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

Detalhes bibliográficos
Autor(a) principal: Pinto, A.
Data de Publicação: 2018
Outros Autores: Alfadhel, M., Akroyd, R., Atik Altınok, Y., Bernabei, S., Bernstein, L., Bruni, G., Caine, G., Cameron, E., Carruthers, R., Cochrane, B., Daly, A., de Boer, F., Delaunay, S., Dianin, A., Dixon, M., Drogari, E., Dubois, S., Evans, S., Gribben, J., Gugelmo, G., Heidenborg, C., Hunjan, I., Kok, I., Kumru, B., Liguori, A., Mayr, D., Megdad, E., Meyer, U., Oliveira, R., Pal, A., Pozzoli, A., Pretese, R., Rocha, J., Rosenbaum-Fabian, S., Serrano-Nieto, J., Sjoqvist, E., Timmer, C., White, L., van den Hurk, T., van Rijn, M., Zweers, H., Ziadlou, M., MacDonald, A.
Tipo de documento: Artigo
Idioma: eng
Título da fonte: Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
Texto Completo: http://hdl.handle.net/10400.16/2310
Resumo: Background: In 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. Methods: 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. Results: 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: <1y, 36% (n = 46); 1-10y, 59% (n = 74); 11-16y, 3% (n = 4); and >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. Conclusions: 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.
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spelling International practices in the dietary management of fructose 1-6 biphosphatase deficiencyDietary restrictionsFasting toleranceFructose 1,6 bisphosphatase deficiencyUncooked cornstarchBackground: In 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. Methods: 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. Results: 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: <1y, 36% (n = 46); 1-10y, 59% (n = 74); 11-16y, 3% (n = 4); and >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. Conclusions: 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.BMCRepositório Científico do Centro Hospitalar Universitário de Santo AntónioPinto, A.Alfadhel, M.Akroyd, R.Atik Altınok, Y.Bernabei, S.Bernstein, L.Bruni, G.Caine, G.Cameron, E.Carruthers, R.Cochrane, B.Daly, A.de Boer, F.Delaunay, S.Dianin, A.Dixon, M.Drogari, E.Dubois, S.Evans, S.Gribben, J.Gugelmo, G.Heidenborg, C.Hunjan, I.Kok, I.Kumru, B.Liguori, A.Mayr, D.Megdad, E.Meyer, U.Oliveira, R.Pal, A.Pozzoli, A.Pretese, R.Rocha, J.Rosenbaum-Fabian, S.Serrano-Nieto, J.Sjoqvist, E.Timmer, C.White, L.van den Hurk, T.van Rijn, M.Zweers, H.Ziadlou, M.MacDonald, A.2020-02-04T10:16:24Z2018-01-252018-01-25T00:00:00Zinfo:eu-repo/semantics/publishedVersioninfo:eu-repo/semantics/articleapplication/pdfhttp://hdl.handle.net/10400.16/2310engPinto A, Alfadhel M, Akroyd R, et al. International practices in the dietary management of fructose 1-6 biphosphatase deficiency. Orphanet J Rare Dis. 2018;13(1):21. Published 2018 Jan 25.1750-117210.1186/s13023-018-0760-3info:eu-repo/semantics/openAccessreponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãoinstacron:RCAAP2023-10-20T11:00:09Zoai:repositorio.chporto.pt:10400.16/2310Portal AgregadorONGhttps://www.rcaap.pt/oai/openaireopendoar:71602024-03-19T20:38:31.498550Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos) - Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informaçãofalse
dc.title.none.fl_str_mv International practices in the dietary management of fructose 1-6 biphosphatase deficiency
title International practices in the dietary management of fructose 1-6 biphosphatase deficiency
spellingShingle International practices in the dietary management of fructose 1-6 biphosphatase deficiency
Pinto, A.
Dietary restrictions
Fasting tolerance
Fructose 1,6 bisphosphatase deficiency
Uncooked cornstarch
title_short International practices in the dietary management of fructose 1-6 biphosphatase deficiency
title_full International practices in the dietary management of fructose 1-6 biphosphatase deficiency
title_fullStr International practices in the dietary management of fructose 1-6 biphosphatase deficiency
title_full_unstemmed International practices in the dietary management of fructose 1-6 biphosphatase deficiency
title_sort International practices in the dietary management of fructose 1-6 biphosphatase deficiency
author Pinto, A.
author_facet Pinto, A.
Alfadhel, M.
Akroyd, R.
Atik Altınok, Y.
Bernabei, S.
Bernstein, L.
Bruni, G.
Caine, G.
Cameron, E.
Carruthers, R.
Cochrane, B.
Daly, A.
de Boer, F.
Delaunay, S.
