Clinical practice: NTBC therapy for tyrosinemia type 1: how much is enough?
Abstract
Unlabelled Four patients with tyrosinemia type 1 (ages 6-32 months) were treated with 2-(2-nitro-4-trifluoro-methylbenzoyl)-1,3-cyclohexandion (NTBC) at Cairo University Children's Hospital, Egypt and followed up for 12-27 months. The recommended average dose of NTBC is 1 mg/kg/day. They were started on the following doses: 0.8, 0.58, 0.5, and 0.625 mg/kg/day, respectively. Two months after start of therapy, succinylacetone was undetectable in patients 1, 2, and 4, while in case 3, it was 5.4 microM. Her NTBC dose was increased from 0.5 to 0.65 mg/kg/day, and succinylacetone was undetectable 1 month later. They were kept on NTBC doses ranging from 0.55 to 0.65 mg/kg/day. These doses allowed catch up growth, normalization of synthetic liver functions, steep drop in serum alpha fetoprotein, reduction in phosphate loss in urine, normalization of serum calcium, phosphate, and alkaline phosphatase, and healing of active rickets. Succinylacetone was undetectable in urine on these doses. In conclusion Doses of NTBC, lower than recommended, may be helpful in treatment of tyrosinemia, on condition that succinylacetone production is suppressed, and AFP is maintained normal or showing a progressive decrease. This cost-effective dose may allow treatment of affected children from economically underprivileged countries, but longer follow up periods are needed.
Integrity signals
Registry
Cites
Statistics
Claims the paper makes
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
Lower doses of nitisinone have been found to be effective.
“However lower doses of nitisinone have been found to be effective [24,25].”
From Recommendations for the management of tyrosinaemia type 1 (2013) · cites this paper as [24]
Cites
Treatment of hereditary tyrosinaemia type I by inhibition of 4-hydroxyphenylpyruvate dioxygenase
LINDSTEDT, S. (1992) · The Lancet · doi:10.1016/0140-6736(92)92685-9 · Cited by 631 · see citing works
Tyrosinaemia type I and NTBC (2‐(2‐nitro‐4‐trifluoromethylbenzoyl)‐1,3‐cyclohexanedione)
Holme, E., & Lindstedt, S. (1998) · Journal of Inherited Metabolic Disease · doi:10.1023/a:1005410820201 · Cited by 264 · see citing works
Flagged first, then by citations
Cited by
Sorted by citations
Chinsky, J. M., Singh, R., Ficicioglu, C., van Karnebeek, C. D. M., Grompe, M., Mitchell, G., Waisbren, S. E., Gucsavas-Calikoglu, M., Wasserstein, M. P., Coakley, K., et al. (2017) · Genetics in Medicine · doi:10.1038/gim.2017.101 · Cited by 247 · see citing works
Recommendations for the management of tyrosinaemia type 1
de Laet, C., Dionisi-Vici, C., Leonard, J. V., McKiernan, P., Mitchell, G., Monti, L., de Baulny, H. O., Pintos-Morell, G., & Spiekerkötter, U. (2013) · Orphanet Journal of Rare Diseases · doi:10.1186/1750-1172-8-8 · Cited by 227 · see citing works
Single dose NTBC‐treatment of hereditary tyrosinemia type I
Schlune, A., Thimm, E., Herebian, D., & Spiekerkoetter, U. (2012) · Journal of Inherited Metabolic Disease · doi:10.1007/s10545-012-9450-9 · Cited by 33 · see citing works
Recomendaciones y manejo de la tirosinemia hereditaria Tipo I o Tirosinemia hepatorrenal
Couce, M. L., Aldámiz-Echevarría, L., Baldellou, A., Blasco, J., Bueno, M. A., Dalmau, J., De La Vega, A., Del Toro, M., Díaz, C., Lama, R., et al. (2010) · Anales de Pediatría · doi:10.1016/j.anpedi.2010.03.005 · Cited by 15 · see citing works
Tyrosinemia type I: long-term outcome in a patient treated with doses of NTBC lower than recommended
D’Eufemia, P., Celli, M., Tetti, M., & Finocchiaro, R. (2011) · European Journal of Pediatrics · doi:10.1007/s00431-011-1419-4 · Cited by 9 · see citing works
- Authors
- El-Karaksy, H., Rashed, M., El-Sayed, R., El-Raziky, M., El-Koofy, N., El-Hawary, M., & Al-Dirbashi, O.
- Affiliations
- Cairo University (EG)
- King Faisal Specialist Hospital & Research Centre (SA)
- Fayoum University (EG)
- Corresponding author
- El-Karaksy, Hanaa
- Venue
- European Journal of Pediatrics
- Published
- 2009-10-31
- Volume
- 169
- Issue
- 6
- Pages
- 689-693
- ISSN
- 0340-6199 (ISSN-L)
- 1432-1076
- OpenAlex
- W1993262647
- Cited by
- 45
- References
- 2
- Citations by year
- 2026: 1 · 2025: 2 · 2024: 2 · 2022: 2 · 2021: 1 · 2020: 2 · 2019: 2 · 2018: 1 · 2017: 7 · 2015: 3 · 2014: 4 · 2013: 2 · 2012: 5
- FWCI
- 3.40
- Type
- journal article
- Language
- en
- Open access
- closed
- Licence
- www.springer.com/tdm (tdm)
- Locations
- European Journal of Pediatrics (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Clinical Biochemistry › Metabolism and Genetic Disorders
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Biochemistry › Amino Acid Enzymes and Metabolism
- Health Sciences › Medicine › Pediatrics, Perinatology and Child Health › Neonatal Health and Biochemistry
- Keywords
- tyrosinemia type I, N-acetylphenylalanine, NTBC, succinylacetone, dose adjustment, alpha-fetoprotein, rickets, phosphate loss, catch-up growth, liver function, cost-effective treatment, children
- MeSH terms
- Child, Preschool, Cost-Benefit Analysis, Cyclohexanones, Dose-Response Relationship, Drug, Egypt, Enzyme Inhibitors, Female, Heptanoates, Humans, Infant, Nitrobenzoates, Drug Costs, Tyrosinemias
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review