1580-P: Hemoglobin A1c (HbA1c) Trajectories of Youth with Type 1 Diabetes (T1D) over 10 Years Postdiagnosis from Three Continents

Author:

SHERR JENNIFER1,SCHWANDT ANKE1,PHELAN HELEN1,CLEMENTS MARK A.1,HOLL REINHARD W.1,BENITEZ-AGUIRRE PAUL Z.1,MILLER KELLEE1,WOELFLE JOACHIM1,DOVER THOMAS1,MAAHS DAVID M.1,FRÖHLICH-REITERER ELKE1,CRAIG MARIA E.1

Affiliation:

1. New Haven, CT, Ulm, Germany, New Lambton, Australia, Kansas City, MO, Sydney, Australia, Tampa, FL, Erlangen, Germany, Brisbane, Australia, Stanford, CA, Graz, Austria, Westmead, Australia

Abstract

Distinct HbA1c trajectories have previously been identified in youth with established T1D. We used data from 3 international registries to evaluate whether distinct HbA1c trajectories occur from T1D onset. Participants were <18 yrs old at diagnosis and had at least 1 HbA1c measured within 12 months post-diagnosis, along with ≥3 duration-year aggregated HbA1c values over 10 yrs of follow-up. 7,292 participants from the Australasian Diabetes Data Network, 39,226 from the German/Austrian Diabetes Prospective Follow-up, and 3,704 from the U.S. T1D Exchange were included. Group-based modelling identified unique HbA1c trajectories from onset of T1D. Five distinct trajectories occurred in all 3 registries (Figure), with similar patterns of proportion by group. Over 50% had stable HbA1c in or near target. Conversely, ∼15% in each registry were characterized by stable HbA1c >8.0%, and ∼11% had values that began in or near target but then increased. Only ∼5% of youth were suboptimal from diagnosis with an increasing HbA1c. This group differed from others with higher rates of minority status and older age at diagnosis across all 3 registries (p≤0.001). We observed similar post-diagnostic HbA1c patterns across 3 international registries. Identifying youth at greatest risk for deterioration in HbA1c over time may allow clinicians to intervene early to avert increasing HbA1c. Disclosure J. Sherr: Advisory Panel; Self; Bigfoot Biomedical, Cecelia Health. Consultant; Self; Eli Lilly and Company, Lexicon Pharmaceuticals, Inc., Medtronic, Sanofi, T1D Exchange. A. Schwandt: None. H. Phelan: None. M.A. Clements: Consultant; Self; Glooko, Inc. Other Relationship; Self; Glooko, Inc. R.W. Holl: None. P.Z. Benitez-Aguirre: None. K. Miller: None. J. Woelfle: Advisory Panel; Self; Novo Nordisk A/S. T. Dover: None. D.M. Maahs: Advisory Panel; Self; Eli Lilly and Company, Insulet Corporation, Medtronic, Novo Nordisk A/S. Consultant; Self; Abbott, Sanofi. Research Support; Self; Bigfoot Biomedical, Dexcom, Inc., Roche Diabetes Care, Tandem Diabetes Care. E. Fröhlich-Reiterer: None. M.E. Craig: None. Funding German Centre for Diabetes Research (FKZ82DZD01402); German Diabetes Association; European Foundation for the Study of Diabetes; INNODIA; The Leona M. and Harry B. Helmsley Charitable Trust

Publisher

American Diabetes Association

Subject

Endocrinology, Diabetes and Metabolism,Internal Medicine

Cited by 3 articles. 订阅此论文施引文献 订阅此论文施引文献,注册后可以免费订阅5篇论文的施引文献,订阅后可以查看论文全部施引文献

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3