Jiangxi Medical College, Nanchang University, Nanchang, Jiangxi, 330006, China.
Department of Nephrology, The First Affiliated Hospital of Nanchang University, Nanchang, Jiangxi, 330006, China.
Nutr Metab Cardiovasc Dis. 2021 Nov 29;31(12):3457-3463. doi: 10.1016/j.numecd.2021.09.008. Epub 2021 Sep 16.
The ratio of high-density lipoprotein cholesterol to apolipoprotein A1 (HAR) is associated with all-cause mortality in nonchronic kidney disease patients, but its role in predicting all-cause mortality in patients undergoing peritoneal dialysis (PD) is still unclear. The purpose of this study was to investigate the relationship between HAR and all-cause mortality in patients with PD.
The medical records of 1199 patients with PD from November 1, 2005, to August 31, 2019, were collected retrospectively. The main outcome was defined as all-cause mortality. The HAR was divided into three groups by X-tile software. The association between HAR and all-cause mortality was evaluated by Cox models. The Kaplan-Meier method was used for the survival curve. The median follow-up period was 35 months (interquartile range: 20-57 months), with a total of 326 deaths recorded. After multiple adjustments, the risk of all-cause mortality in the high HAR group was 1.96-fold higher than that in the low HAR group (hazard ratio: 1.96; 95% CI, 1.22 to 3.15; P = 0.005). The restricted cubic splines showed that the risk of all-cause mortality increased gradually when HAR was >0.37. In the stratified analysis, a high HAR was linked to a high risk of all-cause mortality in males, patients under 55 years old, and patients without diabetes or cardiovascular disease (CVD).
This study suggests that HAR is independently related to all-cause mortality in PD patients, especially in males, patients under 55 years old, and patients without diabetes or CVD.
高密度脂蛋白胆固醇与载脂蛋白 A1 的比值(HAR)与非慢性肾脏病患者的全因死亡率相关,但它在预测腹膜透析(PD)患者全因死亡率中的作用尚不清楚。本研究旨在探讨 HAR 与 PD 患者全因死亡率之间的关系。
回顾性收集了 2005 年 11 月 1 日至 2019 年 8 月 31 日期间 1199 例 PD 患者的病历。主要结局定义为全因死亡率。采用 X-tile 软件将 HAR 分为三组。采用 Cox 模型评估 HAR 与全因死亡率之间的关系。采用 Kaplan-Meier 法绘制生存曲线。中位随访时间为 35 个月(四分位距:20-57 个月),共记录到 326 例死亡。经多次调整后,高 HAR 组的全因死亡风险是低 HAR 组的 1.96 倍(风险比:1.96;95%CI:1.22 至 3.15;P=0.005)。限制性立方样条显示,当 HAR>0.37 时,全因死亡风险逐渐增加。分层分析显示,HAR 较高与男性、55 岁以下患者和无糖尿病或心血管疾病(CVD)的患者全因死亡风险较高相关。
本研究表明,HAR 与 PD 患者的全因死亡率独立相关,尤其是在男性、55 岁以下患者和无糖尿病或 CVD 的患者中。