Literature DB >> 17314188

Long term survival in a patient with variant Creutzfeldt-Jakob disease treated with intraventricular pentosan polysulphate.

A Parry1, I Baker, R Stacey, S Wimalaratna.   

Abstract

Variant Creutzfeldt-Jakob disease (vCJD) is a neurodegenerative disease that principally affects young people and has a median duration of illness of 13 (range 6-39) months. vCJD is incurable and there are currently no treatments that conclusively slow the rate of disease progression. However, recent animal studies and isolated case reports have suggested that treatment with intraventricular pentosan polysulphate (PPS) may be beneficial in the treatment of patients with vCJD. We report a case of a 22-year-old male with vCJD treated 19 months after the onset of clinical symptoms with continuous intraventricular PPS (32 microg/kg/day) over a period of 31 months. Treatment with PPS appeared to be safe and well tolerated and was associated with prolonged survival (51 months) when compared to natural history studies. However, PPS treatment did not appear to arrest the progression of the disease.

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Year:  2007        PMID: 17314188      PMCID: PMC2117700          DOI: 10.1136/jnnp.2006.104505

Source DB:  PubMed          Journal:  J Neurol Neurosurg Psychiatry        ISSN: 0022-3050            Impact factor:   10.154


  3 in total

1.  Cerebroventricular infusion of pentosan polysulphate in human variant Creutzfeldt-Jakob disease.

Authors:  N V Todd; J Morrow; K Doh-ura; S Dealler; S O'Hare; P Farling; M Duddy; N G Rainov
Journal:  J Infect       Date:  2005-06       Impact factor: 6.072

2.  Unsuccessful intraventricular pentosan polysulphate treatment of variant Creutzfeldt-Jakob disease.

Authors:  I R Whittle; R S G Knight; R G Will
Journal:  Acta Neurochir (Wien)       Date:  2006-04-07       Impact factor: 2.216

3.  Treatment of transmissible spongiform encephalopathy by intraventricular drug infusion in animal models.

Authors:  Katsumi Doh-ura; Kensuke Ishikawa; Ikuko Murakami-Kubo; Kensuke Sasaki; Shirou Mohri; Richard Race; Toru Iwaki
Journal:  J Virol       Date:  2004-05       Impact factor: 5.103

  3 in total
  18 in total

Review 1.  Sulfated glycosaminoglycans in protein aggregation diseases.

Authors:  Kazuchika Nishitsuji; Kenji Uchimura
Journal:  Glycoconj J       Date:  2017-04-11       Impact factor: 2.916

Review 2.  Rapidly progressive dementias and the treatment of human prion diseases.

Authors:  Brian S Appleby; Constantine G Lyketsos
Journal:  Expert Opin Pharmacother       Date:  2010-11-23       Impact factor: 3.889

3.  Orally administered amyloidophilic compound is effective in prolonging the incubation periods of animals cerebrally infected with prion diseases in a prion strain-dependent manner.

Authors:  Yuri Kawasaki; Keiichi Kawagoe; Chun-jen Chen; Kenta Teruya; Yuji Sakasegawa; Katsumi Doh-ura
Journal:  J Virol       Date:  2007-09-19       Impact factor: 5.103

4.  Diphenylpyrazole-derived compounds increase survival time of mice after prion infection.

Authors:  Fabienne Leidel; Martin Eiden; Markus Geissen; Hans A Kretzschmar; Armin Giese; Thomas Hirschberger; Paul Tavan; Hermann M Schätzl; Martin H Groschup
Journal:  Antimicrob Agents Chemother       Date:  2011-07-11       Impact factor: 5.191

Review 5.  Therapies for human prion diseases.

Authors:  Peter K Panegyres; Elizabeth Armari
Journal:  Am J Neurodegener Dis       Date:  2013-09-18

6.  Glycosaminoglycan sulphation affects the seeded misfolding of a mutant prion protein.

Authors:  Victoria A Lawson; Brooke Lumicisi; Jeremy Welton; Dorothy Machalek; Katrina Gouramanis; Helen M Klemm; James D Stewart; Colin L Masters; David E Hoke; Steven J Collins; Andrew F Hill
Journal:  PLoS One       Date:  2010-08-23       Impact factor: 3.240

7.  A synthetic heparinoid blocks Tau aggregate cell uptake and amplification.

Authors:  Barbara E Stopschinski; Talitha L Thomas; Sourena Nadji; Eric Darvish; Linfeng Fan; Brandon B Holmes; Anuja R Modi; Jordan G Finnell; Omar M Kashmer; Sandi Estill-Terpack; Hilda Mirbaha; Hung S Luu; Marc I Diamond
Journal:  J Biol Chem       Date:  2020-01-23       Impact factor: 5.157

8.  Toxic effects of intracerebral PrP antibody administration during the course of BSE infection in mice.

Authors:  Maxime Lefebvre-Roque; Elisabeth Kremmer; Sabine Gilch; Wen-Quan Zou; Cécile Féraudet; Chantal Mourton Gilles; Nicole Salès; Jacques Grassi; Pierluigi Gambetti; Thierry Baron; Hermann Schätzl; Corinne Ida Lasmézas
Journal:  Prion       Date:  2007-07-15       Impact factor: 3.931

9.  Heparin binding confers prion stability and impairs its aggregation.

Authors:  Tuane C R G Vieira; Yraima Cordeiro; Byron Caughey; Jerson L Silva
Journal:  FASEB J       Date:  2014-03-19       Impact factor: 5.191

10.  Shortening heparan sulfate chains prolongs survival and reduces parenchymal plaques in prion disease caused by mobile, ADAM10-cleaved prions.

Authors:  Patricia Aguilar-Calvo; Alejandro M Sevillano; Jaidev Bapat; Katrin Soldau; Daniel R Sandoval; Hermann C Altmeppen; Luise Linsenmeier; Donald P Pizzo; Michael D Geschwind; Henry Sanchez; Brian S Appleby; Mark L Cohen; Jiri G Safar; Steven D Edland; Markus Glatzel; K Peter R Nilsson; Jeffrey D Esko; Christina J Sigurdson
Journal:  Acta Neuropathol       Date:  2019-10-31       Impact factor: 17.088

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