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The cognitive developmental profile associated with fragile X syndrome: A longitudinal investigation of cognitive strengths and weaknesses through childhood and adolescence

Published online by Cambridge University Press:  09 December 2015

Eve-Marie Quintin*
Affiliation:
McGill University
Booil Jo
Affiliation:
Stanford University
Scott S. Hall
Affiliation:
Stanford University
Jennifer L. Bruno
Affiliation:
Stanford University
Lindsay C. Chromik
Affiliation:
Stanford University
Mira M. Raman
Affiliation:
Stanford University
Amy A. Lightbody
Affiliation:
Stanford University
Arianna Martin
Affiliation:
Stanford University
Allan L. Reiss
Affiliation:
Stanford University
*
Address correspondence and reprint requests to: Eve-Marie Quintin, Educational and Counseling Psychology Department, McGill University, 3700 McTavish Street, Montreal, QCH3A 1Y2, Canada; E-mail: eve-marie.quintin@mcgill.ca.
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Abstract

Few studies have investigated developmental strengths and weaknesses within the cognitive profile of children and adolescents with fragile X syndrome (FXS), a single-gene cause of inherited intellectual impairment. With a prospective longitudinal design and using normalized raw scores (Z scores) to circumvent floor effects, we measured cognitive functioning of 184 children and adolescents with FXS (ages 6 to 16) using the Wechsler Scale of Intelligence for Children on one to three occasions for each participant. Participants with FXS received lower raw scores relative to the Wechsler Scale of Intelligence for Children normative sample across the developmental period. Verbal comprehension, perceptual organization, and processing speed Z scores were marked by a widening gap from the normative sample, while freedom from distractibility Z scores showed a narrowing gap. Key findings include a relative strength for verbal skills in comparison with visuospatial–constructive skills arising in adolescence and a discrepancy between working memory (weakness) and processing speed (strength) in childhood that diminishes in adolescence. Results suggest that the cognitive profile associated with FXS develops dynamically from childhood to adolescence. Findings are discussed within the context of aberrant brain morphology in childhood and maturation in adolescence. We argue that assessing disorder-specific cognitive developmental profiles will benefit future disorder-specific treatment research.

Information

Type
Regular Articles
Copyright
Copyright © Cambridge University Press 2015 
Figure 0

Table 1. WISC-III index standard scores and full scale IQ for males and females with FXS

Figure 1

Figure 1. (Color online) Observed data and estimated trajectories of the Wechsler Intelligence Scale for Children—Third Edition Z scores based on mixed effects modeling for (a) males and (b) females with fragile X syndrome. The estimated trajectories of quadratic growth for each Wechsler Intelligence Scale for Children index Z score according to age (years) are shown (dark blue lines online only), overlaid onto the observed data (light blue dots and lines online only). Overall, verbal comprehension, perceptual organization, and processing speed Z scores were marked by a widening gap from the normative sample; while freedom from distractibility Z scores showed a narrowing gap.

Figure 2

Table 2. Estimated longitudinal changes in WISC-III index Z scores based on mixed effects modeling

Figure 3

Figure 2. (Color online) Estimated trajectories of the four Wechsler Intelligence Scale for Children—Third Edition Z scores according to age (years) based on mixed effects modeling for (a) males and (b) females with fragile X syndrome. The estimated trajectory of quadratic growth for verbal comprehension is compared to that of perceptual organization, and the estimated trajectory of freedom from distractibility is compared to that of processing speed. Key findings include a relative strength for verbal skills in comparison with visuospatial–constructive skills arising in adolescence and a discrepancy between working memory (weakness) and processing speed (strength) in childhood that diminishes in adolescence.

Figure 4

Table 3. Comparing Z scores between WISC-III indexes among individuals with FXS based on estimated trajectories using mixed effects modeling