83.3%) were on GHT, while 30 patients had never been treated. Overall, 150 subjects (83.3%) were affected by scoliosis, 80.2% of children and adolescents and 87.8% of adults. A mild degree of scoliosis was observed in 58 patients (38.7%), moderate in 43 (28.7%) and severe in 49 (32.6%). Median age at diagnosis of scoliosis was 6.3 years, while the severe forms were diagnosed earlier (median age: 3.8 years). The cumulative probability at 5 years of age was equal to 0.403 and almost doubled at 15 years. No significant associations were found between scoliosis and genotype, gender, pubertal stage, GHT and BMI. A corset was prescribed to 75 subjects (50%) at a median age of 7.5 years, while 26 subjects (17.3%) underwent surgery at a median age of 13.1 years. Our data indicate that scoliosis is one of the major concerns for PWS patients that increases with age, and therefore suggest the need for regular systematic monitoring of spinal deformity from paediatric age.

Indexed as

growth hormone therapyobesityPrader–Willi syndromescoliosis

Identifiers

PMID35329900
PMCPMC8953215
OpenAlexW4220828180

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.