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Factors Associated With the Decline of C-Peptide in a Cohort of Young Children Diagnosed With Type 1 Diabetes

Steck, Andrea K. ; Liu, Xiang ; Krischer, Jeffrey P. ; Haller, Michael J. ; Veijola, Riitta LU ; Lundgren, Markus LU ; Ahmed, Simi ; Akolkar, Beena ; Toppari, Jorma and Hagopian, William A. , et al. (2021) In The Journal of clinical endocrinology and metabolism 106(3). p.1380-1388
Abstract

CONTEXT: Understanding factors involved in the rate of C-peptide decline is needed to tailor therapies for type 1 diabetes (T1D). OBJECTIVE: Evaluate factors associated with rate of C-peptide decline after a T1D diagnosis in young children. DESIGN: Observational study. SETTING: Academic centers. PARTICIPANTS: A total of 57 participants from the Environmental Determinants of Diabetes in the Young (TEDDY) study who were enrolled at 3 months of age and followed until T1D, and 56 age-matched children diagnosed with T1D in the community. INTERVENTION: A mixed meal tolerance test was used to measure the area under the curve (AUC) C-peptide at 1, 3, 6, 12, and 24 months postdiagnosis. OUTCOME: Factors associated with rate of C-peptide decline... (More)

CONTEXT: Understanding factors involved in the rate of C-peptide decline is needed to tailor therapies for type 1 diabetes (T1D). OBJECTIVE: Evaluate factors associated with rate of C-peptide decline after a T1D diagnosis in young children. DESIGN: Observational study. SETTING: Academic centers. PARTICIPANTS: A total of 57 participants from the Environmental Determinants of Diabetes in the Young (TEDDY) study who were enrolled at 3 months of age and followed until T1D, and 56 age-matched children diagnosed with T1D in the community. INTERVENTION: A mixed meal tolerance test was used to measure the area under the curve (AUC) C-peptide at 1, 3, 6, 12, and 24 months postdiagnosis. OUTCOME: Factors associated with rate of C-peptide decline during the first 2 years postdiagnosis were evaluated using mixed effects models, adjusting for age at diagnosis and baseline C-peptide. RESULTS: Adjusted slopes of AUC C-peptide decline did not differ between TEDDY subjects and community controls (P = 0.21), although the former had higher C-peptide baseline levels. In univariate analyses combining both groups (n = 113), younger age, higher weight and body mass index z-scores, female sex, an increased number increased number of islet autoantibodies, and IA-2A or ZnT8A positivity at baseline were associated with a higher rate of C-peptide loss. Younger age, female sex, and higher weight z-score remained significant in multivariate analysis (all P < 0.02). At 3 months after diagnosis, higher HbA1c became an additional independent factor associated with a higher rate of C-peptide decline (P < 0.01). CONCLUSION: Younger age at diagnosis, female sex, higher weight z-score, and HbA1c were associated with a higher rate of C-peptide decline after T1D diagnosis in young children.

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organization
publishing date
type
Contribution to journal
publication status
published
subject
keywords
beta cell decline, C-peptide, new onset, pediatric type 1 diabetes, risk factors
in
The Journal of clinical endocrinology and metabolism
volume
106
issue
3
pages
1380 - 1388
publisher
Oxford University Press
external identifiers
  • scopus:85102909181
  • pmid:33035311
ISSN
1945-7197
DOI
10.1210/clinem/dgaa715
language
English
LU publication?
yes
id
515268dd-a12c-4575-9c10-a0676515c74c
date added to LUP
2021-03-31 09:27:41
date last changed
2024-06-15 08:59:29
@article{515268dd-a12c-4575-9c10-a0676515c74c,
  abstract     = {{<p>CONTEXT: Understanding factors involved in the rate of C-peptide decline is needed to tailor therapies for type 1 diabetes (T1D). OBJECTIVE: Evaluate factors associated with rate of C-peptide decline after a T1D diagnosis in young children. DESIGN: Observational study. SETTING: Academic centers. PARTICIPANTS: A total of 57 participants from the Environmental Determinants of Diabetes in the Young (TEDDY) study who were enrolled at 3 months of age and followed until T1D, and 56 age-matched children diagnosed with T1D in the community. INTERVENTION: A mixed meal tolerance test was used to measure the area under the curve (AUC) C-peptide at 1, 3, 6, 12, and 24 months postdiagnosis. OUTCOME: Factors associated with rate of C-peptide decline during the first 2 years postdiagnosis were evaluated using mixed effects models, adjusting for age at diagnosis and baseline C-peptide. RESULTS: Adjusted slopes of AUC C-peptide decline did not differ between TEDDY subjects and community controls (P = 0.21), although the former had higher C-peptide baseline levels. In univariate analyses combining both groups (n = 113), younger age, higher weight and body mass index z-scores, female sex, an increased number increased number of islet autoantibodies, and IA-2A or ZnT8A positivity at baseline were associated with a higher rate of C-peptide loss. Younger age, female sex, and higher weight z-score remained significant in multivariate analysis (all P &lt; 0.02). At 3 months after diagnosis, higher HbA1c became an additional independent factor associated with a higher rate of C-peptide decline (P &lt; 0.01). CONCLUSION: Younger age at diagnosis, female sex, higher weight z-score, and HbA1c were associated with a higher rate of C-peptide decline after T1D diagnosis in young children.</p>}},
  author       = {{Steck, Andrea K. and Liu, Xiang and Krischer, Jeffrey P. and Haller, Michael J. and Veijola, Riitta and Lundgren, Markus and Ahmed, Simi and Akolkar, Beena and Toppari, Jorma and Hagopian, William A. and Rewers, Marian J. and Elding Larsson, Helena}},
  issn         = {{1945-7197}},
  keywords     = {{beta cell decline; C-peptide; new onset; pediatric type 1 diabetes; risk factors}},
  language     = {{eng}},
  number       = {{3}},
  pages        = {{1380--1388}},
  publisher    = {{Oxford University Press}},
  series       = {{The Journal of clinical endocrinology and metabolism}},
  title        = {{Factors Associated With the Decline of C-Peptide in a Cohort of Young Children Diagnosed With Type 1 Diabetes}},
  url          = {{http://dx.doi.org/10.1210/clinem/dgaa715}},
  doi          = {{10.1210/clinem/dgaa715}},
  volume       = {{106}},
  year         = {{2021}},
}