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FGF-23, Klotho and Vitamin D Levels in Scleroderma
Ravan Ahmadi1,2, Mehrzad Hajialilo2, Amir Ghorbanihaghjo1,2
1Dept. of Clinical Biochemistry and Laboratory Medicine, Tabriz University of Medical Sciences, Tabriz, Iran.
Iranian Journal of Public Health
|May 26, 2017
Summary
Scleroderma patients show lower serum Klotho and vitamin D levels, alongside higher parathyroid hormone (PTH). These altered mineral metabolism markers may play a role in scleroderma pathogenesis and offer potential therapeutic targets.
Area of Science:
- Endocrinology
- Rheumatology
- Mineral Metabolism
Background:
- Scleroderma is a chronic connective tissue disease with unknown causes.
- Vitamin D, parathyroid hormone (PTH), and Klotho are key regulators of calcium and phosphate homeostasis.
- Klotho, a fibroblast growth factor 23 (FGF-23) co-receptor, influences mineral metabolism.
Purpose of the Study:
- To investigate serum levels of Klotho, FGF-23, intact PTH (iPTH), and vitamin D in scleroderma patients compared to healthy controls.
Main Methods:
- Sixty scleroderma patients and 30 healthy controls were enrolled.
- Serum levels of Klotho, FGF-23, 25-hydroxy vitamin D (25-OH Vit D), and iPTH were measured using ELISA.
Main Results:
- Scleroderma patients exhibited significantly lower serum Klotho and 25-OH Vit D levels (P<0.001).
- Patients with scleroderma had significantly higher serum iPTH levels (P<0.001).
- No significant difference in serum FGF-23 levels was observed between scleroderma patients and controls (P=0.202).
Conclusions:
- Decreased serum Klotho, 25-OH Vit D, and elevated iPTH in scleroderma patients suggest a potential association with disease pathogenesis.
- These altered mineral metabolism markers represent potential future therapeutic targets for scleroderma.
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