Literature DB >> 20693542

Peripheral neuropathy in adult type 1 Gaucher disease: a 2-year prospective observational study.

Marieke Biegstraaten1, Eugen Mengel, Laszlo Maródi, Milan Petakov, Claus Niederau, Pilar Giraldo, Derralyn Hughes, Mirando Mrsic, Atul Mehta, Carla E M Hollak, Ivo N van Schaik.   

Abstract

Type 1 Gaucher disease is currently categorized as non-neuronopathic, although recent studies suggest peripheral neurological manifestations. We report prevalence and incidence data for peripheral neuropathy and associated conditions from a multinational, prospective, longitudinal, observational cohort study in patients with type 1 Gaucher disease, either untreated or receiving enzyme replacement therapy. The primary outcome parameters were the prevalence and incidence of polyneuropathy, evaluated by standardized assessments of neurological symptoms and signs, and electrophysiological studies. All diagnoses of polyneuropathy were adjudicated centrally. Secondary outcome parameters included the prevalence and incidence of mononeuropathy, other neurological or electrophysiological abnormalities not fulfilling the criteria for a mono- or polyneuropathy and general type 1 Gaucher disease symptoms. Furthermore, a literature search was performed to identify all studies reporting on prevalence and incidence of polyneuropathy in the general population. One hundred and three patients were enrolled [median (range) age: 42 (18-75) years; disease duration: 15 (0-56) years; 52% female]; 14 (13.6%) were untreated and 89 (86.4%) were on enzyme replacement therapy. At baseline, 11 patients [10.7%; 95% confidence interval (CI): 5.9-18.3] were diagnosed with sensory motor axonal polyneuropathy. Two (1.9%; 95% CI: 0.1-7.2) had a mononeuropathy of the ulnar nerve. The 2-year follow-up period revealed another six cases of polyneuropathy (2.9 per 100 person-years; 95% CI: 1.2-6.3). Patients with polyneuropathy were older than those without (P<0.001). Conditions possibly associated with polyneuropathy were identified in four patients only, being monoclonal gammopathy, vitamin B(1) deficiency, folic acid deficiency, type 2 diabetes mellitus, renal insufficiency, alcohol abuse and exposure to toxins related to profession. The 11 cases of polyneuropathy found at baseline were confirmed during follow-up. According to the literature, the prevalence of polyneuropathy in the general population was estimated between 0.09 and 1.3% and the incidence was estimated between 0.0046 and 0.015 per 100 person-years. Thus, we conclude that the prevalence and incidence of polyneuropathy in patients with type 1 Gaucher disease is increased compared with the general population.

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Year:  2010        PMID: 20693542     DOI: 10.1093/brain/awq198

Source DB:  PubMed          Journal:  Brain        ISSN: 0006-8950            Impact factor:   13.501


  24 in total

Review 1.  Gaucher disease.

Authors:  Aabha Nagral
Journal:  J Clin Exp Hepatol       Date:  2014-04-21

Review 2.  Gaucher disease: the metabolic defect, pathophysiology, phenotypes and natural history.

Authors:  Hagit N Baris; Ian J Cohen; Pramod K Mistry
Journal:  Pediatr Endocrinol Rev       Date:  2014-09

3.  The incidence of Parkinsonism in patients with type 1 Gaucher disease: data from the ICGG Gaucher Registry.

Authors:  Barry Rosenbloom; Manisha Balwani; Jeff M Bronstein; Edwin Kolodny; Swati Sathe; Andrea R Gwosdow; John S Taylor; J Alexander Cole; Ari Zimran; Neal J Weinreb
Journal:  Blood Cells Mol Dis       Date:  2010-11-10       Impact factor: 3.039

4.  Rare Case of Hepatic Gaucheroma in a Child on Enzyme Replacement Therapy.

Authors:  Sophy Korula; Penny Owens; Amanda Charlton; Kaustuv Bhattacharya
Journal:  JIMD Rep       Date:  2016-06-23

Review 5.  Enzyme replacement and substrate reduction therapy for Gaucher disease.

Authors:  Elad Shemesh; Laura Deroma; Bruno Bembi; Patrick Deegan; Carla Hollak; Neal J Weinreb; Timothy M Cox
Journal:  Cochrane Database Syst Rev       Date:  2015-03-27

6.  Long-term effectiveness of enzyme replacement therapy in children with Gaucher disease: results from the NCS-LSD cohort study.

Authors:  L J Anderson; W Henley; K M Wyatt; V Nikolaou; S Waldek; D A Hughes; G M Pastores; S Logan
Journal:  J Inherit Metab Dis       Date:  2014-03-18       Impact factor: 4.982

Review 7.  Gaucher disease - more than just a rare lipid storage disease.

Authors:  Jaehyeok Roh; Subbaya Subramanian; Neal J Weinreb; Reena V Kartha
Journal:  J Mol Med (Berl)       Date:  2022-01-23       Impact factor: 4.599

8.  The cognitive profile of type 1 Gaucher disease patients.

Authors:  Marieke Biegstraaten; Keith A Wesnes; Cécile Luzy; Milan Petakov; Mirando Mrsic; Claus Niederau; Pilar Giraldo; Derralynn Hughes; Atul Mehta; Karl-Eugen Mengel; Carla E M Hollak; László Maródi; Ivo N van Schaik
Journal:  J Inherit Metab Dis       Date:  2012-02-21       Impact factor: 4.982

9.  Peripheral neural response and sex hormones in type 1 Gaucher disease.

Authors:  Milan B Lakočević; Mirjana M Platiša; Zorica R Šumarac; Nada D Suvajdžić; Lana Đ Mačukanović; Milan S Petakov
Journal:  J Med Biochem       Date:  2020-01-10       Impact factor: 3.402

10.  Long-term effectiveness of enzyme replacement therapy in adults with Gaucher disease: results from the NCS-LSD cohort study.

Authors:  L J Anderson; W Henley; K M Wyatt; V Nikolaou; D A Hughes; S Waldek; S Logan
Journal:  J Inherit Metab Dis       Date:  2014-02-11       Impact factor: 4.982

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