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HbA1c underperforms in identifying abnormal glucose tolerance in the presence of G6PD deficiency: Insight from the
Amy R Bentley1, Kauthrah Ntabadde2, Claudine B Kabeza2
1Center for Research on Genomics and Global Health, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, United States of America.
Insights
Glucose tolerance screening using hemoglobin A1c (HbA1c) is unreliable in individuals with Glucose-6-Phosphate Dehydrogenase deficiency (G6PD-D). G6PD-D significantly lowers HbA1c, potentially leading to missed diagnoses of abnormal glucose tolerance.
Area of Science:
- Clinical Biochemistry
- Genetics
- Metabolic Disorders
Background:
- Glucose-6-Phosphate Dehydrogenase deficiency (G6PD-D) is prevalent in African populations, where abnormal glucose tolerance (Abnl-GT) is also common.
- Hemoglobin A1c (HbA1c) is widely used for diagnosing Abnl-GT, but G6PD-D is known to lower HbA1c levels.
- The diagnostic accuracy of HbA1c for Abnl-GT in individuals with G6PD-D remains a concern, particularly in at-risk populations.
Purpose of the Study:
- To evaluate the efficacy of HbA1c in detecting Abnl-GT in individuals with G6PD-D.
- To assess the concordance between genetic testing (genotyping) and enzymatic assays for G6PD-D status.
- To investigate the impact of G6PD-D on HbA1c measurements in sub-Saharan Africans living in the US.
Main Methods:
- A cohort of 534 participants from the Africans in America study was analyzed.
- Abnl-GT was diagnosed using the oral glucose tolerance test (OGTT) as the gold standard.
- HbA1c was compared against OGTT results, and G6PD-D status was determined by genotyping and/or enzymatic assay.
Main Results:
- Participants with G6PD-D exhibited HbA1c levels approximately 0.9% lower than those with normal G6PD activity (4.6% vs. 5.5%).
- HbA1c demonstrated 0% sensitivity and 100% specificity for Abnl-GT in individuals with G6PD-D.
- Genotyping and enzymatic assays for G6PD-D showed 100% concordance, but enzymatic assays are crucial for heterozygous women.
Conclusions:
- HbA1c is an unreliable screening tool for abnormal glucose tolerance in individuals with G6PD-D due to significantly lower HbA1c values.
- The enzymatic assay for G6PD-D is essential for accurate diagnosis, especially in heterozygous women, and is highly concordant with genotyping.
- Failure to account for G6PD-D can lead to underdiagnosis and undertreatment of abnormal glucose tolerance, potentially increasing complication risks.
Abstract:
G6PD deficiency (G6PD-D) variants are associated with lower hemoglobin A1c (HbA1c) concentrations, raising concerns about the diagnostic efficacy of HbA1c for abnormal glucose tolerance (Abnl-GT) in Africans, in whom risk of G6PD-D and Abnl-GT is high. G6PD-D is assessed using genotyping or an enzymatic assay, but because G6PD-D is X-linked, the enzymatic assay is necessary for determining status for women heterozygous for deficiency variants. We assessed: 1) ability of HbA1c to detect Abnl-GT by G6PD-D; 2) concordance of genotyping and enzymatic assay for G6PD-D in sub-Saharan Africans living in the US. 534 participants of the Africans in America study were included, with HbA1c ranging from 3.1-11.3%. Abnl-GT determined by HbA1c (≥5.7%) was compared to the diagnostic standard, the oral glucose tolerance test (fasting glucose≥100 mg/dL and/or 2h glucose≥140 mg/dL). G6PD-D status was determined by genotype (n = 263), enzymatic assay (n = 83), or both (n = 188). G6PD-D could not be determined for 13 women heterozygotes with only genotype data. In the remaining participants, HbA1c was 0.9% lower among those with G6PD-D (4.6 ± 0.5; range 3.1-5.6) compared to those with normal G6PD activity (5.5 ± 0.6; range 4.2-11.3; P < 0.001). Glucose concentrations did not differ between groups. HbA1c sensitivity and specificity for Abnl-GT were 0% (0/17) and 100% (37/37) among those with G6PD-D, and 50% (98/195) and 80% (217/272) among those with normal activity. After excluding women heterozygotes, concordance for G6PD-D detection by genotype and the enzymatic assay was 100%. G6PD-D was associated with ~0.9% lower HbA1c in this study, leading to a failure of HbA1c to identify Abnl-GT in these participants. Such a dramatic difference in a screening tool could have consequences in practice, including late diagnosis, undertreatment, and increased complications among those with G6PD-D. Additionally, the results for the enzymatic assay were perfectly concordant with the genotype results for G6PD-D. However, as genotype alone cannot predict G6PD-D in heterozygous women, the enzymatic assay was more informative.
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