Blood phenylalanine concentrations in patients with PAH-deficient hyperphenylalaninaemia off diet without and with three different single oral doses of tetrahydrobiopterin: Assessing responsiveness in a model of statistical process control
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作者:
Lindner, M.
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Univ Childrens Hosp, Div Metab Disorders, Dept Gen Paediat, D-69120 Heidelberg, GermanyUniv Childrens Hosp, Div Metab Disorders, Dept Gen Paediat, D-69120 Heidelberg, Germany
Lindner, M.
[1
]
Gramer, G.
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Univ Childrens Hosp, Div Metab Disorders, Dept Gen Paediat, D-69120 Heidelberg, GermanyUniv Childrens Hosp, Div Metab Disorders, Dept Gen Paediat, D-69120 Heidelberg, Germany
Gramer, G.
[1
]
Garbade, S. F.
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Univ Childrens Hosp, Div Metab Disorders, Dept Gen Paediat, D-69120 Heidelberg, GermanyUniv Childrens Hosp, Div Metab Disorders, Dept Gen Paediat, D-69120 Heidelberg, Germany
Garbade, S. F.
[1
]
Burgard, P.
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Univ Childrens Hosp, Div Metab Disorders, Dept Gen Paediat, D-69120 Heidelberg, GermanyUniv Childrens Hosp, Div Metab Disorders, Dept Gen Paediat, D-69120 Heidelberg, Germany
Burgard, P.
[1
]
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[1] Univ Childrens Hosp, Div Metab Disorders, Dept Gen Paediat, D-69120 Heidelberg, Germany
Tetrahydrobiopterin (BH(4)) cofactor loading is a standard procedure to differentiate defects of BH(4) metabolism from phenylalanine hydroxylase (PAH) deficiency. BH(4) responsiveness also exists in PAH-deficient patients with high residual PAH activity. Unexpectedly, single cases with presumed nil residual PAH activity have been reported to be BH(4) responsive, too. BH(4) responsiveness has been defined either by a a parts per thousand yen30% reduction of blood Phe concentration after a single BH(4) dose or by a decline greater than the individual circadian Phe level variation. Since both methods have methodological disadvantages, we present a model of statistical process control (SPC) to assess BH(4) responsiveness. Phe levels in 17 adult PKU patients of three phenotypic groups off diet were compared without and with three different single oral dosages of BH(4) applied in a double-blind randomized cross-over design. Results are compared for a parts per thousand yen30% reduction and SPC. The effect of BH(4) by a parts per thousand yen30% reduction was significant for groups (p < 0.01) but not for dose (p = 0.064), with no interaction of group with dose (p = 0.24). SPC revealed significant effects for group (p < 0.01) and the interaction for group with dose (p < 0.05) but not for dose alone (p = 0.87). After one or more loadings, seven patients would be judged to be BH(4) responsive either by the 30% criterion or by the SPC model, but only three by both. Results for patients with identical PAH genotype were not very consistent within (for different BH(4) doses) and between the two models. We conclude that a comparison of protein loadings without and with BH(4) combined with a standardized procedure for data analysis and decision would increase the reliability of diagnostic results.
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Childrens Hosp, Boston, MA 02115 USA
Harvard Univ, Sch Med, Boston, MA USAChildrens Hosp, Boston, MA 02115 USA
Levy, Harvey
;
Burton, Barbara
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Childrens Mem Hosp, Chicago, IL 60614 USA
Northwestern Univ, Feinberg Sch Med, Chicago, IL 60614 USAChildrens Hosp, Boston, MA 02115 USA
Burton, Barbara
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Cederbaum, Stephen
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Univ Calif Los Angeles, David Geffen Sch Med, Div Human Genet, Los Angeles, CA USA
Univ Calif Los Angeles, David Geffen Sch Med, Dept Pediat, Los Angeles, CA USAChildrens Hosp, Boston, MA 02115 USA
Cederbaum, Stephen
;
Scriver, Charles
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McGill Univ, Fac Med, Dept Human Genet & Pediat, Montreal, PQ, CanadaChildrens Hosp, Boston, MA 02115 USA
机构:
Childrens Hosp, Boston, MA 02115 USA
Harvard Univ, Sch Med, Boston, MA USAChildrens Hosp, Boston, MA 02115 USA
Levy, Harvey
;
Burton, Barbara
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机构:
Childrens Mem Hosp, Chicago, IL 60614 USA
Northwestern Univ, Feinberg Sch Med, Chicago, IL 60614 USAChildrens Hosp, Boston, MA 02115 USA
Burton, Barbara
;
Cederbaum, Stephen
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机构:
Univ Calif Los Angeles, David Geffen Sch Med, Div Human Genet, Los Angeles, CA USA
Univ Calif Los Angeles, David Geffen Sch Med, Dept Pediat, Los Angeles, CA USAChildrens Hosp, Boston, MA 02115 USA
Cederbaum, Stephen
;
Scriver, Charles
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McGill Univ, Fac Med, Dept Human Genet & Pediat, Montreal, PQ, CanadaChildrens Hosp, Boston, MA 02115 USA