Cited by 111Cerebrovascular and genetic disordersMetabolism and Genetic DisordersLysosomal Storage Disorders Research

The DOI matches its Crossref record; 41 of the 41 references it cites were found in a registry or an index; none of the 21 sources its claims cite is checked for support yet.

Cathepsin A–related arteriopathy with strokes and leukoencephalopathy (CARASAL)

Open access
Bugiani, Marianna, Kevelam, Sietske H., Bakels, Hannah S., Waisfisz, Quinten, Ceuterick-de Groote, Chantal, Niessen, Hans W.M., Abbink, Truus E.M., Lesnik Oberstein, Saskia A.M.J., van der Knaap, Marjo S.·2016·Neurology

Abstract

OBJECTIVE: To characterize the clinical and MRI features of 2 families with adult-onset dominant leukoencephalopathy and strokes and identify the underlying genetic cause. METHODS: We applied MRI pattern recognition, whole-exome sequencing, and neuropathology. RESULTS: Based on brain imaging, 13 family members of 40 years or older from 2 families were diagnosed with the disease; in 11 family members of the same age, MRI was normal. In the affected family members, MRI showed a leukoencephalopathy that was disproportionately severe compared to the clinical disease. The clinical picture was dominated by ischemic and hemorrhagic strokes, slow and late cognitive deterioration, and therapy-resistant hypertension. With whole-exome sequencing, we identified one variant shared by both families and segregating with the disease: c.973C>T in CTSA. Haplotype analysis revealed a shared 1,145-kb interval encompassing the CTSA variant on chromosome 20q13.12, suggesting a common ancestor. Brain autopsy of 3 patients showed a leukoencephalopathy that was disproportionately extensive compared to the vascular abnormalities. CTSA encodes cathepsin A. Recessive CTSA mutations cause galactosialidosis. One of the numerous cathepsin A functions is to degrade endothelin-1. In the patients, striking endothelin-1 immunoreactivity was found in white matter astrocytes, correlating with increased numbers of premyelinating oligodendrocyte progenitors. This finding supports a role for endothelin-1 in the leukoencephalopathy through inhibition of oligodendrocyte progenitor maturation. CONCLUSIONS: CARASAL (cathepsin A-related arteriopathy with strokes and leukoencephalopathy) is a novel hereditary adult-onset cerebral small vessel disease. It is of interest that, next to the cerebral vascular abnormalities, endothelin-1 may have a role in the pathogenesis of the extensive leukoencephalopathy.

Overview

AI snapshot

Written from the paper’s full text.

TL;DR

CARASAL is a novel adult-onset autosomal dominant cerebral small vessel disease caused by a heterozygous CTSA variant, characterized by leukoencephalopathy, ischemic and hemorrhagic strokes, therapy-resistant hypertension, and late cognitive decline. The authors propose that cathepsin A dysfunction leads to endothelin-1 accumulation, which may impair oligodendrocyte progenitor maturation and contribute to the extensive white matter disease.

Key findings

  • In 2 Dutch families, 13 individuals ≥40 years had MRI-defined disease (11 in F1, 2 in F2), while 11 F1 members ≥40 years had normal MRI; MRI showed frontoparietal periventricular/deep white matter leukoencephalopathy that was disproportionately severe compared with clinical disease, with relative temporal white matter sparing.
  • Whole-exome sequencing identified a heterozygous CTSA variant, c.973C>T p.(Arg325Cys), shared by both families and segregating with disease; two-point linkage in F1 gave a maximal LOD score of 5.4953 at theta 0, and haplotype analysis identified a shared 1,145-kb interval on chromosome 20q13.12 containing CTSA but not TTPAL.
  • Neuropathology showed extensive leukoencephalopathy with myelin pallor, relatively preserved axons, astrogliosis, and unusual asymmetric fibrous thickening and near-total occlusion of distal arterioles; sclerotic index was more severe in patients (mean 0.55) than in sporadic SVD (mean 0.33) or normal controls (mean 0.27).
  • In noninfarcted white matter, patients had increased premyelinating oligodendrocyte progenitor cells compared with sporadic SVD (p<0.05) and nonneurologic controls (p<0.01), lower myelin basic protein, increased CathA 54-kDa precursor, and strikingly increased endothelin-1 immunoreactivity in white matter astrocytes.

