- 1School of Medicine, College of Medicine and Health Science, Wollo University, Dessie, Ethiopia
- 2School of Pharmacy, College of Medicine and Health Science, Wollo University, Dessie, Ethiopia
- 3Department of Pharmacy, Asrat Woldeyes Health Science Campus, Debre Berhan University, Debre Berhan, Ethiopia
- 4School of Medicine, Asrat Woldeyes Health Science Campus, Debre Berhan University, Debre Berhan, Ethiopia
Introduction: Type 1 diabetes mellitus is the most common endocrine–metabolic disorder in children and adolescents worldwide. This study aims to determine the metabolic glycemic control levels and predictors among pediatric type 1 diabetes patients.
Methods: An institution-based prospective cross-sectional study was conducted from July 01, 2022 to October 30, 2022 among patients attending pediatric chronic follow-up at Dessie Comprehensive Specialized Hospital, Northeast Ethiopia. Patients on follow-up for more than 3 months and aged under 18 years were enrolled in the study consecutively based on their visits. Data were entered into Epidata version 3.1 and exported to SPSS version 26 for analysis. Bivariate and multivariate analyses were done to identify the factors affecting glycemic control.
Result: Among 203 patients with type 1 diabetes, the average age was 8.72 ± 4.25 years, with the largest group of participants being over 10 years old (77 patients, 37%). The majority of the patients were female, totaling 126 (62.1%), and about 69 (34.0%) were in grades 7–10. Retinopathy, nephropathy, and diabetic ketoacidosis were commonly observed diabetic-related complications in this study. More than half of the patients, 107 (52.7%), had good diabetic control, while 96 (47.3%) had poor diabetic control. Factors significantly associated with poor glycemic control include having diabetes for more than 5 years (aOR: 1.45; 95% CI: 0.47, 0.91), being a third-born child (aOR: 0.22; 95% CI: 0.05, 0.92), having a comorbid disease condition (aOR: 1.84; 95% CI: 0.29, 0.92), and experiencing diabetes-related complications (aOR: 0.26; 95% CI: 0.08, 0.97).
Conclusion: The study found that glycemic control is significantly poor among pediatric patients with type 1 diabetes. As a result, these patients require special attention to prevent the long-term consequences of diabetes.
Introduction
Diabetes is a metabolic condition characterized by chronic hyperglycemia, resulting from either an absolute or a relative deficiency of insulin, impaired insulin action, or both (1, 2). Type 1 diabetes mellitus (T1DM) is a prevalent endocrine–metabolic disorder among children and adolescents globally. In the USA, the prevalence is 190 per 100,000 school-aged children, with annual incidence rates varying from 1.7 per 100,000 in China (3) to 40 per 100,000 in Finland (4). Over the past 30 years, the incidence of T1DM has been increasing globally (3–5); in some African countries, the incidence ranged from 4.4 per 100,000 in Algeria to 20 per 100,000 in Morocco (6). Whereas in sub-Saharan Africa few studies have been conducted, estimates from Sudan indicate an increase in incidence from 9.5 per 100,000 in 1991 to 10.3 per 100,000 in 1999 (7). A study conducted in Ethiopia found that the average HbA1c level among children was 9.7%, with the majority (85.2%) of the children exhibiting poor glycemic control, defined as a serum HbA1c level greater than 7.5% (8).
Glycemic control is the ultimate goal of diabetes management (9, 10). Type 1 diabetes mellitus is associated with serious macrovascular and microvascular complications, such as nephropathy, retinopathy, and neuropathy (11). Due to the risk of hypoglycemia unawareness in children, the American Diabetes Association (ADA) recommends an HbA1c range of 7.5% to 8.5% for children under 6 years old. For children aged 6 to 12 years, an HbA1c level of less than 8% is advised, while for those over 12 years, a level below 7.5% is considered optimal (12). Various target levels for HbA1c have been proposed, with the goal being to achieve the lowest possible HbA1c without raising the risk of hypoglycemia. Currently, the International Society for Pediatric and Adolescent Diabetes (ISPAD) recommends a target HbA1c of less than 7.5% (58 mmol/mol) for all age groups (13).
