前瞻性队列中血脂对慢性肾脏疾病的影响:基于非连续性回归设计

Kang Lyu, Shaodong Liu, Yanli Liu, Jinlong You, Xue Wang, Min Jiang, Chun Yin, Desheng Zhang, Yana Bai, Minzhen Wang, Shan Zheng
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引用次数: 0

摘要

目的:先前关于脂质谱与慢性肾脏疾病(CKD)之间关系的研究得出了不一致的结果,并且没有明确的血脂阈值。方法:一项前瞻性队列研究,包括32,351名受试者,他们完成了5年的基线和随访调查。使用限制性三次样条和Cox模型来检查脂质谱与CKD之间的关系。采用回归不连续设计来确定与CKD风险增加显著相关的脂质谱的截止值。结果:中位随访时间为2.2年(0.5年,4.2年),648例(2.00%)受试者发生CKD。与CKD显著线性相关的脂质谱包括总胆固醇(TC)、甘油三酯(TG)、高密度脂蛋白胆固醇(HDL-C)、TC/HDL-C和TG/HDL-C,而低密度脂蛋白胆固醇(LDL-C)和LDL-C/HDL-C与CKD呈非线性相关。TC、TG、TC/HDL-C和TG/HDL-C在临界值处呈上升趋势,分别使CKD风险增加0.90%、1.50%、2.30%和1.60%,而HDL-C在临界值处呈下降趋势,使CKD风险降低1.0%。女性和患有血脂异常的参与者患慢性肾病的风险更高,但不同人群特征的临界值不同。结论:在中国西北地区的前瞻性队列中,脂质谱与CKD之间存在显著相关性,而TG、TC/HDL-C和TG/HDL-C表现出更强的风险相关性。脂质谱的特定临界值可为筛查或诊断CKD风险提供临床参考。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The Effect of Blood Lipid Profiles on Chronic Kidney Disease in a Prospective Cohort: Based on a Regression Discontinuity Design.

Objective: Previous studies on the association between lipid profiles and chronic kidney disease (CKD) have yielded inconsistent results and no defined thresholds for blood lipids.

Methods: A prospective cohort study including 32,351 subjects who completed baseline and follow-up surveys over 5 years was conducted. Restricted cubic splines and Cox models were used to examine the association between the lipid profiles and CKD. A regression discontinuity design was used to determine the cutoff value of lipid profiles that was significantly associated with increased the risk of CKD.

Results: Over a median follow-up time of 2.2 (0.5, 4.2) years, 648 (2.00%) subjects developed CKD. The lipid profiles that were significantly and linearly related to CKD included total cholesterol (TC), triglycerides (TG), high-density lipoprotein cholesterol (HDL-C), TC/HDL-C, and TG/HDL-C, whereas low-density lipoprotein cholesterol (LDL-C) and LDL-C/HDL-C were nonlinearly correlated with CKD. TC, TG, TC/HDL-C, and TG/HDL-C showed an upward jump at the cutoff value, increasing the risk of CKD by 0.90%, 1.50%, 2.30%, and 1.60%, respectively, whereas HDL-C showed a downward jump at the cutoff value, reducing this risk by 1.0%. Female and participants with dyslipidemia had a higher risk of CKD, while the cutoff values for the different characteristics of the population were different.

Conclusion: There was a significant association between lipid profiles and CKD in a prospective cohort from Northwest China, while TG, TC/HDL-C, and TG/HDL-C showed a stronger risk association. The specific cutoff values of lipid profiles may provide a clinical reference for screening or diagnosing CKD risk.

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