Expanding association between BICD2 variants and brain malformations and associated lissencephaly

Abstract

The study was approved by the Institutional Review Board (IRB) of Seoul National University Hospital (IRB No. 2010-125-1166). Footnotes Conflicts of interest No potential conflict of interest relevant to this article was reported. Ann Neurol 2020;87:487–96. pmc Jaeso Cho, MD1; Haeryung Kim, MD2; Seoungbok Lee, MD1; Jihoon G Yoon, MD, PhD1; HyeJin Kim, MD2; Minhye Kim, MD2; Seoyun Jang, MD2; Woojoong Kim, MD2; Soo Yeon Kim, MD1; Jong Hee Chae, MD, PhD1 1Department of Genomic Medicine, Seoul National University Hospital, Seoul, Korea 2Department of Pediatrics, Seoul National University College of Medicine, Seoul, Korea

Bicaudal D is an important component of a crucial pathway that involves dynein and dynactin and is responsible for transporting mRNAs and other cellular cargo [1]. Variants in Bicaudal D2 Drosophila homolog 2 (BICD2) were known to be associated with autosomal dominant lower extremity-predominant spinal muscular atrophy 2 (SMALED2A/2B; Online Mendelian Inheritance in Man [OMIM]) [2,3]. After a recent study demonstrating loss of BICD2 function are associated with brain malformations in human [4], 9 patients with BICD2 variants were reported to be associated with brain malformations [5-10]. However, only a few patients have been reported to exhibit lissencephaly in brain imaging, and as such, this phenotype has not yet been added to the OMIM database. We report a case of Korean female patient with novel heterozygous BICD2 variant with developmental regression and lissencephaly, expanding neurologic phenotypic spectrum of BICD2-associated disease.

A 9-month-old female patient visited our outpatient clinic due to developmental delay. At the initial visit, she demonstrated eye contact, social smiles and head control, but was unable to sit unassisted. In neurological examination, spasticity and increased deep tendon reflexes were observed. Facial dysmorphism and joint abnormalities were not noted. Initial examination also revealed microcephaly, as head circumference measured 40.5 cm (-3.7 standard deviation). A brain magnetic resonance imaging taken at 9 months of age showed lissencephaly and corpus callosum hypogenesis (Fig. 1A). Routine laboratory tests, including creatine kinase, showed no notable abnormalities or neutropenia. During follow-up, she was able to sit alone at 14 months of age, crawl at 2 years of age, stand with assistance at 3 years of age, and understand a few commands. However, her developmental milestones regressed when she was 3.5 years old. The initial seizure occurred at 30 months of age, characterized by generalized seizures. A routine baseline electroencephalogram (EEG) at 16 months showed frequent repetitive beta activities, and the EEG at the onset of the first seizure revealed irregular high amplitude delta waves with a few suspicious frontal sharp waves. Initial treatment with valproic acid (up to 70 mg/kg/day) was followed by levetiracetam (up to 50 mg/kg/day) and topiramate (up to 50 mg/kg/day), but was still refractory. At 7 years old, the patient can only sit with assistance and does not understand commands. An EEG taken at 7 years old showed an excessive amount of high amplitude irregular delta waves and some suspicious frontal sharp waves. The patient still suffers from 2–5 generalized seizures per day and did not gain any developmental milestones.

Trio whole exome sequencing (WES) was performed. The detailed method for data generation and processing was described elsewhere [11]. Initial trio WES analysis did not result in likely pathogenic/pathogenic variants linked to patient’s phenotype, asBICD2 was reported to be associated with only spinal muscular atrophy phenotype and not with severe developmental delay and/or lissencephaly. A recent WES reanalysis revealed a novel de novo BICD2 variant (c.2324_2327dupAGAA [p.Thr777fs]) as a likely pathogenic variant with subsequent Sanger sequencing confirmation (Fig. 1B). All known BICD2 variants associated with brain malformations is shown in Fig. 1C.

Written informed consent-to-disclose was obtained from the parent of the patient. The study was approved by the Institutional Review Board (IRB) of Seoul National University Hospital (IRB No. 2010-125-1166).

BICD2 is vital for cerebral cortex development [4]. Only 9 patients with BICD2 variants were reported to have brain malformations (hypogenesis of corpus callosum, polymicrogyria, cerebellar hypoplasia, white matter loss and ventriculomegaly), including lissencephaly in 3 patients. Notably, microcephaly was observed in all BICD2-related lissencephaly cases unlike other BICD2-related brain malformations, while arthrogryposis commonly found in BICD2-related SMALED2A/2B patients was rare in lissencephaly patients. Our patient exhibited microcephaly and lissencephaly, consistent with previous studies [4,9,10]. We observed developmental regression in our patient, a novel occurrence in BICD2-related disease patients during long-term follow-up until age 7 (Table 1). We suspect it may result from refractory seizures not reported before.

We observed significant findings in understanding phenotype-genotype correlations of BICD2-related disorders. Most brain malformation-associated BICD2 variants occur in the conserved CC3 domain. Lissencephaly-related variants are typically heterozygous nonsense variants (p.Lys775Ter) in CC3 or homozygous variants (p.Leu244Pro and p.Gln77Ter) in CC1. Our patient's out-of-frame duplication variant in CC3 (p.Thr777fs) suggests that high-impact variants in CC3 and/or bi-allelic variants in other domains may contribute to the lissencephaly phenotype in BICD2-related disorders. No nonsense or out-of-frame deletion/duplication BICD2 variants associated with SMALED2A/2B phenotypes have been reported in the ClinVar database to date [12]. A recent study revealed interactions between the CC3 domain of BICD2 and 2 nuclear envelope-associated cargos, RanBP2 and Nesprin-2, in neuronal precursor cells in the developing brain. This finding suggests potential phenotype-genotype correlations with variants located in the CC3 domain [13].

In summary, we report a case of novel de novo heterozygous BICD2 variant-associated with lissencephaly and developmental regression. Given that lissencephaly phenotype has not yet been incorporated in the OMIM database, our case significantly contributes to the expanding phenotypic spectrum of BICD2-associated diseases and highlights the importance of raising awareness of the phenotypes reviewed in our study.

Footnotes

Conflicts of interest

No potential conflict of interest relevant to this article was reported.

Funding

This research was supported by a fund (2021-ER0701-01) by Research of Korea Disease Control and Prevention Agency.

Acknowledgments

The authors thank the family for their support.

Fig.1 Radiogenomic findings of patients with BICD2-associated brain malformations in this study. (A) Brain magnetic resonance imaging findings of this patient with lissencephaly and hypogenesis of the corpus callosum (left: T1 sagittal; right: T2 axial). (B) Patient’s pedigree and variant information. Trio-sanger sequencing was performed to confirm the variant. (C) All reported BICD2 variants associated with brain malformations to date. Variants associated with lissencephaly are marked in red.

[Table Omitted; See PDF]

References

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