Evidence map›Paper›PMID 35237541›Full record

ArticleFrontiers in pediatrics2022

The Hyperphagia Questionnaire: Insights From a Multicentric Validation Study in Individuals With Prader Willi Syndrome.

Maria Rosaria Licenziati, Dario Bacchini, Antonino Crinò, Graziano Grugni, Danilo Fintini, Sara Osimani, Letizia Ragusa, Michele Sacco, Lorenzo Iughetti, Luisa De Sanctis and 6 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in pediatrics, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed, 10 citations in OpenAlex.

  1. Article
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  4. Observational
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

16 authors at 13 institutions in 1 country.

Maria Rosaria LicenziatiDepartment of Neurosciences, Obesity and Endocrine Disease Unit, Santobono-Pausilipon Childrens Hospital, Naples, Italy.
Dario BacchiniDepartment of Humanistic Studies, University of Naples "Federico II", Naples, Italy.
Antonino CrinòReference Center for Prader-Willi Syndrome, Research Institute, Bambino Gesù Hospital, Rome, Italy.
Graziano GrugniDepartment of Auxology, Istituto di Ricerca e Cura a Carattere Scientifico Istituto Auxologico Italiano, Verbania, Italy.
Danilo FintiniReference Center for Prader-Willi Syndrome, Research Institute, Bambino Gesù Hospital, Rome, Italy.
Sara OsimaniDepartment of Pediatrics, Scientific Institute San Raffaele, Milan, Italy.
Letizia RagusaOasi Research Institute-IRCCS, Troina, Italy.
Michele SaccoPediatric Unit Scientific Institute "Casa Sollievo Della Sofferenza" San Giovanni Rotondo (FG), San Giovanni Rotondo, Italy.
Lorenzo IughettiPediatric Unit, Department of Medical and Surgical Sciences for Mothers, Children and Adults, University of Modena and Reggio Emilia, Modena, Italy.
Luisa De SanctisDepartment of Public Health and Pediatric Sciences, University of Torino, Turin, Italy.
Adriana FranzeseDepartment of Traslational Sciences, University of Naples Federico II, Naples, Italy.
Malgorzata Gabriela WasniewskaDepartment of Human Pathology of Adulthood and Childhood, University of Messina, Messina, Italy.
Maria Felicia FaienzaDepartment of Biomedical Sciences and Human Oncology, Pediatric Unit, University of Bari "Aldo Moro", Bari, Italy.
Maurizio DelvecchioMetabolic Disorders and Genetics Unit, "Giovanni XXIII" Children's Hospital, Azienda Ospedaliera Universitaria (A.O.U.) Policlinico di Bari, Bari, Italy.
Concetta EspositoDepartment of Humanistic Studies, University of Naples "Federico II", Naples, Italy.
Giuliana ValerioDepartment of Movement Sciences and Wellbeing, Parthenope University of Naples, Naples, Italy.
University of Naples Federico II · ITBambino Gesù Children's Hospital · ITCasa Sollievo della Sofferenza · ITIRCCS Istituto Auxologico Italiano · ITOasi Maria SS · ITOspedale Pediatrico Giovanni XXIII · ITParthenope University of Naples · ITSan Raffaele University of Rome · ITSantobono Children's Hospital · ITUniversity of Bari Aldo Moro · ITUniversity of Messina · ITUniversity of Modena and Reggio Emilia · ITUniversity of Turin · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND/

objectivesThe present study aimed to validate the Italian version of the Hyperphagia Questionnaire (HQ), a 11-items questionnaire developed to assess hyperphagia in individuals with Prader-Willi syndrome (PWS). This is a complex neurodevelopmental disorder characterized by endocrine dysfunction, hypotonia, intellectual disability, psychiatric disorders and obesity.

methodsParents of 219 individuals with PWS (age range 3-54 years; M

resultsConfirmatory factor analysis (CFA) confirmed the three hyperphagic subdimensions of the original structure (behavior, drive, and severity), but one item was dropped out, reducing the final version to 10 items. Using multi-group CFA, HQ showed satisfactory indexes of measurement invariance by age. Good indexes of internal consistency (Cronbach's alpha and McDonald's Omega coefficients) were found for each subdimension. The three hyperphagia subdimensions positively converged with other food-related measures: emotional overeating, food enjoyment, food responsiveness, and satiety responsiveness. A significant increase of all hyperphagic subdimensions was found across age groups. Higher hyperphagic levels were found in participants with higher body mass index. Hyperphagic drive differently increased in function of the interaction between age and underlying genetic mechanisms.

conclusionThe Italian version of the HQ is a psychometrically valid and reliable instrument for assessing hyperphagia in individuals with PWS. This tool may prove useful to evaluate the efficacy of pharmacologic and rehabilitative treatments.

Indexed as

assessmentGenetic Obesityhyperphagiamulticentric studyPrader-Willi syndromeweight status

Identifiers

PMID35237541
PMCPMC8884358
OpenAlexW4213363734

What OpenQuestion holds

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Registered trials

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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.