Aleksandrov V P, Skriabin G N
Urol Nefrol (Mosk). 1993 Mar-Apr(2):25-7.
Phosphorus metabolic disturbances play a great role in the occurrence of urolithiasis. This study covered 150 patients with urolithiasis to establish correlations between the frequency of histocompatibility antigens and the increase in blood and urinary phosphorus levels. The HLA antigens were identified by the routine microlymphocytotoxic method involving a histotyping serum panel. The ABO antigens and rhesus were determined by the agglutination method by using reference sera. The study revealed specific distribution of histocompatibility antigens in urolithiasis patients with disturbed phosphorus metabolism. Hyperphosphatemia correlated with the higher frequency of HLA-B35 (chi 2 = 9.89) and E/E system rhesus (chi 2 = 8.63); hyperphosphaturia showed a negative association with the HLA-A28 antigens (chi 2 = 9.7), as well as with E/e (chi 2 = 14.69) and e/e (chi 2 = 39.36) and a positive association with HLA-B13 (chi 2 = 5.98) and B35 (chi 2 = 36.58). The highest relative risk for hyperphosphatemia associated with the B27 and B35 antigens was observed with genetic predisposition, being 3.63 and 7.13, respectively. B12- and B35-positive individuals were at higher risk for hyperphosphaturia up to 11.25. There were significant differences in antigen frequency, and sex, genetic predisposition to urolithiasis, association of phosphorus metabolic disturbances with other metabolic disorders, and their effects of parathyroid lesions, etc. The findings reveal the immunogenetically induced risk for the occurrence and development of urolithiasis with disturbed phosphorus metabolism to make goal-oriented prophylactic measures.
磷代谢紊乱在尿石症的发生中起重要作用。本研究涵盖了150例尿石症患者,以建立组织相容性抗原频率与血液和尿液磷水平升高之间的相关性。通过使用组织分型血清板的常规微量淋巴细胞毒性方法鉴定HLA抗原。ABO抗原和恒河猴血型通过使用参考血清的凝集法测定。该研究揭示了磷代谢紊乱的尿石症患者中组织相容性抗原的特定分布。高磷血症与HLA - B35(χ2 = 9.89)和恒河猴血型E/E系统(χ2 = 8.63)的较高频率相关;高磷尿症与HLA - A28抗原(χ2 = 9.7)以及E/e(χ2 = 14.69)和e/e(χ2 = 39.36)呈负相关,与HLA - B13(χ2 = 5.98)和B35(χ2 = 36.58)呈正相关。与B27和B35抗原相关的高磷血症的最高相对风险在遗传易感性中观察到,分别为3.63和7.13。B12和B35阳性个体发生高磷尿症的风险高达11.25。在抗原频率、性别、尿石症的遗传易感性、磷代谢紊乱与其他代谢紊乱的关联以及它们对甲状旁腺病变的影响等方面存在显著差异。这些发现揭示了免疫遗传诱导的磷代谢紊乱的尿石症发生和发展的风险,以便制定有针对性的预防措施。