Multiple genomic copy number variants associated with periventricular nodular heterotopia indicate extreme genetic heterogeneity

Elena Cellini, Annalisa Vetro, Valerio Conti, Carla Marini, Viola Doccini, Claudia Clementella, Elena Parrini, Sabrina Giglio, Matteo Della Monica, Marco Fichera, Sebastiano Antonino Musumeci, Renzo Guerrini

Research output: Contribution to journalArticle

2 Citations (Scopus)

Abstract

Periventricular nodular heterotopia (PNH) is a brain malformation in which nodules of neurons are ectopically retained along the lateral ventricles. Genetic causes include FLNA abnormalities (classical X-linked PNH), rare variants in ARFGEF2, DCHS1, ERMARD, FAT4, INTS8, MAPB1, MCPH1, and NEDD4L, as well as several chromosomal abnormalities. We performed array-CGH in 106 patients with different malformations of cortical development (MCD) and looked for common pathways possibly involved in PNH. Forty-two patients, including two parent/proband couples, exhibited PNH associated or not with other brain abnormalities, 44 had polymicrogyria and 20 had rarer MCDs. We found an enrichment of either large rearrangements or cryptic copy number variants (CNVs) in PNH (15/42, 35.7%) vs polymicrogyria (4/44, 9.1%) (i.e., 5.6 times increased risk for PNH of carrying a pathogenic CNV). CNVs in seven genomic regions (2p11.2q12.1, 4p15, 14q11.2q12, 16p13.3, 19q13.33, 20q13.33, 22q11) represented novel, potentially causative, associations with PNH. Through in silico analysis of genes included in imbalances whose breakpoints were clearly detailed, we detected in 9/12 unrelated patients in our series and in 15/24 previously published patients, a significant (P < 0.05) overrepresentation of genes involved in vesicle-mediated transport. Rare genomic imbalances, either small CNVs or large rearrangements, are cumulatively a frequent cause of PNH. Dysregulation of specific cellular mechanisms might play a key pathogenic role in PNH but it remains to be determined whether this is exerted through single genes or the cumulative dosage effect of more genes. Array-CGH should be considered as a first-line diagnostic test in PNH, especially if sporadic and non-classical.

Original languageEnglish
JournalEuropean Journal of Human Genetics
DOIs
Publication statusAccepted/In press - Jan 1 2019

Fingerprint

Periventricular Nodular Heterotopia
Genetic Heterogeneity
Genes
Malformations of Cortical Development
Transport Vesicles
Lateral Ventricles
Brain
Routine Diagnostic Tests
Chromosome Aberrations
Computer Simulation

ASJC Scopus subject areas

  • Genetics
  • Genetics(clinical)

Cite this

Multiple genomic copy number variants associated with periventricular nodular heterotopia indicate extreme genetic heterogeneity. / Cellini, Elena; Vetro, Annalisa; Conti, Valerio; Marini, Carla; Doccini, Viola; Clementella, Claudia; Parrini, Elena; Giglio, Sabrina; Della Monica, Matteo; Fichera, Marco; Musumeci, Sebastiano Antonino; Guerrini, Renzo.

In: European Journal of Human Genetics, 01.01.2019.

Research output: Contribution to journalArticle

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abstract = "Periventricular nodular heterotopia (PNH) is a brain malformation in which nodules of neurons are ectopically retained along the lateral ventricles. Genetic causes include FLNA abnormalities (classical X-linked PNH), rare variants in ARFGEF2, DCHS1, ERMARD, FAT4, INTS8, MAPB1, MCPH1, and NEDD4L, as well as several chromosomal abnormalities. We performed array-CGH in 106 patients with different malformations of cortical development (MCD) and looked for common pathways possibly involved in PNH. Forty-two patients, including two parent/proband couples, exhibited PNH associated or not with other brain abnormalities, 44 had polymicrogyria and 20 had rarer MCDs. We found an enrichment of either large rearrangements or cryptic copy number variants (CNVs) in PNH (15/42, 35.7{\%}) vs polymicrogyria (4/44, 9.1{\%}) (i.e., 5.6 times increased risk for PNH of carrying a pathogenic CNV). CNVs in seven genomic regions (2p11.2q12.1, 4p15, 14q11.2q12, 16p13.3, 19q13.33, 20q13.33, 22q11) represented novel, potentially causative, associations with PNH. Through in silico analysis of genes included in imbalances whose breakpoints were clearly detailed, we detected in 9/12 unrelated patients in our series and in 15/24 previously published patients, a significant (P < 0.05) overrepresentation of genes involved in vesicle-mediated transport. Rare genomic imbalances, either small CNVs or large rearrangements, are cumulatively a frequent cause of PNH. Dysregulation of specific cellular mechanisms might play a key pathogenic role in PNH but it remains to be determined whether this is exerted through single genes or the cumulative dosage effect of more genes. Array-CGH should be considered as a first-line diagnostic test in PNH, especially if sporadic and non-classical.",
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AU - Cellini, Elena

AU - Vetro, Annalisa

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AU - Doccini, Viola

AU - Clementella, Claudia

AU - Parrini, Elena

AU - Giglio, Sabrina

AU - Della Monica, Matteo

AU - Fichera, Marco

AU - Musumeci, Sebastiano Antonino

AU - Guerrini, Renzo

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