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Serum Trace Element Concentrations in Rheumatoid Arthritis.
Maryam Sahebari1, Razie Ayati1, Hamed Mirzaei2
1Rheumatic Diseases Research Center, School of Medicine, Mashhad University of Medical Sciences, Mashhad, Iran.
Biological Trace Element Research
|October 10, 2015
Summary
This study found that low serum zinc and selenium levels, along with high copper levels, are linked to rheumatoid arthritis (RA) disease activity. These trace elements may play a role in RA pathogenesis and progression.
Area of Science:
- Biochemistry
- Immunology
- Clinical Medicine
Background:
- Rheumatoid arthritis (RA) is a chronic inflammatory condition linked to oxidative stress.
- Serum trace elements and transport proteins like albumin and ceruloplasmin are crucial for antioxidant defense.
- Altered trace element status may influence RA pathogenesis or reflect disease activity.
Purpose of the Study:
- To investigate the relationship between serum trace elements (selenium, zinc, copper) and transport proteins (albumin, ceruloplasmin) with rheumatoid arthritis (RA) disease activity.
- To determine if serum trace element concentrations are associated with the presence and severity of RA.
Main Methods:
- Serum concentrations of albumin, ceruloplasmin, selenium, zinc, and copper were measured in 110 RA patients and 100 healthy controls.
- The zinc/copper ratio was calculated.
- Statistical analysis assessed the correlation between these parameters and RA disease activity scores.
Main Results:
- Lower serum albumin, zinc, and selenium concentrations were independently associated with higher RA disease activity.
- Higher serum copper concentrations were linked to the presence of RA.
- Serum copper levels showed a positive correlation with disease activity scores.
Conclusions:
- Low serum zinc and selenium, and high serum copper, may be associated with RA presence or be a consequence of the condition.
- Serum copper concentration is positively correlated with RA disease activity.
- Trace element status is relevant to understanding RA pathogenesis and disease progression.
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