Hepatic glycogen storage diseases type 0, VI and IX: description of an italian cohort.


Journal

Orphanet journal of rare diseases
ISSN: 1750-1172
Titre abrégé: Orphanet J Rare Dis
Pays: England
ID NLM: 101266602

Informations de publication

Date de publication:
19 07 2022
Historique:
received: 18 03 2022
accepted: 30 06 2022
entrez: 19 7 2022
pubmed: 20 7 2022
medline: 22 7 2022
Statut: epublish

Résumé

Glycogen storage disease (GSD) type 0, VI and IX are inborn errors of metabolism involving hepatic glycogen synthesis and degradation. We performed a characterization of a large Italian cohort of 30 patients with GSD type 0a, VI, IXa, IXb and IXc. A retrospective evaluation of genetical, auxological and endocrinological data, biochemical tests, and nutritional intakes was assessed. Eventual findings of overweight/obesity and insulin-resistance were correlated with diet composition. Six GSD-0a, 1 GSD-VI, and 23 GSD-IX patients were enrolled, with an age of presentation from 0 to 72 months (median 14 months). Diagnosis was made at a median age of 30 months, with a median diagnostic delay of 11 months and a median follow-up of 66 months. From first to last visit, patients gained a median height of 0.6 SDS (from - 1.1 to 2.1 SDS) and a median weight of 0.5 SDS (from - 2.5 to 3.3 SDS); mean and minimal glucose values significant improved (p < 0.05). With respect to dietary intakes, protein intake (g/kg) and protein intake (g/kg)/RDA ratio directly correlated with the glucose/insulin ratio (p < 0.05) and inversely correlated with HOMA-IR (Homeostasis model assessment of insulin resistance, p < 0.05), BMI SDS (p < 0.05) and %ibw (ideal body weight percentage, p < 0.01). A prompt establishment of specific nutritional therapy allowed to preserve growth, improve glycemic control and prevent liver complication, during childhood. Remarkably, the administration of a high protein diet appeared to have a protective effect against overweight/obesity and insulin-resistance.

Sections du résumé

BACKGROUND
Glycogen storage disease (GSD) type 0, VI and IX are inborn errors of metabolism involving hepatic glycogen synthesis and degradation. We performed a characterization of a large Italian cohort of 30 patients with GSD type 0a, VI, IXa, IXb and IXc. A retrospective evaluation of genetical, auxological and endocrinological data, biochemical tests, and nutritional intakes was assessed. Eventual findings of overweight/obesity and insulin-resistance were correlated with diet composition.
RESULTS
Six GSD-0a, 1 GSD-VI, and 23 GSD-IX patients were enrolled, with an age of presentation from 0 to 72 months (median 14 months). Diagnosis was made at a median age of 30 months, with a median diagnostic delay of 11 months and a median follow-up of 66 months. From first to last visit, patients gained a median height of 0.6 SDS (from - 1.1 to 2.1 SDS) and a median weight of 0.5 SDS (from - 2.5 to 3.3 SDS); mean and minimal glucose values significant improved (p < 0.05). With respect to dietary intakes, protein intake (g/kg) and protein intake (g/kg)/RDA ratio directly correlated with the glucose/insulin ratio (p < 0.05) and inversely correlated with HOMA-IR (Homeostasis model assessment of insulin resistance, p < 0.05), BMI SDS (p < 0.05) and %ibw (ideal body weight percentage, p < 0.01).
CONCLUSION
A prompt establishment of specific nutritional therapy allowed to preserve growth, improve glycemic control and prevent liver complication, during childhood. Remarkably, the administration of a high protein diet appeared to have a protective effect against overweight/obesity and insulin-resistance.

Identifiants

pubmed: 35854365
doi: 10.1186/s13023-022-02431-5
pii: 10.1186/s13023-022-02431-5
pmc: PMC9295101
doi:

Substances chimiques

Insulins 0
Glucose IY9XDZ35W2

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

285

Informations de copyright

© 2022. The Author(s).

