Journal of Inherited Metabolic Disease 2011-12-01

A quantitative assessment of alkaptonuria: testing the reliability of two disease severity scoring systems.

Trevor F Cox, Lakshminarayan Ranganath

Index: J. Inherit. Metab. Dis. 34(6) , 1153-62, (2011)

Full Text: HTML

Abstract

Alkaptonuria (AKU) is due to excessive homogentisic acid accumulation in body fluids due to lack of enzyme homogentisate dioxygenase leading in turn to varied clinical manifestations mainly by a process of conversion of HGA to a polymeric melanin-like pigment known as ochronosis. A potential treatment, a drug called nitisinone, to decrease formation of HGA is available. However, successful demonstration of its efficacy in modifying the natural history of AKU requires an effective quantitative assessment tool. We have described two potential tools that could be used to quantitate disease burden in AKU. One tool describes scoring the clinical features that includes clinical assessments, investigations and questionnaires in 15 patients with AKU. The second tool describes a scoring system that only includes items obtained from questionnaires used in 44 people with AKU. Statistical analyses were carried out on the two patient datasets to assess the AKU tools; these included the calculation of Chronbach's alpha, multidimensional scaling and simple linear regression analysis. The conclusion was that there was good evidence that the tools could be adopted as AKU assessment tools, but perhaps with further refinement before being used in the practical setting of a clinical trial.


Related Compounds

Related Articles:

Generation of healthy mice from gene-corrected disease-specific induced pluripotent stem cells.

2011-07-01

[PLoS Biol. 9(7) , e1001099, (2011)]

Serum markers in alkaptonuria: simultaneous analysis of homogentisic acid, tyrosine and nitisinone by liquid chromatography tandem mass spectrometry.

2015-09-01

[Ann. Clin. Biochem. 52 , 597-605, (2015)]

A misguided 'pill in the pocket' approach with flecainide leading to cardiac arrest.

2012-01-01

[BMJ Case Rep. 2012 , doi:10.1136/bcr-2012-006868, (2012)]

Single dose NTBC-treatment of hereditary tyrosinemia type I.

2012-09-01

[J. Inherit. Metab. Dis. 35(5) , 831-6, (2012)]

Increase of CSF tyrosine and impaired serotonin turnover in tyrosinemia type I.

2011-02-01

[Mol. Genet. Metab. 102(2) , 122-5, (2011)]

More Articles...