Literature DB >> 26059338

Quality of Life and Its Determinants in a Multicenter Cohort of Children with Alagille Syndrome.

Binita M Kamath1, Zhen Chen2, Rene Romero3, Emily M Fredericks2, Estella M Alonso4, Ronen Arnon5, James Heubi6, Paula M Hertel7, Saul J Karpen3, Kathleen M Loomes8, Karen F Murray9, Philip Rosenthal10, Kathleen B Schwarz11, Girish Subbarao12, Jeffrey H Teckman13, Yumirle P Turmelle14, Kasper S Wang15, Averell H Sherker16, Ronald J Sokol17, John C Magee2.   

Abstract

OBJECTIVES: To assess health-related quality of life (HRQOL) in children with Alagille syndrome (ALGS) in comparison with healthy and other liver disease cohorts, and to identify determinants of HRQOL in patients with ALGS. STUDY
DESIGN: Within the Childhood Liver Disease Research Network prospective study of cholestasis, Pediatric Quality of Life Inventory (PedsQL) questionnaires were administered to 70 children with ALGS, 95 children with alpha-1-antitrypsin deficiency (A1ATD), and 49 children with other causes of chronic intrahepatic cholestasis (IHC) aged 5-18 years. Parent proxy PedsQL scores were recorded for children aged 2-18 years (98 ALGS, 123 A1ATD, and 68 IHC).
RESULTS: Mean ages and total bilirubin (mg/dL) were ALGS 9.4 years; 4.4, A1ATD 9.5 years; 0.7, and IHC 10.3 years; 2.9. ALGS child PedsQL scores were lower than in healthy children and children with A1ATD (mean 73 vs 83; P = .001). Children with ALGS and IHC were similar, except in physical scores (73 vs 79; P = .05). Parents of children with ALGS perceived their children to have worse HRQOL than A1ATD (P ≤ .001) and marginally lower compared with IHC. Univariate analysis revealed ALGS child-reported scores were positively associated with better growth and inversely with total bilirubin. Growth failure, elevated international normalized ratio, and an intracardiac defect were predictive of poor parental scores (P ≤ .05). In multivariate analysis, only weight z-score remained significant for child- and parent-reported scores.
CONCLUSIONS: HRQOL is impaired in children with ALGS compared with healthy and children with A1ATD, similar to children with IHC and is associated with growth failure, which is a potentially treatable cause of impaired HRQOL.
Copyright © 2015 Elsevier Inc. All rights reserved.

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Year:  2015        PMID: 26059338      PMCID: PMC4516587          DOI: 10.1016/j.jpeds.2015.04.077

Source DB:  PubMed          Journal:  J Pediatr        ISSN: 0022-3476            Impact factor:   4.406


  18 in total

1.  Mutations in JAGGED1 gene are predominantly sporadic in Alagille syndrome.

Authors:  C Crosnier; C Driancourt; N Raynaud; S Dhorne-Pollet; N Pollet; O Bernard; M Hadchouel; M Meunier-Rotival
Journal:  Gastroenterology       Date:  1999-05       Impact factor: 22.682

Review 2.  A critical review of the health-related quality of life of children and adolescents after liver transplantation.

Authors:  Rachel Taylor; Linda S Franck; Faith Gibson; Anil Dhawan
Journal:  Liver Transpl       Date:  2005-01       Impact factor: 5.799

3.  Health-related quality of life in long-term survivors of pediatric liver transplantation.

Authors:  D E Midgley; T A Bradlee; C Donohoe; K P Kent; E M Alonso
Journal:  Liver Transpl       Date:  2000-05       Impact factor: 5.799

4.  PedsQL 4.0: reliability and validity of the Pediatric Quality of Life Inventory version 4.0 generic core scales in healthy and patient populations.

Authors:  J W Varni; M Seid; P S Kurtin
Journal:  Med Care       Date:  2001-08       Impact factor: 2.983

5.  Perception of quality of life by patients, partners and treating physicians.

Authors:  K A Wilson; A J Dowling; M Abdolell; I F Tannock
Journal:  Qual Life Res       Date:  2000       Impact factor: 4.147

6.  Health-related quality of life and family function following pediatric liver transplantation.

Authors:  Estella M Alonso; Katie Neighbors; Franca B Barton; Sue V McDiarmid; Stephen P Dunn; George V Mazariegos; Jeanne M Landgraf; John C Bucuvalas
Journal:  Liver Transpl       Date:  2008-04       Impact factor: 5.799

