Remnant cholesterol and the risk of diabetic nephropathy progression to end-stage kidney disease in patients with type 2 diabetes mellitus: a longitudinal cohort study.

IF 3.7 3区 医学 Q2 Medicine
Endocrine Pub Date : 2024-12-01 Epub Date: 2024-07-12 DOI:10.1007/s12020-024-03948-4
Yuancheng Zhao, Ke Liu, Yutong Zou, Yucheng Wu, Jia Yang, Xiang Xiao, Xuegui Ju, Qin Yang, Yanlin Lang, Fang Liu
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引用次数: 0

Abstract

Aim: Diabetic nephropathy (DN) is the most common cause of end-stage kidney disease (ESKD). Remnant cholesterol has been investigated as a predictor for the progression of DN in type 1 diabetes mellitus patients, as well as the incidence of DN in type 2 diabetes mellitus (T2DM) patients. This study aimed to evaluate the longitudinal relationship between baseline remnant cholesterol and kidney outcomes using a Chinese T2DM with biopsy-confirmed DN cohort.

Methods: We included 334 patients with T2DM and biopsy-confirmed DN during 2010-2019 West China Hospital T2DM-DN cohort. Remnant cholesterol was defined by Martin-Hopkins equation. Patients were divided into four groups based on the median (IQR) remnant cholesterol concentration at the time of renal biopsy. The kidney outcome was defined as ESKD, which was defined as the need for chronic kidney replacement therapy or estimated glomerular filtration rate (eGFR) < 15 mL/min/1.73 m2. The relationship between remnant cholesterol and kidney outcome was analyzed using the Kaplan‒Meier method and Cox regression analysis.

Results: The mean age was 51.1 years, and 235 (70%) were men. During follow-up, a total of 121 (36.2%) patients reached ESKD. The Kaplan‒Meier analysis showed that patients in the highest quartile (quartile 4) group had lower cumulative renal survival (log-rank test, p = 0.033) and shorter median renal survival time [34.0 (26.4-41.6) vs. 55.0 (29.8-80.2) months] than patients in the lowest quartile (quartile 1) group. By univariate analysis, the high remnant cholesterol group was associated with a higher risk of progression to ESKD. Moreover, the risk of progression to ESKD in the highest quartile was still 2.857-fold (95% CI 1.305-6.257, p = 0.009) higher than that in the lowest quartile, and one-SD increase of remnant cholesterol was associated with a higher risk (HR = 1.424; 95% CI 1.075-1.886, p = 0.014) of progression to ESKD, after adjusted for confounding factors.

Conclusions: High remnant cholesterol is independently associated with a higher risk of ESKD in patients with T2DM-DN, and it may be a new noninvasive marker of ESKD.

Clinical relevance: Calculated remnant cholesterol has the advantages of being economical and clinically accessible. Moreover, to our knowledge, there are no longitudinal cohort studies for investigating the risk of progression of T2DM-DN to ESKD. In our study, higher remnant cholesterol was associated with a higher risk of ESKD in patients with T2DM-DN, and it may be a new noninvasive predictor of ESKD.

Abstract Image

残留胆固醇与 2 型糖尿病患者糖尿病肾病发展为终末期肾病的风险:一项纵向队列研究。
目的:糖尿病肾病(DN)是终末期肾病(ESKD)最常见的病因。残余胆固醇是预测 1 型糖尿病患者糖尿病肾病进展以及 2 型糖尿病(T2DM)患者糖尿病肾病发病率的指标之一。本研究的目的是通过活检确诊为 DN 的中国 T2DM 患者队列,评估基线残余胆固醇与肾脏预后之间的纵向关系:我们纳入了2010-2019年华西医院T2DM-DN队列中的334例T2DM和活检证实的DN患者。剩余胆固醇用马丁-霍普金斯方程定义。根据肾活检时残余胆固醇浓度的中位数(IQR)将患者分为四组。肾脏结果被定义为 ESKD,即需要慢性肾脏替代治疗或估计肾小球滤过率(eGFR)2。采用 Kaplan-Meier 法和 Cox 回归分析法分析了残余胆固醇与肾脏预后之间的关系:平均年龄为 51.1 岁,男性 235 人(占 70%)。随访期间,共有 121 例(36.2%)患者达到 ESKD。Kaplan-Meier 分析显示,与最低四分位数(四分位数 1)组相比,最高四分位数(四分位数 4)组患者的累积肾脏存活率较低(log-rank 检验,p = 0.033),中位肾脏存活时间较短 [34.0 (26.4-41.6) vs. 55.0 (29.8-80.2) 个月]。通过单变量分析,高残余胆固醇组患者进展为 ESKD 的风险更高。此外,经混杂因素调整后,最高四分位组进展为 ESKD 的风险仍比最低四分位组高出 2.857 倍(95% CI 1.305-6.257,p = 0.009),且残余胆固醇增加一标准差与进展为 ESKD 的更高风险相关(HR = 1.424;95% CI 1.075-1.886,p = 0.014):结论:高残余胆固醇与 T2DM-DN 患者罹患 ESKD 的较高风险独立相关,它可能是 ESKD 的一种新的无创标记物:计算残余胆固醇具有经济和临床可及的优点。此外,据我们所知,目前还没有纵向队列研究来调查 T2DM-DN 发展为 ESKD 的风险。在我们的研究中,较高的残余胆固醇与 T2DM-DN 患者较高的 ESKD 风险相关,它可能是 ESKD 的一种新的非侵入性预测指标。
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来源期刊
Endocrine
Endocrine 医学-内分泌学与代谢
CiteScore
6.40
自引率
5.40%
发文量
0
期刊介绍: Well-established as a major journal in today’s rapidly advancing experimental and clinical research areas, Endocrine publishes original articles devoted to basic (including molecular, cellular and physiological studies), translational and clinical research in all the different fields of endocrinology and metabolism. Articles will be accepted based on peer-reviews, priority, and editorial decision. Invited reviews, mini-reviews and viewpoints on relevant pathophysiological and clinical topics, as well as Editorials on articles appearing in the Journal, are published. Unsolicited Editorials will be evaluated by the editorial team. Outcomes of scientific meetings, as well as guidelines and position statements, may be submitted. The Journal also considers special feature articles in the field of endocrine genetics and epigenetics, as well as articles devoted to novel methods and techniques in endocrinology. Endocrine covers controversial, clinical endocrine issues. Meta-analyses on endocrine and metabolic topics are also accepted. Descriptions of single clinical cases and/or small patients studies are not published unless of exceptional interest. However, reports of novel imaging studies and endocrine side effects in single patients may be considered. Research letters and letters to the editor related or unrelated to recently published articles can be submitted. Endocrine covers leading topics in endocrinology such as neuroendocrinology, pituitary and hypothalamic peptides, thyroid physiological and clinical aspects, bone and mineral metabolism and osteoporosis, obesity, lipid and energy metabolism and food intake control, insulin, Type 1 and Type 2 diabetes, hormones of male and female reproduction, adrenal diseases pediatric and geriatric endocrinology, endocrine hypertension and endocrine oncology.
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