Division of Rheumatology, Department of Medicine, New York University School of Medicine, NYU Hospital for Joint Diseases, New York, NY, USA.
BMC Musculoskelet Disord. 2014 Jan 8;15:8. doi: 10.1186/1471-2474-15-8.
Age, gender and genetic predisposition are major intrinsic risk factors for osteoarthritis (OA). Iron increases are associated with age and gene mutation. In the present study, we examined whether serum ferritin, an indicator of total body iron stores, correlates with clinical features in patients with OA, and whether the hemochromatosis Fe (HFE) gene mutation plays a role.
In a 2-year longitudinal observational study, 127 patients with knee OA and 20 healthy individuals (controls) were enrolled. All patients underwent standardized weight-bearing fixed-flexion posteroanterior knee radiographs. Peripheral blood samples were analyzed for serum ferritin, and genotyped for HFE using allelic discrimination methods.
Higher levels of serum ferritin were found in patients older than 56 years (P =0.0186) and males (P =0.0006), with a trend toward higher ferritin in patients with OA. HFE gene mutation carriers were more prevalent among patients with OA than among healthy controls. When stratified further by gender, we found that male patients with OA had higher levels of serum ferritin than male control subjects [odds ratio = 4.18 (limits of 95% confidence interval: 0.86-27.69, P = 0.048)]. Analyses of radiographic data indicated that higher ferritin was associated with narrower joint space width at baseline (P = 0.032) in male patients. Additionally, among men, risk prediction of radiographic severity [Kellgren-Lawrence (KL) grade >2)] in the higher ferritin group was almost five times that of the lower ferritin group (odds ratio = 4.74, P = 0.023).
Our data suggest that increased ferritin levels are associated with symptomatic knee OA in males. This finding needs to be validated in a larger cohort of patients.
年龄、性别和遗传易感性是骨关节炎(OA)的主要内在危险因素。铁的增加与年龄和基因突变有关。在本研究中,我们检查了血清铁蛋白(一种全身铁储存的指标)是否与 OA 患者的临床特征相关,以及是否铁调素(HFE)基因突变起作用。
在一项为期 2 年的纵向观察性研究中,纳入了 127 名膝关节 OA 患者和 20 名健康个体(对照组)。所有患者均接受了标准化的负重固定屈曲后前位膝关节 X 线检查。分析外周血样本中的血清铁蛋白,并采用等位基因鉴别方法对 HFE 基因进行基因分型。
发现 56 岁以上(P=0.0186)和男性(P=0.0006)患者的血清铁蛋白水平较高,OA 患者的铁蛋白水平呈上升趋势。OA 患者中 HFE 基因突变携带者更为常见。进一步按性别分层后,我们发现男性 OA 患者的血清铁蛋白水平高于男性对照组[比值比=4.18(95%置信区间上限:0.86-27.69,P=0.048)]。对放射学数据的分析表明,在男性患者中,较高的铁蛋白水平与基线时较窄的关节间隙宽度相关(P=0.032)。此外,在男性中,高铁蛋白组预测放射学严重程度(Kellgren-Lawrence(KL)分级>2)的风险几乎是低铁蛋白组的五倍(比值比=4.74,P=0.023)。
我们的数据表明,铁蛋白水平升高与男性症状性膝关节 OA 相关。这一发现需要在更大的患者队列中得到验证。