Impact of age at onset and newborn screening on outcome in organic acidurias

Standard

Impact of age at onset and newborn screening on outcome in organic acidurias. / Heringer, Jana; Valayannopoulos, Vassili; Lund, Allan M; Wijburg, Frits A; Freisinger, Peter; Barić, Ivo; Baumgartner, Matthias R; Burgard, Peter; Burlina, Alberto B; Chapman, Kimberly A; I Saladelafont, Elisenda Cortès; Karall, Daniela; Mühlhausen, Chris; Riches, Victoria; Schiff, Manuel; Sykut-Cegielska, Jolanta; Walter, John H; Zeman, Jiri; Chabrol, Brigitte; Kölker, Stefan; additional individual contributors of the E-IMD consortium.

In: J INHERIT METAB DIS, Vol. 39, No. 3, 2016, p. 341-353.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Heringer, J, Valayannopoulos, V, Lund, AM, Wijburg, FA, Freisinger, P, Barić, I, Baumgartner, MR, Burgard, P, Burlina, AB, Chapman, KA, I Saladelafont, EC, Karall, D, Mühlhausen, C, Riches, V, Schiff, M, Sykut-Cegielska, J, Walter, JH, Zeman, J, Chabrol, B, Kölker, S & additional individual contributors of the E-IMD consortium 2016, 'Impact of age at onset and newborn screening on outcome in organic acidurias', J INHERIT METAB DIS, vol. 39, no. 3, pp. 341-353. https://doi.org/10.1007/s10545-015-9907-8

APA

Heringer, J., Valayannopoulos, V., Lund, A. M., Wijburg, F. A., Freisinger, P., Barić, I., Baumgartner, M. R., Burgard, P., Burlina, A. B., Chapman, K. A., I Saladelafont, E. C., Karall, D., Mühlhausen, C., Riches, V., Schiff, M., Sykut-Cegielska, J., Walter, J. H., Zeman, J., Chabrol, B., ... additional individual contributors of the E-IMD consortium (2016). Impact of age at onset and newborn screening on outcome in organic acidurias. J INHERIT METAB DIS, 39(3), 341-353. https://doi.org/10.1007/s10545-015-9907-8

Vancouver

Heringer J, Valayannopoulos V, Lund AM, Wijburg FA, Freisinger P, Barić I et al. Impact of age at onset and newborn screening on outcome in organic acidurias. J INHERIT METAB DIS. 2016;39(3):341-353. https://doi.org/10.1007/s10545-015-9907-8

Bibtex

@article{c4951bc6a19f49528454bea577842ac7,
title = "Impact of age at onset and newborn screening on outcome in organic acidurias",
abstract = "BACKGROUND AND AIM: To describe current diagnostic and therapeutic strategies in organic acidurias (OADs) and to evaluate their impact on the disease course allowing harmonisation.METHODS: Datasets of 567 OAD patients from the E-IMD registry were analysed. The sample includes patients with methylmalonic (MMA, n = 164), propionic (PA, n = 144) and isovaleric aciduria (IVA, n = 83), and glutaric aciduria type 1 (GA1, n = 176). Statistical analysis included description and recursive partitioning of diagnostic and therapeutic strategies, and odds ratios (OR) for health outcome parameters. For some analyses, symptomatic patients were divided into those presenting with first symptoms during (i.e. early onset, EO) or after the newborn period (i.e. late onset, LO).RESULTS: Patients identified by newborn screening (NBS) had a significantly lower median age of diagnosis (8 days) compared to the LO group (363 days, p < 0.001], but not compared to the EO group. Of all OAD patients 71 % remained asymptomatic until day 8. Patients with cobalamin-nonresponsive MMA (MMA-Cbl(-)) and GA1 identified by NBS were less likely to have movement disorders than those diagnosed by selective screening (MMA-Cbl(-): 10 % versus 39 %, p = 0.002; GA1: 26 % versus 73 %, p < 0.001). For other OADs, the clinical benefit of NBS was less clear. Reported age-adjusted intake of natural protein and calories was significantly higher in LO patients than in EO patients reflecting different disease severities. Variable drug combinations, ranging from 12 in MMA-Cbl(-) to two in isovaleric aciduria, were used for maintenance treatment. The effects of specific metabolic treatment strategies on the health outcomes remain unclear because of the strong influences of age at onset (EO versus LO), diagnostic mode (NBS versus selective screening), and the various treatment combinations used.CONCLUSIONS: NBS is an effective intervention to reduce time until diagnosis especially for LO patients and to prevent irreversible cerebral damage in GA1 and MMA-Cbl(-). Huge diversity of therapeutic interventions hampers our understanding of optimal treatment.",
author = "Jana Heringer and Vassili Valayannopoulos and Lund, {Allan M} and Wijburg, {Frits A} and Peter Freisinger and Ivo Bari{\'c} and Baumgartner, {Matthias R} and Peter Burgard and Burlina, {Alberto B} and Chapman, {Kimberly A} and {I Saladelafont}, {Elisenda Cort{\`e}s} and Daniela Karall and Chris M{\"u}hlhausen and Victoria Riches and Manuel Schiff and Jolanta Sykut-Cegielska and Walter, {John H} and Jiri Zeman and Brigitte Chabrol and Stefan K{\"o}lker and {additional individual contributors of the E-IMD consortium}",
year = "2016",
doi = "10.1007/s10545-015-9907-8",
language = "English",
volume = "39",
pages = "341--353",
journal = "J INHERIT METAB DIS",
issn = "0141-8955",
publisher = "Springer Netherlands",
number = "3",

