Hemoglobin A1c Patterns of Youth With Type 1 Diabetes 10 Years Post Diagnosis From 3 Continents

Author:

Sherr Jennifer L.1,Schwandt Anke23,Phelan Helen45,Clements Mark A.67,Holl Reinhard W.23,Benitez-Aguirre Paul Z.58,Miller Kellee M.9,Woelfle Joachim10,Dover Thomas1112,Maahs David M.1314,Fröhlich-Reiterer Elke15,Craig Maria E.58

Affiliation:

1. Division of Pediatric Endocrinology, Department of Pediatrics, Yale School of Medicine, Yale University, New Haven, Connecticut

2. Institute of Epidemiology and Medical Biometry, Zentralinstitut für Biomedizinische Technik, Ulm University, Ulm, Germany

3. German Centre for Diabetes Research, Munich-Neuherberg, Germany

4. John Hunter Children’s Hospital, Newcastle, Australia

5. Division of Child and Adolescent Health, The University of Sydney, Sydney, Australia

6. Children’s Mercy Hospital, Kansas City, Missouri

7. Department of Pediatrics, University of Missouri-Kansas City, Kansas City, Missouri

8. Children’s Hospital at Westmead, Sydney, Australia

9. Jaeb Center for Health Research, Tampa, Florida

10. Children’s Hospital, University of Erlangen, Erlangen, Germany

11. Ipswich Hospital, Brisbane, Australia

12. Mater Hospitals, Brisbane, Australia

13. Stanford Diabetes Research Center

14. Division of Endocrinology and Diabetes, Department of Pediatrics, School of Medicine, Stanford University, Stanford, California

15. Department of Pediatrics and Adolescent Medicine, Medical University of Graz, Graz, Austria

Abstract

OBJECTIVES Distinct hemoglobin A1c (HbA1c) trajectories during puberty are identified in youth with established type 1 diabetes (T1D). We used data from 3 international registries to evaluate whether distinct HbA1c trajectories occur from T1D onset. METHODS Participants were <18 years old at diagnosis with at least 1 HbA1c measured within 12 months post diagnosis, along with ≥3 duration-year–aggregated HbA1c values over 10 years of follow-up. Participants from the Australasian Diabetes Data Network (n = 7292), the German-Austrian-Luxembourgian-Swiss diabetes prospective follow-up initiative (Diabetes Patienten Verlaufsdokumentation) (n = 39 226) and the US-based Type 1 Diabetes Exchange Clinic Registry (n = 3704) were included. With group-based trajectory modeling, we identified unique HbA1c patterns from the onset of T1D. RESULTS Five distinct trajectories occurred in all 3 registries, with similar patterns of proportions by group. More than 50% had stable HbA1c categorized as being either low stable or intermediate stable. Conversely, ∼15% in each registry were characterized by stable HbA1c >8.0% (high stable), and ∼11% had values that began at or near the target but then increased (target increase). Only ∼5% of youth were above the target from diagnosis, with an increasing HbA1c trajectory over time (high increase). This group differed from others, with higher rates of minority status and an older age at diagnosis across all 3 registries (P ≤ .001). CONCLUSIONS Similar postdiagnostic HbA1c patterns were observed across 3 international registries. Identifying the youth at the greatest risk for deterioration in HbA1c over time may allow clinicians to intervene early, and more aggressively, to avert increasing HbA1c.

Publisher

American Academy of Pediatrics (AAP)

Subject

Pediatrics, Perinatology and Child Health

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