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Digit Span Performance in Children with Dystrophinopathy: A Verbal Span or Working Memory Contribution?

Published online by Cambridge University Press:  08 June 2016

Emily B. Leaffer
Affiliation:
Sergievsky Center & Department of Neurology, Columbia University, New York, New York Department of Psychology, Queens College & The Graduate Center, City University of New York, New York, New York
Robert J. Fee
Affiliation:
Sergievsky Center & Department of Neurology, Columbia University, New York, New York Department of Psychology, Queens College & The Graduate Center, City University of New York, New York, New York
Veronica J. Hinton*
Affiliation:
Sergievsky Center & Department of Neurology, Columbia University, New York, New York
*
Correspondence and reprint requests to: Veronica J. Hinton, GH Sergievsky Center, Columbia University, P & S Unit 16, 630 West 168th Street, New York, New York 10032. E-mail: [email protected]

Abstract

Objectives: In a large cohort of boys with dystrophinopathies and their unaffected siblings, we examined whether consistently observed performance on digit span is due primarily to a verbal span or executive deficit. We additionally assessed whether digit span performance contributed to the observed variability in reading performance noted in this population. Methods: Performance of 170 boys with dystrophinopathy was compared to 95 unaffected sibling controls on measures of verbal function, reading, and digit span. Maximum digit span forward (DSF) and backward (DSB) lengths were converted to Z-scores using normative data. Independent sample t tests, analysis of variance, and hierarchical multiple regression were run (α=0.05). Results: Probands performed worse than controls on digit span, even after accounting for differences in general verbal function (p<.0001). Differences were significant for both DSF (p<.005) and DSB (p<.0001) span length, and an interaction effect yielded significantly worse DSB compared with DSF (p=.01). Reading performance was also lower in probands (p<.0001). The contribution of general level of verbal function, and forward and backward span lengths, did not vary between groups. Conclusions: In boys with dystrophinopathy, decreased performance on digit span appears to be due to both decreased span forward (measuring verbal span only) and backward (measuring verbal span and working memory). The extent to which sibling controls exhibited better performance compared to the probands was significantly greater for backward span when compared with forward span. Thus, immediate verbal memory and executive control are differentially compromised among boys with dystrophinopathy, and both of these abilities independently contribute to reading performance. (JINS, 2016, 22, 777–784)

Type
Research Articles
Copyright
Copyright © The International Neuropsychological Society 2016 

