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International practices in the dietary management of fructose 1-6 biphosphatase deficiency.

dc.contributor.authorPinto, A
dc.contributor.authorAlfadhel, M
dc.contributor.authorAkroyd, R
dc.contributor.authorAtik-Altınok, Y
dc.contributor.authorBernabei, S M
dc.contributor.authorBernstein, L
dc.contributor.authorBruni, G
dc.contributor.authorCaine, G
dc.contributor.authorCameron, E
dc.contributor.authorCarruthers, R
dc.contributor.authorCochrane, B
dc.contributor.authorDaly, A
dc.contributor.authorde-Boer, F
dc.contributor.authorDelaunay, S
dc.contributor.authorDianin, A
dc.contributor.authorDixon, M
dc.contributor.authorDrogari, E
dc.contributor.authorDubois, S
dc.contributor.authorEvans, S
dc.contributor.authorGribben, J
dc.contributor.authorGugelmo, G
dc.contributor.authorHeidenborg, C
dc.contributor.authorHunjan, I
dc.contributor.authorKok, I L
dc.contributor.authorKumru, B
dc.contributor.authorLiguori, A
dc.contributor.authorMayr, D
dc.contributor.authorMegdad, E
dc.contributor.authorMeyer, U
dc.contributor.authorOliveira, R B
dc.contributor.authorPal, A
dc.contributor.authorPozzoli, A
dc.contributor.authorPretese, R
dc.contributor.authorRocha, J C
dc.contributor.authorRosenbaum-Fabian, S
dc.contributor.authorSerrano-Nieto, J
dc.contributor.authorSjoqvist, E
dc.contributor.authorTimmer, C
dc.contributor.authorWhite, L
dc.contributor.authorvan-den-Hurk, T
dc.contributor.authorvan-Rijn, M
dc.contributor.authorZweers, H
dc.contributor.authorZiadlou, M
dc.contributor.authorMacDonald, A
dc.contributor.funderERDF
dc.contributor.funderPrograma Operacional Competitividade e Internacionalização– COMPETE2020
dc.contributor.funderNational Funds through FCT- Fundação para a Ciência e a Tecnologia within CINTESIS,
dc.date.accessioned2023-01-25T10:03:03Z
dc.date.available2023-01-25T10:03:03Z
dc.date.issued2018-01-25
dc.description.abstractIn fructose 1,6 bisphosphatase (FBPase) deficiency, management aims to prevent hypoglycaemia and lactic acidosis by avoiding prolonged fasting, particularly during febrile illness. Although the need for an emergency regimen to avoid metabolic decompensation is well established at times of illness, there is uncertainty about the need for other dietary management strategies such as sucrose or fructose restriction. We assessed international differences in the dietary management of FBPase deficiency. A cross-sectional questionnaire (13 questions) was emailed to all members of the Society for the Study of Inborn Errors of Metabolism (SSIEM) and a wide database of inherited metabolic disorder dietitians. Thirty-six centres reported the dietary prescriptions of 126 patients with FBPase deficiency. Patients' age at questionnaire completion was: 1-10y, 46% (n = 58), 11-16y, 21% (n = 27), and >16y, 33% (n = 41). Diagnostic age was: 16y, 33% (n = 41). Diagnostic age was: 16y, 2% (n = 2). Seventy-five per cent of centres advocated dietary restrictions. This included restriction of: high sucrose foods only (n = 7 centres, 19%); fruit and sugary foods (n = 4, 11%); fruit, vegetables and sugary foods (n = 13, 36%). Twenty-five per cent of centres (n = 9), advised no dietary restrictions when patients were well. A higher percentage of patients aged >16y rather than ≤16y were prescribed dietary restrictions: patients aged 1-10y, 67% (n = 39/58), 11-16y, 63% (n = 17/27) and >16y, 85% (n = 35/41). Patients classified as having a normal fasting tolerance increased with age from 30% in 1-10y, to 36% in 11-16y, and 58% in >16y, but it was unclear if fasting tolerance was biochemically proven. Twenty centres (56%) routinely prescribed uncooked cornstarch (UCCS) to limit overnight fasting in 47 patients regardless of their actual fasting tolerance (37%). All centres advocated an emergency regimen mainly based on glucose polymer for illness management. Although all patients were prescribed an emergency regimen for illness, use of sucrose and fructose restricted diets with UCCS supplementation varied widely. Restrictions did not relax with age. International guidelines are necessary to help direct future dietary management of FBPase deficiency.
dc.description.versionSi
dc.identifier.citationPinto A, Alfadhel M, Akroyd R, Atik Altınok Y, Bernabei SM, Bernstein L, et al. International practices in the dietary management of fructose 1-6 biphosphatase deficiency. Orphanet J Rare Dis. 2018 Jan 25;13(1):21
dc.identifier.doi10.1186/s13023-018-0760-3
dc.identifier.essn1750-1172
dc.identifier.pmcPMC5785792
dc.identifier.pmid29370874
dc.identifier.pubmedURLhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5785792/pdf
dc.identifier.unpaywallURLhttps://doi.org/10.1186/s13023-018-0760-3
dc.identifier.urihttp://hdl.handle.net/10668/12050
dc.issue.number1
dc.journal.titleOrphanet journal of rare diseases
dc.journal.titleabbreviationOrphanet J Rare Dis
dc.language.isoen
dc.organizationHospital Universitario Regional de Málaga
dc.page.number6
dc.provenanceRealizada la curación de contenido 18/02/2025
dc.publisherBioMed Central
dc.pubmedtypeJournal Article
dc.relation.projectIDPOCI-01-0145-FEDER007746
dc.relation.projectIDUID/IC/4255/2013
dc.relation.publisherversionhttps://ojrd.biomedcentral.com/articles/10.1186/s13023-018-0760-3
dc.rightsAttribution 4.0 International
dc.rights.accessRightsopen access
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectDietary restrictions
dc.subjectFasting tolerance
dc.subjectFructose 1,6 bisphosphatase deficiency
dc.subjectUncooked cornstarch
dc.subject.decsAyuno
dc.subject.decsDietoterapia
dc.subject.decsAlimentos
dc.subject.decsSacarosa
dc.subject.decsUrgencias médicas
dc.subject.decsErrores innatos del metabolismo
dc.subject.meshAcidosis, Lactic
dc.subject.meshCross-Sectional Studies
dc.subject.meshDietary Carbohydrates
dc.subject.meshDietary Supplements
dc.subject.meshFasting
dc.subject.meshFructose-1,6-Diphosphatase Deficiency
dc.subject.meshHumans
dc.subject.meshHypoglycemia
dc.subject.meshSurveys and Questionnaires
dc.titleInternational practices in the dietary management of fructose 1-6 biphosphatase deficiency.
dc.typeresearch article
dc.type.hasVersionVoR
dc.volume.number13
dspace.entity.typePublication

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