Methods

  • Clinical and imaging study of 2 Caucasian Dutch families: F1 included 22 members ≥40 years (11 affected, 11 unaffected by MRI), and F2 included 2 affected patients; MRI pattern recognition was used to classify disease.
  • Genetic analysis used whole-exome sequencing in 3 F1 members (2 affected, 1 unaffected), Sanger sequencing of CTSA and TTPAL, two-point linkage analysis, and microsatellite haplotype analysis around chromosome 20q13.12.
  • Neuropathology included brain autopsy in 3 patients, body autopsy in 1, immunohistochemistry for CathA, GFAP, endothelin-1, β-amyloid, phosphorylated tau, Olig2, and PDGFRα, electron microscopy, Western blotting/SDS-PAGE, sclerotic index quantification, and leukocyte enzyme activity assays for carboxypeptidase, β-galactosidase, and neuraminidase-1.

Limitations

  • The paper states that the possible functional role of the CTSA mutation in CARASAL is presently unexplained; nonreducing SDS-PAGE did not support misfolding of mutant CathA, and reduced CathA carboxypeptidase activity was not found in leukocytes.
  • The authors state that further studies should determine whether only the p.(Arg325Cys) CTSA variant is associated with CARASAL or whether other mutations also increase small vessel disease risk.
  • Evident limitations include the very small sample (2 families, 3 autopsied patients), limited F2 availability, and reliance on postmortem and immunohistochemical associations rather than direct functional proof that endothelin-1 accumulation causes the leukoencephalopathy.

Model-written summary. Check it against the paper before relying on it.

Integrity signals

Registry

Crossref · 10.1212/wnl.0000000000003251

Cites

41 of 41 references verified0 citation errors · 0 not checkable

Statistics

Nothing to recompute.

Verification

Claims the paper makes

52 Own result · 16 Sources not found · 13 Own interpretation · 2 Own method · 1 No basis given

Show all 57 claims

  • It may state two separate claims as one. 19
  • Probably not a substantial claim. 10
27 of 27
  • The paper relies on this without support.

    Family members aged 40 years or older with a normal brain MRI are unaffected by the disease.

    “Family members younger than 40 years without MRI or with normal MRI were considered to have unknown status and were excluded; 22 family members of 40 years or older were included.Based on MRI, 11 were diagnosed with vascular leukoencephalopathy and 11 were unaffected.”
  • The paper relies on this without support.

    Heterozygous CTSA mutations have not been associated with disease.

    “Heterozygous CTSA mutations have hitherto not been associated with disease.”
  • The paper relies on this without support.

    The functional role of the CTSA mutation in CARASAL is unexplained.

    “The possible functional role of the CTSA mutation in CARASAL is presently unexplained.”
  • The paper relies on this without support.

    Parents of patients with galactosialidosis, who are obligatory CTSA mutation carriers, are not known to have increased risk of hypertension and SVD.

    “Parents of patients with galactosialidosis, who are obligatory CTSA mutation carriers, are not known to have increased risk of hypertension and SVD.”
  • The paper relies on this without support.

    Gaucher disease is caused by recessive mutations in GBA1, encoding glucocerebrosidase.

    “It is long known that Gaucher disease is caused by recessive mutations in GBA1, encoding glucocerebrosidase.”
  • The paper relies on this without support.

    Mature CathA is mainly found in lysosomes, where it stabilizes a multienzyme complex with b-galactosidase and neuraminidase-1.

    “Mature CathA is mainly found in lysosomes, where it stabilizes a multienzyme complex with b-galactosidase and neuraminidase-1.”
6 of 6

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

Each contradiction between two passages listed here was confirmed by an independent check.

