Evidence map›Paper›PMID 24692796›Full record

ArticleCurrent therapeutic research, clinical and experimental2008

Genistin-rich soy isoflavone extract in substrate reduction therapy for Sanfilippo syndrome: An open-label, pilot study in 10 pediatric patients.

Ewa Piotrowska, Joanna Jakóbkiewicz-Banecka, Anna Tylki-Szymanska, Anna Liberek, Agnieszka Maryniak, Marcelina Malinowska, Barbara Czartoryska, Ewa Puk, Anna Kloska, Tomasz Liberek and 3 more

Open access · goldAbstract read
In one paragraph

Article in Current therapeutic research, clinical and experimental, 2008. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 39 papers.

0numbers the graph read from it
0cells of the map it votes in
39citing papers in PubMed
4.7field-weighted citation impact, top 5% 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

39 citing papers in PubMed, 105 citations in OpenAlex.

  1. Genistein supplementation in patients affected by Sanfilippo disease.Journal of inherited metabolic disease · 2011
    Trial
  2. Trial
  3. Advances in Therapies for Mucopolysaccharidoses.Current issues in molecular biology · 2026
    Review
  4. Review
  5. Article
  6. Targeting Neurological Aspects of Mucopolysaccharidosis Type II: Enzyme Replacement Therapy and Beyond.BioDrugs : clinical immunotherapeutics, biopharmaceuticals and gene therapy · 2024
    Review
  7. Article
  8. Article
  9. Article
  10. Review
  11. Innate Immunity in Mucopolysaccharide Diseases.International journal of molecular sciences · 2022
    Review
  12. Article
  13. Article
  14. Novel therapies for mucopolysaccharidosis type III.Journal of inherited metabolic disease · 2021
    Review
  15. Mucopolysaccharidosis III: Molecular basis and treatment.Pediatric endocrinology, diabetes, and metabolism · 2021
    Review
  16. Article
  17. Review
  18. Lysosomes as a therapeutic target.Nature reviews. Drug discovery · 2019
    Review
  19. Comparison among Activities and Isoflavonoids fromMolecules (Basel, Switzerland) · 2019
    Article
  20. 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

13 authors at 5 institutions in 1 country.

Ewa PiotrowskaDepartment of Molecular Biology, University of Gdansk, Gdansk, Poland.
Joanna Jakóbkiewicz-BaneckaDepartment of Molecular Biology, University of Gdansk, Gdansk, Poland ; Laboratory of Molecular Biology, Institute of Biochemistry and Biophysics, Polish Academy of Sciences, Gdansk, Poland.
Anna Tylki-SzymanskaThe Children's Memorial Health Institute, Warsaw, Poland.
Anna LiberekDepartment of Pediatrics, Children's Gastroenterology and Oncology, Medical University of Gdansk, Gdansk, Poland.
Agnieszka MaryniakThe Children's Memorial Health Institute, Warsaw, Poland.
Marcelina MalinowskaDepartment of Molecular Biology, University of Gdansk, Gdansk, Poland.
Barbara CzartoryskaDepartment of Genetics, Institute of Psychiatry and Neurology, Warsaw, Poland.
Ewa PukBiofarm, Poznan, Poland.
Anna KloskaDepartment of Molecular Biology, University of Gdansk, Gdansk, Poland.
Tomasz LiberekDepartment of Nephrology, Transplantation, and Internal Medicine, Medical University of Gdansk, Gdansk, Poland.
Sylwia BaranskaDepartment of Molecular Biology, University of Gdansk, Gdansk, Poland.
Alicja WegrzynLaboratory of Molecular Biology, Institute of Biochemistry and Biophysics, Polish Academy of Sciences, Gdansk, Poland.
Grzegorz WegrzynDepartment of Molecular Biology, University of Gdansk, Gdansk, Poland.
University of Gdańsk · PLChildren's Memorial Health Institute · PLGdańsk Medical University · PLInstitute of Biochemistry and Biophysics, Polish Academy of Sciences · PLInstitute of Psychiatry and Neurology · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundMucopolysaccharidoses (MPSs) are a group of severe metabolic disorders caused by deficiencies in enzymes involved in the degradation of glycosaminoglycans (GAGs)-long chains of sugar carbohydrates in cells that help build bone, cartilage, tendons, corneas, skin, and connective tissue. Although enzyme replacement therapy has become available for the treatment of some types of MPS, effective treatment of neurodegenerative forms of MPS has yet to be determined. Recently, genistein (4',5,7-trihydroxyisoflavone), a specific inhibitor of protein tyrosine kinase, has been found to inhibit GAG synthesis and to reduce GAG concentrations in cultures of fibroblasts of MPS patients. Therefore, a potential substrate reduction therapy has been proposed.

objectiveThe aim of this study was to examine urinary GAG concentration, hair morphology, and cognitive function in patients receiving genistin treatment for Sanfilippo syndrome (MPS type III).

methodsPatients aged 3 to 14 years with a biochemically confirmed diagnosis of MPS IIIA or MPS IIIB were eligible to enroll in this open-label, pilot study. Genistin-rich soy isoflavone extract 5 mg/kg/d was administered PO for 12 months. Urinary GAG concentration, hair morphology,and cognitive function (measured using a modified version of the Brief Assessment Examination [BAE] and parent observations)were measured at baseline and after 12 months of treatment.

resultsTen patients (6 girls, 4 boys; mean age, 8 years [range,3\2-14 years];mean weight, 28 kg [range, 17\2-43 kg]) were included in the study. All patients had Sanfilippo syndrome; 5 patients had MPS IIIA and 5 had MPS IIIB. After 1 year, statistically significant improvement was found in urinary GAG concentration, hair morphology, and cognitive function. Urinary GAG concentration decreased significantly in all 5 patients with MPS IIIA and in 2 patients with MPS IIIB (P = 0.028). Hair morphology improved significantly in all 5 MPS IIIA patients and in 3 MPS IIIB patients (P = 0.012). A significant increase in the BAE score (by 2-6 points) was noted in 8 patients, while the scores of 2 patients did not change after 12 months of treatment (P = 0.012). No adverse events (AEs) considered related to treatment were reported. Moreover, no AEs not related to the treatment (apart from classical symptoms of MPS III) were noted.

conclusionsThis pilot study found some improvements in GAG concentration, hair morphology, and cognitive function in these pediatric patients with Sanfilippo syndrome treated with genistin-rich soy isoflavone extract for 1 year. Clinical trials are needed to evaluate the efficacy and safety of this potential treatment.

Indexed as

gene expressiongenisteingenistinmucopolysaccharidosissubstrate reduction therapy

Identifiers

PMID24692796
PMCPMC3969963
OpenAlexW2119181048

What OpenQuestion holds

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Registered trials

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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.