数据挖掘聚类分类方法在反应性关节炎与慢性肾盂肾炎结缔组织代谢相互加重机制研究中的应用

O. Zaliavska, O. Khukhlina, Y. Tkach, O. Nika
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引用次数: 0

摘要

反应性关节炎(ReA)患者的“蛋白聚糖-胶原”系统代谢过程紊乱,酶反应的改变通常伴随着许多并发症,包括肾功能受损。经典回归方法在确定ReA和慢性肾盂肾炎(CP)的相互负担以及疾病的原发性方面并不是很有用。目的:探讨ReA与CP之间可能存在的关系,以结缔组织代谢指标为背景,建立早期预测CP发展的标准。材料和方法。113例患者被分为两组:第一组-尿源性ReA患者,活动I-III。FTS I-III st. (n = 65);第二组为尿源性肾病肾病合并急性期肾盂肾炎患者(48例)。对照组由20名健康个体组成。患者平均病程为24.4±4.7个月。患者平均年龄32.5±1.2岁。采用数据挖掘聚类和分类方法对得到的研究结果进行处理。采用k-means聚类和模糊聚类两种聚类方法,得到了相同的聚类隶属度结果。其中,ReA病确诊48例,占全部确诊病例的74%,17例(26%)归为聚类“2”。在第二个集群中也存在不匹配。特别是,经数学计算,在确诊为ReA + CP的32人中,有28人(88%)属于这一群体。4例患者(13%)被分配到“1”组,即只应诊断一种ReA疾病的组。这表明ReA和ReA + CP簇之间的界限有些模糊。这是确立ReA疾病可逐渐导致cp的基础。采用DataMining聚类方法,确定游离氧脯氨酸(FOP)、蛋白结合氧脯氨酸(PBOP)、胶原溶解活性度(CLA)(偶氮醇溶解强度)等指标在ReA进展诊断算法中的最显著性,这些指标与炎症过程的活性程度直接相关。1 h内FOP> 13.8 μmol/l、PBOP> 65.0 μmol/l、CLA (azocol)> 0.85 μmol/ ml的升高可能是病情进展的危险因素,也是严重ReA和CP的早期诊断标准。
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Application of DataMining clustering and classification methods in the study of the mechanisms of mutual burdening of reactive arthritis and chronic pyelonephritis in terms of connective tissue metabolism
Disorders of metabolic processes in the "proteoglycans-collagen" system, changes in enzymatic reactions in patients with reactive arthritis (ReA) are often preceded by many complications, including impaired renal function. Classical regression methods are not very informative in determining the mutual burden of ReA and chronic pyelonephritis (CP), as well as the primacy of the disease.Objective - to investigate the possible relationship between ReA and CP in order to establish early criteria for predicting the development of CP on the background of ReA on the indicators of connective tissue metabolism. Material and methods. 113 patients were examined, which were divided into two groups: the first group - patients with urogenic ReA, activity I-III. FTS I-III st. (n = 65); the second group - patients with urogenic ReA and CKD I-II: pyelonephritis in the acute phase (n = 48). The control group consisted of 20 healthy individuals. The average duration of the disease of the examined patients was 24.4 ± 4.7 months. The mean age of patients was 32.5 ± 1.2 years. DataMining clustering and classification methods were used to process the obtained research results.Results. As a result of clustering methods (k-means and fuzzy clustering), the same results of cluster membership were obtained. In particular, ReA disease was correctly diagnosed in 48 cases, which is 74% of all diagnosed, 17 people (26%) were assigned to cluster "2". There is also a mismatch in the second cluster. In particular, out of 32 people diagnosed with ReA + CP, according to mathematical calculations, 28 people (88%) got into this cluster. Four patients (13%) were assigned to cluster "1" – to the group of persons in whom only one ReA disease should be diagnosed. This indicates that the boundary between the ReA and ReA + CP clusters are somewhat blurred. And this is the basis for establishing the fact that ReA disease can gradually lead to CP.Conclusions. Using DataMining clustering methods the greatest significance was defined in the diagnostic algorithm of ReA progression of such indicators as free oxyproline (FOP), protein-bound oxyproline (PBOP), the degree of collagenolytic activity (CLA) (intensity of azocol lysis), which showed a direct dependence on the degree of activity of the inflammatory process. Increases in FOP> 13.8 μmol/l, PBOP> 65.0 μmol/l and CLA (azocol)> 0.85 μg / ml in 1 h are probable risk factors for progression and early criteria for severe ReA and CP.
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