4 of 4

Citations

Cites

Show all 40 references

Cited by

Sorted by citations

See all 111

Metadata

Authors
Bugiani, M., Kevelam, S. H., Bakels, H. S., Waisfisz, Q., Ceuterick-de Groote, C., Niessen, H. W. M., Abbink, T. E. M., Lesnik Oberstein, S. A. M. J., & van der Knaap, M. S.
Affiliations
  • University of Antwerp (BE)
  • From the Departments of Child Neurology (M.B., S.H.K., H.S.B., T.E.M.A., M.S.v.d.K.) and Pathology (M.B., H.W.M.N.), Neuroscience Campus Amsterdam, VU University Medical Center, Amsterdam; Department of Clinical Genetics (Q.W.), VU University Medical Center, Amsterdam, the Netherlands; Laboratory for Ultrastructural Neuropathology (C.C.-d.G.), Institute Born-Bunge and University of Antwerp, Belgium; Department of Clinical genetics (S.A.M.J.L.O.), Leiden University Medical Center, Leiden; and...
Venue
Neurology
Published
2016-10-25
Volume
87
Issue
17
Pages
1777-1786
ISSN
  • 0028-3878 (ISSN-L)
  • 1526-632X
OpenAlex
W2522033536
Cited by
111
References
40
Citations by year
2026: 3 · 2025: 6 · 2024: 16 · 2023: 10 · 2022: 16 · 2021: 9 · 2020: 13 · 2019: 13 · 2018: 13 · 2017: 9 · 2016: 1
FWCI
9.02
Type
journal article
Language
en
Locations
  • Neurology (publishedVersion)
  • PubMed (publishedVersion)
  • Amsterdam UMC (VU Amsterdam) - Institutional Repository (publishedVersion)
  • Leiden Repository (Leiden University) (submittedVersion)
  • Data Archiving and Networked Services (DANS) (submittedVersion)
Topics
  • Health Sciences › Medicine › Clinical Neurology › Cerebrovascular and genetic disorders
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Clinical Biochemistry › Metabolism and Genetic Disorders
  • Health Sciences › Medicine › Genetics (clinical) › Lysosomal Storage Disorders Research
Keywords
cathepsin A, Clinical and Translational Science Awards, leukoencephalopathy, cerebral small vessel disease, ischemic stroke, hemorrhagic stroke, endothelin-1, oligodendrocyte progenitors, white matter astrocytes, familial stroke, treatment-resistant hypertension, cognitive decline, haplotype analysis
MeSH terms
Adult, Aged, Brain, Family Health, Female, Hemorrhage, Humans, Magnetic Resonance Imaging, Male, Middle Aged, Mutation, Neurologic Examination, Endothelins, Microsatellite Repeats, Stroke, Cathepsin A, Vascular Malformations, Genome-Wide Association Study, Leukoencephalopathies

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

A language model drew the claims from the paper on 2026-11-02, under version 3 of the claim definition (model deepseek-v4.1-flash, prompt extract-v3).

A second model labelled each claim on 2026-11-02 (model jev-1.13-20260917, definition revision gold-guideline-v0.2).

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review

How to cite

Cite CoChat for the checks on this page, and the paper for its own findings.

This page
CoChat. (2026). Citation check: Cathepsin A–related arteriopathy with strokes and leukoencephalopathy (CARASAL). https://app.cochat.ai/papers/10.1212/wnl.0000000000003251
The paper
Bugiani, M., Kevelam, S. H., Bakels, H. S., Waisfisz, Q., Ceuterick-de Groote, C., Niessen, H. W. M., Abbink, T. E. M., Lesnik Oberstein, S. A. M. J., & van der Knaap, M. S. (2016). Cathepsin A–related arteriopathy with strokes and leukoencephalopathy (CARASAL). Neurology. https://doi.org/10.1212/wnl.0000000000003251