Evidence map›Paper›PMID 41272630›Full record

ArticleBMC endocrine disorders2025

Glucotypes in patients with type 2 diabetes and either diabetic kidney disease or end stage kidney disease under different anti-diabetic treatments.

Yu-Yun Chou, Feng-Hsuan Liu, Chia-Hung Lin

Abstract read
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Article in BMC endocrine disorders, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Yu-Yun ChouDivision of Endocrinology and Metabolism, Department of Internal Medicine, Chang Gung Memorial Hospital, Linkou, Taoyuan City, Taiwan.
Feng-Hsuan LiuDivision of Endocrinology and Metabolism, Department of Internal Medicine, Chang Gung Memorial Hospital, Linkou, Taoyuan City, Taiwan.
Chia-Hung LinDivision of Endocrinology and Metabolism, Department of Internal Medicine, Chang Gung Memorial Hospital, Linkou, Taoyuan City, Taiwan. adronlin@cgmh.org.tw.

Funding

Chang Gung Memorial Hospital CMRPG3M0881, CMRPG3M0882, CMRPG3M2141, CORPG3P0181National Science and Technology Council, ROC NSTC 112-2314-B-182-038
6 · The paper itself

Abstract

backgroundThe profile of glycemic changes in diabetic kidney disease (DKD) remains unclear. Therefore, we aimed to evaluate glucotypes in patients with type 2 diabetes and end stage kidney disease (ESKD) and those with DKD through continuous glucose monitoring (CGM).

methodsWe analyzed ambulatory glucose profiles. The primary outcome was time in range (TIR) and the secondary outcomes included hypoglycemia and glucose variability.

resultsTwenty-one patients with ESKD and 42 patients with DKD were enrolled after matching for age and gender. There was no significant difference in TIR between the ESKD and DKD groups. However, patients with ESKD exhibited higher standard deviation (SD), and nocturnal glucose levels compared to those with DKD. For different dialysis treatments, patients undergoing peritoneal dialysis (PD) had higher continuous overlapping net glycemic action (CONGA), J-Index, high blood glucose index (HBGI), glycemic risk assessment in diabetes equation (GRADE), and M-value than those undergoing HD. Additionally, higher all day glycemic values were observed in the PD group. Patients with ESKD on premixed insulin therapy had higher standard deviation of sensor glucose across 24 h and lower nocturnal glucose levels compared with those on Multiple daily injection (MDI).

conclusionsPatients with ESKD exhibited higher glucose variability and nocturnal glucose levels compared with those with DKD. Patients receiving PD showed higher glycemic variability and glucose levels compared with those undergoing HD.

Indexed as

BiomarkersBlood GlucoseDiabetes Mellitus, Type 2Diabetic NephropathiesHypoglycemic AgentsKidney Failure, ChronicAgedBlood Glucose Self-MonitoringFemaleFollow-Up StudiesHumansMaleMiddle AgedPrognosisRenal DialysisBiomarkersBlood GlucoseHypoglycemic AgentsContinuous glucose monitoringDiabetesDiabetic kidney disease

Identifiers

PMID41272630
PMCPMC12751554

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.