Evidence map›Paper›PMID 40401429›Full record

ArticleHuman molecular genetics2025

Improving genetic diagnostic yield in familial and sporadic cerebral cavernous malformations: detection of copy number and deep Intronic variants.

Neblina Sikta, Samuel Gooley, Timothy E Green, Olivia Hoeper, Tom Witkowski, Caitlin Bennett, David Francis, Joshua Reid, Kevin Mao, Mohammed Awad and 9 more

Abstract read
In one paragraph

Article in Human molecular genetics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Review
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

19 authors.

Neblina SiktaEpilepsy Research Centre, Department of Medicine, The University of Melbourne, Austin Health, 245 Burgundy St, Heidelberg, VIC 3084, Australia.
Samuel GooleyEpilepsy Research Centre, Department of Medicine, The University of Melbourne, Austin Health, 245 Burgundy St, Heidelberg, VIC 3084, Australia.
Timothy E GreenEpilepsy Research Centre, Department of Medicine, The University of Melbourne, Austin Health, 245 Burgundy St, Heidelberg, VIC 3084, Australia.
Olivia HoeperEpilepsy Research Centre, Department of Medicine, The University of Melbourne, Austin Health, 245 Burgundy St, Heidelberg, VIC 3084, Australia.
Tom WitkowskiEpilepsy Research Centre, Department of Medicine, The University of Melbourne, Austin Health, 245 Burgundy St, Heidelberg, VIC 3084, Australia.
Caitlin BennettEpilepsy Research Centre, Department of Medicine, The University of Melbourne, Austin Health, 245 Burgundy St, Heidelberg, VIC 3084, Australia.
David FrancisVictorian Clinical Genetics Services and Murdoch Children's Research Institute, The Royal Children's Hospital, 50 Flemington Rd, Parkville, VIC 3052, Australia.
Joshua ReidEpilepsy Research Centre, Department of Medicine, The University of Melbourne, Austin Health, 245 Burgundy St, Heidelberg, VIC 3084, Australia.
Kevin MaoEpilepsy Research Centre, Department of Medicine, The University of Melbourne, Austin Health, 245 Burgundy St, Heidelberg, VIC 3084, Australia.
Mohammed AwadDepartment of Neurosurgery, The Royal Melbourne hospital, 300 Grattan St, Parkville, VIC 3052, Australia.
Samuel Roberts-ThomsonAnatomical Pathology, The Royal Melbourne hospital, 300 Grattan St, Parkville, VIC 3052, Australia.
Kristian BullussDepartment of Neurosurgery, Austin Health, 145 Studley Rd, Heidelberg, VIC 3084, Australia.
Jonathan ClarkAnatomical Pathology, Austin Health, Heidelberg, 145 Studley Rd. VIC 3084, Australia.
Ingrid E SchefferEpilepsy Research Centre, Department of Medicine, The University of Melbourne, Austin Health, 245 Burgundy St, Heidelberg, VIC 3084, Australia.
Piero PeruccaEpilepsy Research Centre, Department of Medicine, The University of Melbourne, Austin Health, 245 Burgundy St, Heidelberg, VIC 3084, Australia.
Mark F BennettEpilepsy Research Centre, Department of Medicine, The University of Melbourne, Austin Health, 245 Burgundy St, Heidelberg, VIC 3084, Australia.
Melanie BahloPopulation Health and Immunity Division, The Walter and Eliza Hall Institute of Medical Research, 1G Royal Parade, Parkville, VIC 3052, Australia.ORCID 0000-0001-5132-0774
Samuel F BerkovicEpilepsy Research Centre, Department of Medicine, The University of Melbourne, Austin Health, 245 Burgundy St, Heidelberg, VIC 3084, Australia.
Michael S HildebrandEpilepsy Research Centre, Department of Medicine, The University of Melbourne, Austin Health, 245 Burgundy St, Heidelberg, VIC 3084, Australia.ORCID 0000-0003-2739-0515

Funding

Austin Medical Research FoundationInstitute Infrastructure Support SchemeMedical Research Future Fund AustraliaMRFF Genomics Health Futures Mission Grant 2007707National Health and Medical Research Council AustraliaNHMRC Investigator 1172897NHMRC Investigator 1195236NHMRC Investigator 2017651Norman Beischer Medical Research FoundationSynergy Grant 2010562University of Melbourne, Monash UniversityVictorian State Government Operational Infrastructure Support and Australian Government National Health and Medical Research Council
6 · The paper itself

Abstract

Cerebral cavernous malformations (CCMs) are intracranial vascular lesions associated with risk of haemorrhages and seizures. While the majority are sporadic and often associated with somatic variants in PIK3CA and MAP3K3, around 20% are familial with germline variants in one of three CCM genes-KRIT1/CCM1, CCM2 and PDCD10/CCM3. We performed comprehensive phenotyping and genetic analysis of nine multiplex families and ten sporadic individuals with CCM. In the familial cases, initial standard analyses had a low yield, we therefore searched for small copy number changes and deep intronic variants. Subsequently, pathogenic germline variants in KRIT1/CCM1 or CCM2 were identified in all 9 multiplex families. Single or multiple exon deletions or splice site variants in KRIT1/CCM1 were found in 3/9 families. Where cavernous malformation tissue was available, second hit somatic PIK3CA variants were identified in 4/7 individuals. These 4 individuals were from separate families with germline KRIT1/CCM1 variants. In 8/10 sporadic cases, we detected recurrent pathogenic somatic PIK3CA, MAP3K3 or CCM2 variants. All familial cases had multiple CCMs, whereas the sporadic cases had a single lesion only, which was in the temporal lobe in 9/10 individuals. Our comprehensive approach interrogating deep intronic variants combined with detection of small copy number variants warrants implementation in standard clinical genetic testing pipelines to increase diagnostic yield. We also build on the established second hit germline and somatic variant mechanism in some CCM lesions. Genetic diagnosis has clinical implications such as reproductive counselling and provides potential eligibility for precision medicine therapies to treat rapidly growing CCMs.

Indexed as

Carrier ProteinsDNA Copy Number VariationsHemangioma, Cavernous, Central Nervous SystemAdolescentAdultApoptosis Regulatory ProteinsChildClass I Phosphatidylinositol 3-KinasesFemaleGerm-Line MutationHumansIntronsKRIT1 ProteinMaleMAP Kinase Kinase Kinase 3Membrane ProteinsApoptosis Regulatory ProteinsCarrier ProteinsCCM2 protein, humanClass I Phosphatidylinositol 3-KinasesKRIT1 ProteinKRIT1 protein, humanMAP3K3 protein, humanMAP Kinase Kinase Kinase 3Membrane ProteinsPDCD10 protein, humanPIK3CA protein, humanProto-Oncogene ProteinsCerebral cavernous malformationsCopy number variantDeep intronic variantGermline variantSomatic mosaicism

Identifiers

PMID40401429
PMCPMC12278727

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.