Evidence map›Paper›PMID 36917420›Full record

ArticleJournal of endocrinological investigation2023

High levels of LIGHT/TNFSF14 in patients with Prader-Willi syndrome.

M F Faienza, G Brunetti, D Fintini, G Grugni, M G Wasniewska, A Crinò, G D'Amato, L Piacente, A Oranger, M Dicarlo and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Journal of endocrinological investigation, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
2.2field-weighted citation impact, top 12% 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

5 citing papers in PubMed, 7 citations in OpenAlex.

  1. Article
  2. Article
  3. Review
  4. LIGHT/TNFSF14 Affects Adipose Tissue Phenotype.International journal of molecular sciences · 2024
    Article
  5. Review
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

12 authors at 4 institutions in 1 country.

M F Faienza *Department of Precision and Regenerative Medicine and Ionian Area, Section of Human Anatomy and Histology, University of Bari 'A. Moro', Bari, Italy.
G Brunetti *Department of Biosciences, Biotechnologies and Environment, University of Bari Aldo Moro, Via Orabona, 4, 70125, Bari, Italy. giacomina.brunetti@uniba.it.ORCID http://orcid.org/0000-0002-0681-1432
D FintiniEndocrinology Unit, Pediatric University Department, Bambino Gesù Children's Hospital, Rome, Italy.
G GrugniDivision of Auxology, Istituto Auxologico Italiano, Research Institute, Verbania, Italy.
M G WasniewskaPediatric Unit, Department of Human Pathology in Adulthood and Childhood, University of Messina, Messina, Italy.
A CrinòReference Center for Prader-Willi Syndrome, Bambino Gesù Children's Hospital, Research Institute, Rome, Italy.
G D'AmatoNeonatal Intensive Care Unit, Di Venere Hospital, Bari, Italy.
L PiacenteDepartment of Precision and Regenerative Medicine and Ionian Area, Section of Human Anatomy and Histology, University of Bari 'A. Moro', Bari, Italy.
A OrangerDepartment of Precision and Regenerative Medicine and Ionian Area, Section of Human Anatomy and Histology, University of Bari 'A. Moro', Bari, Italy.
M DicarloDepartment of Translational Biosciences and Neurosciences, Section of Human Anatomy and Histology, University of Bari 'A. Moro', Bari, Italy.
S ColucciDepartment of Translational Biosciences and Neurosciences, Section of Human Anatomy and Histology, University of Bari 'A. Moro', Bari, Italy.
M GranoDepartment of Precision and Regenerative Medicine and Ionian Area, Section of Human Anatomy and Histology, University of Bari 'A. Moro', Bari, Italy.
University of Bari Aldo Moro · ITBambino Gesù Children's Hospital · ITIRCCS Istituto Auxologico Italiano · ITUniversity of Messina · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

PURPOSE/

methodsPrader-Willi syndrome (PWS) is a rare genetic disorder displaying different clinical features, including obesity and bone impairment. LIGHT/TNFSF14 is a cytokine produced by immune cells affecting both fat and bone metabolism. The present study aimed to evaluate LIGHT serum levels in 28 children and 52 adult PWS patients compared to age and sex-matched controls, as well as correlations with parameters of bone and fat metabolism.

resultsMedian serum LIGHT levels were significantly increased in pediatric PWS with respect to controls [255.82 (284.43) pg/ml vs 168.11 (76.23) pg/ml, p ≤ 0.02] as well as in adult PWS compared to controls [296.85 (895.95) pg/ml vs 134.18 (141.18) pg/ml, p ≤ 0.001]. In pediatric PWS, LIGHT levels were positively correlated with weight-SDS, height-SDS, and glucose levels, and negatively with total 25 (OH) vitamin D, cholesterol, LDL cholesterol and triglycerides. Additionally, LIGHT levels were negatively correlated with total BMD and fat mass. In adult PWS, LIGHT levels were positively correlated with weight, HDL cholesterol and PTH, and negatively with glucose, insulin, HOMA-IR, total cholesterol, LDL cholesterol, triglycerides, calcium, phosphorus, 25(OH)Vitamin D as well as with instrumental parameters of bone and fat quality. Consistently, multiple regression analysis showed that LIGHT serum levels in pediatric and adult PWS were predicted by different parameters including 25 (OH) Vitamin D as well as DXA parameters of bone and fat quality.

conclusionsIn PWS children and adults the high levels of LIGHT could represent a marker of the altered bone and fat metabolism.

Indexed as

Prader-Willi SyndromeAdultChildCholesterol, LDLGlucoseHumansTriglyceridesTumor Necrosis Factor Ligand Superfamily Member 14Vitamin DVitaminsCholesterol, LDLGlucoseTNFSF14 protein, humanTriglyceridesTumor Necrosis Factor Ligand Superfamily Member 14Vitamin DVitaminsBone diseaseDXALIGHT/TNFSF14Prader–Willi syndrome

Identifiers

PMID36917420
PMCPMC10371899
OpenAlexW4324129367

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.