Evidence map›Paper›PMID 33124662›Full record

ArticleThe Journal of clinical endocrinology and metabolism2021

Hypercalcemia in Children Using the Ketogenic Diet: A Multicenter Study.

Colin P Hawkes, Sani M Roy, Bassem Dekelbab, Britney Frazier, Monica Grover, Jaime Haidet, James Listman, Sarianne Madsen, Marian Roan, Celia Rodd and 3 more

Open access · bronzeAbstract readMulticenter Study
In one paragraph

Article in The Journal of clinical endocrinology and metabolism, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing papers in PubMed
1.6field-weighted citation impact, top 17% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

11 citing papers in PubMed, 24 citations in OpenAlex.

  1. Article
  2. Treatment of pediatric epilepsy.Pediatric investigation · 2026
    Review
  3. Ketogenic diet in neonates: effects, pitfalls, and a paradigm from a preterm newborn affected by pyruvate dehydrogenase deficiency.Journal of perinatology : official journal of the California Perinatal Association · 2025
    Review
  4. Article
  5. Article
  6. Breaking the Cycle of Recurrent Calcium Stone Disease.Advances in kidney disease and health · 2023
    Review
  7. Review
  8. Molecular mechanisms altering tubular calcium reabsorption.Pediatric nephrology (Berlin, Germany) · 2022
    Review
  9. Fad Diets: Facts and Fiction.Frontiers in nutrition · 2022
    Review
  10. A Novel Germline Mutation ofInternational journal of molecular sciences · 2021
    Article
  11. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

13 authors at 11 institutions in 2 countries.

Colin P HawkesDivision of Endocrinology and Diabetes, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Sani M RoyDivision of Endocrinology and Diabetes, Cook Children's Medical Center, Fort Worth, Texas.
Bassem DekelbabDivision of Endocrinology and Diabetes, Beaumont Children's, Royal Oak, Michigan.
Britney FrazierMulticare Mary Bridge Children's Hospital and Health Center, Tacoma, Washington.
Monica GroverDivision of Pediatric Endocrinology, Stanford University, Stanford, California.
Jaime HaidetCenter for Diabetes and Endocrinology, Akron Children's Hospital, Akron, Ohio 44308.
James ListmanPediatric Nephrology Group, Albany Medical College, Albany, New York.
Sarianne MadsenUCSF Benioff Children's Hospital, San Francisco, California.
Marian RoanDepartment of Clinical Nutrition, UCSF Benioff Children's Hospital, Oakland, California.
Celia RoddDepartment of Pediatrics and Child Health, The Children's Hospital Research Institute of Manitoba, Winnipeg, MB, Canada.
Aviva SopherDivision of Pediatric Endocrinology Diabetes and Metabolism, Columbia University Irving Medical Center, New York, New York.
Peter TebbenDivision of Pediatric Endocrinology and Metabolism, Department of Pediatric and Adolescent Medicine, Mayo Clinic, Rochester, Minnesota.
Michael A LevineDivision of Endocrinology and Diabetes, The Children's Hospital of Philadelphia, Philadelphia, Pennsylvania.
Children's Hospital of Philadelphia · USUCSF Benioff Children's Hospital · USAkron Children's Hospital · USAlbany Medical Center Hospital · USChildren's Hospital Research Institute of Manitoba · CAColumbia University Irving Medical Center · USCook Children's Medical Center · USCorewell Health Children's · USMayo Clinic in Florida · USMultiCare Health System · USStanford University · US

Funding

Repurposing rifampin to reduce elevated levels of blood and urine calcium in patients with inactivating mutations of CYP24A1R01DK112955 · NIDDK · CHILDREN'S HOSP OF PHILADELPHIA · PI Michael A. Levine, David R Weber · 2017 to 2026
$5.1M
The Role of GCM2 in Parathyroid Gland HomeostasisR01DK079970 · NIDDK · CHILDREN'S HOSP OF PHILADELPHIA · PI LEVINE, MICHAEL A. · 2009 to 2015
$3.2M
NIDDK NIH HHS R01 DK079970NIDDK NIH HHS R01 DK112955
6 · The paper itself

Abstract

contextThe ketogenic diet is associated with progressive skeletal demineralization, hypercalciuria, and nephrolithiasis. Acute hypercalcemia has been described as a newly recognized complication of this treatment.

objectiveTo describe the clinical characteristics of acute hypercalcemia in children on the ketogenic diet through analysis of the presentation, response to treatment, and natural history in a large cohort of patients.

designA multicenter case series was performed including children who developed acute hypercalcemia while treated with the ketogenic diet. Information on clinical presentation, treatment, and course of this complication was collated centrally.

resultsThere were 14 patients (median (range) age 6.3 (0.9 to 18) years) who developed hypercalcemia 2.1 (range, 0.2-12) years after starting the ketogenic diet. All had low levels of parathyroid hormone and levels of 1,25-dihydroxyvitamin D were low in all except one. Seven (50%) had impaired renal function at presentation. All except the 2 oldest had low alkaline phosphatase levels for age. Once normocalcemia was achieved, hypercalcemia recurred in only 2 of these patients over observation of up to 9.8 years. One patient discontinued the ketogenic diet prior to achieving normocalcemia while 4 more stopped the diet during follow-up after resolution of hypercalcemia.

conclusionsKetotic hypercalcemia can occur years after starting the ketogenic diet, especially in the setting of renal impairment. The mechanism is unknown but appears to be due to reduced osteoblast activity and impaired bone formation. We recommend close attention to optimizing bone health in these children, and screening for the development of ketotic hypercalcemia.

Indexed as

Acute DiseaseAdolescentAge FactorsAicardi SyndromeCalciumChildChild, PreschoolCohort StudiesDiet, KetogenicDrug Resistant EpilepsyFemaleHumansHypercalcemiaHypercalciuriaInfantInfant, NewbornCalciumParathyroid Hormonehypercalcemiahypercalciuriaketogenic dietnephrocalcinosis

Identifiers

PMID33124662
PMCPMC7823241
OpenAlexW3094995846

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.