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Approach to Diagnosing a Pediatric Patient With Severe Insulin Resistance in Low- or Middle-income Countries
Alise A van Heerwaarde1, Renz C W Klomberg1, Conny M A van Ravenswaaij-Arts1,2
1Department of Pediatrics, Academic Pediatric Center Suriname, Academic Hospital Paramaribo, Paramaribo, Suriname.
Insights
Diagnosing insulin-resistant diabetes mellitus in children is crucial for effective treatment. A detailed medical history and physical exam can identify severe insulin resistance, even in resource-limited settings.
Area of Science:
- Pediatric Endocrinology
- Metabolic Disorders
Background:
- Diabetes mellitus (DM) in children often stems from impaired insulin secretion (Type 1 DM).
- Increased insulin resistance presents a distinct challenge, with higher insulin needs (>2.0 U/kg/day) signifying severe cases.
- Early diagnosis of severe insulin resistance is vital for targeted therapies and preventing complications.
Observation:
- A case study of a Surinamese adolescent with severe insulin-resistant DM revealed autosomal recessive congenital generalized lipodystrophy (Berardinelli-Seip syndrome).
- Many disorders causing severe insulin resistance in pediatric patients require advanced diagnostics, often unavailable in low- and middle-income countries.
- Clinical presentation and physical examination are key to identifying insulin-resistant DM.
Findings:
- A systematic approach, prioritizing medical history and physical examination, can accurately diagnose insulin-resistant DM in children.
- This diagnostic strategy is particularly relevant for resource-limited healthcare settings.
- The case highlights the importance of considering rare genetic disorders like Berardinelli-Seip syndrome.
Implications:
- This approach facilitates early and accurate diagnosis of insulin-resistant DM in diverse healthcare settings.
- It enables timely initiation of appropriate management strategies for pediatric patients with severe insulin resistance.
- Improved diagnostic accessibility can lead to better outcomes and reduced long-term complications of pediatric diabetes.
Abstract:
Diabetes mellitus (DM) in children is most often caused by impaired insulin secretion (type 1 DM). In some children, the underlying mechanism for DM is increased insulin resistance, which can have different underlying causes. While the majority of these children require insulin dosages less than 2.0 U/kg/day to achieve normoglycemia, higher insulin requirements indicate severe insulin resistance. Considering the therapeutic challenges in patients with severe insulin resistance, early diagnosis of the underlying cause is essential in order to consider targeted therapies and to prevent diabetic complications. Although rare, several disorders can attribute to severe insulin resistance in pediatric patients. Most of these disorders are diagnosed through advanced diagnostic tests, which are not commonly available in low- or middle-income countries. Based on a case of DM with severe insulin resistance in a Surinamese adolescent who was later confirmed to have autosomal recessive congenital generalized lipodystrophy, type 1 (Berardinelli-Seip syndrome), we provide a systematic approach to the differential diagnosis and work-up. We show that a thorough review of medical history and physical examination generally provide sufficient information to diagnose a child with insulin-resistant DM correctly, and, therefore, our approach is especially applicable to low- or middle-income countries.
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