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References

Anderson, S.W., Routh, D.K., & Ionasescu, V.V. (1988). Serial position memory of boys with Duchenne muscular dystrophy. Developmental Medicine & Child Neurology, 30(3), 328333. Retrieved from http://www.ncbi.nlm.nih.gov/pubmed/3402674 Google Scholar
Baddeley, A. (2012). Working memory: Theories, models, and controversies. Annual Review of Psychology, 63, 129. doi:10.1146/annurev-psych-120710-100422 Google Scholar
Baddeley, A.D., Allen, R.J., & Hitch, G.J. (2011). Binding in visual working memory: The role of the episodic buffer. Neuropsychologia, 49(6), 13931400. doi:10.1016/j.neuropsychologia.2010.12.042 Google Scholar
Billard, C., Gillet, P., Barthez, M., Hommet, C., & Bertrand, P. (1998). Reading ability and processing in Duchenne muscular dystrophy and spinal muscular atrophy. Developmental Medicine & Child Neurology, 40(1), 1220. Retrieved from http://www.ncbi.nlm.nih.gov/pubmed/9459212 Google Scholar
Billard, C., Gillet, P., Signoret, J.L., Uicaut, E., Bertrand, P., Fardeau, M., & Santini, J.J. (1992). Cognitive functions in Duchenne muscular dystrophy: A reappraisal and comparison with spinal muscular atrophy. Neuromuscular Disorders, 2(5-6), 371378. Retrieved from http://www.ncbi.nlm.nih.gov/pubmed/1300185 Google Scholar
Cotton, S., Crowe, S.F., & Voudouris, N. (1998). Neuropsychological profile of Duchenne muscular dystrophy. Child Neuropsychology, 4, 110117.Google Scholar
Cotton, S., Voudouris, N.J., & Greenwood, K.M. (2001). Intelligence and Duchenne muscular dystrophy: Full-scale, verbal, and performance intelligence quotients. Developmental Medicine & Child Neurology, 43(7), 497501. Retrieved from http://www.ncbi.nlm.nih.gov/pubmed/11463183 Google Scholar
Cyrulnik, S.E., Fee, R.J., De Vivo, D.C., Goldstein, E., & Hinton, V.J. (2007). Delayed developmental language milestones in children with Duchenne’s muscular dystrophy. Journal of Pediatrics, 150(5), 474478. doi:10.1016/j.jpeds.2006.12.045 Google Scholar
Cyrulnik, S.E., & Hinton, V.J. (2008). Duchenne muscular dystrophy: A cerebellar disorder? Neuroscience & Biobehavioral Reviews, 32(3), 486496. doi:10.1016/j.neubiorev.2007.09.001 Google Scholar
D’Angelo, M.G., Lorusso, M.L., Civati, F., Comi, G.P., Magri, F., Del Bo, R., & Bresolin, N. (2011). Neurocognitive profiles in Duchenne muscular dystrophy and gene mutation site. Pediatric Neurology, 45(5), 292299. doi:10.1016/j.pediatrneurol.2011.08.003 Google Scholar
Daneman, M.C., & Carpenter, P.A. (1980). Individual differnces in working memory and reading. Journal of Verbal Learning and Verbal Behavior, 19, 450466.CrossRefGoogle Scholar
Donders, J., & Taneja, C. (2009). Neurobehavioral characteristics of children with Duchenne muscular dystrophy. Child Neuropsychology, 15(3), 295304. doi:10.1080/09297040802665777 Google Scholar
Dorman, C., Hurley, A.D., & D’Avignon, J. (1988). Language and learning disorders of older boys with Duchenne muscular dystrophy. Developmental Medicine & Child Neurology, 30(3), 316327. Retrieved from http://www.ncbi.nlm.nih.gov/pubmed/3402673 Google Scholar
Dunn, L.M., & Dunn, L. (1997). Examiner’s manual for the Peabody Picture Vocabulary Test (3rd ed.). Circle Pines, MN: American Guidance Service.Google Scholar
Emery, A.E. (1991). Population frequencies of inherited neuromuscular diseases--A world survey. Neuromuscular Disorders, 1(1), 1929. Retrieved from http://www.ncbi.nlm.nih.gov/pubmed/1822774 Google Scholar
Engle, R.W., Tuholski, S.W., Laughlin, J.E., & Conway, A.R. (1999). Working memory, short-term memory, and general fluid intelligence: A latent-variable approach. Journal of Experimental Psychology: General, 128(3), 309331. Retrieved from http://www.ncbi.nlm.nih.gov/pubmed/10513398 Google Scholar
Hinton, V.J., De Vivo, D.C., Fee, R., Goldstein, E., & Stern, Y. (2004). Investigation of poor academic achievement in children with Duchenne muscular dystrophy. Learning Disabilities & Research Practice, 19(3), 146154. doi:10.1111/j.1540-5826.2004.00098.x Google Scholar
Hinton, V.J., De Vivo, D.C., Nereo, N.E., Goldstein, E., & Stern, Y. (2000). Poor verbal working memory across intellectual level in boys with Duchenne dystrophy. Neurology, 54(11), 21272132. Retrieved from http://www.ncbi.nlm.nih.gov/pubmed/10851376 Google Scholar
Hinton, V.J., De Vivo, D.C., Nereo, N.E., Goldstein, E., & Stern, Y. (2001). Selective deficits in verbal working memory associated with a known genetic etiology: The neuropsychological profile of duchenne muscular dystrophy. Journal of the International Neuropsychological Society, 7(1), 4554. Retrieved from http://www.ncbi.nlm.nih.gov/pubmed/11253841 Google Scholar
Hinton, V.J., Fee, R.J., Goldstein, E.M., & De Vivo, D.C. (2007). Verbal and memory skills in males with Duchenne muscular dystrophy. Developmental Medicine & Child Neurology, 49(2), 123128. doi:10.1111/j.1469-8749.2007.00123.x Google Scholar
Mento, G., Tarantino, V., & Bisiacchi, P.S. (2011). The neuropsychological profile of infantile Duchenne muscular dystrophy. Clinical Neuropsychology, 25(8), 13591377. doi:10.1080/13854046.2011.617782 Google Scholar
Ogasawara, A. (1989). Downward shift in IQ in persons with Duchenne muscular dystrophy compared to those with spinal muscular atrophy. American Journal of Mental Retardation, 93(5), 544547. Retrieved from http://www.ncbi.nlm.nih.gov/pubmed/2706122 Google Scholar
Siegel, L.S. (1994). Working memory and reading: A life-span perspective. International Journal of Behavioral Development, 17, 109124.Google Scholar
Swanson, H.L. (1994). Short-term memory and working memory: Do both contribute to our understanding of academic achievement in children and adults with learning disabilities? Journal of Learning Disabilities, 27(1), 3450. Retrieved from http://www.ncbi.nlm.nih.gov/pubmed/8133185 Google Scholar
Swanson, H.L., & Berninger, V. (1995). The role of working memory in skilled and less skilled readers’ comprehension. Intelligence, 21, 83108.Google Scholar
Swanson, H.L., Xinhua, Z., & Jerman, O. (2009). Working memory, short-term memory, and reading disabilities: A selective meta-analysis of the literature. Journal of Learning Disabilities, 42(3), 260287. doi:10.1177/0022219409331958 Google Scholar
Wechsler, D. (1991). Wechsler Intelligence Scale for Children (3rd ed.). San Antonio: Psychological Corporation.Google Scholar
Wechsler, D. (2003). Wechsler Intelligence Scale for Children (4th ed.). San Antonio: Psychological Corporation.Google Scholar
Whelan, T.B. (1987). Neuropsychological performance of children with Duchenne muscular dystrophy and spinal muscle atrophy. Developmental Medicine & Child Neurology, 29(2), 212220. Retrieved from http://www.ncbi.nlm.nih.gov/pubmed/3582791 Google Scholar
Wicksell, R.K., Kihlgren, M., Melin, L., & Eeg-Olofsson, O. (2004). Specific cognitive deficits are common in children with Duchenne muscular dystrophy. Developmental Medicine & Child Neurology, 46(3), 154159. Retrieved from http://www.ncbi.nlm.nih.gov/pubmed/14995084 Google Scholar
Wingeier, K., Giger, E., Strozzi, S., Kreis, R., Joncourt, F., Conrad, B., & Steinlin, M. (2011). Neuropsychological impairments and the impact of dystrophin mutations on general cognitive functioning of patients with Duchenne muscular dystrophy. Journal of Clinical Neuroscience, 18(1), 9095. doi:10.1016/j.jocn.2010.07.118 Google Scholar
Woodcock, R.W., & Johnson, M.B. (1977). The Woodcock-Johnson psycho-educational battery. Allen, TX: DLM.Google Scholar
Woodcock, R.W., McGrew, K.S., & Mather, N. (2001). Woodcock Johnson Psychoeducational Battery (3rd ed.). Chicago: Riverside.Google Scholar