Published online Nov 6, 2021. doi: 10.12998/wjcc.v9.i31.9520
Peer-review started: February 24, 2021
First decision: April 20, 2021
Revised: May 4, 2021
Accepted: September 10, 2021
Article in press: September 10, 2021
Published online: November 6, 2021
Processing time: 247 Days and 9.1 Hours
Glycated albumin (GA), the non-enzymatic glycation product of albumin in plasma, was first introduced as a glycemic marker in the beginning of the 21st century. GA is not affected by hemoglobin levels and reflects glycemic status over a shorter period (2-4 wk) as compared to HbA1c measurements. GA has been verified for various aspects in the management of diabetes mellitus (DM) in clinical chemistry.
This study is the first systematic review and meta-analysis on the diagnostic accuracy of GA for DM. GA may contribute as an intermediate glucose index in the current DM diagnostic system.
Our main purpose was to summarize and assess the diagnostic data to evaluate the suitability of GA in the diagnosis of DM.
The Quality Assessment of Diagnostic Accuracy Studies-2 tool was applied for the assessment of quality. The bivariate model was used to pool sensitivity and specificity, and the hierarchical summary receiver operator characteristic curve (HSROC) model was utilized to estimate the summary receiver operating characteristics curve (SROC). The results account for the correlation between sensitivity and specificity across the studies, while the HSROC model also considered the variations between the functional relationship and thresholds in each study.
The average cut-off values of GA reported for gestational diabetes mellitus (GDM) diagnosis were much lower than those for non-GDM. Diagnosing DM with a circulating GA cut-off of 14.0% had a summary sensitivity of 0.766 (95%CI: 0.539, 0.901), specificity of 0.687 (95%CI: 0.364, 0.894), and area under the curve (AUC) of 0.80 (95%CI: 0.76, 0.83) for SROC. The estimated SROC at different GA cut-off values for non-GDM exhibited that the average location parameter lambda was 2.354 (95%CI: 2.002, 2.707) and the scale parameter beta was -0.163 (95%CI: -0.614, 0.288).
GA should be used as an additional test rather than an alternative to HbA1c or OGTT, considering its moderate accuracy in diagnosing non-GDM. Its use as the sole DM diagnostic test should be interpreted with caution to assure the correct classification of diabetic individuals.
Further research on the diagnostic accuracy of GA for GDM and combinational measurements of GA with other assays has been suggested. Besides, it is pertinent for researchers to unify international standards and optimize GA detection methods.