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Infant and toddler type 1 diabetes: complications after 20 years' duration
Silvana Salardi1, Massimo Porta, Giulio Maltoni
1Department of Pediatrics, S.Orsola-Malpighi Hospital, University of Bologna, Bologna, Italy. silvana.salardi@unibo.it
Insights
Early diabetes diagnosis in toddlers may protect against diabetic retinopathy (DR), but poor metabolic control negates this benefit. Pubertal onset increases DR risk, potentially linked to blood pressure.
Area of Science:
- Endocrinology
- Ophthalmology
- Pediatrics
Background:
- Type 1 diabetes onset timing influences long-term complication risk.
- Understanding the impact of prepubertal versus pubertal diabetes onset is crucial for managing diabetic complications.
Purpose of the Study:
- To compare the effect of prepubertal diabetes duration on complication occurrence.
- To evaluate diabetic retinopathy (DR) and other complications based on diabetes onset during prepuberty versus puberty.
Main Methods:
- Multicenter study of 105 patients (aged 16-40.3 years) divided into prepubertal (n=53) and pubertal (n=52) onset groups.
- Assessed retinal photographs, urinary albumin excretion (UAE), blood pressure (BP), and lifetime HbA(1c).
Main Results:
- Higher prevalence of any-grade DR (71% vs. 40%) and mild-to-severe DR (P=0.005) in pubertal onset patients.
- No significant difference in abnormal UAE between groups.
- Elevated lifetime HbA(1c) in prepubertal onset patients with moderate-to-severe DR (P < 0.01).
Conclusions:
- Long prepubertal diabetes duration may offer protection against DR, especially with good metabolic control.
- Pubertal onset is associated with higher DR risk, potentially influenced by factors like BP.
- Metabolic control significantly impacts DR risk, particularly in those with early-onset diabetes.
Objective:
To compare the effect of the prepubertal duration of diabetes on the occurrence of complications in two groups of patients after the same number of years of the disease.
Research Design And Methods:
This multicenter study enrolled 105 patients aged 16-40.3 years; 53 were prepubertal at diagnosis (aged 0-3) and 52 were pubertal (Tanner stage) and aged 9-14.9. The mean duration of disease was 19.8 and 19.5 years for prepubertal and pubertal patients, respectively. In all patients, retinal photographs were taken and centrally graded. Urinary albumin excretion (UAE; 86 case subjects), blood pressure (BP; 89 case subjects), and lifetime HbA(1c) (72 case subjects) were also evaluated.
Results:
The prevalence of diabetic retinopathy (DR) was higher in pubertal than in prepubertal patients, both for any grade DR (71 vs. 40%, P = 0.002) and for mild or more severe DR (P = 0.005). The prevalence of abnormal UAE was not different in the two groups. Hypertension was found only in three patients, all pubertal at diagnosis. In the small group with moderate-to-severe DR, lifetime HbA(1c) levels, as percentages above the upper normal reference value, were higher (P < 0.01) in prepubertal than in pubertal patients.
Conclusions:
If diabetes is diagnosed in infants or toddlers and the prepubertal duration of diabetes is very long, the patients seem to be protected against DR. This protection disappears if lifetime metabolic control is bad. Instead, when onset is at puberty, the DR risk is higher and less dependent on metabolic control and may be influenced by age-related factors, such as BP.
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