dc.contributor.author | Giovannini, M. | |
dc.contributor.author | Fiori, L. | |
dc.contributor.author | Fiege, B. | |
dc.contributor.author | Ozen, I. | |
dc.contributor.author | Zurfluh, M. R. | |
dc.contributor.author | Demirkol, M. | |
dc.contributor.author | Gartner, K. H. | |
dc.contributor.author | Thony, B. | |
dc.contributor.author | Blau, N. | |
dc.date.accessioned | 2021-03-05T14:17:15Z | |
dc.date.available | 2021-03-05T14:17:15Z | |
dc.date.issued | 2006 | |
dc.identifier.citation | Zurfluh M. R. , Fiori L., Fiege B., Ozen I., Demirkol M., Gartner K. H. , Thony B., Giovannini M., Blau N., "Pharmacokinetics of orally administered tetrahydrobiopterin in patients with phenylalanine hydroxylase deficiency", JOURNAL OF INHERITED METABOLIC DISEASE, cilt.29, ss.725-731, 2006 | |
dc.identifier.issn | 0141-8955 | |
dc.identifier.other | vv_1032021 | |
dc.identifier.other | av_b65f046c-dddd-4d5e-8cca-79986d855e11 | |
dc.identifier.uri | http://hdl.handle.net/20.500.12627/121391 | |
dc.identifier.uri | https://doi.org/10.1007/s10545-006-0425-6 | |
dc.description.abstract | The oral loading test with tetrahydrobiopterin (BH4) is used to discriminate between variants of hyper-phenylalaninaemia and to detect BH4-responsive patients. The outcome of the loading test depends on the genotype, dosage of BH4, and BH4 pharmacokinetics. A total of 71 patients with hyperphenylaianinaemia (mild to classic) were challenged with BH4 (20 mg/kg) according to different protocols (1 x 20 mg or 2 x 20 mu) and blood BH4 concentrations were measured in dried blood spots at different time points (T-0, T-2, T-4, T-8, T-12, T-14, T-32 and T-48h). Maximal BH4 concentrations (median 22.69 nmol/g Hb) were measured 4 h after BH4 administration in 63 out of 7 1 patients. Eight patients presented with maximal BH4 concentrations similar to 44% higher at 8 h than at 4 h. After 24 h, BH4 blood concentrations dropped to 11% of maximal values. This profile was similar using different protocols. The following pharmacokinetic parameters were calculated for BH4 in blood: t(max) = 4h, AUC (T0-32) = 370 nmol x h/g Hb, and t(1/2) for absorption (1.1 h), distribution (2.5 h), and elimination (46.0 h) phases. Maximal BH4 blood concentrations were not significantly lower in non-responders and there was no correlation between blood concentrations and responsiveness. Of mild PKU patients, 97% responded to BH4 administration, while one was found to be a non-responder. Only 10/19 patients (53%) with Phe concentrations of 600-1200 mu mol/L responded to BH4 administration, and of the patients with the severe classical phenotype (blood Phe > 1200 mu mol/L) only 4 out of 17 patient responded. An additional 36 patients with mild hyperphenylalaninaemia (HPA) who underwent the combined loading test with Phe+BH4 were all responders. Slow responders and non-responders were found in all groups of HPA. | |
dc.language.iso | eng | |
dc.subject | Tıbbi Genetik | |
dc.subject | Tıbbi Ekoloji ve Hidroklimatoloji | |
dc.subject | Yaşam Bilimleri | |
dc.subject | Moleküler Biyoloji ve Genetik | |
dc.subject | Temel Bilimler | |
dc.subject | GENETİK VE HAYAT | |
dc.subject | Moleküler Biyoloji ve Genetik | |
dc.subject | Yaşam Bilimleri (LIFE) | |
dc.subject | TIP, ARAŞTIRMA VE DENEYSEL | |
dc.subject | Tıp | |
dc.subject | Sağlık Bilimleri | |
dc.subject | Dahili Tıp Bilimleri | |
dc.subject | İç Hastalıkları | |
dc.subject | Endokrinoloji ve Metabolizma Hastalıkları | |
dc.subject | ENDOKRİNOLOJİ VE METABOLİZMA | |
dc.subject | Klinik Tıp | |
dc.subject | Klinik Tıp (MED) | |
dc.title | Pharmacokinetics of orally administered tetrahydrobiopterin in patients with phenylalanine hydroxylase deficiency | |
dc.type | Makale | |
dc.relation.journal | JOURNAL OF INHERITED METABOLIC DISEASE | |
dc.contributor.department | , , | |
dc.identifier.volume | 29 | |
dc.identifier.issue | 6 | |
dc.identifier.startpage | 725 | |
dc.identifier.endpage | 731 | |
dc.contributor.firstauthorID | 180613 | |