Evidence map›Paper›PMID 27375477›Full record

ArticleFrontiers in aging neuroscience2016

Tendon Extracellular Matrix Alterations in Ullrich Congenital Muscular Dystrophy.

Francesca Sardone, Francesco Traina, Alice Bondi, Luciano Merlini, Spartaco Santi, Nadir Mario Maraldi, Cesare Faldini, Patrizia Sabatelli

Open access · goldAbstract read
In one paragraph

Article in Frontiers in aging neuroscience, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
1.1field-weighted citation impact, top 23% 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

13 citing papers in PubMed, 14 citations in OpenAlex.

  1. Review
  2. Myopathic Ehlers-Danlos Syndrome (mEDS) Related toInternational journal of molecular sciences · 2025
    Review
  3. Article
  4. Article
  5. Article
  6. Collagen VI in the Musculoskeletal System.International journal of molecular sciences · 2023
    Review
  7. Review
  8. Genetic Disorders of the Extracellular Matrix.Anatomical record (Hoboken, N.J. : 2007) · 2020
    Review
  9. Article
  10. Article
  11. Review
  12. Article
  13. Article
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

8 authors at 6 institutions in 1 country.

Francesca SardoneDepartment of Biomedical Sciences, University of PadovaPadova, Italy; National Research Council of Italy, Institute of Molecular GeneticsBologna, Italy.
Francesco TrainaRizzoli Orthopaedic Institute, University of Bologna Bologna, Italy.
Alice BondiRizzoli Orthopaedic Institute, University of Bologna Bologna, Italy.
Luciano MerliniMuscle Clinic, Villa Erbosa Hospital, Gruppo San Donato Bologna, Italy.
Spartaco SantiNational Research Council of Italy, Institute of Molecular GeneticsBologna, Italy; SC Laboratory of Musculoskeletal Cell Biology, IOR-IRCCSBologna, Italy.
Nadir Mario MaraldiNational Research Council of Italy, Institute of Molecular GeneticsBologna, Italy; SC Laboratory of Musculoskeletal Cell Biology, IOR-IRCCSBologna, Italy.
Cesare FaldiniRizzoli Orthopaedic Institute, University of Bologna Bologna, Italy.
Patrizia SabatelliNational Research Council of Italy, Institute of Molecular GeneticsBologna, Italy; SC Laboratory of Musculoskeletal Cell Biology, IOR-IRCCSBologna, Italy.
Istituto Ortopedico Rizzoli · ITNational Research Council · ITIstituti di Ricovero e Cura a Carattere Scientifico · ITUniversity of Bologna · ITUniversity of Padua · ITVilla Torri Hospital · IT

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Collagen VI (COLVI) is a non-fibrillar collagen expressed in skeletal muscle and most connective tissues. Mutations in COLVI genes cause two major clinical forms, Bethlem myopathy and Ullrich congenital muscular dystrophy (UCMD). In addition to congenital muscle weakness, patients affected by COLVI myopathies show axial and proximal joint contractures and distal joint hypermobility, which suggest the involvement of the tendon function. We examined a peroneal tendon biopsy and tenocyte culture of a 15-year-old patient affected by UCMD with compound heterozygous COL6A2 mutations. In patient's tendon biopsy, we found striking morphological alterations of tendon fibrils, consisting in irregular profiles and reduced mean diameter. The organization of the pericellular matrix of tenocytes, the primary site of collagen fibril assembly, was severely affected, as determined by immunoelectron microscopy, which showed an abnormal accumulation of COLVI and altered distribution of collagen I (COLI) and fibronectin (FBN). In patient's tenocyte culture, COLVI web formation and cell surface association were severely impaired; large aggregates of COLVI, which matched with COLI labeling, were frequently detected in the extracellular matrix. In addition, metalloproteinase MMP-2, an extracellular matrix-regulating enzyme, was increased in the conditioned medium of patient's tenocytes, as determined by gelatin zymography and western blot. Altogether, these data indicate that COLVI deficiency may influence the organization of UCMD tendon matrix, resulting in dysfunctional fibrillogenesis. The alterations of tendon matrix may contribute to the complex pathogenesis of COLVI related myopathies.

Indexed as

Collagen VImetalloproteinasespericellular matrixtendonUllrich congenital muscular dystrophy (UCMD)

Identifiers

PMID27375477
PMCPMC4896961
OpenAlexW2414169119

What OpenQuestion holds

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LicenceCC BY
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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.