Cited by 21Adrenal Hormones and DisordersGrowth Hormone and Insulin-like Growth FactorsDiabetes Management and Research

Nocturnal hypoglycaemia in ACTH and GH deficient children: role of continuous glucose monitoring

Open access
Cambiaso, Paola, Schiaffini, Riccardo, Pontrelli, Giuseppe, Carducci, Chiara, Ubertini, Graziamaria, Crea, Francesca, Cappa, Marco·2013·Clinical Endocrinology

Abstract

Summary: Objectives: To evaluate the usefulness of continuous glucose monitoring (CGM) to identify nocturnal hypoglycaemia in children affected by combined ACTH and GH deficiency and to optimize the hydrocortisone replacement therapy in these patients. Study design: Eleven patients with ACTH and GH deficiency (five boys and six girls, age 1·6–16·8 years) underwent CGM for 36 h, including two nights. At least two consecutive glucose levels <2·78 m m were considered hypoglycaemic episodes. The differences in age and doses of hydrocortisone and recombinant human growth hormone (rh GH) between children with and without hypoglycaemia were analysed. The percentage of the glucose values <3·33 m m and the mean glucose levels were also evaluated. Results: Continuous glucose monitoring demonstrated nocturnal hypoglycaemia lasting from 30 to 155 min (1·5% of the total monitoring time) in three cases (27%). No statistically significant differences in age and rh GH dose were observed between children with or without hypoglycaemia. Conversely, the difference in the hydrocortisone doses between the patients with and without hypoglycaemia resulted statistically significant (5·9 vs 8·5 mg/m²/day; P = 0·04). Eight patients presented glucose values less than 3·33 m m during 5% of the total monitoring time. Hydrocortisone dose showed significant positive linear relation with mean glucose level (r = 0·79, P = 0·0035) and inverse relation with time lags of glucose levels under 3·33 m m (r = −0·65, P = 0·03). Conclusions: Our study shows that CGM may represent a valuable tool to detect nocturnal asymptomatic hypoglycaemic episodes and optimize the hydrocortisone therapeutic regimen in children with ACTH and GH deficiency.

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Integrity signals

Registry

Crossref · 10.1111/cen.12123

Cites

4 of 4 references verified0 citation errors · 0 not checkable

Statistics

Claims the paper makes

The claims and statistics of this paper haven’t been checked yet.

Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.

A few free checks a day · papers already verified open instantly · results are public

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

  • Due to gastric acids and hepatic first-pass effect, the recommended glucocorticoid treatment in children with primary adrenal insufficiency is slightly higher, ranging between 6-12mg/m2/day.

    “Due to gastric acids and hepatic first-pass effect, the recommended glucocorticoid treatment in children with primary AI is slightly higher, ranging between 6-12mg/m2/day (1, 49).”

    From Hypoglycaemia in adrenal insufficiency (2023) · cites this paper as [49]

    The Introduction (page unavailable) recommends hydrocortisone replacement for children, but specifies 6–8 mg/m²/day for central adrenal insufficiency, not 6–12 mg/m²/day for primary adrenal insufficiency. The cited paper does not give gastric acids or hepatic first-pass metabolism as the reason for a higher dose. (LLM, conf=0.87)

    Experimental — accuracy not yet measured
  • Children with secondary adrenal insufficiency may require a lower daily replacement dose (6-8mg/m2/day).

    “Children with secondary AI may require a lower daily replacement dose (6-8mg/m2/day) (49).”

    From Hypoglycaemia in adrenal insufficiency (2023) · cites this paper as [49]

    The Introduction states that 6–8 mg/m²/day of hydrocortisone is considered an optimal replacement regimen for children with central adrenal insufficiency. It does not establish that this dose is lower than a dose required by another group. The Discussion also notes hypoglycaemia near the lower end of the range and favors 8 mg/m²/day to reduce that risk. (LLM, conf=0.84)

    Experimental — accuracy not yet measured
  • Continuous glucose monitoring in children with combined congenital central adrenal insufficiency and growth hormone deficiency identified severe asymptomatic nocturnal hypoglycaemia (< 2.7 mmol/L) in 3 out of 11 children, with the period of hypoglycaemia ranging from 30 to 150 minutes.

    “CGM in children with combined congenital central adrenal insufficiency and growth hormone deficiency have identified severe asymptomatic nocturnal hypoglycaemia (< 2.7mmol/L) in 3 out of 11 children, with the period of hypoglycaemia ranging from 30 to 150 minutes.”

    From Hypoglycaemia in adrenal insufficiency (2023) · cites this paper as [49]

    The Results report CGM-detected hypoglycaemia in three of 11 children, predominantly in the early morning, and the Discussion describes it as asymptomatic. The cited paper defines the threshold as <2.78 mmol/L and gives a duration of 30–155 minutes, rather than <2.7 mmol/L and 30–150 minutes. (LLM, conf=0.90)

    Experimental — accuracy not yet measured
  • In those children, daily doses of hydrocortisone were significantly lower in the 3 children with hypoglycaemia.