}

RIS

TY - JOUR

T1 - Impact of age at onset and newborn screening on outcome in organic acidurias

AU - Heringer, Jana

AU - Valayannopoulos, Vassili

AU - Lund, Allan M

AU - Wijburg, Frits A

AU - Freisinger, Peter

AU - Barić, Ivo

AU - Baumgartner, Matthias R

AU - Burgard, Peter

AU - Burlina, Alberto B

AU - Chapman, Kimberly A

AU - I Saladelafont, Elisenda Cortès

AU - Karall, Daniela

AU - Mühlhausen, Chris

AU - Riches, Victoria

AU - Schiff, Manuel

AU - Sykut-Cegielska, Jolanta

AU - Walter, John H

AU - Zeman, Jiri

AU - Chabrol, Brigitte

AU - Kölker, Stefan

AU - additional individual contributors of the E-IMD consortium

PY - 2016

Y1 - 2016

N2 - BACKGROUND AND AIM: To describe current diagnostic and therapeutic strategies in organic acidurias (OADs) and to evaluate their impact on the disease course allowing harmonisation.METHODS: Datasets of 567 OAD patients from the E-IMD registry were analysed. The sample includes patients with methylmalonic (MMA, n = 164), propionic (PA, n = 144) and isovaleric aciduria (IVA, n = 83), and glutaric aciduria type 1 (GA1, n = 176). Statistical analysis included description and recursive partitioning of diagnostic and therapeutic strategies, and odds ratios (OR) for health outcome parameters. For some analyses, symptomatic patients were divided into those presenting with first symptoms during (i.e. early onset, EO) or after the newborn period (i.e. late onset, LO).RESULTS: Patients identified by newborn screening (NBS) had a significantly lower median age of diagnosis (8 days) compared to the LO group (363 days, p < 0.001], but not compared to the EO group. Of all OAD patients 71 % remained asymptomatic until day 8. Patients with cobalamin-nonresponsive MMA (MMA-Cbl(-)) and GA1 identified by NBS were less likely to have movement disorders than those diagnosed by selective screening (MMA-Cbl(-): 10 % versus 39 %, p = 0.002; GA1: 26 % versus 73 %, p < 0.001). For other OADs, the clinical benefit of NBS was less clear. Reported age-adjusted intake of natural protein and calories was significantly higher in LO patients than in EO patients reflecting different disease severities. Variable drug combinations, ranging from 12 in MMA-Cbl(-) to two in isovaleric aciduria, were used for maintenance treatment. The effects of specific metabolic treatment strategies on the health outcomes remain unclear because of the strong influences of age at onset (EO versus LO), diagnostic mode (NBS versus selective screening), and the various treatment combinations used.CONCLUSIONS: NBS is an effective intervention to reduce time until diagnosis especially for LO patients and to prevent irreversible cerebral damage in GA1 and MMA-Cbl(-). Huge diversity of therapeutic interventions hampers our understanding of optimal treatment.

AB - BACKGROUND AND AIM: To describe current diagnostic and therapeutic strategies in organic acidurias (OADs) and to evaluate their impact on the disease course allowing harmonisation.METHODS: Datasets of 567 OAD patients from the E-IMD registry were analysed. The sample includes patients with methylmalonic (MMA, n = 164), propionic (PA, n = 144) and isovaleric aciduria (IVA, n = 83), and glutaric aciduria type 1 (GA1, n = 176). Statistical analysis included description and recursive partitioning of diagnostic and therapeutic strategies, and odds ratios (OR) for health outcome parameters. For some analyses, symptomatic patients were divided into those presenting with first symptoms during (i.e. early onset, EO) or after the newborn period (i.e. late onset, LO).RESULTS: Patients identified by newborn screening (NBS) had a significantly lower median age of diagnosis (8 days) compared to the LO group (363 days, p < 0.001], but not compared to the EO group. Of all OAD patients 71 % remained asymptomatic until day 8. Patients with cobalamin-nonresponsive MMA (MMA-Cbl(-)) and GA1 identified by NBS were less likely to have movement disorders than those diagnosed by selective screening (MMA-Cbl(-): 10 % versus 39 %, p = 0.002; GA1: 26 % versus 73 %, p < 0.001). For other OADs, the clinical benefit of NBS was less clear. Reported age-adjusted intake of natural protein and calories was significantly higher in LO patients than in EO patients reflecting different disease severities. Variable drug combinations, ranging from 12 in MMA-Cbl(-) to two in isovaleric aciduria, were used for maintenance treatment. The effects of specific metabolic treatment strategies on the health outcomes remain unclear because of the strong influences of age at onset (EO versus LO), diagnostic mode (NBS versus selective screening), and the various treatment combinations used.CONCLUSIONS: NBS is an effective intervention to reduce time until diagnosis especially for LO patients and to prevent irreversible cerebral damage in GA1 and MMA-Cbl(-). Huge diversity of therapeutic interventions hampers our understanding of optimal treatment.

U2 - 10.1007/s10545-015-9907-8

DO - 10.1007/s10545-015-9907-8

M3 - SCORING: Journal article

C2 - 26689403

VL - 39

SP - 341

EP - 353

JO - J INHERIT METAB DIS

JF - J INHERIT METAB DIS

SN - 0141-8955

IS - 3

ER -