Different factors may contribute to poor metabolic glycemic control, such as unmet basic food needs, mothers’ low level of education (14), being female, having a greater body mass index, and low medication adherence (15). Additionally, a duration of diabetes >8 years, diabetes complications, and poor self-care behavior were significant predictors of poor glycemic control (16). Factors contributing to poor glycemic control in children with T1DM include insulin dose determination and administration as well as factors such as being separated from their mothers, being over 1 year old, having diabetes for more than 5 years, and having elevated serum triglyceride levels (1).
To prevent complications, it is recommended to begin screening for albuminuria through urine analysis to detect diabetic nephropathy, conduct annual eye examinations for diabetic retinopathy, and screen for peripheral neuropathy starting at the age of 11 for those with 2–5 years of diabetes duration. These screenings should be repeated annually thereafter (17). Despite different strategies being applied to prevent complications, good glycemic control is a crucial parameter (18). This study focused on the level of glycemic control and the factors that predict glycemic control among patients with T1DM.
Methods
Study area and study design
The study was conducted at the South Wollo Dessie Comprehensive Specialized Hospital, located in Dessie, a city in northeastern Ethiopia, 401 km north of Addis Ababa and 476 km east of Bahir Dar. The hospital serves over 10 million people from the South Wollo zone and other regions of Ethiopia. It operates a follow-up clinic three times a week—on Mondays, Wednesdays, and Fridays. A facility-based cross-sectional study was conducted involving all pediatric diabetic patients attending follow-up appointments from July 1, 2022 to October 30, 2022.
Sample size determination and sampling technique
During the study period, 203 pediatric patients with type 1 diabetes met the selection criteria. The study was conducted over four 4-month periods, with the patients returning for follow-up visits every 1 to 3 months. All patients who attended follow-up visits during the study period were included in the study, with the participants selected based on their convenient visit times.
Eligibility criteria
Children and adolescents with diabetes who have been on insulin treatment for ≥3 months of age and age <18 years were included in the study.
Variables of the study
Metabolic–glycemic control, either good or poor control level, is the dependent variable.
Independent variables
Demographic factors: age, sex, address, level of education of the caregiver, occupation of the caregiver, marital status of the caregiver, family history of diabetes, and socioeconomic state of the family.
Disease-related characteristics: age at onset of disease, duration of the disease, type and frequency of insulin injection, presence of comorbidity, diabetic complication, types of insulin, doses of insulin, injection site, and frequency of checkup are independent variables.
Data collection tool and procedures
The patients and caregivers were interviewed, and the patients’ medical records were reviewed to gather relevant clinical information from their charts. A data collection tool was developed to include questions about sociodemographic details and diabetes-related information. Sociodemographic data collected included age, sex, address, primary caregiver, level of parental/caregiver education, and the occupation of the parents/caregivers.
Data on diabetes-related information were collected, including age at diagnosis, condition at initial presentation, duration of illness, insulin regimen, frequency of insulin injections, total daily insulin dose, and number of meals per day. The presence of diabetes-related complications was assessed through the patients’ medical history, physical exams, and relevant investigations. In the diabetes clinic, children were screened for chronic complications according to the screening criteria set by the American Diabetes Association (ADA) (19). Diabetic retinopathy was evaluated using fundus photography to assess for hemorrhages, edema, new vessel formation, and exudates in the eye and was performed by an ophthalmologist at the ophthalmology clinic, which operates on Mondays through Fridays. Diabetic neuropathy was assessed by screening for symptoms and signs of neuropathy, along with a comprehensive foot examination. HbA1c tests were conducted at the DCSH laboratory unit during the patients’ routine follow-up visits. A less stringent HbA1c goal of <7.5% was used to classify patients as having good or poor glycemic control. Specifically, an HbA1c value <7.5% was considered indicative of good glycemic control, while a value ≥7.5% (58 mmol/mol) was regarded as indicative of poor control (13).
