Navarro-Blackaller G, Benitez-Renteria A S, Hernández-Morales K, Rico-Fontalvo J, Daza-Arnedo R, Gómez-Ramírez G G, Camacho-Guerrero J R, Pérez-Venegas M A, Carmona-Morales J, Oseguera-González A N, Murguía-Soto C, Chávez-Alonso G, García-Peña F, Barrera-Torres C J, Orozco-Chan E, Arredondo-Dubois M, Gallardo-González A Martínez, Gómez-Fregoso J A, Rodríguez-García F G, Luquin-Arellano V H, Abundis-Mora G, Alcantar-Vallin L, Medina-González R, García-García G, Chávez-Iñiguez J S
Nephrology Service, Hospital Civil de Guadalajara Fray Antonio Alcalde, Guadalajara, Jalisco, Mexico.
University of Guadalajara Health Sciences Center, Guadalajara, Jalisco, Mexico.
Int J Endocrinol. 2025 May 4;2025:9919963. doi: 10.1155/ije/9919963. eCollection 2025.
In subjects with type 2 diabetes (DM), poor glycemic control, and advanced chronic kidney disease (CKD), the kidney benefit of the reduction of glycated hemoglobin (HbA1c) is not well established. In a retrospective cohort, we included patients with DM, CKD grade 3b-5, and HbA1c > 9% to evaluate the risk of developing major adverse kidney events (MAKE) defined as the start of kidney replacement therapy (KRT), ≥ 25% or ≥ 40% decline in the glomerular filtration rate (eGFR) from baseline, and death; patients were divided according to the HbA1c levels at the end of the follow-up into the following groups: > 75 mmol/mol (≥ 9.0%), 74-64 mmol/mol (8.9%-8.0%), 64-53 mmol/mol (7.9%-7.0%), and < 52 mmol/mol (< 7.0%). We described their characteristics and analyzed their risks, adjusting for confounding variables. From 2015 to 2023, 111 patients were included. In 46 patients (41.4%), the HbA1c at the end of follow-up (60 months) was still > 75 mmol/mol (≥ 9%), and each patient had a mean of 4.9 HbA1c measurements. The mean age was 59 years, and 46% were male; the baseline eGFR was 25 mL/min/1.73 m. MAKE occurred in 67% of cases. In a multivariate analysis, the risk of MAKE was not associated with the HbA1c groups, nor was it associated with any of the MAKE components individually, nor in certain subgroups. When evaluating the magnitude of percentage changes in HbA1 with the initiation of KRT, we did not find any association. With advanced CKD and poor glycemic control, changes in HbA1c during long follow-up are not associated with MAKE or its individual components.
在2型糖尿病(DM)、血糖控制不佳且患有晚期慢性肾脏病(CKD)的患者中,糖化血红蛋白(HbA1c)降低对肾脏的益处尚未明确。在一项回顾性队列研究中,我们纳入了患有DM、CKD 3b - 5级且HbA1c>9%的患者,以评估发生主要不良肾脏事件(MAKE)的风险,MAKE定义为开始肾脏替代治疗(KRT)、肾小球滤过率(eGFR)较基线下降≥25%或≥40%以及死亡;根据随访结束时的HbA1c水平将患者分为以下几组:>75 mmol/mol(≥9.0%)、74 - 64 mmol/mol(8.9% - 8.0%)、64 - 53 mmol/mol(7.9% - 7.0%)和<52 mmol/mol(<7.0%)。我们描述了他们的特征并分析了他们的风险,对混杂变量进行了调整。2015年至2023年,共纳入111例患者。46例患者(41.4%)在随访结束时(60个月)的HbA1c仍>75 mmol/mol(≥9%),每位患者平均进行了4.9次HbA1c测量。平均年龄为59岁,46%为男性;基线eGFR为25 mL/min/1.73m²。67%的病例发生了MAKE。在多变量分析中,MAKE的风险与HbA1c分组无关,也与任何一个MAKE组成部分无关,在某些亚组中也无关联。在评估开始KRT时HbA1的百分比变化幅度时,我们未发现任何关联。对于晚期CKD和血糖控制不佳的情况,长期随访期间HbA1c的变化与MAKE或其各个组成部分无关。