Dianin, A.
Dixon, M.
Drogari, E.
Dubois, S.
Evans, S.
Gribben, J.
Gugelmo, G.
Heidenborg, C.
Hunjan, I.
Kok, I.
Kumru, B.
Liguori, A.
Mayr, D.
Megdad, E.
Meyer, U.
Oliveira, R.
Pal, A.
Pozzoli, A.
Pretese, R.
Rocha, J.
Rosenbaum-Fabian, S.
Serrano-Nieto, J.
Sjoqvist, E.
Timmer, C.
White, L.
van den Hurk, T.
van Rijn, M.
Zweers, H.
Ziadlou, M.
MacDonald, A.
author_role author
author2 Alfadhel, M.
Akroyd, R.
Atik Altınok, Y.
Bernabei, S.
Bernstein, L.
Bruni, G.
Caine, G.
Cameron, E.
Carruthers, R.
Cochrane, B.
Daly, A.
de Boer, F.
Delaunay, S.
Dianin, A.
Dixon, M.
Drogari, E.
Dubois, S.
Evans, S.
Gribben, J.
Gugelmo, G.
Heidenborg, C.
Hunjan, I.
Kok, I.
Kumru, B.
Liguori, A.
Mayr, D.
Megdad, E.
Meyer, U.
Oliveira, R.
Pal, A.
Pozzoli, A.
Pretese, R.
Rocha, J.
Rosenbaum-Fabian, S.
Serrano-Nieto, J.
Sjoqvist, E.
Timmer, C.
White, L.
van den Hurk, T.
van Rijn, M.
Zweers, H.
Ziadlou, M.
MacDonald, A.
author2_role author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
author
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author
author
author
author
author
author
dc.contributor.none.fl_str_mv Repositório Científico do Centro Hospitalar Universitário de Santo António
dc.contributor.author.fl_str_mv Pinto, A.
Alfadhel, M.
Akroyd, R.
Atik Altınok, Y.
Bernabei, S.
Bernstein, L.
Bruni, G.
Caine, G.
Cameron, E.
Carruthers, R.
Cochrane, B.
Daly, A.
de Boer, F.
Delaunay, S.
Dianin, A.
Dixon, M.
Drogari, E.
Dubois, S.
Evans, S.
Gribben, J.
Gugelmo, G.
Heidenborg, C.
Hunjan, I.
Kok, I.
Kumru, B.
Liguori, A.
Mayr, D.
Megdad, E.
Meyer, U.
Oliveira, R.
Pal, A.
Pozzoli, A.
Pretese, R.
Rocha, J.
Rosenbaum-Fabian, S.
Serrano-Nieto, J.
Sjoqvist, E.
Timmer, C.
White, L.
van den Hurk, T.
van Rijn, M.
Zweers, H.
Ziadlou, M.
MacDonald, A.
dc.subject.por.fl_str_mv Dietary restrictions
Fasting tolerance
Fructose 1,6 bisphosphatase deficiency
Uncooked cornstarch
topic Dietary restrictions
Fasting tolerance
Fructose 1,6 bisphosphatase deficiency
Uncooked cornstarch
description Background: In 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. Methods: 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. Results: 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: <1y, 36% (n = 46); 1-10y, 59% (n = 74); 11-16y, 3% (n = 4); and >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. Conclusions: 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.
publishDate 2018
dc.date.none.fl_str_mv 2018-01-25
2018-01-25T00:00:00Z
2020-02-04T10:16:24Z
dc.type.status.fl_str_mv info:eu-repo/semantics/publishedVersion
dc.type.driver.fl_str_mv info:eu-repo/semantics/article
format article
status_str publishedVersion
dc.identifier.uri.fl_str_mv http://hdl.handle.net/10400.16/2310
url http://hdl.handle.net/10400.16/2310
dc.language.iso.fl_str_mv eng
language eng
dc.relation.none.fl_str_mv Pinto A, Alfadhel M, Akroyd R, et al. International practices in the dietary management of fructose 1-6 biphosphatase deficiency. Orphanet J Rare Dis. 2018;13(1):21. Published 2018 Jan 25.
1750-1172
10.1186/s13023-018-0760-3
dc.rights.driver.fl_str_mv info:eu-repo/semantics/openAccess
eu_rights_str_mv openAccess
dc.format.none.fl_str_mv application/pdf
dc.publisher.none.fl_str_mv BMC
publisher.none.fl_str_mv BMC
dc.source.none.fl_str_mv reponame:Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
instname:Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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instname_str Agência para a Sociedade do Conhecimento (UMIC) - FCT - Sociedade da Informação
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reponame_str Repositório Científico de Acesso Aberto de Portugal (Repositórios Cientìficos)
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