Data quality control
The questionnaire was initially developed in English, then translated into Amharic, and subsequently back-translated into English to ensure consistency and accuracy. The language translation was carried out by two research experts familiar with the study area and who were proficient in both the local language and culture. They independently translated the text from English to Amharic and vice versa. A pretest was conducted with 5% of the total sample size at Borumeda Hospital, and necessary changes and modifications were made to the questionnaire based on the feedback from the pretest. Data collectors received 3 days of training on the entire data collection process. During the data collection period, supervisors visited the study sites on each follow-up day to review the completed questionnaires for completeness, accuracy, and clarity.
Data processing and analysis
Data were entered using EpiData version 3.1 for cleaning and then exported to SPSS version 26 for analysis. Descriptive statistics were performed for all variables. Bivariable and multivariable binary logistic regression analyses were used to identify factors associated with glycemic control. Bivariate regression was employed to examine the association between dependent and independent variables. During the bivariate analysis, variables with p-values less than 0.25 were included in the multivariable analysis. The direction and strength of the associations were determined using crude odds ratios and adjusted odds ratios, along with their 95% CIs. In the multivariable analysis, variables with p-values less than 0.05 were considered statistically significant for the outcome variable. Hosmer and Lemeshow’s test was used to assess whether the independent variables adequately predicted the outcome variable. Variables were considered statistically significant if the p-value was less than 0.05. In addition to identifying significant variables, interactions and potential confounders were examined during the model-building process.
Result
A total of 203 patients with type 1 diabetes had an average age of 8.72 ± 4.25 years, with the highest proportion (77, 37%) of participants being above 10 years of age. The majority of the patients were female, with 126 (62.1%) being girls. Approximately 69 (34.0%) of the patients were in grades 7 to 10. About 82 (40.4%) were first-born children, and 186 (91.6%) lived with their parents. Of those, 138 (68.0%) had their mothers as the primary caregivers (Table 1).
Table 1. Sociodemographic characteristics of the study participants in Northeast Ethiopia (N = 203).
Drug and disease characteristics
Most patients (94, 46.3%) were diagnosed with diabetes at ages 5 to 10, while the duration of diabetes for 109 (53.7%) patients ranged from 2 to 5 years. Regarding the initial presentation, around 129 (63.5%) patients presented with various diabetic symptoms at the time of diagnosis. A total of 107 (52.7%) patients achieved adequate metabolic control (HbA1c <7.5%). Among all participants, 142 (70.0%) had regular follow-up visits. Additionally, diabetic-related complications were observed in the participants, with seven (3.4%) having retinopathy, nine (4.4%) with nephropathy, and 10 (4.9%) experiencing diabetic ketoacidosis (Table 2).
Table 2. Disease and drug-related characteristics of the study participants in Northeast Ethiopia (N = 203).
Glycemic control
Among the participants, 107 (52.7%) had good diabetic control, while 96 (47.3%) had poor glycemic control. Poor glycemic control was more prevalent in patients with 2–5 years of diabetes duration, accounting for 52 (25.1%) of the participants (Figure 1).
Predictors of glycemic control
The logistic regression analysis of factors associated with glycemic control revealed that the education level of patients, birth order, education level of the caregiver, duration of diabetes, diabetes-related complications, comorbidities, and daily insulin dose were variables significantly associated with poor glycemic control, with p-values <0.25 (Table 3). All variables that showed significant associations in the bivariate logistic analysis were further analyzed using multivariable logistic regression. In the multivariable analysis, three variables were found to be significantly associated with poor glycemic control: being a third-born child, having diabetes-related complications, and having other comorbid conditions.
Table 3. Predictors of poor glycemic control in the study participants—Northeast Ethiopia (N = 203).
Patients with diabetes for more than 5 years were 1.45 times more likely to experience poor glycemic control compared to those with less than 2 years of diabetes duration. Similarly, the presence of comorbid conditions increased the likelihood of poor glycemic control by 1.84 times. Being the third-born child was associated with 78% higher probability of poor glycemic control compared to being the first-born. Conversely, patients who developed diabetes-related complications had 71.5% lower probability of poor glycemic control (Table 3).
