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.

Plos One
|January 23, 2026
PubMed

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.

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