“…Based on these two values the presence and duration of PR were determined. PR was defined as a period with insulin requirements of less than 0.5 U/kg/day accompanied by hemoglobin A1c (HbA1c) level of less or equal to 7%; 53 mmol/mol (ISPAD Consensus Guidelines 2018) …”
Background/Objective
The study aimed to analyze the frequency of partial remission (PR) and its association with chosen clinical and laboratory factors among pediatric patients with newly diagnosed type 1 diabetes (T1D). The long‐term effect of PR on chosen parameters was also investigated.
Methods
In 194 patients (95 girls) aged 8.1 ± 4.3 years, we analyzed data at T1D onset: glycemia, pH, C‐peptide, antibodies, weight, and concomitant autoimmune diseases. Anthropometric parameters, daily insulin requirement (DIR), and HbA1c 2 and 4 years after T1D diagnosis were also analyzed. We determined PR based on HbA1c and DIR measurements at least every 3 months.
Results
PR occurred in 59% of patients. Remitters had significantly higher pH (7.33 vs 7.28, P = 0.03), weight SD score (SDS) (0.25 vs −0.24, P = 0.002), and body mass index SDS (0.19 vs −0.66, P = 0.02) compared with non‐remitters. Concomitant diseases correlated negatively with PR. Multivariate analysis indicated only pH at onset was an independent predictor of PR. pH was the most important factor associated with the beginning of PR. There was a positive correlation between the start and duration of PR. Four years after T1D onset remitters had lower HbA1c (7.24% vs 8.05%, 53 vs 63.9 mmol/mol, P < 0.001) and DIR (0.81 vs 1.08, P = 0.005).
Conclusions
PR occurred quite often and developed more frequently in children with higher: weight and BMI SDS, but the main factor influencing PR presence and duration was higher pH at T1D onset. There was a beneficial impact of PR on HbA1c and DIR after 4 years of treatment.
“…Based on these two values the presence and duration of PR were determined. PR was defined as a period with insulin requirements of less than 0.5 U/kg/day accompanied by hemoglobin A1c (HbA1c) level of less or equal to 7%; 53 mmol/mol (ISPAD Consensus Guidelines 2018) …”
Background/Objective
The study aimed to analyze the frequency of partial remission (PR) and its association with chosen clinical and laboratory factors among pediatric patients with newly diagnosed type 1 diabetes (T1D). The long‐term effect of PR on chosen parameters was also investigated.
Methods
In 194 patients (95 girls) aged 8.1 ± 4.3 years, we analyzed data at T1D onset: glycemia, pH, C‐peptide, antibodies, weight, and concomitant autoimmune diseases. Anthropometric parameters, daily insulin requirement (DIR), and HbA1c 2 and 4 years after T1D diagnosis were also analyzed. We determined PR based on HbA1c and DIR measurements at least every 3 months.
Results
PR occurred in 59% of patients. Remitters had significantly higher pH (7.33 vs 7.28, P = 0.03), weight SD score (SDS) (0.25 vs −0.24, P = 0.002), and body mass index SDS (0.19 vs −0.66, P = 0.02) compared with non‐remitters. Concomitant diseases correlated negatively with PR. Multivariate analysis indicated only pH at onset was an independent predictor of PR. pH was the most important factor associated with the beginning of PR. There was a positive correlation between the start and duration of PR. Four years after T1D onset remitters had lower HbA1c (7.24% vs 8.05%, 53 vs 63.9 mmol/mol, P < 0.001) and DIR (0.81 vs 1.08, P = 0.005).
Conclusions
PR occurred quite often and developed more frequently in children with higher: weight and BMI SDS, but the main factor influencing PR presence and duration was higher pH at T1D onset. There was a beneficial impact of PR on HbA1c and DIR after 4 years of treatment.
“…Inclusion criteria were as follows: age at trial onset between 7 and 18 years, diagnosis of T1D according to the ISPAD 2014 guidelines, treatment with insulin pump therapy or basal‐prandial insulin regimen with multiple daily injections (MDI), T1D outside of partial remission phase (defined according to the insulin dose‐adjusted A1C [IDAA1C] definition, being equal to HbA1c (%) + [4 × insulin dose (units/kg/24 h)] and at least >2 years after T1D diagnosis (defined as the first day of insulin therapy) and/or diagnosis of T1D for more than 2 years (based on the first day of insulinotherapy), HbA1c level ≤9.5% during the last control visit. Criteria for exclusion were: patients with non‐T1D, patients not treated with insulin pump therapy or basal‐prandial insulin regimen, history of recurrent severe hypoglycemia, presence of specific co‐morbidities as severe neonatal asphyxia (defined as Apgar score ≤3 after 5 minutes), children born small for gestational age, chronic systemic disease, active malignancy, hypothyroidism, hypopituitarism, developmental delay, bladder dysfunction, obesity (ie, body mass index [BMI] >95th percentile according to Belgian reference charts) intake of drugs interfering with insulin sensitivity (eg, corticosteroids or human recombinant growth hormone), carnitine deficiency, β‐oxidation defect, cardiac malformation, dysrhythmia, or any medical condition not suitable for completing the exercise protocol on a treadmill.…”
Section: Methodsmentioning
confidence: 99%
“…Inclusion criteria were as follows: age at trial onset between 7 and 18 years, diagnosis of T1D according to the ISPAD 2014 guidelines, 19…”
In our pediatric cohort, algorithmic adaptations of insulin doses were associated with better outcomes in terms of postexercise glucose control in patients with CSII therapy but not with MDI treatment.
“…Youth progress through three stages at variable rates: stage 1 is characterized by the presence of β‐cell autoimmunity with normoglycemia and a lack of clinical symptoms, which can last for months to many years, stage 2 is progresses to dysglycemia but remains asymptomatic, and stage 3 is defined as the onset of symptomatic disease . The phases of diabetes are discussed in chapter 3 (add ref) …”
Section: Pathogenesis Of Type 1 Diabetesmentioning
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