    “On further review, they found that the daily doses of hydrocortisone were significantly lower in the 3 children and resolution of hypoglycaemia was seen when the doses were increased (49).”

    From Hypoglycaemia in adrenal insufficiency (2023) · cites this paper as [49]

  • Resolution of hypoglycaemia was seen when the hydrocortisone doses were increased in those children.

    “On further review, they found that the daily doses of hydrocortisone were significantly lower in the 3 children and resolution of hypoglycaemia was seen when the doses were increased (49).”

    From Hypoglycaemia in adrenal insufficiency (2023) · cites this paper as [49]

Self-check

Percentages, sums and reported differences re-computed from the paper’s own numbers.

The self-check needs the paper’s full text.

Cites

Flagged first, then by citations

Research works printed but not linked: 11

  1. Crown, A. & Lightman, S. (2005) Why is the management of glucocorticoid deficiency still controversial: a review of the litera- ture. Clinical Endocrinology (Oxford), 63, 483-492.
  2. Harris, D.L., Battin, M.R., Weston, P.J. et al. (2010) Continuous glucose monitoring in newborn babies at risk of hypoglycemia. Journal of Pediatrics, 157, 198-202.
  3. Hershkovitz, E., Rachmel, A., Ben-Zaken, H. et al. (2001) Contin- uous glucose monitoring in children with glycogen storage disease type I. Journal of Inherited Metabolic Disease, 24, 863-869.
  4. Conrad, S.C., Mastrototaro, J. & Gitelman, S.E. (2004) The use of a continuous glucose monitoring system in hypoglycemic dis- orders. Journal of Pediatric Endocrinology and Metabolism, 17, 281-288.
  5. Mastrototaro, J. (1999) The MiniMed Continuous Glucose Mon- itoring System (CGMS). Journal of Pediatric Endocrinology and Metabolism, 12(Suppl. 3), 751-758.
  6. Blasetti, A., Chiuri, R.M., Tocco, A.M. et al. (2011) The effect of recurrent severe hypoglycemia on cognitive performance in children with type 1 diabetes: a meta-analysis. Journal of Child Neurology, 26, 1383-1391.
  7. DeVile, C.J. & Stanhope, R. (1997) Hydrocortisone replacement therapy in children and adolescents with hypopituitarism. Clini- cal Endocrinology (Oxford), 47, 37-41.
  8. Johnstone, H.C., McNally, R.J. & Cheetham, T.D. (2008) The impact of fasting and treatment omission on susceptibility to hypoglycaemia in children and adolescents with GH and cortisol insufficiency. Clinical Endocrinology (Oxford), 69, 436-442.
  9. Newell-Price, J., Whiteman, M., Rostami-Hodjegan, A. et al. (2008) Modified-release hydrocortisone for circadian therapy: a proof-of-principle study in dexamethasone-suppressed normal volunteers. Clinical Endocrinology (Oxford), 68, 130-135.
  10. Johannsson, G., Bergthorsdottir, R., Nilsson, A.G. et al. (2009) Improving glucocorticoid replacement therapy using a novel modified-release hydrocortisone tablet: a pharmacokinetic study. European Journal of Endocrinology, 161, 119-130.
  11. Debono, M., Ghobadi, C., Rostami-Hodjegan, A. et al. (2009) Modified-release hydrocortisone to provide circadian cortisol profiles. Journal of Clinical Endocrinology and Metabolism, 94, 1548-1554.

Cited by

Sorted by citations

Authors
Cambiaso, P., Schiaffini, R., Pontrelli, G., Carducci, C., Ubertini, G., Crea, F., & Cappa, M.
Affiliations
Bambino Gesù Children's Hospital (IT)
Corresponding author
Cambiaso, Paola
Venue
Clinical Endocrinology
Publisher
Wiley
Published
2013-05-06
Volume
79
Issue
2
Pages
232-237
ISSN
  • 0300-0664 (ISSN-L)
  • 1365-2265
OpenAlex
W2049826219
Cited by
21
References
4
Citations by year
2026: 1 · 2025: 1 · 2023: 2 · 2022: 1 · 2021: 3 · 2020: 3 · 2019: 1 · 2018: 1 · 2017: 5 · 2016: 2 · 2015: 1
FWCI
0.26
Type
journal article
Language
en
Open access
Locations
  • Clinical Endocrinology (publishedVersion)
  • PubMed (publishedVersion)
Topics
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Adrenal Hormones and Disorders
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Growth Hormone and Insulin-like Growth Factors
  • Health Sciences › Medicine › Endocrinology, Diabetes and Metabolism › Diabetes Management and Research
Keywords
nocturnal hypoglycemia, ACTH deficiency, growth hormone deficiency, combined pituitary hormone deficiency, continuous glucose monitoring, hydrocortisone replacement, recombinant human growth hormone, children
MeSH terms
Adolescent, Adrenal Insufficiency, Adrenocorticotropic Hormone, Blood Glucose, Child, Child, Preschool, Female, Humans, Hydrocortisone, Hypoglycemia, Infant, Male, Monitoring, Physiologic, Biosensing Techniques, Human Growth Hormone

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review