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Published on: November 16, 2011
Idiopathic postprandial hyperinsulinaemic hypoglycaemia
Insights
Idiopathic postprandial hyperinsulinaemic hypoglycaemia (PPHH) in children is rare. Diagnosis requires a prolonged oral glucose tolerance test (OGTT), and while acarbose shows promise, frequent feeding alone is insufficient for management.
Area of Science:
- Pediatric Endocrinology
- Metabolic Disorders
- Clinical Research
Background:
- Idiopathic postprandial hyperinsulinaemic hypoglycaemia (PPHH) is infrequently documented in pediatric populations.
- This study focuses on characterizing PPHH in children, including its clinical presentation, diagnostic approaches, and therapeutic strategies.
Purpose of the Study:
- To describe the clinical features, diagnostic methods, and management outcomes of pediatric patients diagnosed with PPHH.
- To evaluate the efficacy of prolonged oral glucose tolerance tests (OGTT) in diagnosing PPHH in children.
Main Methods:
- A cohort of six pediatric patients with PPHH was studied at a single tertiary center.
- Diagnostic tools included 24-hour blood glucose monitoring, diagnostic fasting tests, and prolonged oral glucose tolerance tests (OGTT) or mixed meal (MM) tests.
Main Results:
- All patients exhibited symptomatic hypoglycemia after 120 minutes during prolonged OGTT, accompanied by detectable serum insulin levels.
- Acarbose demonstrated efficacy in glycemic and symptom control for some patients but was limited by side effects; diazoxide was beneficial in one case.
- Management with frequent feeds alone did not resolve hypoglycemia during prolonged OGTT/MM tests.
Conclusions:
- Prolonged OGTT is essential for diagnosing PPHH in pediatric cases.
- Acarbose can be beneficial for PPHH in children, though tolerance may be an issue.
- The etiology of PPHH in the studied pediatric cohort remains undetermined.
Background:
Idiopathic postprandial hyperinsulinaemic hypoglycaemia (PPHH) has rarely been reported in the paediatric age. The objective of this study was to describe the clinical characteristics, diagnosis and management in a group of children with PPHH.
Methods:
Six children (three females) with a mean follow-up of 3.5±3.0 years at a single tertiary paediatric hospital. All had 24-h blood glucose monitoring, diagnostic fast and prolonged oral glucose tolerance test (OGTT). Follow-up included: 24-h blood glucose monitoring or continuous glucose monitoring system, prolonged OGTT and/or mixed meal (MM) test.
Results:
Age at diagnosis ranged from 5.4 to 15.7 years and auxology parameters were within normal range in all subjects. All the children had a normal fasting tolerance for age. Prolonged OGTT demonstrated symptomatic hypoglycaemia after 120 min in all the patients with simultaneous detectable serum insulin concentration. Acarbose was tried in three patients, having a positive effect on glycaemic and symptom control, but due to side effects, only two patients continued acarbose in the long run. Diazoxide proved to be beneficial in one patient. The rest of the patients were managed with frequent feeds but despite this, prolonged OGTT/MM demonstrated on-going PPHH.
Conclusions:
Prolonged OGTT is necessary to diagnose PPHH in children. Acarbose is beneficial in children with PPHH, although not well tolerated. Patients managed exclusively on frequent feeds demonstrated persistent hypoglycaemia on OGTT. The underlying cause of the PPHH in these patients remains unknown.
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