Relation of plasma fibroblast growth factor-23 (FGF-23) to radiographic severity in primary knee osteoarthritis patients

被引:8
|
作者
Mohammed, Mai A. [1 ]
Rady, Shaimaa A. K. [2 ]
Mohammed, Rabab A. [3 ]
Fadda, Samia M. H. [4 ]
机构
[1] Minist Hlth, Beni Suef Hosp, Bani Suwayf, Egypt
[2] Beni Suef Univ, Fac Med, Rheumatol Dept, Bani Suwayf, Egypt
[3] Beni Suef Univ, Fac Med, Clin Pathol Dept, Bani Suwayf, Egypt
[4] Cairo Univ, Fac Med, Rheumatol Dept, Cairo, Egypt
来源
EGYPTIAN RHEUMATOLOGIST | 2018年 / 40卷 / 04期
关键词
Fibroblast growth factor-23; Osteoarthritis; KL score; WOMAC score;
D O I
10.1016/j.ejr.2018.01.007
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Aim of the work: This study aimed to investigate the plasma level of fibroblast growth factor-23 (FGF-23) in patients with primary knee osteoarthritis (KOA) and to elaborate its relation with radiographic and symptomatic severity of OA. Patients and methods: 50 KOA patients were recruited from the Rheumatology and Rehabilitation Department, Beni-Suef University Hospital and 20 matched controls were also included. Plasma FGF23 level was estimated by ELISA. Severity of the disease was assessed clinically by Western Ontario and McMaster Universities Osteoarthritis (WOMAC) score and radiologically by Kellgren-Lawrence (KL) grading scale. Results: The mean age of the patients was 59.8 +/- 8.02 years (51-75 years) and disease duration 3.8 +/- 2.1 years (1-9 years); they were 8 males (16%) and 42 (84%) females with a body mass index of 34.04 +/- 5.3 (23.6-48.4). FGF-23 level was higher in KOA patients (96.2 +/- 148.9 pg/ml; 3.4-14814.6pg/ml) than in control (18.3 +/- 11.1pg/ml; 5-38.4 pg/ml) (p = .023). There was no significant difference in FGF-23 between males and females. FGF-23 was significantly increased in patients who had effusion (p = .004) or bilateral involvement (p = .023). Plasma FGF-23 level significantly correlated with disease severity sores; WOMAC and KL (p = .009, p = .01 respectively) and also with the age (p = .016), disease duration (p = .006) and body mass idex (p = .008) Conclusions: FGF-23 might be a potential biomarker for diagnosing and evaluating the onset and development of KOA and significantly correlated with the symptomatic and radiographic severity of the disease. Controlling KOA progression by inhibitors of FGF23 may be an issue of interest in further studies. (C) 2018 Publishing services provided by Elsevier B.V. on behalf of Egyptian Society of Rheumatic Diseases.
引用
收藏
页码:261 / 264
页数:4
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