Références

Mol Genet Metab. 2006 Apr;87(4):284-8
pubmed: 16337419
Arch Med Sci. 2019 Feb 18;17(2):304-313
pubmed: 33747265
Acta Endocrinol (Buchar). 2019 Oct-Dec;15(4):526-530
pubmed: 32377253
J Pediatr Pharmacol Ther. 2019 Sep-Oct;24(5):421-430
pubmed: 31598106
Genet Med. 2015 May;17(5):405-24
pubmed: 25741868
Eur J Pediatr. 1990 Jan;149(4):268-71
pubmed: 2303074
Mol Genet Metab. 2013 Jun;109(2):179-82
pubmed: 23578772
Eur J Pediatr. 2020 Mar;179(3):405-413
pubmed: 31768638
J Sport Health Sci. 2021 Dec;10(6):675-689
pubmed: 34237456
Eur J Nutr. 2021 Aug;60(5):2435-2447
pubmed: 33145643
World J Gastroenterol. 2007 May 14;13(18):2541-53
pubmed: 17552001
BBA Clin. 2016 Feb 27;5:85-100
pubmed: 27051594
J Int Med Res. 2020 Aug;48(8):300060520936857
pubmed: 32779500
J Endocrinol Invest. 2006 Jul-Aug;29(7):581-93
pubmed: 16957405
JIMD Rep. 2020 Feb 25;53(1):39-44
pubmed: 32395408
JAMA Pediatr. 2019 Jun 1;173(6):597-598
pubmed: 30933264
J Inherit Metab Dis. 2007 Oct;30(5):722-34
pubmed: 17705025
Front Biosci. 1999 Sep 15;4:D618-41
pubmed: 10487978
J Pediatr Endocrinol Metab. 2017 Apr 1;30(4):459-462
pubmed: 28245189
Genet Med. 2019 Apr;21(4):772-789
pubmed: 30659246
Gastroenterology. 2017 Feb;152(3):571-585.e8
pubmed: 27765690
JIMD Rep. 2017;37:63-72
pubmed: 28283841
Mol Genet Metab. 2014 Nov;113(3):171-6
pubmed: 25266922
J Pediatr Gastroenterol Nutr. 2012 Jul;55(1):90-2
pubmed: 21857251
Ann Transl Med. 2018 Dec;6(24):474
pubmed: 30740405
Bioinformatics. 2019 Jun 1;35(11):1978-1980
pubmed: 30376034

Auteurs

Francesco Tagliaferri (F)

Division of Metabolism, Department of Pediatric Subspecialties, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
SCDU of Pediatrics, Azienda Ospedaliero-Universitaria Maggiore Della Carità, University of Piemonte Orientale, Novara, Italy.

Miriam Massese (M)

Division of Metabolism, Department of Pediatric Subspecialties, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.
Center for Rare Diseases and Birth Defects, Department of Woman and Child Health and Public Health, Fondazione Policlinico Universitario A. Gemelli IRCCS, Rome, Italy.

Luisa Russo (L)

Division of Metabolism, Department of Pediatric Subspecialties, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.

Anna Commone (A)

Division of Metabolism, Department of Pediatric Subspecialties, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.

Serena Gasperini (S)

Metabolic Unit Rare Disease, Pediatric Department, Fondazione MBBM, San Gerardo Hospital, Monza, Italy.

Roberta Pretese (R)

Metabolic Unit Rare Disease, Pediatric Department, Fondazione MBBM, San Gerardo Hospital, Monza, Italy.

Carlo Dionisi-Vici (C)

Division of Metabolism, Department of Pediatric Subspecialties, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy.

Arianna Maiorana (A)

Division of Metabolism, Department of Pediatric Subspecialties, Bambino Gesù Children's Hospital, IRCCS, Rome, Italy. arianna.maiorana@opbg.net.

Articles similaires

[Redispensing of expensive oral anticancer medicines: a practical application].

Lisanne N van Merendonk, Kübra Akgöl, Bastiaan Nuijen
1.00
Humans Antineoplastic Agents Administration, Oral Drug Costs Counterfeit Drugs

Smoking Cessation and Incident Cardiovascular Disease.

Jun Hwan Cho, Seung Yong Shin, Hoseob Kim et al.
1.00
Humans Male Smoking Cessation Cardiovascular Diseases Female
Humans United States Aged Cross-Sectional Studies Medicare Part C
1.00
Humans Yoga Low Back Pain Female Male

Classifications MeSH