Glycemic control in youth-onset type 2 diabetes correlates with weight loss.


Journal

Pediatric diabetes
ISSN: 1399-5448
Titre abrégé: Pediatr Diabetes
Pays: Denmark
ID NLM: 100939345

Informations de publication

Date de publication:
11 2020
Historique:
received: 14 05 2020
revised: 19 07 2020
accepted: 28 07 2020
entrez: 26 10 2020
pubmed: 27 10 2020
medline: 21 8 2021
Statut: ppublish

Résumé

To identify risk factors for glycemic failure in youth with type 2 diabetes (T2D). A retrospective review of HbA1c, anthropomorphic measures, medication records, and laboratory studies was performed using registry data from a dedicated pediatric T2D clinic. Latent profile analysis (LPA) was performed to model longitudinal trajectory of HbA1c over 5 years. The registry includes 229 youth with T2D, of whom 80% self-identify as Latinx. The odds ratio (OR) for uncontrolled diabetes 5 years after diagnosis correlated with diagnostic HbA1c, with OR of 2.41 if HbA1c at diagnosis >8.5% (sensitivity 68%, specificity 54%, P = .015). LPA modeling identified three HbA1c profiles: (a) mean HbA1c <8% throughout the 5 years, (b) persistent elevation of mean HbA1c >9%, and (c) mean HbA1c of 12% at diagnosis, rapid decline to 6.4% by 4 to 6 months, and increase to 11% by 18 months. Our analysis of medication regimen showed that, amongst patients treated with metformin, the addition of multiple daily injections (MDI) did not improve HbA1c compared to those on basal insulin. Finally, weight loss over the 1 year after diagnosis correlated with improvement in HbA1c in both subjects prescribed metformin monotherapy, as well as insulin-containing regimen. Youth with T2D exhibit distinct HbA1c profiles. Patients with diagnostic HbA1c >8.5% are at high risk for glycemic failure, irrespective of short-term improvement in HbA1c. Weight management has the potential to improve short-term HbA1c outcome in youth with T2D. Additional studies are needed to determine the role of medication adherence on glycemic control.

Identifiants

pubmed: 33103329
doi: 10.1111/pedi.13093
pmc: PMC8629030
mid: NIHMS1747539
doi:

Substances chimiques

Glycated Hemoglobin A 0
Hypoglycemic Agents 0
Insulin 0
Metformin 9100L32L2N

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

1116-1125

Subventions

Organisme : NCATS NIH HHS
ID : UL1 TR000130
Pays : United States
Organisme : NCATS NIH HHS
ID : UL1 TR001855
Pays : United States

Informations de copyright

© 2020 John Wiley & Sons A/S . Published by John Wiley & Sons Ltd.

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Auteurs

Nancy Chang (N)

The Center for Endocrinology, Diabetes, and Metabolism, Department of Pediatrics, Children's Hospital Los Angeles, Los Angeles, California, USA.
The Saban Research Institute, Children's Hospital Los Angeles, Los Angeles, California, USA.

Mei Yu Yeh (MY)

Biostatistics Core, The Saban Research Institute, Children's Hospital Los Angeles, Los Angeles, California, USA.

Jennifer K Raymond (JK)

The Center for Endocrinology, Diabetes, and Metabolism, Department of Pediatrics, Children's Hospital Los Angeles, Los Angeles, California, USA.
The Saban Research Institute, Children's Hospital Los Angeles, Los Angeles, California, USA.

Mitchell E Geffner (ME)

The Center for Endocrinology, Diabetes, and Metabolism, Department of Pediatrics, Children's Hospital Los Angeles, Los Angeles, California, USA.
The Saban Research Institute, Children's Hospital Los Angeles, Los Angeles, California, USA.

Ji Hoon Ryoo (JH)

Biostatistics Core, The Saban Research Institute, Children's Hospital Los Angeles, Los Angeles, California, USA.
Department of Education, College of Educational Sciences, Yonsei University, Seoul, South Korea.

Lily C Chao (LC)

The Center for Endocrinology, Diabetes, and Metabolism, Department of Pediatrics, Children's Hospital Los Angeles, Los Angeles, California, USA.
The Saban Research Institute, Children's Hospital Los Angeles, Los Angeles, California, USA.

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