Cognitive Profiles and Brain Volume Are Affected in Patients with Silver–Russell Syndrome

Author:

Patti Giuseppa12ORCID,De Mori Letizia2,Tortora Domenico3,Severino Mariasavina3,Calevo Mariagrazia4,Russo Silvia5,Napoli Flavia1,Confalonieri Laura12,Schiavone Maurizio12,Thiabat Hanan F12,Casalini Emilio12,Morana Giovanni3,Rossi Andrea3,Ramenghi Luca Antonio6,Maghnie Mohamad12,Di Iorgi Natascia12

Affiliation:

1. Department of Pediatrics, IRCCS Istituto Giannina Gaslini, Genova, Italy

2. Department of Neuroscience, Rehabilitation, Ophtalmology, Genetics, Maternal and Child Health, University of Genova, Genova, Italy

3. Pediatric Neuroradiology Unit, IRCCS Istituto Giannina Gaslini, Genova, Italy

4. Epidemiology and Biostatistics Unit, IRCCS Istituto Giannina Gaslini, Genova, Italy

5. Cytogenetic and Molecular Genetics Laboratory, Istituto Auxologico Italiano, Milano, Italy

6. Department of Mother and Child, Neonatal Intensive Care Unit, IRCCS Istituto Giannina Gaslini, Italy

Abstract

Abstract Context There is little information on cognitive function in Silver–Russell syndrome (SRS), and no neuroimaging studies are available so far. Objective To assess cognitive function and brain volumes in patients with SRS. Design/Setting Wechsler Intelligence Scale and brain magnetic resonance on a 3-Tesla scanner with Voxel-based morphometry analysis were performed between 2016 and 2018 in a single tertiary university center. Partecipants 38 white subjects with clinical diagnosis of SRS confirmed by molecular analysis: 30 of these patients (mean age 12.6 ± 10 years) were enrolled for cognitive assessment; 23 of the 30 performed neuroimaging sequences. A control group of 33 school-aged children performed cognitive assessment while 65 age and sex-matched volunteers were included for the neuroradiological assessment. Main Outcomes Intelligence quotient, Verbal Comprehension Index (VCI), Perceptual Reasoning Index (PRI), Working Memory Index (WMI), Processing Speed Index, and brain volume. Results The mean overall IQ score was 87.2 ± 17, and it was significantly lower in the maternal uniparental disomy of chromosome 7 (mUPD7) group at the age of 6 to 16 years compared to loss of methylation on chromosome 11p15 (11p15 LOM) group and to controls. VCI, PRI, and WMI were significantly higher in 11p15 LOM group and in control group than in mUPD7 group at the age of 6 to 16 years. There were no significant differences in cognitive scores between 11p15 LOM school-aged patients and the control group. SRS patients showed lower brain volume compared to controls at the frontal/temporal poles and globi pallidi. Conclusions Patients with mUPD7 had an impaired cognitive profile. The brain volume at the frontal/temporal lobes and at the globi pallidi was reduced in patients with SRS.

Funder

Ministero Dell’Istruzione, dell’Università e della Ricerca

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

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