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Review
. 2018 Jul;48(4):259-270.
doi: 10.1007/s10519-018-9903-5. Epub 2018 Jun 19.

Neurocognitive Functioning in Patients with 22q11.2 Deletion Syndrome: A Meta-Analytic Review

Affiliations
Review

Neurocognitive Functioning in Patients with 22q11.2 Deletion Syndrome: A Meta-Analytic Review

Paul J Moberg et al. Behav Genet. 2018 Jul.

Abstract

The 22q11.2 deletion syndrome (22q11.2DS) is a known risk factor for development of schizophrenia and is characterized by a complex neuropsychological profile. To date, a quantitative meta-analysis examining cognitive functioning in 22q11.2DS has not been conducted. A systematic review of cross-sectional studies comparing neuropsychological performance of individuals with 22q11.2DS with age-matched healthy typically developing and sibling comparison subjects was carried out. Potential moderators were analyzed. Analyses included 43 articles (282 effects) that met inclusion criteria. Very large and heterogeneous effects were seen for global cognition (d = - 1.21) and in specific neuropsychological domains (intellectual functioning, achievement, and executive function; d range = - 0.51 to - 2.43). Moderator analysis revealed a significant role for type of healthy comparison group used (typically developing or siblings), demographics (age, sex) and clinical factors (externalizing behavior). Results revealed significant differences between pediatric and adult samples, with isolated analysis within the pediatric sample yielding large effects in several neuropsychological domains (intellectual functioning, achievement, visual memory; d range = - 0.56 to - 2.50). Large cognitive deficits in intellectual functioning and specific neuropsychological variables in individuals with 22q11.2DS represent a robust finding, but these deficits are influenced by several factors, including type of comparison group utilized, age, sex, and clinical status. These findings highlight the clinical relevance of characterizing cognitive functioning in 22q11.2DS and the importance of considering demographic and clinical moderators in future analyses.

Keywords: 22q11.2 Deletion syndrome; Cognitive; Meta-analysis; Neuropsychology; Velocardiofacial syndrome.

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Conflict of interest statement

Conflict of interest P.J. Moberg, M.J. Richman, D.R. Roalf, C.L. Morse, A.C. Graefe, L. Brennan, K. Vickers, W. Tsering, V. Kamath, B.I. Turetsky, R.C. Gur, and R.E. Gur declare that they have no conflict of interest.

Figures

Fig. 1
Fig. 1
Search and selection criteria
Fig. 2
Fig. 2
Effect sizes for neuropsychological domains for entire sample. Error bars represent 95% Confidence Intervals. Key: FSIQ > achievement, attention, emotion, executive function, language, motor, processing speed, verbal memory, VIQ, visual memory, visuospatial, p < .05. VIQ > achievement, attention, emotion, executive function, motor, processing speed, verbal memory, visual memory, visuospatial, p < .05. PIQ > achievement, attention, emotion, executive function, motor, processing speed, verbal memory, visual memory, visuospatial, p < .05. Executive function > attention, processing speed, visuospatial, p < .05. Achievement > attention, processing speed, visuospatial, p < .05
Fig. 3
Fig. 3
Effect sizes for neuropsychological domains in pediatric-only sample. Error bars represent 95% Confidence Intervals. FSIQ > achievement, attention, emotion, executive function, language, motor, processing speed, verbal memory, visual memory, visuospatial, p < .05. VIQ > achievement, attention, emotion, executive function, language, motor, processing speed, verbal memory, visual memory, visuospatial, p < .05. PIQ > achievement, attention, emotion, executive function, language, motor, processing speed, verbal memory, visual memory, visuospatial, p < .05. Achievement > attention, processing speed, p < .05. Visual memory > attention, processing speed, p < .05

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