Publication

1-h Glucose During Oral Glucose Tolerance Test Predicts Hyperglycemia Relapse-Free Survival in Obese Black Patients With Hyperglycemic Crises

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Last modified
  • 05/22/2025
Type of Material
Authors
    Ram Jagannathan, Emory UniversityDarko Stefanovski, University of PennsylvaniaDawn D Smiley, Emory UniversityOmolade Oladejo, Emory UniversityLucia F Cotten, Emory UniversityGuillermo Umpierrez, Emory UniversityPriyathama Vellanki, Emory University
Language
  • English
Date
  • 2022-06-02
Publisher
  • FRONTIERS MEDIA SA
Publication Version
Copyright Statement
  • © 2022 Jagannathan, Stefanovski, Smiley, Oladejo, Cotten, Umpierrez and Vellanki
License
Final Published Version (URL)
Title of Journal or Parent Work
Volume
  • 13
Start Page
  • 871965
End Page
  • 871965
Grant/Funding Information
  • PV is funded in part by NIH/NIDDK K23 DK 11324-01A1.
  • This study was funded by NIH K08 DK083036 to DDS. GU is partly supported by research grants from the NIH/NATS UL1 TR002378 from the Clinical and Translational Science Award program and 1P30DK111024-01 from NIH and National Center for Research Resources.
Supplemental Material (URL)
Abstract
  • Objective: Approximately 50% of obese Black patients with unprovoked diabetic ketoacidosis (DKA) or severe hyperglycemia (SH) at new-onset diabetes achieve near-normoglycemia remission with intensive insulin treatment. Despite the initial near-normoglycemia remission, most DKA/SH individuals develop hyperglycemia relapse after insulin discontinuation. Traditional biomarkers such as normal glucose tolerance at the time of remission were not predictive of hyperglycemia relapse. We tested whether 1-h plasma glucose (1-h PG) at remission predicts hyperglycemia relapse in Black patients with DKA/SH. Methods: Secondary analysis was performed of two prospective randomized controlled trials in 73 patients with DKA/SH at the safety net hospital with a median follow-up of 408 days. Patients with DKA/SH underwent a 5-point, 2-h 75-g oral glucose tolerance test after hyperglycemia remission. Hyperglycemia relapse is defined by fasting blood glucose (FBG) > 130 mg/dl, random blood glucose (BG) >180 mg/dl, or HbA1c > 7%. Results: During the median 408 (interquartile range: 110–602) days of follow-up, hyperglycemia relapse occurred in 28 (38.4%) participants. One-hour PG value ≥199 mg/dl discriminates hyperglycemia relapse (sensitivity: 64%; specificity: 71%). Elevated levels of 1-h PG (≥199 mg/dl) were independently associated with hyperglycemia relapse (adjusted hazard ratio: 2.40 [95% CI: 1.04, 5.56]). In a multivariable model with FBG, adding 1-h PG level enhanced the prediction of hyperglycemia relapse, with significant improvements in C-index (Δ: +0.05; p = 0.04), net reclassification improvement (NRI: 48.7%; p = 0.04), and integrated discrimination improvement (IDI: 7.8%; p = 0.02) as compared with the addition of 2-h PG (NRI: 20.2%; p = 0.42; IDI: 1.32%; p = 0.41) or HbA1c (NRI: 35.2%; p = 0.143; IDI: 5.8%; p = 0.04). Conclusion: One-hour PG at the time of remission is a better predictor of hyperglycemia relapse than traditional glycemic markers among obese Black patients presenting with DKA/SH. Testing 1-h PG at insulin discontinuation identifies individuals at high risk of developing hyperglycemia relapse.
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Research Categories
  • Biology, Biostatistics

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