Discussion
The results of this study suggest that in pediatric patients with T1DM, the level of glucose control was determined based on a glycosylated hemoglobin (HbA1c) level of ≥7.5% as indicative of poor control, and efforts were made to identify the factors contributing to poor control. This study assessed the extent of poor glycemic control and identified the factors contributing to it among children with diabetes attending routine follow-ups in northeastern Ethiopia.
According to this study, out of the total sample of 203 participants, 107 (52.7%) had good glycemic control, while 96 (47.3%) had poor glycemic control. This finding was compared with a previous study conducted in Egypt, which reported that 45.8% of the participants had poor glycemic control (20). This figure is lower than the previous study report in Hawasa in southern Ethiopia (83.6%) (18), in Harar in eastern Ethiopia (71.9%) (21), in Addis Ababa, Ethiopia (85.2%) (8), in Sudan (76%) (22), and in Iran (23). However, this figure is slightly higher compared to a finding in northwest Ethiopia (39.3%) (24). The discrepancy in the proportion of patients with poor glycemic control may be attributed to differences in the study setting, study design, sample size, and the level of diabetic care provided. Additionally, factors such as variations in the population served by the study setting, the education level of caregivers, and the availability of resources like insulin may also contribute to this difference.
Focusing on the determinants of poor glycemic control, the birth order of the child, specifically being a third-born, was found to have a significant role in poor glucose control (aOR: 0.22; 95% CI: 0.05, 0.92). Interestingly, being a third-born child appeared to have a protective effect against poor glycemic control. This could be explained by parental caregiving behavior, as parents may become more experienced and attentive in managing diabetes with subsequent children. The increased caregiving practices and attention toward the third child might result in better glycemic control compared to the firstborn.
Patients with diabetes for more than 5 years had an increased probability of poor glycemic control (aOR: 1.45; 95% CI: 0.47, 0.91). This finding is consistent with previous studies, which have suggested that a longer duration of diabetes is associated with a higher likelihood of poor glycemic control in pediatric patients. As the disease progresses, managing blood glucose levels effectively can become more challenging, potentially leading to poorer control over time (8, 25). In addition, the increased duration of diabetes may lead to financial challenges for families, as parents may struggle to afford the cost of medications (such as insulin) and ongoing care. This is supported by the findings of Shibeshi et al., which indicated that families who cannot afford insulin were more likely to have poor glycemic control. Financial constraints can limit access to necessary treatments and regular follow-up care, contributing to suboptimal diabetes management (18). Furthermore, the patients’ and caregivers’ attention on the disease condition may decrease, and they may consider it as a normal condition.
Indeed the presence of comorbid disease conditions (aOR: 1.84; 95% CI: 0.29, 0.92) was significantly associated with poor glycemic control, while diabetes-related complications (AOR: 0.26; 95% CI: 0.08, 0.97) were linked to better glycemic control. This may be explained by the increased attention and care that parents, caregivers, and patients themselves tend to provide once diabetes-related complications such as diabetic ketoacidosis (DKA), retinopathy, and nephropathy develop. The recognition of these serious complications often prompts more diligent management of the disease, resulting in improved glycemic control.
The strengths of the study include its observational design, the involvement of trained data collectors, and a relatively long data collection period. However, the study’s limitations include its single-center, cross-sectional nature, which restricts the generalizability of the findings. Therefore, the researchers suggest that future studies adopt a more robust cohort and follow-up design as well as a multicenter approach. Additionally, exploring other continuous glucose monitoring metrics would help develop stronger scientific evidence.
Conclusion
In conclusion, glycemic control is significantly poor among the pediatric patients with T1DM in this study. The findings indicate that a longer duration of diabetes mellitus and the presence of comorbid disease conditions are associated with poorer glycemic control. Therefore, special attention and focused care are essential for these patients to prevent diabetes-related consequences and complications.
Data availability statement
The raw data supporting the conclusions of this article will be made available by the authors, without undue reservation.
