Cited by 79Dementia and Cognitive Impairment ResearchAlzheimer's disease research and treatmentsClusterin in disease pathology

The Role of Clusterin in Amyloid-β–Associated Neurodegeneration

Open access
Desikan, Rahul S., Thompson, Wesley K., Holland, Dominic, Hess, Christopher P., Brewer, James B., Zetterberg, Henrik, Blennow, Kaj, Andreassen, Ole A. +3 more·2014·JAMA Neurology

Abstract

IMPORTANCE: Converging evidence indicates that clusterin, a chaperone glycoprotein, influences Alzheimer disease neurodegeneration. However, the precise role of clusterin in Alzheimer disease pathogenesis is still not well understood. OBJECTIVE: To elucidate the relationship between clusterin, amyloid-β (Aβ), phosphorylated tau (p-tau), and the rate of brain atrophy over time among nondemented older individuals. DESIGN, SETTING, AND PARTICIPANTS: This longitudinal cohort included cognitively normal older participants and individuals with mild cognitive impairment assessed with baseline lumbar puncture and longitudinal structural magnetic resonance imaging. We examined 241 nondemented older individuals from research centers across the United States and Canada (91 participants with a Clinical Dementia Rating score of 0 and 150 individuals with a Clinical Dementia Rating score of 0.5). MAIN OUTCOMES AND MEASURES: Using linear mixed-effects models, we investigated interactions between cerebrospinal fluid (CSF) clusterin, CSF Aβ1-42, and CSF p-tau at threonine 181 (p-tau181p) on the atrophy rate of the entorhinal cortex and hippocampus. RESULTS: Across all participants, we found a significant interaction between CSF clusterin and CSF Aβ1-42 on the entorhinal cortex atrophy rate but not on the hippocampal atrophy rate. Cerebrospinal fluid clusterin was associated with the entorhinal cortex atrophy rate among CSF Aβ1-42-positive individuals but not among CSF Aβ1-42-negative individuals. In secondary analyses, we found significant interactions between CSF Aβ1-42 and CSF clusterin, as well as CSF Aβ1-42 and CSF p-tau181p, on the entorhinal cortex atrophy rate. We found similar results in subgroup analyses within the mild cognitive impairment and cognitively normal cohorts. CONCLUSIONS AND RELEVANCE: In nondemented older individuals, Aβ-associated volume loss occurs in the presence of elevated clusterin. The effect of clusterin on Aβ-associated brain atrophy is not confounded or explained by p-tau. These findings implicate a potentially important role for clusterin in the earliest stages of the Alzheimer disease neurodegenerative process and suggest independent effects of clusterin and p-tau on Aβ-associated volume loss.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1001/jamaneurol.2013.4560

Cites

28 of 28 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • Elevated CSF clusterin together with elevated amyloid-beta is associated with greater entorhinal atrophy.

    “Increased cerebrospinal fluid (CSF) CLU levels combined with increased amyloid-beta (Aβ) levels were associated with increased entorhinal atrophy (Desikan, et al., 2014)”

    From A potential endophenotype for Alzheimer's disease: cerebrospinal fluid clusterin (2016) · cites this paper as Desikan, et al., 2014

Self-check

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

The self-check needs the paper’s full text.

Cites

Flagged first, then by citations

Cited by

Sorted by citations

Authors
Desikan, R. S., Thompson, W. K., Holland, D., Hess, C. P., Brewer, J. B., Zetterberg, H., Blennow, K., Andreassen, O. A., McEvoy, L. K., Hyman, B. T., & Dale, A. M.
Affiliations
  • University of California San Diego (US)
  • University of California, San Francisco (US)
  • National Hospital for Neurology and Neurosurgery (GB)
  • University of Gothenburg (SE)
  • Oslo University Hospital (NO)
  • Massachusetts General Hospital (US)
Corresponding author
Desikan, Rahul S.
Venue
JAMA Neurology
Published
2014-02-01
Volume
71
Issue
2
Pages
180
ISSN
2168-6149 (ISSN-L)
OpenAlex
W2167538572
Cited by
79
References
28
Citations by year
2026: 1 · 2025: 6 · 2024: 2 · 2023: 3 · 2022: 3 · 2021: 5 · 2020: 10 · 2019: 4 · 2018: 9 · 2017: 6 · 2016: 9 · 2015: 12 · 2014: 9
FWCI
7.11
Type
journal article
Language
en
Open access
Locations
  • JAMA Neurology (publishedVersion)
  • PubMed (publishedVersion)
  • Europe PMC (PubMed Central) (acceptedVersion)
  • PubMed Central (acceptedVersion)
  • eScholarship (California Digital Library) (submittedVersion)
  • NORA - Norwegian Open Research Archives (submittedVersion, other-oa)
Funders
  • Alzheimer's Association (U01 AG024904)
  • Alzheimer's Disease Neuroimaging Initiative (U01AG024904, AG024904)
  • Norges Forskningsråd
  • National Institutes of Health (5u01ag024904-10, U01-AG024904, AG024904)
  • Canadian Institutes of Health Research
  • National Institute on Aging (U01-AG-024904, P30AG010129, R01AG031224, P50AG005131, K01AG030514, K01AG029218, U19AG024904)
  • National Institute of Neurological Disorders and Stroke (K02NS067427)
  • National Institute of Biomedical Imaging and Bioengineering (T32EB005970)
Topics
  • Health Sciences › Medicine › Psychiatry and Mental health › Dementia and Cognitive Impairment Research
  • Health Sciences › Medicine › Physiology › Alzheimer's disease research and treatments
  • Health Sciences › Medicine › Oncology › Clusterin in disease pathology
Keywords
clusterin, amyloid-beta, phosphorylated tau, Alzheimer's disease, neurodegeneration, brain atrophy, entorhinal cortex, hippocampus, cerebrospinal fluid biomarkers, mild cognitive impairment, cognitively normal older adults, amyloid-beta 42
MeSH terms
Aged, Aged, 80 and over, Alzheimer Disease, Female, Follow-Up Studies, Humans, Longitudinal Studies, Male, Peptide Fragments, Cohort Studies, Biomarkers, Amyloid beta-Peptides, Neurodegenerative Diseases, Clusterin

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.

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