Cited by 40Adrenal Hormones and DisordersSexual Differentiation and DisordersMetabolism and Genetic Disorders

Frequency of hypoglycemia in children with adrenal insufficiency

Artavia-Loria, E., Chaussain, J.L., Bougnères, P.F., Job, J.C.·1986·Acta Endocrinologica

Abstract

The frequency of hypoglycemia in 165 children with primary adrenal insufficiency, 118 of whom had Congenital Adrenal Hyperplasia and 47 Addison's Disease, was 18%. Half of the hypoglycemic episodes occurred in the neonatal period. Hypoglycemia was isolated in 13 children, revealing the disease in 4 newborns with Congenital Adrenal Hypoplasia and in a boy with 11 B Hydroxylase deficiency. Basal plasma cortisol levels were significantly lower in those of subjects who experienced hypoglycemia (47.1 +/- 28.6 ng/ml vs. 106.0 +/- 86.6 ng/ml, p less than 0.001). A significant correlation (p less than 0.001) was found between the plasma concentration of glucose and cortisol at time of hypoglycemia.

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Crossref · 10.1530/acta.0.112s275

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  • Children and infants with primary adrenal insufficiency who experienced hypoglycaemia had a significantly lower basal cortisol level.

    “Those who experienced hypoglycaemia had a significantly lower basal cortisol level.”

    From Hypoglycaemia in adrenal insufficiency (2023) · cites this paper as [38]

  • In a study conducted in France, 30 out of 165 (18%) children and infants with primary adrenal insufficiency experienced hypoglycaemic episodes.

    “In children, a study conducted in France reported 30 out of 165 (18%) children and infants with PAI experienced hypoglycaemic episodes.”

    From Hypoglycaemia in adrenal insufficiency (2023) · cites this paper as [38]

  • All hypoglycaemic episodes in that French study were associated with prior fasting or poor oral intake due to vomiting or viral illness.

    “Additionally, all of these hypoglycaemic episodes were associated with prior fasting or poor oral intake due to vomiting or viral illness (38).”

    From Hypoglycaemia in adrenal insufficiency (2023) · cites this paper as [38]

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Authors
Artavia-Loria, E., Chaussain, J. L., Bougnères, P. F., & Job, J. C.
Affiliations
Hôpital Saint-Vincent-de-Paul (FR)
Venue
Acta Endocrinologica
Published
1986-12
Volume
113
Issue
4_Suppl
Pages
S275-S278
ISSN
  • 0804-4643 (ISSN-L)
  • 1479-683X
OpenAlex
W2107961995
Cited by
40
References
0
Citations by year
2025: 1 · 2023: 2 · 2021: 3 · 2020: 1 · 2017: 2 · 2016: 1 · 2015: 3 · 2014: 2 · 2012: 2
FWCI
0.00
Type
journal article
Language
en
Open access
closed
Locations
  • European Journal of Endocrinology (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Adrenal Hormones and Disorders
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Sexual Differentiation and Disorders
  • Life Sciences › Biochemistry, Genetics and Molecular Biology › Clinical Biochemistry › Metabolism and Genetic Disorders
Keywords
hypoglycemia, Addison's disease, congenital adrenal hyperplasia, congenital adrenal hypoplasia, 11beta-hydroxylase deficiency, plasma cortisol, neonatal hypoglycemia, children
MeSH terms
Addison Disease, Adolescent, Adrenal Insufficiency, Adrenal Hyperplasia, Congenital, Child, Child, Preschool, Humans, Hydrocortisone, Hypoglycemia, Infant, Infant, Newborn

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