血清标志物在结节病加重诊断中的作用

Yu. Yu. Garmash, L. N. Novikova, A. M. Ryzhov
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引用次数: 0

摘要

为了提高接受包括皮质类固醇在内的综合治疗的患者结节病加重和活动性的诊断,303例呼吸道结节病患者在初次就诊(治疗前)和每2个月治疗2年进行检查。1-193例结节病无加重;2-51例结节病加重患者,未使用皮质类固醇(GCS);3-59组结节病加重,长期服用皮质类固醇的患者。为了提高接受包括糖皮质激素在内的综合治疗的患者结节病加重和活动性的诊断,303例呼吸道结节病患者在初次就诊(治疗前)和每2个月治疗2年进行检查。1-193例无加重;2-51组未服用皮质类固醇(GCS)的加重患者;3-59组患者病情加重,长期服用皮质激素。进行临床及血液生化检查,呼吸器官计算机断层扫描,肺活量图,超声心动图,静息心电图。研究各组血清标志物的变化:自由基(RwR)、血管紧张素转换酶(ACE)、腺苷脱氨酶(ADA)、血管紧张素转换酶(ACE)、血管紧张素转换酶(ADA)、相关系数(CC),根据开发的公式计算(专利):CC =任意单位的ACE/ADA (KKnorm = 1.2-2.4),测定脂质代谢紊乱标志物,评估内源性炎症活性,脂质沉积活性指标(PAL)根据先前开发的公式(专利)计算:PAL = TC/LDLxc + TGL。在治疗前,100%的结节病患者表现出中度内源性炎症、活跃的肉芽肿过程、低氧血症和身体抗氧化防御能力下降的迹象。血清腺苷脱氨酶(ADA)对结节病加重的敏感性为31%,特异性为48%。相关系数(CC)敏感性为85.0%;特异性78.8%;诊断效率80.0%,临床价值高于ACE、ADA、PAL、SVR、UKO。因此,血清酶腺苷脱氨酶(ADA)应包括在结节病患者的强制性最低实验室方法。
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Role of serum markers in diagnosis of exacerbations of sarcoidosis
In order to improve the diagnosis of exacerbation and activity of sarcoidosis in patients receiving complex treatment, including corticosteroids, 303 patients with respiratory sarcoidosis were examined at the initial visit (before treatment) and every 2 months of treatment for 2 years. Group 1–193 patients without exacerbation of sarcoidosis; group 2–51 patients with exacerbation of sarcoidosis, who did not take corticosteroids (GCS); group 3–59 patients with exacerbation of sarcoidosis, long-term taking corticosteroids. In order to improve the diagnosis of exacerbation and activity of sarcoidosis in patients receiving complex treatment, including glucocorticosteroids, 303 patients with respiratory sarcoidosis were examined at the initial visit (before treatment) and every 2 months of treatment for 2 years. Group 1–193 patients without exacerbation; group 2–51 patients with exacerbation who did not take corticosteroids (GCS); group 3–59 patients with exacerbation, long-term taking corticosteroids. Conducted clinical and biochemical blood tests, computed tomography of the respiratory organs, spirography, echocardiography, electrocardiography at rest. Changes in the following serum markers were studied: free radicals (RwR), resistance to oxidative stress calculated by trolox equivalent (UcE), angiotensin-converting enzyme (ACE), adenosine deaminase (ADA), the correlation coefficient (CC) was calculated according to the developed formula (patent): CC = ACE/ADA in arbitrary units (KKnorm = 1.2–2.4), markers of lipid metabolism disorders were determined, to assess the activity of endogenous inflammation, the indicator of lipoidosis activity (PAL) was calculated according to the previously developed formula (patent): PAL = TC/LDLxc + TGL. Before treatment, 100 % of patients with sarcoidosis showed signs of moderate endogenous inflammation, an active granulomatous process, hypoxemia, and a decrease in the body’s antioxidant defense. The sensitivity of the serum adenosine deaminase (ADA) enzyme in exacerbations of sarcoidosis was 31 %, and the specificity was 48 %. The correlation coefficient (CC) had a sensitivity of 85.0 %; specificity 78.8 %; diagnostic efficiency of 80.0 % and higher clinical value than ACE, ADA, PAL, SVR, UKO. Thus, the serum enzyme adenosine deaminase (ADA) should be included in the mandatory minimum of laboratory methods in patients with sarcoidosis.
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