Evidence map›Paper›PMID 25421091›Full record

ArticleJournal of inherited metabolic disease2015

Evaluation of enzyme dose and dose-frequency in ameliorating substrate accumulation in MPS IIIA Huntaway dog brain.

Barbara King, Neil Marshall, Helen Beard, Sofia Hassiotis, Paul J Trim, Marten F Snel, Tina Rozaklis, Robert D Jolly, John J Hopwood, Kim M Hemsley

Abstract read
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In one paragraph

Article in Journal of inherited metabolic disease, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.

0numbers the graph read from it
0cells of the map it votes in
10citing papers in PubMed
1.2field-weighted citation impact, top 22% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

10 citing papers in PubMed, 21 citations in OpenAlex.

  1. Article
  2. Novel therapies for mucopolysaccharidosis type III.Journal of inherited metabolic disease · 2021
    Review
  3. Article
  4. Diagnosis of Mucopolysaccharidoses.Diagnostics (Basel, Switzerland) · 2020
    Review
  5. Article
  6. Article
  7. Review
  8. Review
  9. Article
  10. Sanfilippo syndrome: causes, consequences, and treatments.The application of clinical genetics · 2015
    Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors at 2 institutions in 2 countries.

Barbara KingLysosomal Diseases Research Unit, South Australian Health and Medical Research Institute, PO Box 11060, Adelaide, SA, 5001, Australia.
Neil Marshall
Helen Beard
Sofia Hassiotis
Paul J Trim
Marten F Snel
Tina Rozaklis
Robert D Jolly
John J Hopwood
Kim M Hemsley
South Australian Health and Medical Research Institute · AUMassey University · NZ

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Intracerebrospinal fluid (CSF) infusion of replacement enzyme is under evaluation for amelioration of disease-related symptoms and biomarker changes in patients with the lysosomal storage disorder mucopolysaccharidosis type IIIA (MPS IIIA; www.clinicaltrials.gov ; NCT#01155778; #01299727). Determining the optimal dose/dose-frequency is important, given the invasive method for chronically supplying recombinant protein to the brain, the main site of symptom generation. To examine these variables, we utilised MPS IIIA Huntaway dogs, providing recombinant human sulphamidase (rhSGSH) to young pre-symptomatic dogs from an age when MPS IIIA dog brain exhibits significant accumulation of primary (heparan sulphate) and secondary (glycolipid) substrates. Enzyme was infused into CSF via the cisterna magna at one of two doses (3 mg or 15 mg/infusion), with the higher dose supplied at two different intervals; fortnightly or monthly. Euthanasia was carried out 24 h after the final injection. Dose- and frequency-dependent reductions in heparan sulphate were observed in CSF and deeper layers of cerebral cortex. When we examined the amount of immunostaining of the general endo/lysosomal marker, LIMP-2, or quantified activated microglia, the higher fortnightly dose resulted in superior outcomes in affected dogs. Secondary lesions such as accumulation of GM3 ganglioside and development of GAD-reactive axonal spheroids were treated to a similar degree by both rhSGSH doses and dose frequencies. Our findings indicate that the lower fortnightly dose is sub-optimal for ameliorating existing and preventing further development of disease-related pathology in young MPS IIIA dog brain; however, increasing the dose fivefold but halving the frequency of administration enabled near normalisation of disease-related biomarkers.

Indexed as

Enzyme Replacement TherapyAnimalsBiomarkersBrainDisease Models, AnimalDogsDrug Administration ScheduleDrug Dosage CalculationsGlycolipidsHeparan SulfateHydrolasesInfusions, IntraventricularLysosomal-Associated Membrane Protein 2Mucopolysaccharidosis IIIRecombinant ProteinsTime FactorsBiomarkersGlycolipidsHeparan SulfateHydrolasesLysosomal-Associated Membrane Protein 2N-sulfoglucosamine sulfohydrolaseRecombinant Proteins

Identifiers

PMID25421091
OpenAlexW2016596347

What OpenQuestion holds

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Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.