7.  Functional outcomes of pediatric liver transplantation.

Authors:  E M Alonso; K Neighbors; C Mattson; E Sweet; H Ruch-Ross; C Berry; J Sinacore
Journal:  J Pediatr Gastroenterol Nutr       Date:  2003-08       Impact factor: 2.839

8.  Impact of liver transplantation on HRQOL in children less than 5 years old.

Authors:  Conrad R Cole; John C Bucuvalas; Richard W Hornung; Susan Krug; Frederick C Ryckman; Harry Atherton; Maria P Alonso; William F Balistreri; Uma Kotagal
Journal:  Pediatr Transplant       Date:  2004-06

9.  The PedsQL 4.0 as a pediatric population health measure: feasibility, reliability, and validity.

Authors:  James W Varni; Tasha M Burwinkle; Michael Seid; Douglas Skarr
Journal:  Ambul Pediatr       Date:  2003 Nov-Dec

10.  Outcome of syndromic paucity of interlobular bile ducts (Alagille syndrome) with onset of cholestasis in infancy.

Authors:  E J Hoffenberg; M R Narkewicz; J M Sondheimer; D J Smith; A Silverman; R J Sokol
Journal:  J Pediatr       Date:  1995-08       Impact factor: 4.406

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  7 in total

1.  Development of a Novel Tool to Assess the Impact of Itching in Pediatric Cholestasis.

Authors:  Binita M Kamath; Linda Abetz-Webb; Ciara Kennedy; Bonnie Hepburn; Martha Gauthier; Nathan Johnson; Sharon Medendorp; Alejandro Dorenbaum; Lora Todorova; Benjamin L Shneider
Journal:  Patient       Date:  2018-02       Impact factor: 3.883

2.  Unraveling the Relationship Between Itching, Scratch Scales, and Biomarkers in Children With Alagille Syndrome.

Authors:  Binita M Kamath; Cathie Spino; Richard McLain; John C Magee; Emily M Fredericks; Kenneth D Setchell; Alexander Miethke; Jean P Molleston; Cara L Mack; Robert H Squires; Estella M Alonso; Karen F Murray; Kathleen M Loomes; M Kyle Jensen; Saul J Karpen; Philip Rosenthal; Danny Thomas; Ronald J Sokol; Benjamin L Shneider
Journal:  Hepatol Commun       Date:  2020-05-26

Review 3.  Potential of ileal bile acid transporter inhibition as a therapeutic target in Alagille syndrome and progressive familial intrahepatic cholestasis.

Authors:  Binita M Kamath; Philip Stein; Roderick H J Houwen; Henkjan J Verkade
Journal:  Liver Int       Date:  2020-06-22       Impact factor: 5.828

Review 4.  Epidemiology and burden of progressive familial intrahepatic cholestasis: a systematic review.

Authors:  Tracey Jones-Hughes; Jo Campbell; Louise Crathorne
Journal:  Orphanet J Rare Dis       Date:  2021-06-03       Impact factor: 4.123

5.  Evaluation of nutritional adjustment program on quality of life in children with chronic liver disease.

Authors:  Seyed Ali Jafari; Aramesh Rezaeian; Zahra Namjou; Majid Ghayour-Mobarhan; Zahra Ghaneifar
Journal:  J Educ Health Promot       Date:  2021-05-20

6.  Neurodevelopmental Outcomes in Children With Inherited Liver Disease and Native Liver.

Authors:  Daniel H Leung; Lisa G Sorensen; Wen Ye; Kieran Hawthorne; Vicky L Ng; Kathleen M Loomes; Emily M Fredericks; Estella M Alonso; James E Heubi; Simon P Horslen; Saul J Karpen; Jean P Molleston; Philip Rosenthal; Ronald J Sokol; Robert H Squires; Kasper S Wang; Binita M Kamath; John C Magee
Journal:  J Pediatr Gastroenterol Nutr       Date:  2022-01-01       Impact factor: 3.288

7.  Impact of progressive familial intrahepatic cholestasis on caregivers: caregiver-reported outcomes from the multinational PICTURE study.

Authors:  Claudia Mighiu; Sonia O'Hara; Enrico Ferri Grazzi; Karen F Murray; Jörn M Schattenberg; Emily Ventura; Melanie Karakaidos; Alison Taylor; Harpreet Brrang; Anil Dhawan; Jose Willemse; Alan Finnegan
Journal:  Orphanet J Rare Dis       Date:  2022-02-02       Impact factor: 4.123

  7 in total

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