Correlation between glycaemic variability and prognosis in diabetic patients with CKD
Mingshuang Gao1,2, Zhihua Zhong3, Ya Yue4
1Nephrology Department, Jinan University First Affiliated Hospital, Guangzhou, China. 904025298@qq.com.
Insights
Glycaemic variability (GV), measured by the coefficient of glucose variation (GLUCV), is a significant risk factor for mortality in patients with diabetes mellitus and chronic kidney disease. Monitoring and managing GV may improve patient outcomes.
Area of Science:
- Nephrology
- Endocrinology
- Critical Care Medicine
Background:
- Glycaemic variability (GV), assessed by the coefficient of glucose variation (GLUCV), is linked to in-hospital mortality.
- The role of GLUCV as a predictor of adverse outcomes in patients with both diabetes mellitus (DM) and chronic kidney disease (CKD) remains unclear.
Purpose of the Study:
- To investigate the association between GLUCV and in-hospital and 30-day mortality in adult patients with DM and CKD.
- To determine if GLUCV is an independent risk factor for mortality in this patient population.
Main Methods:
- Retrospective analysis of adult DM patients with CKD from the MIMIC-IV database.
- Kaplan-Meier analysis and Cox regression models were employed to assess mortality risks.
- Patients were stratified into four groups based on GLUCV quartiles.
Main Results:
- 1572 DM patients with CKD were analyzed.
- Cox regression identified GLUCV as an independent risk factor for in-hospital and 30-day mortality.
- Survival rates decreased in a time-dependent manner, particularly in the lowest and highest GLUCV groups.
Conclusions:
- GV, quantified by GLUCV, is validated as a mortality risk factor in hospitalized DM patients with CKD.
- Clinical monitoring and adjustment of GV may offer significant therapeutic benefits for these patients.
Introduction:
Glycaemic variability (GV), rather than glucose level, has been shown to be an important factor associated with in-hospital mortality. The coefficient of variation of glucose (GLUCV) is one of the methods used to evaluate GV. However, the clinical significance of GLUCV in diabetes mellitus (DM) patients diagnosed with chronic kidney disease (CKD) as a risk factor for long-term adverse changes is unknown.
Material And Methods:
In this retrospective study, we extracted data of adult DM patients diagnosed with CKD from the Medical Information Mart for Intensive Care (MIMIC-IV). We sought to investigate the relationship between GV and in-hospital mortality as well as 30-day mortality. A non-parametric test was used to compare baseline characteristics between groups. Kaplan-Meier analysis and Cox regression model were used to analyse the risk factors associated with in-hospital and 30-day mortality.
Results:
A total of 1572 DM patients with CKD were included in our data analysis. The quartile of the GLUCV values was used to assign subjects to 4 groups: GLUCV1 (GLUCV < 24), GLUCV2 (24 ≤ GLUCV < 31), GLUCV3 (31 ≤ GLUCV < 39) and GLUCV 4 (GLUCV ≥ 39). COX regression analysis revealed that the GLUCV was an independent risk factor for in-hospital and 30-day mortality [GLUCV2 group (HR = 0.639, 95% CI: 0.454-0.899, p = 0.010), GLUCV3 group (HR = 0.668, 95% CI: 0.476-0.936, p = 0.019), and GLUCV3 group (HR = 0.726, 95% CI: 0.528-0.999, p = 0.049)]. The Kaplan-Meier survival curve was steeper in the GLUCV1 and GLUCV4 groups, and the survival rate decreased in a time-dependent manner.
Conclusions:
Herein, we validated GV as a mortality risk factor for DM patients with CKD. Therefore, monitoring and adjusting GV in hospitalized patients might have a significant treatment benefit.
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