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Haemoglobin A1c or Glycated Albumin for Diagnosis and Monitoring Diabetes: An African Perspective
11Department of Chemical Pathology, National Health Laboratory Services and University of Witwatersrand, Johannesburg, South Africa.
Insights
Glycated haemoglobin (HbA1c) monitoring for diabetes in Africa is limited by conditions like sickle cell anemia. Glycated albumin and fructosamine offer alternative, more reliable measures for diabetes management in African patients.
Area of Science:
- Endocrinology
- Clinical Chemistry
- Public Health
Background:
- Diabetes mellitus (DM) is a global epidemic, with sub-Saharan Africa experiencing significant increases.
- Poorly controlled diabetes is prevalent among diagnosed individuals in the region.
- Existing diagnostic and monitoring methods for DM in Africa face limitations.
Purpose of the Study:
- To review the limitations of glycated haemoglobin (HbA1c) for diabetes monitoring in Africa.
- To assess the utility of glycated albumin and fructosamine in African patients.
- To highlight alternative biomarkers for diabetes management in specific African contexts.
Main Methods:
- Literature review focusing on glycated haemoglobin (HbA1c), glycated albumin, and fructosamine.
- Analysis of factors affecting HbA1c accuracy in African populations.
- Discussion of enzymatic measurement methods for glycated albumin.
Main Results:
- Conditions common in Africa, such as sickle cell anemia, chronic kidney disease, and HIV infection, compromise HbA1c accuracy.
- Glycated albumin reflects short-term glycaemia and is less affected by these interfering conditions.
- Fructosamine also offers an alternative for monitoring glycaemic control.
Conclusions:
- Standard HbA1c monitoring may be unreliable for diabetes management in many African patients.
- Glycated albumin and fructosamine present viable alternatives for assessing glycaemic control in this population.
- Further research and implementation of these alternative markers are crucial for improving diabetes care in Africa.
Abstract:
Diabetes mellitus (DM) has reached epidemic proportions across the globe with the largest increases seen in sub-Saharan Africa. Those that are diagnosed are largely poorly controlled. This review summarizes the limitations of the use of glycated haemoglobin (HBA1c) in Africa and current knowledge on the utility of glycated albumin and fructosamine in African patients. The diagnosis and monitoring of DM in African patients may be compromised by associated conditions like sickle cell anaemia, chronic kidney disease and HIV infection. Glycated albumin reflects short term glycaemia and is not affected by many conditions that alter HbA1c. It can be measured enzymatically, and this review discusses methods for analysis, and discusses the advantages and limitations in specific situations with an emphasis on conditions that also affect HbA1c.
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