外周单核细胞计数是2型糖尿病伴大血管并发症的全因死亡率的独立预测因子。

Lina Yang, Jinbo Hu, Zhihong Wang, Xiangjun Chen, Yue Wang, Shumin Yang, Ting Luo, Mei Mei, Qingfeng Cheng, Zhixin Xu, Zhipeng Du, Lilin Gong, Rong Luo, Qifu Li
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引用次数: 4

摘要

单核细胞计数与死亡率之间的关系似乎在不同的疾病中有所不同,但在2型糖尿病(T2D)中仍不清楚。我们进行了一项前瞻性研究,探讨单核细胞计数是否能预测T2D患者的全因死亡率。在这项前瞻性研究中,共有1073名T2D患者在基线时入组,880名患者完成了随访。中位随访时间为47个月。基线时,记录临床特征包括身高、体重、腰围、血压。测定各组白细胞(WBCC)、中性粒细胞(NC)、单核细胞(MC)、血脂、糖化血红蛋白(HbA1c)、血清肌酐等生化指标。Charlson共病指数(CCI)基于年龄和共病计算。根据基线MC将参与者分为低、中、高三位数。回归模型用于分析外周MC与全因死亡率的关系。与存活者相比,随访期间死亡患者的基线MC显著高于存活者(0.45±0.16 vs 0.37±0.15 × 10/L, P = 0.003)。在多因素Cox风险模型中,经性别、体重指数、CCI、T2D病程、高血压和代谢综合征史、药物、高敏c反应蛋白水平、收缩压、HbA1c、WBCC、NC等因素调整后,高MC分位数的受试者全因死亡风险较高(以低分位数为参照,风险比[HR] 95%CI分别为2.65[0.84,8.31]和3.73[1.14,12.24])。在基线时伴有大血管并发症的T2D患者中,MC增加1-SD导致全因死亡风险增加1.92倍。然而,在基线时无大血管并发症的受试者中,这种关系消失(1.13 [0.72,1.78],P = .591)。外周单核细胞计数是T2D患者全因死亡率的独立预测因子,特别是对于有大血管并发症的患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Peripheral monocyte count is an independent predictor of all-cause mortality in type 2 diabetes with macro-vascular complications.

Peripheral monocyte count is an independent predictor of all-cause mortality in type 2 diabetes with macro-vascular complications.

Peripheral monocyte count is an independent predictor of all-cause mortality in type 2 diabetes with macro-vascular complications.

Peripheral monocyte count is an independent predictor of all-cause mortality in type 2 diabetes with macro-vascular complications.

The relationship between monocyte count and mortality seemed to be varied in different diseases, and it remains unclear in type 2 diabetes (T2D). We conducted a prospective study to investigate whether monocyte count predict all-cause mortality in patients with T2D.In this prospective study, a total of 1073 patients with T2D were enrolled at baseline and 880 patients completed the follow up. The median follow-up time was 47 months. At baseline, clinical characteristics including height, weight, waist circumference, blood pressure were recorded. Biochemical parameters including counts of white blood cells (WBCC), neutrophil (NC) and monocyte (MC), lipid profiles, glycated hemoglobin (HbA1c), serum creatinine were measured. Charlson comorbidity index (CCI) was calculated based on age and comorbidities. Participants were stratified into low, median, and high tertiles according to the baseline MC. Regression models were used to analyze the associations of peripheral MC and the all-cause mortality.Compared to the survived subjects, the baseline MC was significantly higher in patients who deceased during the follow-up (0.45 ± 0.16 vs 0.37 ± 0.15 × 10/L, P = .003). In the multivariate Cox hazard models, subjects in higher MC tertile showed higher risks of all-cause mortality (low tertile as the reference, hazard ratio [HR] 95%CI 2.65 [0.84,8.31] and 3.73 [1.14,12.24] for middle and high MC tertile, respectively) after adjusted for gender, body mass index, CCI, duration of T2D, history of hypertension and metabolic syndrome, drugs, levels of high-sensitivity C-reactive protein, systolic blood pressure, HbA1c, WBCC, and NC. In T2D patients with macro-vascular complications at baseline, 1-SD increment of MC resulted in 1.92-fold higher risk of all-cause mortality. However, the relationship disappeared in subjects without macro-vascular complications at baseline (1.13 [0.72, 1.78], P = .591).Peripheral monocyte count is an independent predictor of all-cause mortality in T2D, especially for subjects with macro-vascular complications.

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