Evidence map›Paper›PMID 41484600›Full record

ReviewNeurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology2026

Late-onset intracerebral hemorrhage associated with COL4A1 variants: clinical and genetic perspectives.

Xinting Zhuang, Shuyan Xu, Chaohan Chen, Ying Wang, Fangwei Hu, Bin Cai

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Review in Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Xinting Zhuang *Department of Neurology and Institute of Neurology, Institute of Neuroscience, and Fujian Key Laboratory of Molecular Neurology, the First Affiliated Hospital, Fujian Medical University, 20 Chazhong Road, Fuzhou, 350005, Fujian, China.
Shuyan Xu *Department of Neurology and Institute of Neurology, Institute of Neuroscience, and Fujian Key Laboratory of Molecular Neurology, the First Affiliated Hospital, Fujian Medical University, 20 Chazhong Road, Fuzhou, 350005, Fujian, China.
Chaohan ChenDepartment of Neurology and Institute of Neurology, Institute of Neuroscience, and Fujian Key Laboratory of Molecular Neurology, the First Affiliated Hospital, Fujian Medical University, 20 Chazhong Road, Fuzhou, 350005, Fujian, China.
Ying WangDepartment of Neurology and Institute of Neurology, Institute of Neuroscience, and Fujian Key Laboratory of Molecular Neurology, the First Affiliated Hospital, Fujian Medical University, 20 Chazhong Road, Fuzhou, 350005, Fujian, China.
Fangwei HuDepartment of Neurology and Institute of Neurology, Institute of Neuroscience, and Fujian Key Laboratory of Molecular Neurology, the First Affiliated Hospital, Fujian Medical University, 20 Chazhong Road, Fuzhou, 350005, Fujian, China.
Bin CaiDepartment of Neurology and Institute of Neurology, Institute of Neuroscience, and Fujian Key Laboratory of Molecular Neurology, the First Affiliated Hospital, Fujian Medical University, 20 Chazhong Road, Fuzhou, 350005, Fujian, China. caibin@fjmu.edu.cn.ORCID http://orcid.org/0000-0003-2659-9376

Funding

Joint Funds for the innovation of science and Technology, Fujian province 2018Y9084 (BC)Joint Funds for the innovation of science and Technology, Fujian province 2023Y9039 (BC)Natural Science Foundation of China 82071277 (BC)Natural Science Foundation of China 82471299 (BC)
6 · The paper itself

Abstract

backgroundPathogenic variants in the COL4A1 gene, which encodes a key structural component of the vascular basement membrane, compromise vascular integrity and contribute to a broad spectrum of cerebrovascular disorders. COL4A1-related intracerebral hemorrhage (ICH) demonstrates a distinct bimodal age distribution, characterized by early-onset (perinatal/childhood) and late-onset (adulthood) presentations.Although early-onset phenotypes have been extensively characterized, late-onset intracerebral hemorrhage linked to COL4A1 mutations remains underrecognized, frequently obscured by coexisting vascular risk factors.

methodWe reported two probands with late-onset intracerebral hemorrhage associated with COL4A1. Structural modeling was performed to assess the potential impact of these variants on collagen stability. Additionally, we reviewed 27 previously published cases to evaluate the association between COL4A1 mutations and ICH.

resultsWe identified two probands with heterozygous COL4A1 missense variants: c.2086G > A (p.Gly696Ser) and a novel c.3110C > T (p.Pro1037Leu). Notably, the patient with the Pro1037Leu variant remained asymptomatic until experiencing a hemorrhagic event.Structural modeling suggests that these variants may induce subtle conformational changes that impair collagen stability. A review of 27 published cases further supports the notion that such intrinsic structural abnormalities, in combination with vascular risk factors (e.g., arterial hypertension), may increase susceptibility to intracerebral hemorrhage.

conclusionThe results underscore the importance of considering genetic testing in patients with unexplained or recurrent intracerebral hemorrhage, particularly those with a positive family history or syndromic features. While disease-specific therapies are currently lacking, early molecular diagnosis and rigorous control of modifiable risk factors may improve long-term outcomes and support informed genetic counseling.

Indexed as

Cerebral HemorrhageCollagen Type IVAge of OnsetFemaleHumansMaleMiddle AgedMutationMutation, MissenseCOL4A1 protein, humanCollagen Type IVCOL4A1 geneDiagnosisLate-onset intracerebral hemorrhageMissense variantProtein structure simulation

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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.