scholarly journals Evaluation of Children with Type 1 Diabetes Mellitus in terms of Overweight / Obesity in Tertiary Care Hospital

Author(s):  
Eda Çelebi Bitkin ◽  
Cengiz Kara ◽  
Gülay Can Yılmaz ◽  
Jamala Mammadova ◽  
Hasan Murat Aydın

Abstract Objective: Obesity was once a rare problem in Type 1 diabetes mellitus, but is a growing problem today. The aim of our study is to determine the frequency of overweight / obesity at the time of diagnosis and during follow-up in children with type 1 diabetes mellitus as well as review the conditions that may accompany. Methods: 315 patients with type 1 diabetes mellitus were retrospectively analyzed. The patients were divided into two groups according to the last examination as normal weight and overweight / obese. The two groups were compared in terms of age at diagnosis, gender, birth weight, family history, anthropometric measurements, insulin dose used and blood pressure measurements, and insulin, c-peptide, hemoglobin A1c, triglyceride, and high-density lipoprotein levels at the time of diagnosis and follow-up. Results: The prevalence of overweight / obese in all patients was 4.8% at the time of diagnosis, while it was 9.8% at the last examination. The height, weight and BMI SD scores and c-peptide levels at the time of diagnosis of the overweight / obese group were higher than those with normal weight (p <0.001 and p = 0.008, respectively). The frequency of dyslipidemia and hypertension was higher in the overweight / obese group than in the normal weight group [18.2% versus 5% (p = 0.015) and 10% versus 1.5% (p = 0.003), respectively]. Conclusion: In our study, the fact that the overweight / obese group had higher BMI and c-peptide and lower HDL values at the time of diagnosis can be evaluated as indicators that insulin resistance syndrome can accompany T1DM from the beginning (double diabetes). When determining the treatment and follow-up strategies of patients with type 1 diabetes mellitus, considering the risk of obesity and taking the necessary precautions is very important in terms of morbidity.

Author(s):  
Eda Celebi Bitkin ◽  
Cengiz Kara ◽  
Gülay Can Yılmaz ◽  
Jamala Mammadova ◽  
Hasan Murat Aydın

Abstract Objectives Obesity is a growing problem in type 1 diabetes mellitus (T1DM) today. The aim of our study is to determine the frequency of overweight/obesity at the time of diagnosis and during follow-up in children with T1DM as well as review the conditions that may accompany. Methods A total of 315 patients with T1DM were retrospectively analyzed. The patients were divided into two groups as normal weight and overweight/obese. The two groups were compared in terms of age at diagnosis, birth weight, anthropometric measurements, insulin dose used and blood pressure measurements, and insulin, c-peptide, hemoglobin A1c, triglyceride, and high-density lipoprotein levels at the time of diagnosis and follow-up. Results The height, weight and body mass index standard deviation (BMI SD) scores, and c-peptide levels at the time of diagnosis of the overweight/obese group were higher than those with normal weight (p<0.001 and p = 0.008, respectively). The frequency of dyslipidemia and hypertension was higher in the overweight/obese group than in the normal weight group [18.2 vs. 5% (p = 0.015) and 10 vs. 1.5% (p = 0.003), respectively]. Conclusions In our study, the fact that the overweight/obese group had higher BMI and c-peptide and lower HDL values at the time of diagnosis can be evaluated as indicators that insulin resistance syndrome can accompany T1DM from the beginning (double diabetes). When determining the treatment and follow-up strategies of patients with T1DM, considering the risk of obesity and taking the necessary precautions is very important in terms of morbidity.


2021 ◽  
Vol 15 (11) ◽  
pp. 3340-3342
Author(s):  
Irum Rafique ◽  
Roshia Parveen ◽  
Zubair Khoso ◽  
Shazia Mahar ◽  
Versha Rani ◽  
...  

Introduction: Cardiac arrhythmias and arrest have been described in children with diabetic ketoacidosis and generally have been presumed to be caused by electrolyte abnormalities. The rationale of this study was to assess the role and importance of ECG monitoring, as a simple, quick, non-invasive and readily available tool in the diagnosis and confirmation of hypokalemia and hyperkalemia in patients with DKA in the Emergency Department Objective: To Assess the Frequency of electrocardiographic changes in Type-1 diabetes mellitus children with diabetic ketoacidosis presenting to tertiary care hospital, Karachi. Materials and Methods: This retrospective cross sectional study was carried out at the department of pediatric medicine, NICH Karachi. At the time of presentation, the standard 12-lead ECG was recorded by a single pediatric cardiologist having more than 2 years of experience, QT and RR intervals were measured. Three separate measurements were obtained from each ECG, and the mean of these measurements was used as the value for QTC. QTC of at least 0.45s (450ms) was considered as prolonged QTC. QTD was also assessed at the same time and QTD>50 ms was considered as prolonged QTD. Results: One hundred cases of T1DM with DKA were included in this study. Average age of children was 7.9 ±3.5 years (Min – Max = 0.5 – 14 years), male to female ratio was 1: 0.96. Prolong QTc and QTd interval was observed in (56%) and (38%) children respectively, Mean (±SD) QTc and QTd interval was 449.4 ±36.6 mc and 39.3 ±16.1 mc respectively. While ECG changes were found in (58%) cases. Association between ECG changes and the cases with higher RBS (>350 mg/dl) was statistically significant 81 (81%) cases with ECG changes had higher RBS (p<0.0001) while ECG changes were statistically similar in both age groups and gender (p-values > 0.05). Conclusion: The frequency of ECG changes was higher in T1DM children with diabetic ketoacidosis. ECG changes was significantly associated with higher RBS (>350 mg/dl). Key words: T1DM, Diabetic Ketoacidosis, ECG, QTc, QTd


2015 ◽  
Vol 36 (2) ◽  
pp. 146-149 ◽  
Author(s):  
Ayyagari Mythili ◽  
K. Dileep Kumar ◽  
B. Vivekananda ◽  
K. A. V. Subrahmanyam

Blood ◽  
2014 ◽  
Vol 124 (21) ◽  
pp. 1191-1191
Author(s):  
Olga Graciela Cantú-Rodríguez ◽  
Fernando Lavalle-Gonzalez ◽  
Miguel Angel Herrera-Rojas ◽  
Cesar H Gutiérrez-Aguirre ◽  
Consuelo Mancías-Guerra ◽  
...  

