Type 2 & other diabetes

Racial differences in measures of glycemia in the Vitamin D and Type 2 Diabetes (D2d) Study: a secondary analysis of a randomized trial

BMJ Open Diabetes Res CarePublished Secondary analysis of the D2d randomised trial

Authors' conclusion

Use of additional testing beyond A1c to screen for diabetes may better stratify diabetes risk in the diverse US population.

Study context

Population
Persons at risk of diabetes with concurrently measured HbA1c and oral glucose tolerance test (OGTT), 22 US clinical sites; subset with high-risk prediabetes followed longitudinally2,154 followed
Participants
1,016 / 2,658 / 193
Comparison
Black and Asian vs white participants
  • Blackn = 1,016
  • Whiten = 2,658reference
  • Asiann = 193
Primary endpoint
Glucose levels during OGTT (AUCglu) for a given HbA1c level, and HbA1c for a given AUCglu, by race
Methodological detailscross-sectional analysis, observational longitudinal follow-up, multicentre (22 US clinical sites)
  • Cross-sectional analysis
  • Observational longitudinal follow-up
  • Multicentre (22 US clinical sites)

Primary result

As reported in the abstract

HbA1c for a given AUCglu quintile, adjusted

Difference

0.15-0.20 percentage points

P < 0.05

Black · higher with Black

Difference

0.02-0.19 percentage points

P < 0.05

Asian · higher with Asian

Further findings

Diabetes diagnosed by fasting glucose (longitudinal) · 2.5 years — Black vs White · Black and Asian less likely than White

P < 0.05

OutcomeBlackWhiteAsianP value
Diabetes diagnosed by HbA1c (longitudinal) · 2.5 yearsBlack vs White28%10%— not stated in the abstractP < 0.01

— not stated in the abstract

Change in HbA1c over time

Black participants with HbA1c in lower-level quintiles had greater increase in HbA1c over time vs white participants

Original publication

Racial differences in measures of glycemia in the Vitamin D and Type 2 Diabetes (D2d) Study: a secondary analysis of a randomized trial. BMJ Open Diabetes Res Care. Published 12 February 2024. doi:10.1136/bmjdrc-2023-003613

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