Ethics statement
The studies involving humans were approved by Ethics committee of Wollo University College of Medicine and Health Sciences. The studies were conducted in accordance with the local legislation and institutional requirements. Written informed consent for participation was not required from the participants or the participants’ legal guardians/next of kin in accordance with the national legislation and institutional requirements.
Author contributions
HA: Conceptualization, Methodology, Project administration, Software, Writing – original draft. GG: Data curation, Writing – original draft. ASA: Formal analysis, Writing – original draft. MTK: Methodology, Writing – review & editing. BLE: Methodology, Validation, Software, Project administration, Writing – review & editing.
Funding
The author(s) declare that no financial support was received for the research, authorship, and/or publication of this article.
Conflict of interest
The authors declare that no the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest.
Publisher’s note
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References
1. WHO. Diagnosis of diabetes mellitus and intermediate hyperglycemia: report of a WHO/IDF consultation Vol. 3. Geneva: World Health Organization (2006).
2. Saeedi P, Petersohn I, Salpea P, Malanda B, Karuranga S, Unwin N, et al. Global and regional diabetes prevalence estimates for 2019 and projections for 2030 and 2045: Results from the International Diabetes Federation Diabetes Atlas. Diabetes Res. Clin. pract. (2019) 157:107843. doi: 10.1016/j.diabres.2019.107843
3. Gong C, Meng X, Jiang Y, Wang X, Cui H, Chen X. Trends in childhood type 1 diabetes mellitus incidence in Beijing from 1995 to 2010: a retrospective multicenter study based on hospitalization data. Diabetes Technol. Ther. (2015) 17:159–65. doi: 10.1089/dia.2014.0205
4. Tuomilehto J, Virtala E, Karvonen M, Lounamaa R, Pitkāniemi J, Reunanen A, et al. Increase in incidence of insulin-dependent diabetes mellitus among children in Finland. Int. J. Epidemiol. (1995) 24:984–92. doi: 10.1093/ije/24.5.984
5. Dabelea D, Bell RA, D’Agostino RB Jr, Imperatore G, Johansen JM, Linder B, et al. Incidence of diabetes in youth in the United States. Jama. (2007) 297:2716–24. doi: 10.1001/jama.297.24.2716
6. Ngwiri T, Were F, Predieri B, Ngugi P, Iughetti L. Glycemic control in Kenyan children and adolescents with type 1 diabetes mellitus. Int. J. Endocrinol. (2015) 2015:1–7. doi: 10.1155/2015/761759
7. Swai A, Lutale JL, McLarty DG. Prospective study of incidence of juvenile diabetes mellitus over 10 years in Dar es Salaam, Tanzania. Br. Med. J. (1993) 306:1570–2. doi: 10.1136/bmj.306.6892.1570
8. Fantahun B, Leulseged TW. Glycemic control among children with type 1 diabetes mellitus and its determinants in a resource-limited setting. J. Pediatr. Endocrinol. Metab. (2022) 35:813–7. doi: 10.1515/jpem-2022-0144
9. ADA. Classification and diagnosis of diabetes: standards of medical care in diabetes—2019. Diabetes Care. (2019) 42:S13–28. doi: 10.2337/dc19-S002
10. Imran SA, Agarwal G, HS B, Ross S. Targets for glycemic control. Can. J. diabet. (2018) 42:S42–S6. doi: 10.1016/j.jcjd.2017.10.030
11. Brink SJ. Complications of pediatric and adolescent type 1 diabetes mellitus. Curr. Diabetes Rep. (2001) 1:47–55. doi: 10.1007/s11892-001-0010-1
12. ADA. Children and Adolescents: standard of care in diabetes. Diabetes Care. (2023) 46:S230–S253. doi: 10.2337/dc23-Sint
