scholarly journals - To: Pundziute - Lycka. A et al. (2002) The incidence of type 1 diabetes has not increased but shifted to a younger age at diagnosis in the 0-34 years group in Sweden 1983-1998. Diabetologia 45: 783-791

Diabetologia ◽  
2002 ◽  
Vol 45 (12) ◽  
pp. 1734-1734
Author(s):  
Wilkin T.
2004 ◽  
Vol 27 (10) ◽  
pp. 913-918 ◽  
Author(s):  
F. Cadario ◽  
◽  
A. Vercellotti ◽  
M. Trada ◽  
M. Zaffaroni ◽  
...  

2021 ◽  
Vol 21 (1) ◽  
Author(s):  
Sureka Bhola ◽  
Eleanor M Cave ◽  
Sindeep Bhana ◽  
Nigel J Crowther ◽  
Carolyn J Padoa

Abstract Background Autoantibodies to β-cell specific antigens are markers of type 1 diabetes. The most recently identified autoantibodies are targeted to the zinc transporter 8 (ZnT8) protein located in the membrane of β-cell insulin secretory granules. The prevalence of ZnT8 autoantibodies in newly diagnosed participants with type 1 diabetes has been found to range from 33 to 80 %. Due to the lack of data on the immunological aetiology of type 1 diabetes in African populations, this study aimed to determine the prevalence of ZnT8 autoantibodies in black South Africans with type 1 diabetes and whether ZnT8 autoantibody positivity was associated with age at diagnosis and disease duration. Methods Participants with type 1 diabetes and controls were recruited from the greater Johannesburg area, South Africa. Positivity for ZnT8, GAD65 and IA2 autoantibodies was determined by ELISA. Results Participants with type 1 diabetes (n = 183) and controls (n = 49) were matched for age (29.1 ± 9.53 vs. 27.3 ± 7.29, respectively; p = 0.248). The mean age at diagnosis for participants with type 1 diabetes was 20.8 ± 8.46 years. The prevalence of ZnT8 autoantibody positivity was 17.5 % (32 of 183) in participants with type 1 diabetes with a median disease duration of 7.00 [2.00; 11.0] years. ZnT8 autoantibody prevalence in newly diagnosed participants (< 1 year duration) was 27.3 % (6 of 22). Logistic regression analysis found an association between ZnT8 autoantibody positivity and shorter disease duration (OR: 0.9 (0.81-1.00); p = 0.042). In addition, ZnT8 autoantibody positivity was significantly associated with an increased chance of being GAD65 (OR: 3.37 (1.10–10.3)) and IA2 (OR: 8.63 (2.82–26.4)) autoantibody positive. Multiple regression analysis found no association between ZnT8 autoantibody positivity and age at diagnosis. However, the presence of ≥ 2 autoantibodies was associated with a younger age at diagnosis of type 1 diabetes when compared to participants with ≤ 1 autoantibody (B = -5.270; p = 0.002). Conclusions The presence of ZnT8 autoantibodies was not related to a younger age at diagnosis in black South African patients with type 1 diabetes. However, the greater the numbers of autoantibodies present in an individual the earlier the age at diagnosis. ZnT8 autoantibodies decline with disease duration in the black South African population.


2009 ◽  
Vol 4 (S 01) ◽  
Author(s):  
L Gerber ◽  
M Penna-Martinez ◽  
K Badenhoop ◽  
E Ramos-Lopez

Author(s):  
Andrea K Steck ◽  
Xiang Liu ◽  
Jeffrey P Krischer ◽  
Michael J Haller ◽  
Riitta Veijola ◽  
...  

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 T1D diagnosis in young children. Design Observational study. Setting Academic centers. Participants 57 participants in The Environmental Determinants of Diabetes in the Young (TEDDY) 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 post-diagnosis. Outcome Factors associated with rate of C-peptide decline during the first 2 years post-diagnosis 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 BMI z-scores, female sex, increased number of islet autoantibodies, and IA-2A or ZnT8A positivity at baseline were associated with 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 three months after diagnosis, higher HbA1c became an additional independent factor associated with 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 higher rate of C-peptide decline after T1D diagnosis in young children.


2021 ◽  
Vol 12 ◽  
Author(s):  
Meenal Mavinkurve ◽  
Muhammad Yazid Jalaludin ◽  
Elaine Wan Ling Chan ◽  
Mazidah Noordin ◽  
Nurshadia Samingan ◽  
...  

BackgroundChildren with Type 1 diabetes (T1DM) commonly present in diabetic ketoacidosis (DKA) at initial diagnosis. This is likely due to several factors, one of which includes the propensity for T1DM to be misdiagnosed. The prevalence of misdiagnosis has been reported in non-Asian children with T1DM but not in Asian cohorts.AimTo report the rate of misdiagnosis and its associated risk factors in Malaysian children and adolescents with T1DM.MethodsA retrospective analysis of children with T1DM below 18 years of age over a 10 year period was conducted.ResultsThe cohort included 119 children (53.8% female) with a mean age 8.1 SD ± 3.9 years. 38.7% of cases were misdiagnosed, of which respiratory illnesses were the most common (37.0%) misdiagnosis. The rate of misdiagnosis remained the same over the 10 year period. Among the variables examined, younger age at presentation, DKA at presentation, healthcare professional (HCP) contact and admission to the intensive care unit were significantly different between the misdiagnosed and correctly diagnosed groups (p &lt;0.05).ConclusionMisdiagnosis of T1DM occurs more frequently in Malaysian children &lt;5 years of age. Misdiagnosed cases are at a higher risk of presenting in DKA with increased risk of ICU admission and more likely to have had prior HCP contact. Awareness of T1DM amongst healthcare professionals is crucial for early identification, prevention of DKA and reducing rates of misdiagnosis


Diabetes Care ◽  
2014 ◽  
Vol 38 (3) ◽  
pp. 476-481 ◽  
Author(s):  
Asa K. Davis ◽  
Stephanie N. DuBose ◽  
Michael J. Haller ◽  
Kellee M. Miller ◽  
Linda A. DiMeglio ◽  
...  

2008 ◽  
Vol 9 (4pt1) ◽  
pp. 303-307 ◽  
Author(s):  
Carl J Hochhauser ◽  
Robert Rapaport ◽  
Eyal Shemesh ◽  
James Schmeidler ◽  
Claude M Chemtob

2014 ◽  
Vol 40 (2) ◽  
pp. 167-177 ◽  
Author(s):  
Ariana Chao ◽  
Robin Whittemore ◽  
Karl E. Minges ◽  
Kathryn M. Murphy ◽  
Margaret Grey

2010 ◽  
Vol 64 (Suppl 1) ◽  
pp. A8-A8
Author(s):  
K. Harron ◽  
P. A. McKinney ◽  
R. G. Feltbower ◽  
C. R. Stephenson ◽  
H. J. Bodansky ◽  
...  

2008 ◽  
Vol 40 (1) ◽  
pp. 66-68 ◽  
Author(s):  
D. Pitocco ◽  
E. DiStasio ◽  
A. Crinò ◽  
S. Manfrini ◽  
C. Guglielmi ◽  
...  

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