Cargando…

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

PURPOSE/METHODS: Prader–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 i...

Descripción completa

Detalles Bibliográficos
Autores principales:	Faienza, M. F., Brunetti, G., Fintini, D., Grugni, G., Wasniewska, M. G., Crinò, A., D’Amato, G., Piacente, L., Oranger, A., Dicarlo, M., Colucci, S., Grano, M.
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	Springer International Publishing 2023
Materias:	Original Article
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10371899/ https://www.ncbi.nlm.nih.gov/pubmed/36917420 http://dx.doi.org/10.1007/s40618-023-02050-2

Ejemplares similares

The genetic background and vitamin D supplementation can affect irisin levels in Prader–Willi syndrome
por: Faienza, M. F., et al.
Publicado: (2021)

Obesity management in Prader–Willi syndrome: current perspectives
por: Crinò, Antonino, et al.
Publicado: (2018)

Shedding “LIGHT” on the Link between Bone and Fat in Obese Children and Adolescents
por: Brunetti, Giacomina, et al.
Publicado: (2020)

The Hyperphagia Questionnaire: Insights From a Multicentric Validation Study in Individuals With Prader Willi Syndrome
por: Licenziati, Maria Rosaria, et al.
Publicado: (2022)

Congenital hypothyroidism due to ectopic sublingual thyroid gland in Prader-Willi Syndrome: a case report
por: Bocchini, Sarah, et al.
Publicado: (2017)

Angiopoietin-like 8 (ANGPTL8) as a potential predictor of NAFLD in paediatric patients with Prader-Willi Syndrome
por: Mele, C., et al.
Publicado: (2020)

LIGHT/TNFSF14 increases osteoclastogenesis and decreases osteoblastogenesis in multiple myeloma-bone disease
por: Brunetti, Giacomina, et al.
Publicado: (2014)

The Italian registry for patients with Prader–Willi syndrome
por: Salvatore, Marco, et al.
Publicado: (2023)

Hyperprolactinemia in Adults with Prader-Willi Syndrome
por: Sjöström, Anna, et al.
Publicado: (2021)

Growth hormone therapy for Prader–willi syndrome: challenges and solutions
por: Grugni, Graziano, et al.
Publicado: (2016)

High Prevalence of Scoliosis in a Large Cohort of Patients with Prader-Willi Syndrome
por: Crinò, Antonino, et al.
Publicado: (2022)

Circulating Irisin in Children and Adolescents With Prader-Willi Syndrome: Relation With Glucose Metabolism
por: Mai, Stefania, et al.
Publicado: (2022)

LIGHT/TNFSF14 as a New Biomarker of Bone Disease in Multiple Myeloma Patients Experiencing Therapeutic Regimens
por: Brunetti, Giacomina, et al.
Publicado: (2018)

Long-term effects of GH therapy in adult patients with Prader-Willi syndrome: a longitudinal study
por: Grugni, Graziano, et al.
Publicado: (2023)

Central Adrenal Insufficiency Is Rare in Adults With Prader–Willi Syndrome
por: Rosenberg, Anna G W, et al.
Publicado: (2020)

Caring and living with Prader-Willi syndrome in Italy: integrating children, adults and parents’ experiences through a multicentre narrative medicine research
por: Ragusa, Letizia, et al.
Publicado: (2020)

Hyponatremia in Children and Adults with Prader–Willi Syndrome: A Survey Involving Seven Countries
por: Coupaye, Muriel, et al.
Publicado: (2021)

Role of Wnt-signaling inhibitors DKK-1 and sclerostin in bone fragility associated with Turner syndrome
por: Chiarito, M., et al.
Publicado: (2022)

SUN-308 Central Adrenal Insufficiency Is Rare in Adults with Prader-Willi Syndrome
por: Rosenberg, Anna G W, et al.
Publicado: (2020)

Gait patterns in Prader-Willi and Down syndrome patients
por: Cimolin, Veronica, et al.
Publicado: (2010)

Gait initiation and termination strategies in patients with Prader-Willi syndrome
por: Cimolin, Veronica, et al.
Publicado: (2017)

EEG Patterns in Patients with Prader–Willi Syndrome
por: Elia, Maurizio, et al.
Publicado: (2021)

Malignancies in Prader-Willi Syndrome: Results From a Large International Cohort and Literature Review
por: Pellikaan, Karlijn, et al.
Publicado: (2023)

Causes of Death in Prader-Willi Syndrome: Prader-Willi Syndrome Association (USA) 40-Year Mortality Survey
por: Butler, Merlin G., et al.
Publicado: (2016)

Postural adaptations to long-term training in Prader-Willi patients
por: Capodaglio, Paolo, et al.
Publicado: (2011)

A rare occurrence of non-classic congenital adrenal hyperplasia and type 1 diabetes mellitus in a girl with Prader-Willi Syndrome: Case report and review of the literature
por: Aureli, Alessia, et al.
Publicado: (2023)

Three Siblings with Prader-Willi Syndrome: Brief Review of Sleep and Prader-Willi Syndrome
por: Bingeliene, Arina, et al.
Publicado: (2015)

Hedonic eating in Prader–Willi syndrome is associated with blunted PYY secretion
por: Rigamonti, A. E., et al.
Publicado: (2017)

Kidney disease in adults with Prader-Willi syndrome: international cohort study and systematic literature review
por: van Abswoude, Denise H., et al.
Publicado: (2023)

Learning by observation and learning by doing in Prader-Willi syndrome
por: Foti, Francesca, et al.
Publicado: (2015)

Epigenetics in Prader-Willi Syndrome
por: Mendiola, Aron Judd P., et al.
Publicado: (2021)

Fractal dimension approach in postural control of subjects with Prader-Willi Syndrome
por: Cimolin, Veronica, et al.
Publicado: (2011)

Prader–Willi Syndrome in Adults: An Update On Nutritional Treatment and Pharmacological Approach
por: Barrea, Luigi, et al.
Publicado: (2022)

Glucocorticoid-Induced Osteoporosis in Children with 21-Hydroxylase Deficiency
por: Ventura, Annamaria, et al.
Publicado: (2013)

Mechanisms Involved in Childhood Obesity-Related Bone Fragility
por: Faienza, Maria Felicia, et al.
Publicado: (2019)

Strength characterization of knee flexor and extensor muscles in Prader-Willi and obese patients
por: Capodaglio, Paolo, et al.
Publicado: (2009)

Special Issue: Genetics of Prader–Willi Syndrome
por: Godler, David E., et al.
Publicado: (2021)

Clinical implications of gait analysis in the rehabilitation of adult patients with "Prader-Willi" Syndrome: a cross-sectional comparative study ("Prader-Willi" Syndrome vs matched obese patients and healthy subjects)
por: Vismara, Luca, et al.
Publicado: (2007)

Pharmacodynamic Gene Testing in Prader-Willi Syndrome
por: Forster, Janice, et al.
Publicado: (2020)

OR27-5 Malignancies in Prader-Willi Syndrome: Practical Recommendations Based on a Large International Cohort
por: Caixàs, Assumpta, et al.
Publicado: (2022)

Cannot write session to /tmp/vufind_sessions/sess_46kp9am7u7eu2vgiavfu6aq64o