Literature DB >> 27206562

Defining the Phenotype and Assessing Severity in Phosphoglucomutase-1 Deficiency.

Sunnie Yan-Wai Wong1, Lesa J Beamer2, Therese Gadomski3, Tomas Honzik4, Miski Mohamed5, Saskia B Wortmann6, Katja S Brocke Holmefjord7, Marit Mork7, Francis Bowling8, Jolanta Sykut-Cegielska9, Dieter Koch10, Amanda Ackermann11, Charles A Stanley11, Daisy Rymen12, Avraham Zeharia13, Moeen Al-Sayed14, Thomas Marquardt15, Jaak Jaeken16, Dirk Lefeber17, Donald F Conrad18, Tamas Kozicz3, Eva Morava19.   

Abstract

OBJECTIVE: To define phenotypic groups and identify predictors of disease severity in patients with phosphoglucomutase-1 deficiency (PGM1-CDG). STUDY
DESIGN: We evaluated 27 patients with PGM1-CDG who were divided into 3 phenotypic groups, and group assignment was validated by a scoring system, the Tulane PGM1-CDG Rating Scale (TPCRS). This scale evaluates measurable clinical features of PGM1-CDG. We examined the relationship between genotype, enzyme activity, and TPCRS score by using regression analysis. Associations between the most common clinical features and disease severity were evaluated by principal component analysis.
RESULTS: We found a statistically significant stratification of the TPCRS scores among the phenotypic groups (P < .001). Regression analysis showed that there is no significant correlation between genotype, enzyme activity, and TPCRS score. Principal component analysis identified 5 variables that contributed to 54% variance in the cohort and are predictive of disease severity: congenital malformation, cardiac involvement, endocrine deficiency, myopathy, and growth.
CONCLUSIONS: We established a scoring algorithm to reliably evaluate disease severity in patients with PGM1-CDG on the basis of their clinical history and presentation. We also identified 5 clinical features that are predictors of disease severity; 2 of these features can be evaluated by physical examination, without the need for specific diagnostic testing and thus allow for rapid assessment and initiation of therapy.
Copyright © 2016 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  bifid uvula; cleft palate; coagulopathy; congenital disorder of glycosylation; congenital malformation; dilated cardiomyopathy; hepatopathy; hormonal deficiency; hypoglycemia; myopathy; small stature

Mesh:

Substances:

Year:  2016        PMID: 27206562     DOI: 10.1016/j.jpeds.2016.04.021

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


  20 in total

Review 1.  Glycogen metabolism and glycogen storage disorders.

Authors:  Shibani Kanungo; Kimberly Wells; Taylor Tribett; Areeg El-Gharbawy
Journal:  Ann Transl Med       Date:  2018-12

Review 2.  Nutrient sensing in pancreatic islets: lessons from congenital hyperinsulinism and monogenic diabetes.

Authors:  Ming Lu; Changhong Li
Journal:  Ann N Y Acad Sci       Date:  2017-10-16       Impact factor: 5.691

Review 3.  Liver involvement in congenital disorders of glycosylation (CDG). A systematic review of the literature.

Authors:  D Marques-da-Silva; V Dos Reis Ferreira; M Monticelli; P Janeiro; P A Videira; P Witters; J Jaeken; D Cassiman
Journal:  J Inherit Metab Dis       Date:  2017-01-20       Impact factor: 4.982

Review 4.  Congenital hyperinsulinism disorders: Genetic and clinical characteristics.

Authors:  Elizabeth Rosenfeld; Arupa Ganguly; Diva D De Leon
Journal:  Am J Med Genet C Semin Med Genet       Date:  2019-08-14       Impact factor: 3.908

5.  A Hotspot for Disease-Associated Variants of Human PGM1 Is Associated with Impaired Ligand Binding and Loop Dynamics.

Authors:  Kyle M Stiers; Lesa J Beamer
Journal:  Structure       Date:  2018-08-16       Impact factor: 5.006

6.  The Metabolic Map into the Pathomechanism and Treatment of PGM1-CDG.

Authors:  Silvia Radenkovic; Matthew J Bird; Tim L Emmerzaal; Sunnie Y Wong; Catarina Felgueira; Kyle M Stiers; Leila Sabbagh; Nastassja Himmelreich; Gernot Poschet; Petra Windmolders; Jan Verheijen; Peter Witters; Ruqaiah Altassan; Tomas Honzik; Tuba F Eminoglu; Phillip M James; Andrew C Edmondson; Jozef Hertecant; Tamas Kozicz; Christian Thiel; Pieter Vermeersch; David Cassiman; Lesa Beamer; Eva Morava; Bart Ghesquière
Journal:  Am J Hum Genet       Date:  2019-04-11       Impact factor: 11.025

Review 7.  Cardiac complications of congenital disorders of glycosylation (CDG): a systematic review of the literature.

Authors:  D Marques-da-Silva; R Francisco; D Webster; V Dos Reis Ferreira; J Jaeken; T Pulinilkunnil
Journal:  J Inherit Metab Dis       Date:  2017-07-19       Impact factor: 4.982

8.  Disruption of the Responsible Gene in a Phosphoglucomutase 1 Deficiency Patient by Homozygous Chromosomal Inversion.

Authors:  Katsuyuki Yokoi; Yoko Nakajima; Tamae Ohye; Hidehito Inagaki; Yoshinao Wada; Tokiko Fukuda; Hideo Sugie; Isao Yuasa; Tetsuya Ito; Hiroki Kurahashi
Journal:  JIMD Rep       Date:  2018-05-12

9.  Induced Structural Disorder as a Molecular Mechanism for Enzyme Dysfunction in Phosphoglucomutase 1 Deficiency.

Authors:  Kyle M Stiers; Bailee N Kain; Abigail C Graham; Lesa J Beamer
Journal:  J Mol Biol       Date:  2016-03-10       Impact factor: 5.469

Review 10.  Consensus guideline for the diagnosis and management of mannose phosphate isomerase-congenital disorder of glycosylation.

Authors:  Anna Čechová; Ruqaiah Altassan; Delphine Borgel; Arnaud Bruneel; Joana Correia; Muriel Girard; Annie Harroche; Beata Kiec-Wilk; Klaus Mohnike; Tiffany Pascreau; Łukasz Pawliński; Silvia Radenkovic; Sandrine Vuillaumier-Barrot; Luis Aldamiz-Echevarria; Maria Luz Couce; Esmeralda G Martins; Dulce Quelhas; Eva Morava; Pascale de Lonlay; Peter Witters; Tomáš Honzík
Journal:  J Inherit Metab Dis       Date:  2020-04-21       Impact factor: 4.982

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.