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单核细胞计数改变了慢性肾病与死亡风险之间的关联。

Monocyte count modifies the association between chronic kidney disease and risk of death
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作者信息

Koraishy Farrukh M, Bowe Benjamin, Xie Yan, Xian Hong, Al-Aly Ziyad

出版信息

Clin Nephrol. 2018 Sep;90(3):194-208. doi: 10.5414/CN109434.

Abstract

BACKGROUND

Chronic kidney disease (CKD) is associated with increased all-cause mortality. How non-traditional risk factors modify the mortality risk associated with CKD has not been studied. We approached this question using elevated monocyte count, which is associated with increased risk of death in the general population; however, there is very limited data in CKD.

MATERIALS AND METHODS

A national cohort of 1,706,589 U.S. veterans without end-stage renal disease (ESRD) was followed over a median of 9.16 years. Estimated glomerular filtration rate (eGFR; mL/min/1.73m2) was divided into 6 categories: 15 - 30, 30 - 45, 45 - 60, 60 - 90, 90 - 105 (reference), and > 105. Monocyte count (k/cmm) was grouped into quartiles: 0.00 - 0.40 (reference), 0.40 - 0.56, 0.56 - 0.70, and > 0.70. Multinomial logistic regression, Cox proportional hazard regression, and formal interaction analyses on both the multiplicative and additive scales were undertaken.

RESULTS

Monocyte count > 0.56 k/cmm was associated with increased risk of death overall (hazard ratio (HR) 1.40, confidence interval (CI) 1.38, 1.41 in monocyte quartile 4) and across each eGFR category. Very high (> 105 mL/min/1.73m2) and low (15 - 30 mL/min/1.73m2) eGFR categories were associated with increased mortality risk (HR 1.40, CI 1.38, 1.42 and HR 2.07, CI 2.03, 2.11, respectively). The mortality risk associated with high monocyte count and low eGFR exhibited a strong negative interaction (p < 0.001). No interaction was noted at very high eGFR.

CONCLUSION: While low and very high eGFR were both associated with increased mortality risk, a monocyte count > 0.56 k/cmm only modified the risk associated with low eGFR. This suggests a shared underlying mechanism of death between CKD and high monocyte count.
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摘要

背景

慢性肾脏病(CKD)与全因死亡率增加相关。非传统风险因素如何改变与CKD相关的死亡风险尚未得到研究。我们使用单核细胞计数升高来探讨这个问题,单核细胞计数升高与普通人群死亡风险增加相关;然而,在CKD患者中相关数据非常有限。

材料与方法

对1706589名无终末期肾病(ESRD)的美国退伍军人组成的全国队列进行了为期9.16年的中位数随访。估计肾小球滤过率(eGFR;mL/min/1.73m²)分为6类:15 - 30、30 - 45、45 - 60、60 - 90、90 - 105(参照)和>105。单核细胞计数(k/cmm)分为四分位数:0.00 - 0.40(参照)、0.40 - 0.56、0.56 - 0.70和>0.70。进行了多项逻辑回归、Cox比例风险回归以及乘法和加法尺度上的正式交互分析。

结果

单核细胞计数>0.56 k/cmm与总体死亡风险增加相关(风险比(HR)1.40,置信区间(CI)1.38, 1.41,在单核细胞四分位数4中),并且在每个eGFR类别中均如此。非常高(>105 mL/min/1.73m²)和低(15 - 30 mL/min/1.73m²)的eGFR类别与死亡风险增加相关(HR分别为1.40,CI 1.38, 1.42和HR 2.07,CI 2.03, 2.11)。与高单核细胞计数和低eGFR相关的死亡风险表现出强烈的负交互作用(p<0.001)。在非常高的eGFR水平未观察到交互作用。

结论

虽然低和非常高的eGFR均与死亡风险增加相关,但单核细胞计数>0.56 k/cmm仅改变了与低eGFR相关的风险。这表明CKD和高单核细胞计数之间存在共同的潜在死亡机制。

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