Evidence map›Paper›PMID 31455779›Full record

ArticleScientific reports2019

CCM1 and CCM2 variants in patients with cerebral cavernous malformation in an ethnically Chinese population in Taiwan.

Chun-Wei Chang, Peng-Wei Hsu, Kuo-Chen Wei, Chia-Wen Chang, Hon-Chung Fung, Mo-Song Hsih, Wen-Chuin Hsu, Long-Sun Ro, Chen-Nen Chang, Jiun-Jie Wang and 2 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.8field-weighted citation impact, top 27% of its field
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

4 citing papers in PubMed, 10 citations in OpenAlex.

  1. Review
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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

12 authors at 2 institutions in 2 countries.

Chun-Wei ChangDepartment of Neurology, Chang Gung Memorial Hospital - Linkou Medical Center, Taoyuan, Taiwan.ORCID http://orcid.org/0000-0003-3384-0199
Peng-Wei HsuDepartment of Neurosurgery, Chang Gung Memorial Hospital - Linkou Medical Center, Taoyuan, Taiwan.
Kuo-Chen WeiDepartment of Neurosurgery, Chang Gung Memorial Hospital - Linkou Medical Center, Taoyuan, Taiwan.
Chia-Wen ChangDepartment of Neurology, Chang Gung Memorial Hospital - Linkou Medical Center, Taoyuan, Taiwan.
Hon-Chung FungDepartment of Neurology, Chang Gung Memorial Hospital - Linkou Medical Center, Taoyuan, Taiwan.
Mo-Song HsihDepartment of Neurology, Chang Gung Memorial Hospital - Linkou Medical Center, Taoyuan, Taiwan.
Wen-Chuin HsuDepartment of Neurology, Chang Gung Memorial Hospital - Linkou Medical Center, Taoyuan, Taiwan.
Long-Sun RoDepartment of Neurology, Chang Gung Memorial Hospital - Linkou Medical Center, Taoyuan, Taiwan.
Chen-Nen ChangDepartment of Neurosurgery, Chang Gung Memorial Hospital - Linkou Medical Center, Taoyuan, Taiwan.
Jiun-Jie WangDepartment of Medical Imaging and Radiological Sciences, Chang Gung University, Taoyuan, Taiwan.
Yih-Ru WuDepartment of Neurology, Chang Gung Memorial Hospital - Linkou Medical Center, Taoyuan, Taiwan. yihruwu@cgmh.org.tw.
Sien-Tsong ChenDepartment of Neurology, Chang Gung Memorial Hospital - Linkou Medical Center, Taoyuan, Taiwan. chen0050@cgmh.org.tw.
Chang Gung Memorial Hospital · TWChang Gung University · TW

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cerebral cavernous malformation (CCM) is a vascular malformation characterized by clustered enlarged capillary-like channels in the central nervous system. The genes harboring variants in patients with CCM include CCM1/Krev interaction trapped-1, CCM2/MGC4607, and CCM3/programmed cell death protein 10. We aimed to identify pathogenic variants in an ethnic Chinese population in Taiwan. We recruited 95 patients with multiple CCMs or a single lesion with a relevant family history. Sanger sequencing was performed for 41 patients. Variants were identified using sequence alignment tools, and the clinical significance of these variants was determined using American College of Medical Genetics and Genomics standards and guidelines. Several pathogenic variants were found in six patients, including three unrelated patients and three affected members of one family. Two novel pathogenic variants leading to early truncation comprised a deletion variant in exon 18 of CCM1 (c.1846delA; p.Glu617LysfsTer44) and an insertion variant in exon 4 of CCM2 (c.401_402insGCCC; p.Ile136AlafsTer4). One novel pathogenic splice site variant was c.485 + 1G > C at the beginning of intron 8 of CCM1. In this study, we identified novel variants related to CCM in an ethnically Chinese population in Taiwan.

Indexed as

AdultAsian PeopleBrainCarrier ProteinsDNA Mutational AnalysisExonsFemaleHemangioma, Cavernous, Central Nervous SystemHeterozygoteHumansINDEL MutationKRIT1 ProteinMagnetic Resonance ImagingMaleMiddle AgedMutation, MissenseCarrier ProteinsCCM2 protein, humanKRIT1 ProteinKRIT1 protein, humanRNA Splice Sites

Identifiers

PMID31455779
PMCPMC6712018
OpenAlexW2970677111

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.