Machado C S, Ortiz K, Martins A de L, Martins R S, Machado N C
Faculdade de Medicina de Botucatu, SP, Brazil.
J Pediatr (Rio J). 2001 Mar-Apr;77(2):105-11. doi: 10.2223/jped.185.
To determine ASO titer profile by establishing ARF differential diagnoses of other diseases with high levels of ASO antibodies. METHODS: We investigated 78 patients with ARF at onset and follow-up, 22 with isolated chorea at onset, 45 with recurrent oropharyngeal tonsillitis, and 23 with recent flare of juvenile idiopathic arthritis. We tested ASO with automated particle-enhanced immunonephelometric assay (Behring(R)-Germany). The ASO (IU/ml) titers were assessed at the following time intervals: 0-7 days, 1-2 weeks, 2-4 weeks, 1-2 months, 2-4 months, 4-6 months, 6-12 months, 1-2 years, 2-3 years, 3-4 years, and 4-5 years after onset of ARF. RESULTS: ASO titers in patients diagnosed with ARF had a significant increase up to the 2-4-month time interval (P<0.0001). Baseline levels were observed afterwards in patients under regular penicillin prophylaxis. The levels of ASO in ARF were also significantly higher than in patients with isolated chorea, recurrent oropharyngeal infections or juvenile idiopathic arthritis (P=0.0025), when age-matched samples of these groups were compared. The testacute;s sensitivity was 73.3% and the specificity was 57.6%, and it was calculated taking into account the upper limit of normality at 320 IU/ml, as well as the established diagnosis of ARF. The testacute;s specificity and positive predictive value increased with rising or higher titers, being higher with titers above 960 UI/ml. CONCLUSION: This reappraisal of ASO profile in ARF patients indicates a remarkable response during the acute phase, and that points to the extent to which ASO levels may differentiate ARF from other diseases with high levels of ASO antibodies, as coincidental but unrelated streptococcal infection or chronic arthritis flareup.
通过对其他ASO抗体水平高的疾病进行急性风湿热(ARF)鉴别诊断来确定ASO滴度特征。方法:我们调查了78例发病时及随访期的ARF患者、22例发病时仅有舞蹈症的患者、45例复发性口咽扁桃体炎患者以及23例近期幼年特发性关节炎发作的患者。我们采用自动颗粒增强免疫比浊法(德国贝林公司)检测ASO。在以下时间间隔评估ASO(IU/ml)滴度:ARF发病后0 - 7天、1 - 2周、2 - 4周、1 - 2个月、2 - 4个月、4 - 6个月、6 - 12个月、1 - 2年、2 - 3年、3 - 4年和4 - 5年。结果:诊断为ARF的患者ASO滴度在2 - 4个月时间间隔内显著升高(P<0.0001)。之后在接受常规青霉素预防的患者中观察到基线水平。当比较这些组年龄匹配的样本时,ARF患者的ASO水平也显著高于仅有舞蹈症、复发性口咽感染或幼年特发性关节炎的患者(P = 0.0025)。该检测的敏感性为73.3%,特异性为57.6%,计算时考虑了正常上限为320 IU/ml以及已确立的ARF诊断。该检测的特异性和阳性预测值随滴度升高而增加,滴度高于960 UI/ml时更高。结论:对ARF患者ASO特征的这一重新评估表明急性期有显著反应,这表明ASO水平在区分ARF与其他ASO抗体水平高的疾病(如巧合但无关的链球菌感染或慢性关节炎发作)方面的程度。