Abstract
The data on the congenital hyperinsulinism (CHI) in Asian Indian patients is
limited. Diazoxide is often unavailable in India, which poses challenge in
managing CHI. The study was aimed to present our experience with CHI with a
special focus on the effectiveness and cost-effectiveness of octreotide
long-acting release (OCT-LAR) among diazoxide-responsive CHI. The data of 14
index cases with CHI registered at our center were retrospectively analyzed. The
diagnosis of CHI was based on elevated serum insulin (3.4–32.5
μIU/ml) and C-peptide (0.58–1.98 ng/ml) at the time of
symptomatic hypoglycemia (BG≤41 mg/dl). Fourteen patients (13
males) presented at a median (range) age of 3 (1–270) days, seizures
being the most common mode of presentation (78.6%). Ten patients were
diazoxide-responsive, two were partially responsive, while two were
unresponsive. Genetics was available for eight patients; ABCC8
(n=3, 1 novel) and HADH (n=2, both novel) were the most
commonly mutated genes. OCT-LAR was offered to eight patients including four
with diazoxide-responsive disease and was universally effective. We propose a
cost-effective approach to use OCT-LAR in the management of CHI, which may also
make it more cost-effective than diazoxide for diazoxide-responsive disease.
Five of the 11 (45.5%) patients had evidence of neurological impairment;
notably, two patients with HADH mutations had intellectual disability
despite diazoxide-responsiveness. We report three novel mutations in
CHI-associated genes. We demonstrate the effectiveness of and propose a
cost-effective approach to use OCT-LAR in diazoxide-responsive CHI. Mutations in
HADH may be associated with abnormal neurodevelopmental outcomes
despite diazoxide-responsiveness.
Key words
congenital hyperinsulinemic hypoglycemia -
ABCC8
-
HADH
- diazoxide - octreotide-LAR