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With this in mind, it could be interesting to investigate whether the accumulated Treg cells in patients with arthritis function properly in vivo and whether these patients could really benefit from a therapeutic enhancement of Treg function, as suggested by some enthusiastic investigators in this field.
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A recent review pooling results of four NSAID trials indicated that NSAIDs were superior to placebo in improving spinal pain, peripheral arthritis, and function in AS patients over a 6-week period (Zochling et al. 2006a).
Subsets of CD4+ T cells with regulatory capacity, such as CD25+ regulatory T (Treg) cells and Th2 cells, have been identified, and recent observations suggest that in rheumatoid arthritis the function of these regulatory T cells is severely impaired.
A validated native language version for performance tests may not be a prerequisite, but since the validated and currently used performance test were quick and easy to perform, we refrained from introducing new instruments such as the Sequential occupational dexterity assessment (SODA) [ 30], and the Arthritis hand function test [ 31].
Our results highlight a paradoxical arthritis-regulatory function of exogenous TNFα.
There were also trends for improvements in self-efficacy towards managing arthritis-related functioning (P = 0.06), in self-efficacy towards physical activity (P = 0.07) and in symptoms of anxiety and depression (P = 0.08).
End-stage ankle arthritis impairs joint function and patients' mobility.
Moreover long immobilization has been correlated with high percentages of arthritis and decreased function rating between 50 80% [6, 15, 17].
PRO assessments included HRQoL, fatigue, physical function, arthritis pain and disease activity.
We included comorbidities that may impact physical function: arthritis, stroke, diabetes mellitus, chronic bronchitis, emphysema, asthma, myocardial infarction, congestive heart failure, and cancer (excluding skin cancer).
We analyzed the fraction of animals with arthritis as a function of time, by fitting time-response models to our data.
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