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Intrathecal enzyme replacement therapy in a patient with mucopolysaccharidosis type I and symptomatic spinal cord compression
American journal of medical genetics. Part A, 2008-10, Vol.146A (19), p.2538-2544
Munoz‐Rojas, Maria‐Veronica
Vieira, Taiane
Costa, Ronaldo
Fagondes, Simone
John, Angela
Jardim, Laura Bannach
Vedolin, Leonardo M.
Raymundo, Marcia
Dickson, Patricia I.
Kakkis, Emil
Giugliani, Roberto
2008
Volltextzugriff (PDF)
Details
Autor(en) / Beteiligte
Munoz‐Rojas, Maria‐Veronica
Vieira, Taiane
Costa, Ronaldo
Fagondes, Simone
John, Angela
Jardim, Laura Bannach
Vedolin, Leonardo M.
Raymundo, Marcia
Dickson, Patricia I.
Kakkis, Emil
Giugliani, Roberto
Titel
Intrathecal enzyme replacement therapy in a patient with mucopolysaccharidosis type I and symptomatic spinal cord compression
Ist Teil von
American journal of medical genetics. Part A, 2008-10, Vol.146A (19), p.2538-2544
Ort / Verlag
Hoboken: Wiley Subscription Services, Inc., A Wiley Company
Erscheinungsjahr
2008
Quelle
Wiley Online Library - AutoHoldings Journals
Beschreibungen/Notizen
In mucopolysaccharidosis I, deficiency of α‐L‐iduronidase can cause spinal cord compression (SCC) due to storage of glycosaminoglycans (GAGs) within the cervical meninges. As intravenous enzyme replacement therapy (ERT) is not likely to provide enzyme across the blood–brain barrier, standard treatment for this complication is usually surgical, which has a high morbidity and mortality risk. We report on the use of intrathecal (IT) laronidase in a MPS I patient with SCC who refused the surgical treatment. Assessments were performed at baseline, with clinical and biochemical evaluations, 4‐extremity somatosensory evoked potentials, 12 min walk test and MRI studies of the CNS. Changes on these parameters were evaluated after 4 IT infusions of laronidase administered monthly via lumbar puncture. To our knowledge, this was the first MPS patient who received IT ERT. No major adverse events were observed. There were no clinically significant changes in serum chemistries. CSF GAG results revealed pretreatment values slightly above normal standards: 13.3 mg/L (NV < 12 mg/L) which after IT laronidase infusions were within normal levels (10.3 mg/L). 12MWT presented a 14% improvement, with better performance on stability and gait control. Maximum voluntary ventilation showed 55.6% improvement considering the percentage of predicted (26.7% at baseline compared to 41.9%); Maximum Inspiration Pressure improved 36.6% of predicted (26.8% at baseline to 36.7%); Pulmonary diffusion improved 17.6% of predicted %. In conclusion, although the improvement observed in this case with IT laronidase should be confirmed in further patients, this procedure seems to be a safe treatment for SCC in MPS I. © 2008 Wiley‐Liss, Inc.
Sprache
Englisch
Identifikatoren
ISSN: 1552-4825
eISSN: 1552-4833
DOI: 10.1002/ajmg.a.32294
Titel-ID: cdi_proquest_miscellaneous_20118739
Format
–
Schlagworte
Adult
,
Biological and medical sciences
,
Carbohydrates (enzymatic deficiencies). Glycogenosis
,
Cerebrospinal fluid. Meninges. Spinal cord
,
Drug Administration Schedule
,
enzyme replacement therapy
,
Errors of metabolism
,
Humans
,
Iduronidase - administration & dosage
,
Iduronidase - genetics
,
Iduronidase - therapeutic use
,
Injections, Spinal - adverse effects
,
Injections, Spinal - methods
,
intrathecal treatment
,
lysomal storage diseases
,
Male
,
Medical genetics
,
Medical sciences
,
Metabolic diseases
,
mucopolysaccharidosis
,
mucopolysaccharidosis I
,
Mucopolysaccharidosis I - complications
,
Mucopolysaccharidosis I - therapy
,
Nervous system (semeiology, syndromes)
,
Neurology
,
Radiography
,
Recombinant Proteins - administration & dosage
,
Recombinant Proteins - therapeutic use
,
Scheie syndrome
,
spinal cord compression
,
Spinal Cord Compression - complications
,
Spinal Cord Compression - diagnostic imaging
,
Spinal Cord Compression - therapy
,
Spinal Puncture - methods
,
Treatment Outcome
,
α‐L‐iduronidase
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