Lin Jieshan, Tang Wenfang, Liu Wei, Yu Feng, Wu Yanhua, Fang Xiaowu, Zhou Maohua, Hao Wenke, Hu Wenxue
Department of Nephrology, Guangdong Provincial People's Hospital, Guangdong Academy of Medical Sciences, Guangdong Provincial Geriatrics Institute, Guangzhou, China.
Shantou University Medical College, Shantou, China.
Front Med (Lausanne). 2020 Mar 20;7:75. doi: 10.3389/fmed.2020.00075. eCollection 2020.
Loss of renal function is associated with immune deficiency; however, few studies have addressed the role of B lymphocytes in elderly patients with chronic kidney disease (CKD). In this study, we examined the distribution and the relationship of the B lymphocyte subpopulation with clinical outcomes in elderly CKD patients. In this study, a total of 380 patients (312 CKD patients and 68 non-CKD controls) were recruited. Venous blood samples were analyzed by flow cytometry to determine the following B cell subsets: total B cells (CD19+), innate B1 cells (CD19+CD5+), and conventional B2 cells (CD19+CD5-). Correlations between the B cell subsets with clinical features and patient prognosis were analyzed. A total of 380 patients (mean age 82.29 ± 6.22 years, 76.3% male) were included. The median follow-up time was 37.0 months (range, 1-109 months); 109 (28.7%) patients died. The main causes of death were infections (59.6%) and cardiovascular diseases (22.9%). Correlation analysis showed that levels of serum creatinine (SCr), blood urea nitrogen (BUN), and CKD were negatively associated with B1 cells. However, lymphocytes, T lymphocytes, and estimated glomerular filtration rate (eGFR) were positively correlated with B1 cells (all < 0.05). B2 cells were negatively associated with age, SCr, cystatin C, BUN, and CKD, and were positively correlated with hemoglobin, lymphocytes, T lymphocytes, NK cells, and eGFR (all < 0.05). Patient survival was significantly better in patients with B cells > 0.05 × 10/L, B1 cells > 0.02 × 10/L, and B2 cells > 0.04 × 10/L. Multivariate Cox regression analysis showed that B1 cells > 0.02 × 10/L [hazard ratio (HR) = 0.502, 95% confidence interval (CI): 0.297-0.851, = 0.010] and B2 cells > 0.04 × 10/L (HR = 0.536, 95% CI: 0.319-0.901, = 0.019) were independent protective factors for all-cause mortality. Our results showed that B1 and B2 cells exhibited a significantly negative correlation with the progression of CKD in elderly patients. Moreover, B1 and B2 cells were independent prognostic factors for survival, which indicates that the decrease in B cells may be associated with the progression of kidney diseases.
肾功能丧失与免疫缺陷相关;然而,很少有研究探讨B淋巴细胞在老年慢性肾脏病(CKD)患者中的作用。在本研究中,我们检测了老年CKD患者B淋巴细胞亚群的分布及其与临床结局的关系。本研究共纳入380例患者(312例CKD患者和68例非CKD对照)。通过流式细胞术分析静脉血样本,以确定以下B细胞亚群:总B细胞(CD19+)、固有B1细胞(CD19+CD5+)和传统B2细胞(CD19+CD5-)。分析了B细胞亚群与临床特征及患者预后之间的相关性。共纳入380例患者(平均年龄82.29±6.22岁,76.3%为男性)。中位随访时间为37.0个月(范围1 - 109个月);109例(28.7%)患者死亡。主要死亡原因是感染(59.6%)和心血管疾病(22.9%)。相关性分析显示,血清肌酐(SCr)、血尿素氮(BUN)水平及CKD分期与B1细胞呈负相关。然而,淋巴细胞、T淋巴细胞及估算肾小球滤过率(eGFR)与B1细胞呈正相关(均P<0.05)。B2细胞与年龄、SCr、胱抑素C、BUN及CKD分期呈负相关,与血红蛋白、淋巴细胞、T淋巴细胞、NK细胞及eGFR呈正相关(均P<0.05)。B细胞>0.05×10⁹/L、B1细胞>0.02×10⁹/L及B2细胞>0.04×10⁹/L的患者生存情况明显更好。多因素Cox回归分析显示,B1细胞>0.02×10⁹/L[风险比(HR)=0.502,95%置信区间(CI):0.297 - 0.851,P=0.010]和B2细胞>0.04×10⁹/L(HR = 0.536,95%CI:0.319 - 0.901,P=0.019)是全因死亡率的独立保护因素。我们的结果表明,B1和B2细胞与老年患者CKD的进展呈显著负相关。此外,B1和B2细胞是生存的独立预后因素,这表明B细胞减少可能与肾脏疾病的进展有关。