袁铭, 刘亚, 戴春. 免疫球蛋白A肾病患者全身免疫炎症指数与低蛋白血症的关系[J]. 实用临床医药杂志, 2022, 26(11): 127-132. DOI: 10.7619/jcmp.20214452
引用本文: 袁铭, 刘亚, 戴春. 免疫球蛋白A肾病患者全身免疫炎症指数与低蛋白血症的关系[J]. 实用临床医药杂志, 2022, 26(11): 127-132. DOI: 10.7619/jcmp.20214452
YUAN Ming, LIU Ya, DAI Chun. Correlation of systemic immune-inflammation index with hypoproteinemia in immunoglobulin A nephrology patients[J]. Journal of Clinical Medicine in Practice, 2022, 26(11): 127-132. DOI: 10.7619/jcmp.20214452
Citation: YUAN Ming, LIU Ya, DAI Chun. Correlation of systemic immune-inflammation index with hypoproteinemia in immunoglobulin A nephrology patients[J]. Journal of Clinical Medicine in Practice, 2022, 26(11): 127-132. DOI: 10.7619/jcmp.20214452

免疫球蛋白A肾病患者全身免疫炎症指数与低蛋白血症的关系

Correlation of systemic immune-inflammation index with hypoproteinemia in immunoglobulin A nephrology patients

  • 摘要:
    目的 探讨免疫球蛋白A肾病(IgAN)患者全身免疫炎症指数(SII)与低蛋白血症的关系。
    方法 选取143例IgAN患者作为研究对象,根据血清白蛋白水平是否>35 g/L将患者分为正常组和低蛋白血症组,比较2组患者的临床资料和SII水平(SII=血小板×中性粒细胞/淋巴细胞)。根据SII中位数将143例患者分为低SII组和高SII组,比较2组患者的临床资料。采用Logistic回归分析探讨IgAN患者发生低蛋白血症的危险因素,并采用Spearman相关分析法分析血清白蛋白与其他指标的相关性。
    结果 143例患者中, 35例发生低蛋白血症,占24.48%; 低蛋白血症组年龄、病理分型为E1者占比和白细胞、中性粒细胞、血小板、总胆固醇、24 h尿蛋白定量(24 hUTP)、低密度脂蛋白、SII、血小板与淋巴细胞比值(PLR)、中性粒细胞与淋巴细胞比值(NLR)水平高于正常组,血红蛋白、白蛋白、估算肾小球滤过率(eGFR)水平低于正常组,差异均有统计学意义(P < 0.05); 高SII组年龄和白细胞、中性粒细胞、血小板、24 hUTP、总胆固醇、PLR、NLR水平高于低SII组,白蛋白、eGFR水平和病理分型为T0者占比低于低SII组,病理分型为E1者占比、T1~T2者占比高于低SII组,差异均有统计学意义(P < 0.05); 相关性分析结果显示,血清白蛋白与SII、PLR、中性粒细胞均呈显著负相关(P < 0.05), 与肌酐呈显著正相关(P < 0.05); 多因素Logistic回归分析显示,年龄较大(OR=1.060, 95%CI: 1.012~1.101, P=0.013)、低水平eGFR(OR=0.974, 95%CI: 0.953~0.996, P=0.019)、高水平SII(OR=1.001, 95%CI: 1.000~1.003, P=0.028)为IgAN患者发生低蛋白血症的独立危险因素。
    结论 高水平SII是IgAN患者发生低蛋白血症的独立危险因素,临床可通过监测SII水平判断疾病进展情况,从而提前采取措施预防IgAN患者低蛋白血症的发生。

     

    Abstract:
    Objective To investigate the relationship between systemic immune inflammatory index (SII) and hypoalbuminemia in patients with immunoglobulin A nephropathy (IgAN).
    Methods A total of 143 patients with IgAN were selected as study objects. According to whether serum albumin was more than 35 g/L or not, the patients were divided into hypoalbuminemia group and normal group. The SII level (SII=platelet×neutrophils/lymphocytes) and clinical data of the two groups were compared. According to the median SII, these 143 patients were divided into low SII group and high SII group, and clinical data of the two groups were compared. Logistic regression analysis was used to explore the risk factors of hypoproteinemia in patients with IgAN, and Spearman correlation analysis was used to analyze the correlations of related indexes with serum albumin.
    Results There were 35 of 143 patients with hypoproteinemia (24.48%). Age, proportion of patients with pathological classification of E1, leukocyte, neutrophil, platelet, total cholesterol, 24-hour urinary protein quantity (24 hUTP), low density lipoprotein, SII, platelet to lymphocyte ratio (PLR) and neutrophil to lymphocyte ratio (NLR) in the hypoproteinemia group were higher than those in the normal group, while the levels of hemoglobin, albumin and estimated glomerular filtration rate (eGFR) were lower than those in the normal group, and the differences were statistically significant (P < 0.05). Age, levels of leukocyte, neutrophils, platelets, 24 hUTP, total cholesterol, PLR and NLR in the high SII group were higher than those in the low SII group, albumin, eGFR level and the proportions of patients with pathological type of T0 were lower than those in the low SII group, and the proportion of patients with pathological types of E1 and T1 to T2 was higher than that in the low SII group(P < 0.05). The results of correlation analysis showed that serum albumin was negatively correlated with SII, PLR, and neutrophils (P < 0.05), and positively correlated with creatinine (P < 0.05); multiple Logistic regression analysis showed that older age (OR=1.060, 95%CI, 1.012 to 1.101, P=0.013), low level of eGFR (OR=0.974, 95%CI, 0.953 to 0.996, P=0.019), and high level of SII (OR=1.001, 95%CI, 1.000 to 1.003, P=0.028) were independent risk factors for occurrence of hypoalbuminemia in IgAN patients.
    Conclusion High level of SII is an independent risk factor for hypoalbuminemia in patients with IgAN. In clinical practice, the disease progression can be judged by monitoring the SII level, so that measures can be taken in advance to prevent the occurrence of hypoalbuminemia in patients with IgAN.

     

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