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Does thiol-disulphide balance show oxidative stress in different MEFV mutations?
Burhan Balta1, Murat Erdogan2, Murat Alisik3
1Department of Medical Genetics, Kayseri Training and Research Hospital, Kayseri, Turkey. burhan0629@gmail.com.
Rheumatology International
|December 21, 2017
Summary
Familial Mediterranean Fever (FMF) patients exhibit altered thiol-disulphide homeostasis, with lower thiol and disulfide levels compared to controls. Different MEFV gene mutations did not significantly impact these oxidative stress markers.
Area of Science:
- Biochemistry
- Genetics
- Immunology
Background:
- Oxidative stress is elevated in Familial Mediterranean Fever (FMF).
- Thiols are crucial antioxidants that combat free radicals.
- The impact of specific MEFV gene mutations on thiol-disulphide balance in FMF is not well understood.
Purpose of the Study:
- To investigate thiol-disulphide homeostasis in FMF patients.
- To examine how different MEFV gene mutations affect thiol-disulphide balance.
Main Methods:
- Compared thiol-disulphide parameters in FMF patients and healthy controls.
- Categorized FMF patients into groups based on MEFV gene mutations (exon 10 and non-exon 10).
- Utilized an automated spectrophotometric method to measure thiol-disulphide homeostasis.
Main Results:
- FMF patients showed significantly lower native thiol, total thiol, and disulphide levels compared to controls.
- Disulphide/native thiol and disulphide/total thiol ratios were lower in FMF patients.
- Native thiol/total thiol ratios were higher in FMF patients.
- No significant differences in thiol-disulphide parameters were observed among different groups of MEFV gene mutations.
Conclusions:
- FMF is associated with a disturbed thiol-disulphide balance, indicating increased oxidative stress.
- Specific MEFV gene mutations do not appear to differentially affect thiol-disulphide homeostasis.
- Thiol-disulphide balance may not serve as a marker for oxidative damage across different FMF mutations.
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