Evidence map›Paper›PMID 40700473›Full record

ArticleJournal of neuropathology and experimental neurology2025

Intracellular amyloidosis in peripheral nerve and skeletal muscle.

Grace K Grafham, Gloria Mak, Sandra Grant, Alison Murphy, Steven K Baker, Mark Tarnopolsky, Jian-Qiang Lu

Abstract read
In one paragraph

Article in Journal of neuropathology and experimental neurology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing 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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

7 authors.

Grace K GrafhamDepartment of Pathology and Molecular Medicine, McMaster University, Hamilton, ON, Canada.
Gloria MakDivision of Neurology, Department of Medicine, University of Alberta, Edmonton, AB, Canada.
Sandra GrantDepartment of Pathology and Molecular Medicine, McMaster University, Hamilton, ON, Canada.
Alison MurphyDepartment of Pathology and Molecular Medicine, McMaster University, Hamilton, ON, Canada.
Steven K BakerDivision of Physical Medicine & Rehabilitation, Department of Medicine, McMaster University, Hamilton, ON, Canada.
Mark TarnopolskyDivision of Neurology, Department of Medicine, McMaster University, Hamilton, ON, Canada.
Jian-Qiang LuDepartment of Pathology and Molecular Medicine, McMaster University, Hamilton, ON, Canada.ORCID 0000-0003-1945-5569

Funding

Department of Pathology and Molecular Medicine, McMaster UniversityMcMaster UniversityResident ResearchResident Research Grant from Department of Pathology and Molecular Medicine
6 · The paper itself

Abstract

Amyloidosis is an etiologically heterogeneous group of disorders pathologically characterized by the extracellular deposition of amyloid fibrils, leading to tissue damage. It commonly affects the peripheral nervous system and occasionally involves skeletal muscle. The pathogenic mechanisms driving cellular injury in amyloidosis remain elusive. In this study, we examined 3 sural nerve and 5 skeletal muscle biopsies from patients with amyloidosis to localize the deposition of amyloid fibrils. Histologically, the nerve biopsies showed axonal degeneration and Schwann cell (SC) changes; muscle biopsies demonstrated variable myopathic and neurogenic features with multifocal amyloid deposition, including within intramuscular nerves. Electron microscopy identified both intracellular and extracellular amyloid deposition in all 8 biopsies. The ultrastructural localization of amyloid fibrils included the nerve and muscle extracellular matrix, as well as the SC processes, peri-/sub-sarcolemmal region of non-necrotic myofibers, and endoneurial and endomysial/perimysial blood vessel cells. Notably, SC processes, particularly bands of Büngner, formed amyloid-related complex inclusions in all 3 nerve cases. These findings suggest that intracellular amyloid deposition is common in peripheral nerve and skeletal muscle and may play a significant role in cellular injury and degeneration, and ultimately the progression of neuropathy and myopathy.

Indexed as

AmyloidosisMuscle, SkeletalPeripheral NervesSural NerveAdultAgedFemaleHumansMaleMiddle Agedamyloid fibrilamyloidosiselectron microscopyintracellular pathologymyopathyneuropathytissue biopsy

Identifiers

PMID40700473
PMCPMC12531485

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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.