13. Rewers M, Pihoker C, Donaghue K, Hanas R, Swift P, Klingensmith GJ. Assessment and monitoring of glycemic control in children and adolescents with diabetes. Pediatr. diabet. (2009) 10:71–81. doi: 10.1111/j.1399-5448.2009.00582.x
14. Araujo MB, Mazza CS. Assessment of risk factors of poor metabolic control in type 1 diabetic children assisted in a public hospital in Argentina. Pediatr. diabet. (2008) 9:480–7. doi: 10.1111/j.1399-5448.2008.00388.x
15. Demoz GT, Gebremariam A, Yifter H, Alebachew M, Niriayo YL, Gebreslassie G, et al. Predictors of poor glycemic control among patients with type 2 diabetes on follow-up care at a tertiary healthcare setting in Ethiopia. BMC Res. notes. (2019) 12:1–7. doi: 10.1186/s13104-019-4248-6
16. Oluma A, Abadiga M, Mosisa G, Etafa W. Magnitude and predictors of poor glycemic control among patients with diabetes attending public hospitals of Western Ethiopia. PloS One. (2021) 16:e0247634. doi: 10.1371/journal.pone.0247634
17. Codner E, Acerini CL, Craig ME, Hofer SE, Maahs DM. ISPAD Clinical Practice Consensus Guidelines 2018: limited care guidance appendix. Pediatr. Diabetes. (2018) 19:328–38. doi: 10.1111/pedi.12767
18. Shibeshi MS, Daba AK, Meiso KM, Tadesse BT. Glycemic control among children and adolescents with diabetes in Southern Ethiopia: a cross-sectional study. BMC Endocr Disord. (2022) 22:161. doi: 10.1186/s12902-022-01070-y
19. ADA. Children and adolescents: standards of medical care in diabetes– 2020. Diabetes Care. (2020) 43:S163–S82. doi: 10.2337/dc20-S013
20. Mohammad HA, Farghaly HS, Metwalley KA, Monazea EM, Abd El-Hafeez HA. Predictors of glycemic control in children with Type 1 diabetes mellitus in Assiut-Egypt. Indian J. Endocrinol. Metab. (2012) 16:796–802. doi: 10.4103/2230-8210.100679
21. Habteyohans BD, Hailu BS, Meseret F, Mohammed A, Berhanu Y, Alemu A, et al. Poor glycemic control and its associated factors among children with type 1 diabetes mellitus in Harar, eastern Ethiopia: A cross-sectional study. BMC endocr Disord. (2023) 23:208. doi: 10.1186/s12902-023-01453-9
22. Taha Z, Eltoum Z, Washi S. Predictors of glucose control in children and adolescents with type 1 diabetes: results of a cross-sectional study in Khartoum, Sudan. Open Access Macedonian J. Med. Sci. (2018) 6:2035–9. doi: 10.3889/oamjms.2018.423
23. Ghazaiean M, Najafi B, Zamanfar D, Alipour MJ. Risk factors for suboptimal glycemic control in pediatrics with type 1 diabetes mellitus: a cross-sectional study. Sci. Rep. (2024) 14:7492. doi: 10.1038/s41598-024-57205-9
24. Kidie AA, Ayal BG, Ayele T, Fentie EA, Lakew AM. Poor glycemic control and associated factors among pediatric diabetes mellitus patients in northwest Ethiopia, 2020: facility-based cross sectional retrospective study design. Sci. Rep. (2022) 12:15664. doi: 10.1038/s41598-022-19909-8
Keywords: glycemic control, pediatrics, type 1 DM, northeast, Ethiopia
Citation: Adege H, Getnet G, Ambaye AS, Kassa MT and Endalifer BL (2025) Predictors of glycemic control among type 1 pediatric diabetes patients—Northeast Ethiopia. Front. Clin. Diabetes Healthc. 5:1449641. doi: 10.3389/fcdhc.2024.1449641
Received: 08 July 2024; Accepted: 20 December 2024;
Published: 17 January 2025.
Edited by:
Stavros Liatis, Laiko General Hospital of Athens, GreeceReviewed by:
Silvia Pieralice, Campus Bio-Medico University, ItalyKayla Nguyen, George Washington University, United States
Copyright © 2025 Adege, Getnet, Ambaye, Kassa and Endalifer. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
*Correspondence: Bedilu Linger Endalifer, bGluZ2VyZW5kYWxpZmVyQGdtYWlsLmNvbQ==