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Giant cell arteritis: laboratory tests at the time of diagnosis in a series of 240 patients.

机译:巨细胞动脉炎:在诊断时对一系列240例患者进行实验室检查。

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The outcome of a patient with giant cell arteritis (GCA) is closely related to the development of severe ischemic manifestations. In the current study we analyzed the implications of routine laboratory tests obtained at the time of diagnosis in the clinical spectrum of a series of 240 consecutive patients with biopsy-proven GCA at the single hospital for a defined population. We also examined whether the laboratory markers of inflammation may be predictors of severe ischemic manifestations (visual ischemic events, cerebrovascular accidents, jaw claudication, or large-artery stenosis of the extremities of recent onset), and their potential correlation. Anemia (hemoglobin <12 g/dL) was observed in 131 (54.6%) and thrombocytosis in 117 (48.8%) patients. Sixty-eight (28.3%) patients had leukocytosis. The percentage of patients showing a significant increase of alkaline phosphatase and hypoalbuminemia was similar (25% and 27.8%, respectively). The mean values of erythrocyte sedimentation rate (ESR) and C-reactive protein were 93 +/- 23 mm/h and 94 +/- 63 mg/L, respectively. A strong correlation among most laboratory markers of inflammation was observed. Anemia was more commonly observed in patients without severe ischemic manifestations (61.5% versus 48.9% in those with severe ischemic manifestation; p = 0.05) and in patients with constitutional syndrome or fever (p < 0.001). Patients with ESR greater than 100 mm/h exhibited more commonly constitutional syndrome (p < 0.001) and had a statistically significant reduction in the incidence of visual ischemic events (p < 0.025). Only 7 (22.6%) of the 31 patients who suffered permanent visual loss had an ESR at the time of disease diagnosis greater than 100 mm/h. However, in a multivariate logistic regression analysis, only anemia was found to be a negative predictor for the development of severe ischemic manifestations of GCA (odds ratio, 0.53; 95% confidence intervals, 0.30-0.94; p = 0.03). In conclusion, our results suggest that some laboratory markers of inflammation, in particular the presence of anemia, may negatively predict the risk of severe ischemic complications in GCA patients.
机译:巨细胞动脉炎(GCA)患者的预后与严重缺血性表现的发展密切相关。在当前的研究中,我们分析了在诊断时获得的常规实验室检查在单一医院针对一系列特定人群对240例经活检证实的GCA的连续患者的临床范围所产生的影响。我们还检查了炎症的实验室标记物是否可能是严重缺血性表现(视觉缺血性事件,脑血管意外,下颌骨lau行或近期发作的四肢大动脉狭窄)的预测因素,以及它们的潜在相关性。 131例(54.6%)出现贫血(血红蛋白<12 g / dL),117例(48.8%)观察到血小板增多。六十八(28.3%)位患者患有白细胞增多症。碱性磷酸酶和低白蛋白血症显着增加的患者百分比相似(分别为25%和27.8%)。红细胞沉降率(ESR)和C反应蛋白的平均值分别为93 +/- 23 mm / h和94 +/- 63 mg / L。观察到大多数炎症实验室标记之间有很强的相关性。在没有严重缺血表现的患者中,贫血的发生率更高(61.5%,而在具有严重缺血表现的患者中为48.9%; p = 0.05)以及患有体质综合症或发烧的患者(p <0.001)。 ESR大于100 mm / h的患者表现出更常见的体质综合征(p <0.001),并且视觉缺血事件的发生率在统计学上显着降低(p <0.025)。在永久性视力丧失的31例患者中,只有7例(22.6%)在疾病诊断时的ESR大于100 mm / h。然而,在多因素logistic回归分析中,仅贫血被发现是严重缺血性GCA表现的阴性预测因子(几率0.53; 95%置信区间0.30-0.94; p = 0.03)。总之,我们的结果表明,某些炎症的实验室指标,尤其是贫血的存在,可能会对GCA患者发生严重缺血性并发症的危险性产生负面影响。

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