Abstract Introduction Type 1 diabetes mellitus (T1DM) is a disease characterized by the attack of pancreatic islet B cells by anti-glutamic acid decarboxylase (GAD) antibodies.1 In the search for a solution, Voltarelli et al. performed peripheral blood autologous stem cells transplant (PBASCT) in patients with newly diagnosed T1DM with encouraging results.2,3 These results have been replicated.4,5 Intensive conditioning using 200 mg/kg of cyclophosphamide plus antithymocyte globulin employed are not without serious risk and several complications have occurred including one death, extended hospital management and higher costs.3,6 Therefore, we decided to carry out an PBASCT, using a less costly and outpatient- simplify method.7,8 Patients and Methods This phase 3, single-arm study was performed at Hospital Universitario in Monterrey, México. Between January 2010 and July 2013, we included patients within first 3 months of type 1 diabetes diagnoses, 8 to 25 years old, with positive antibodies anti GAD, C peptide levels > 1.0 ng/mL, with or without previous ketoacidotic crisis. Ethics committee approved and written informed consent was obtained (www.clinicaltrials.gov as NCT01121029). The objectives were to determine baseline and 3-month serum levels of C-peptide, glycated hemoglobin (HbA1c), anti-GAD, quantify the insulin levels needed during the follow-up period, the morbidity associated with the procedure and the need for inhospital management. PBASCT was performed at the outpatient setting. Stem cells were mobilized using CFM 1.5 g/m2 I.V./day, 2 consecutive days, GCS-F , 10 µg/kg/day 6 days. In All patients we collected at least 2.0 x 106 CD34+ cells/kg. The conditioning consisted in CFM 500 mg/m2/day IV + fludarabine 30 mg/m2/day PO for 4 days. Cells were infused 24 hours after the last dose of chemotherapy. Ciprofloxacin (500 mg/bid), fluconazole (100 mg/qd), and acyclovir (400 mg/bid) were prescribed to all patients until the graft was reached. After the 3 months of follow-up, patients were categorized in 3 groups: Complete responders (CR) defined as total independence of insulin , non-responders (NR) those achieving <10% reduction in insulin requirements and partial responders (PR) those achieving a reduction of 11 to 90% of insulin. Results Fifteen patients were included, 6 women and 9 men. Mean time from diagnosis was 80.06 days (SD ± 44.81). The mean AUC of the C-peptide level was 283.28 (SD 213.58). Baseline measurements of anti-GAD and HbA1c showed means of 10.42 U/mL (SD ± 13.26) and 7.94% (SD ± 1.93%), respectively. A mean of 12.12 x 106 CD34+ (SD ± 8.2) was obtained. A statistically significant difference was found in the number of CD34+ cells collected between both sexes. In males a mean of 15.84x106/kg was obtained versus 6.54x106/kg in the female subgroup (p = 0.026). The myeloid engraftment was noticed in a median of 14 days (range 11-20 days) and the lower platelet count was 63x106/ml. Grade I-II adverse events occurs in 40% and were mainly nausea, vomiting, fever, alopecia and one case of hemorrhagic cystitis that resolved rapidly. Four patients developed fever during the period of neutropenia, and all improved with oral antibiotics and without hospitalization. Transplant related mortality at 100 days was 0%. A median follow-up of patients included in this analysis was 441 days (148-1261). Anti-GAD titers were reduced overall by 93.83% (p = 0.016). HbA1c values were modified downward by 15.01%, (p = 0.093). A1c levels showed a mean decrease of 0.87% in the 3 months of study. Overall, the daily insulin requirements decreased from 0.41 U/kg to 0.32 U/kg at the third month (p=0.46). Six patients achieved insulin independence. As mentioned, 3 were non-responders, and the rest were partial responders. Conclusion A simplify PBASCT in a outpatient setting is secure and a potential therapeutic strategy for early onset type 1diabetes. Disclosures No relevant conflicts of interest to declare.


2013 ◽  
Vol 172 (12) ◽  
pp. 1581-1585 ◽  
Author(s):  
Maja D. Ješić ◽  
Miloš M. Ješić ◽  
Dejana Stanisavljević ◽  
Vera Zdravković ◽  
Vladislav Bojić ◽  
...  

2019 ◽  
Vol 47 (1) ◽  
pp. 721-726 ◽  
Author(s):  
Michelle T. Alves ◽  
Amanda C. S. Chaves ◽  
Ana Paula M. Almeida ◽  
Ana Cristina Simões e Silva ◽  
Stanley de A. Araújo ◽  
...  

2021 ◽  
Vol 173 ◽  
pp. 108680
Author(s):  
Ricardo Rodrigues ◽  
Isabela Cristina Borges Rossi ◽  
Bruno Franco Rossi ◽  
Débora Cristiane Gomes ◽  
Nilson Penha-Silva

PLoS ONE ◽  
2018 ◽  
Vol 13 (11) ◽  
pp. e0207065 ◽  
Author(s):  
Catherine A. Sullivan ◽  
Jose M. Cacicedo ◽  
Iniya Rajendran ◽  
Devin W. Steenkamp

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