Long-Term Results of Long-Acting Somatostatin Analog Therapy in Children with Congenital Hyperinsulinism

Background and objectives: Congenital hyperinsulinism (CHI) is a rare condition caused by dysregulation of pancreatic insulin secretion, leading to severe hypoglycemia in children. In diazoxide-unresponsive patients, somatostatin analogs are recommended as a treatment option. The aim of the present study was to evaluate the clinical characteristics, growth patterns, side effect profiles, and long-term follow-up of CHI patients who received octreotide long-acting release (octreotide-LAR) therapy. Methods: In the study, data from 23 CHI patients (F/M: 9/14) who received octreotide-LAR therapy between 2010 and 2025 were collected retrospectively. Data regarding glycemic control, growth parameters, and treatment-related adverse events were collected. The initial dose of octreotide-LAR was calculated as the total monthly dose of short-acting octreotide and was thereafter adjusted based on blood glucose monitoring results. Results: quartiles: 9-24) months, and the mean treatment duration was 71.6±38.2 months (min-max: 7-162). Initial dose was calculated as total monthly dose of short acting octreotide which was adjusted per blood glucose monitoring results. Mean growth velocity during treatment was 6.4±1.1 cm/year with no concern of negative growth outcome. Neurodevelopmental delay was observed in 10 patients (43.4%). Apart from gallstones in three patients and mild, transiently elevated liver enzyme levels in six patients, no serious treatment-related side effects were observed. Conclusion: In our cohort, long-term octreotide-LAR therapy achieved normoglycemia in the majority of patients without negativegrowth outcome. Transient elevations in liver enzymes and cholelithiasis were the most frequently observed side effects, indicating a safety profile comparable to that of short-acting octreotide. These results suggested that octreotide-LAR therapy is an effective and safe treatment option for diazoxide-unresponsive patients with CHI.

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Journal
Journal of Clinical Research in Pediatric Endocrinology
Published
2026-08-20
DOI
https://doi.org/10.4274/jcrpe.galenos.2026.2026-3-12
Primary Topic
Hyperglycemia and glycemic control in critically ill and hospitalized patients
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article
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article

Long-Term Results of Long-Acting Somatostatin Analog Therapy in Children with Congenital Hyperinsulinism

Funda Feryal Taş, Mehmet Nuri Özbek, Hüseyin Demirbilek, Şervan Özalkak et al.
Journal of Clinical Research in Pediatric Endocrinology
Hyperglycemia and glycemic control in critically ill and hospitalized patients
article

Long-Term Results of Long-Acting Somatostatin Analog Therapy in Children with Congenital Hyperinsulinism

Funda Feryal Taş, Mehmet Nuri Özbek, Hüseyin Demirbilek, Şervan Özalkak, Ruken Yıldırım, EDİP ÜNAL, Amine Aktar Karakaya
article en

Abstract

Background and objectives: Congenital hyperinsulinism (CHI) is a rare condition caused by dysregulation of pancreatic insulin secretion, leading to severe hypoglycemia in children. In diazoxide-unresponsive patients, somatostatin analogs are recommended as a treatment option. The aim of the present study was to evaluate the clinical characteristics, growth patterns, side effect profiles, and long-term follow-up of CHI patients who received octreotide long-acting release (octreotide-LAR) therapy. Methods: In the study, data from 23 CHI patients (F/M: 9/14) who received octreotide-LAR therapy between 2010 and 2025 were collected retrospectively. Data regarding glycemic control, growth parameters, and treatment-related adverse events were collected. The initial dose of octreotide-LAR was calculated as the total monthly dose of short-acting octreotide and was thereafter adjusted based on blood glucose monitoring results. Results: quartiles: 9-24) months, and the mean treatment duration was 71.6±38.2 months (min-max: 7-162). Initial dose was calculated as total monthly dose of short acting octreotide which was adjusted per blood glucose monitoring results. Mean growth velocity during treatment was 6.4±1.1 cm/year with no concern of negative growth outcome. Neurodevelopmental delay was observed in 10 patients (43.4%). Apart from gallstones in three patients and mild, transiently elevated liver enzyme levels in six patients, no serious treatment-related side effects were observed. Conclusion: In our cohort, long-term octreotide-LAR therapy achieved normoglycemia in the majority of patients without negativegrowth outcome. Transient elevations in liver enzymes and cholelithiasis were the most frequently observed side effects, indicating a safety profile comparable to that of short-acting octreotide. These results suggested that octreotide-LAR therapy is an effective and safe treatment option for diazoxide-unresponsive patients with CHI.

Journal of Clinical Research in Pediatric Endocrinology
Dicle University (TR), Mardin Artuklu University (TR), Diyarbakır Gazi Yaşargil Eğitim ve Araştırma Hastanesi (TR), Children's Research Hospital (JP), Hacettepe University (TR)
Good health and well-being
Openalex Percentile: Top 10%
Hyperglycemia and glycemic control in critically ill and hospitalized patients
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