Literature DB >> 31182507

Motor function impairment is an early sign of CLN3 disease.

Willemijn F E Kuper1, Claudia van Alfen1, Linda van Eck1, Barbara C H Huijgen1, Edward E S Nieuwenhuis1, Marco van Brussel1, Peter M van Hasselt2.   

Abstract

OBJECTIVE: To delineate timing of motor decline in CLN3 disease.
METHODS: Motor function, assessed by the 6-Minute Walk Test (6MWT), was evaluated repeatedly in 15 patients with CLN3 disease, resulting in 65 test results and during one occasion in 2 control cohorts. One control cohort (n = 14) had isolated visual impairment; a second cohort (n = 12) exhibited visual impairment in combination with neurologic impairments. Based on 6MWT reference values in healthy sighted children, z scores of 6MWT results in patients with CLN3 disease and control cohort individuals were calculated. 6MWT results were correlated with age-including multilevel modeling analysis allowing assessment of imbalanced repeated measurements-and with Unified Batten Disease Rating Scale (UBDRS) scores.
RESULTS: In CLN3 disease, 6MWT scores were already impaired from first testing near diagnosis (mean z scores of -3.6 and -4.7 at 7 and 8 years of age, respectively). Afterwards, 6MWT scores continuously declined with age (r = -0.64, p < 0.0001) and with increasing UBDRS scores (r = -0.60, p = 0.0001), confirming correlation with disease progression. The decrease was more pronounced at a later age, as shown by the nonlinear multilevel model for 6MWT results in CLN3 disease (y = 409.18 - [0.52 × age2]). In contrast, an upward trend of 6MWT scores with age was observed in the control cohort with isolated visual impairment (r = 0.56; p = 0.04) similar to healthy, sighted children. The control cohort with additional neurologic impairments displayed a slightly decreased 6MWT walking distance independent of age.
CONCLUSIONS: The 6MWT unveils early onset of motor decline in CLN3 disease.
© 2019 American Academy of Neurology.

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Year:  2019        PMID: 31182507     DOI: 10.1212/WNL.0000000000007773

Source DB:  PubMed          Journal:  Neurology        ISSN: 0028-3878            Impact factor:   9.910


  6 in total

1.  Use of the Vineland-3, a measure of adaptive functioning, in CLN3.

Authors:  An N Dang Do; Audrey E Thurm; Cristan A Farmer; Ariane G Soldatos; Colby E Chlebowski; Julie K O'Reilly; Forbes D Porter
Journal:  Am J Med Genet A       Date:  2021-12-16       Impact factor: 2.578

2.  Quantifying lymphocyte vacuolization serves as a measure of CLN3 disease severity.

Authors:  Willemijn F E Kuper; Marlies Oostendorp; Brigitte T A van den Broek; Karin van Veghel; Lourens J P Nonkes; Edward E S Nieuwenhuis; Sabine A Fuchs; Tineke Veenendaal; Judith Klumperman; Albert Huisman; Stefan Nierkens; Peter M van Hasselt
Journal:  JIMD Rep       Date:  2020-06-02

3.  Towards Understanding Behaviour and Emotions of Children with CLN3 Disease (Batten Disease): Patterns, Problems and Support for Child and Family.

Authors:  Aline K Honingh; Yvonne L Kruithof; Willemijn F E Kuper; Peter M van Hasselt; Paula S Sterkenburg
Journal:  Int J Environ Res Public Health       Date:  2022-05-12       Impact factor: 4.614

Review 4.  Neuronal Ceroid Lipofuscinosis: Potential for Targeted Therapy.

Authors:  Nicola Specchio; Alessandro Ferretti; Marina Trivisano; Nicola Pietrafusa; Chiara Pepi; Costanza Calabrese; Susanna Livadiotti; Alessandra Simonetti; Paolo Rossi; Paolo Curatolo; Federico Vigevano
Journal:  Drugs       Date:  2021-01       Impact factor: 9.546

5.  Characterizing upper limb function in the context of activities of daily living in CLN3 disease.

Authors:  Hanna Hildenbrand; Jordan Wickstrom; Rebecca Parks; Cris Zampieri; Thuy-Tien Nguyen; Audrey Thurm; Kisha Jenkins; Katharine E Alter; Jesse Matsubara; Dylan Hammond; Ariane Soldatos; Forbes D Porter; An N Dang Do
Journal:  Am J Med Genet A       Date:  2021-02-08       Impact factor: 2.578

6.  The c.1A > C start codon mutation in CLN3 is associated with a protracted disease course.

Authors:  Willemijn F E Kuper; Claudia van Alfen; Linda van Eck; Stella A de Man; Marjolein H Willemsen; Koen L I van Gassen; Monique Losekoot; Peter M van Hasselt
Journal:  JIMD Rep       Date:  2020-02-07
  6 in total

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