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Elevated Plasma Levels of TIMP-1 in Patients With Rotator Cuff Tear

Completed
Conditions
Rotator Cuff Tear
Interventions
Procedure: Blood sampling
Registration Number
NCT01562145
Lead Sponsor
University Hospital, Linkoeping
Brief Summary

The aim of the study was to investigate the levels of matrixmetalloproteinases and their inhibitors in blood samples from patients with rotator cuff tears and compare with blood samples from healthy matched controls.

Detailed Description

Background: Extracellular matrix remodeling is altered in rotator cuff tears, partly due to altered expression of matrix metalloproteinases (MMPs) and their inhibitors. It is unclear if this altered expression can be traced as changes in plasma protein levels. We measured the plasma level of MMPs and their tissue inhibitors (TIMPs) in patients with rotator cuff tears.

Material and methods: Blood samples were collected from 17 patients, median 61 (range 39-77) years, with sonographically verified rotator cuff tears (partial- or full-thickness). These were compared with 16 gender and age matched control persons with sonographically intact rotator cuffs. Plasma levels of MMPs and TIMPs were measured simultaneously using Luminex technology.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
34
Inclusion Criteria
  • degenerative rotator cuff tear verified by ultrasound
Exclusion Criteria
  • systemic joint disease such as rheumatoid arthritis
  • a fracture non-union
  • dupuytrens disease
  • frozen shoulder
  • tendinosis or rupture of any other tendons than in the rotator cuff
  • disorders of the spine such as disc disease,idiopathic scoliosis, spondylitis
  • cerebral or cardiovascular disease during the past year
  • abdominal or bowel disease
  • surgery or trauma during the past year
  • any infection during the last month
  • malignancy
  • treatment for the last month with medications that may affect MMPs or TIMPs (tetracycline, bisphosphonates, anti-inflammatory drugs, statins)
  • vigorous physical activity during the last 24 hours
  • inability to understand written and spoken Swedish

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Patients with rotator cuff tearsBlood samplingPatients with ultrasound verified rotator cuff tears
Healthy controlsBlood samplingAge and gender matched controls with ultrasound verified intact rotator cuff
Primary Outcome Measures
NameTimeMethod
Level of MMP and TIMP in plasmaMeasaured at one time point

Four mL venous blood samples were collected from all study participants after inclusion, and centrifuged to plasma that was stored at -70 degrees until the analysis.

Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (1)

University clinic of orthopeadics Linkoeping

πŸ‡ΈπŸ‡ͺ

Linkoeping, Oestergoetland, Sweden

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