Level of purposeful hand function as a marker of clinical severity in Rett syndrome

Aim - We investigated relationships between hand function and genotype and aspects of phenotype in Rett syndrome. Method - Video assessment in naturalistic settings was supplemented by parent-reported data in a cross-sectional study of 144 females with a mean age of 14 years 10 months (SD 7y 10mo; r...

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Main Authors: Downs, J., Bebbington, A., Jacoby, P., Williams, A., Ghosh, Soumya, Kaufmann, W., Leonard, H.
Format: Journal Article
Published: Wiley-Blackwell Publishing Ltd. 2010
Online Access:http://hdl.handle.net/20.500.11937/21837
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author Downs, J.
Bebbington, A.
Jacoby, P.
Williams, A.
Ghosh, Soumya
Kaufmann, W.
Leonard, H.
author_facet Downs, J.
Bebbington, A.
Jacoby, P.
Williams, A.
Ghosh, Soumya
Kaufmann, W.
Leonard, H.
author_sort Downs, J.
building Curtin Institutional Repository
collection Online Access
description Aim - We investigated relationships between hand function and genotype and aspects of phenotype in Rett syndrome. Method - Video assessment in naturalistic settings was supplemented by parent-reported data in a cross-sectional study of 144 females with a mean age of 14 years 10 months (SD 7y 10mo; range 2y–31y 10mo), 110 of whom had a mutation of the methyl CpG binding protein 2 (MECP2) gene. Ordinal logistic regression was used to assess relationships between hand function and MECP2 mutation, age, a modified Kerr score, Functional Independence Measure for Children (WeeFIM), ambulation level, and frequency of hand stereotypies. Results - Approximately two-thirds of participants demonstrated purposeful hand function, ranging from simple grasping skills to picking up and manipulating small objects. In participants with a confirmed MECP2 mutation, those with the p.R168X mutation had the poorest hand function on multivariate analysis with C-terminal deletion as the baseline (odds ratio [OR] 0.19; 95% confidence interval [CI] 0.04–0.95), whereas those with the p.R133C or p.R294X mutation had better hand function. Participants aged 19 years or older had lower hand function than those aged less than 8 years (OR 0.36; 95% CI 0.14–0.92). Factors that were associated with better hand function were lower Kerr scores for a 1-point increase in score (OR 0.77; 95% CI 0.69–0.86), higher WeeFIM scores for a 1-point increase in score (OR 1.08; 95% CI 1.04–1.12), and greater ambulation than those completely dependent on carers for mobility (OR 22.64; 95% CI 7.02–73.08). The results for participants with a confirmed pathogenic mutation were similar to results obtained when participants without a mutation were also included. Interpretation - Our novel assessment of hand function in Rett syndrome correlated well with known profiles of common MECP2 mutations and overall clinical severity. This promising assessment could measure clinical responses to therapy.
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spelling curtin-20.500.11937-218372017-09-13T13:52:23Z Level of purposeful hand function as a marker of clinical severity in Rett syndrome Downs, J. Bebbington, A. Jacoby, P. Williams, A. Ghosh, Soumya Kaufmann, W. Leonard, H. Aim - We investigated relationships between hand function and genotype and aspects of phenotype in Rett syndrome. Method - Video assessment in naturalistic settings was supplemented by parent-reported data in a cross-sectional study of 144 females with a mean age of 14 years 10 months (SD 7y 10mo; range 2y–31y 10mo), 110 of whom had a mutation of the methyl CpG binding protein 2 (MECP2) gene. Ordinal logistic regression was used to assess relationships between hand function and MECP2 mutation, age, a modified Kerr score, Functional Independence Measure for Children (WeeFIM), ambulation level, and frequency of hand stereotypies. Results - Approximately two-thirds of participants demonstrated purposeful hand function, ranging from simple grasping skills to picking up and manipulating small objects. In participants with a confirmed MECP2 mutation, those with the p.R168X mutation had the poorest hand function on multivariate analysis with C-terminal deletion as the baseline (odds ratio [OR] 0.19; 95% confidence interval [CI] 0.04–0.95), whereas those with the p.R133C or p.R294X mutation had better hand function. Participants aged 19 years or older had lower hand function than those aged less than 8 years (OR 0.36; 95% CI 0.14–0.92). Factors that were associated with better hand function were lower Kerr scores for a 1-point increase in score (OR 0.77; 95% CI 0.69–0.86), higher WeeFIM scores for a 1-point increase in score (OR 1.08; 95% CI 1.04–1.12), and greater ambulation than those completely dependent on carers for mobility (OR 22.64; 95% CI 7.02–73.08). The results for participants with a confirmed pathogenic mutation were similar to results obtained when participants without a mutation were also included. Interpretation - Our novel assessment of hand function in Rett syndrome correlated well with known profiles of common MECP2 mutations and overall clinical severity. This promising assessment could measure clinical responses to therapy. 2010 Journal Article http://hdl.handle.net/20.500.11937/21837 10.1111/j.1469-8749.2010.03636.x Wiley-Blackwell Publishing Ltd. unknown
spellingShingle Downs, J.
Bebbington, A.
Jacoby, P.
Williams, A.
Ghosh, Soumya
Kaufmann, W.
Leonard, H.
Level of purposeful hand function as a marker of clinical severity in Rett syndrome
title Level of purposeful hand function as a marker of clinical severity in Rett syndrome
title_full Level of purposeful hand function as a marker of clinical severity in Rett syndrome
title_fullStr Level of purposeful hand function as a marker of clinical severity in Rett syndrome
title_full_unstemmed Level of purposeful hand function as a marker of clinical severity in Rett syndrome
title_short Level of purposeful hand function as a marker of clinical severity in Rett syndrome
title_sort level of purposeful hand function as a marker of clinical severity in rett syndrome
url http://hdl.handle.net/20.500.11937/21837