Rusu Tania-Elena, Murgu Alina, Moraru Evelina, Florea Maria-Magdalena, Ioniuc Ileana, Alexoaie Monica, Rugină Aurica, Goţia Stela
Universitatea de Medicină şi Farmacie Gr.T. Popa" Iaşi, Facultatea de Medicină, Clinica a IIa Pediatrie.
Rev Med Chir Soc Med Nat Iasi. 2008 Jan-Mar;112(1):88-93.
The aim of the study was to evaluate the presence and etiopathogenesis of osteopenia in 41 children with Juvenile Idiopathic Arthritis (JIA).
Bone status was evaluated by quantitative ultrasound using a Sunlight Omnisense 7000s Ultrasound Bone Sonometer. Measurements were performed at the distal radius and midshaft tibia. Results were obtained as Speed of sound (SOS) and Z-score. We used standardised clinical evaluation (modified Giannini's criteria, CHAQ). ESR, Fibrinogen, serum calcium, magnesium, alkaline phosphatase, protein electrophoresis, 25-OH vitamin D (RIA) and urinary Hydroxyproline were obtained in all patients. Osteopenia was present in 15 (36.5%) patients. Statistical analysis was performed with SPSS 13.0.
Age, sex, age at onset, disease duration, life standards and duration of corticotherapy and methotrexate treatment were not related to osteopenia in our study. The disease activity, evaluated by clinical criteria, ESR and Fibrinogen, was strongly associated with osteopenia (p<0.001). Nutritional status was an independent risk factor for osteopenia (p<0.001). Low serum calcium (p=0.034), magnesium (p=0.010), 25-OH vitamin D (p=0.091) and alkaline phosphatase (p=0.31) were more frequent in patients with osteopenia. Hydroxyproline was increased in all patients with osteopenia (p<0.001).
Osteopenia was a frequent (36.5%) complication of JIA in our study. The disease activity and nutritional status were the most important risk factors for osteopenia. The increase of bone reabsorption was the main pathogenic mechanism of osteopenia in our study. Calcium and magnesium deficits were related to osteopenia. Decrease of bone synthesis was not associated with osteopenia in the present study.
本研究旨在评估41例幼年特发性关节炎(JIA)患儿骨质疏松症的存在情况及其发病机制。
采用Sunlight Omnisense 7000s超声骨密度仪通过定量超声评估骨状况。测量部位为桡骨远端和胫骨中段。结果以声速(SOS)和Z值表示。我们采用标准化临床评估(改良詹尼尼标准,CHAQ)。所有患者均检测了红细胞沉降率(ESR)、纤维蛋白原、血清钙、镁、碱性磷酸酶、蛋白电泳、25-羟维生素D(放射免疫分析)和尿羟脯氨酸。15例(36.5%)患者存在骨质疏松症。使用SPSS 13.0进行统计分析。
在我们的研究中,年龄、性别、发病年龄、病程、生活水平以及皮质激素治疗和甲氨蝶呤治疗的持续时间与骨质疏松症无关。通过临床标准、ESR和纤维蛋白原评估的疾病活动度与骨质疏松症密切相关(p<0.001)。营养状况是骨质疏松症的独立危险因素(p<0.001)。骨质疏松症患者血清钙(p=0.034)、镁(p=0.010)、25-羟维生素D(p=0.091)和碱性磷酸酶(p=0.31)水平较低更为常见。所有骨质疏松症患者尿羟脯氨酸均升高(p<0.001)。
在我们的研究中,骨质疏松症是JIA常见的(36.5%)并发症。疾病活动度和营养状况是骨质疏松症最重要的危险因素。骨吸收增加是我们研究中骨质疏松症的主要发病机制。钙和镁缺乏与骨质疏松症有关。在本研究中,骨合成减少与骨质疏松症无关。