Evidence map›Paper›PMID 34788830›Full record

ArticleThe Journal of clinical endocrinology and metabolism2022

Optimizing the Timing of Highest Hydrocortisone Dose in Children and Adolescents With 21-Hydroxylase Deficiency.

Mariska A M Schröder, Antonius E van Herwaarden, Paul N Span, Erica L T van den Akker, Gianni Bocca, Sabine E Hannema, Hetty J van der Kamp, Sandra W K de Kort, Christiaan F Mooij, Dina A Schott and 5 more

Open access · hybridAbstract read
In one paragraph

Article in The Journal of clinical endocrinology and metabolism, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 14 papers.

0numbers the graph read from it
0cells of the map it votes in
14citing papers in PubMed
0.1field-weighted citation impact, top 55% 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

14 citing papers in PubMed, 1 citations in OpenAlex.

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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

15 authors at 9 institutions in 1 country.

Mariska A M SchröderAmalia Children's Hospital, Department of Pediatrics, Radboud University Medical Center, HB Nijmegen, the Netherlands.ORCID 0000-0003-2139-9076
Antonius E van HerwaardenDepartment of Laboratory Medicine, Radboud Institute for Molecular Life Sciences (RIMLS), Radboud University Medical Center, HB Nijmegen, the Netherlands.
Paul N SpanRadiotherapy & OncoImmunology Laboratory, Department of Radiation Oncology, Radboud Institute for Molecular Life Sciences (RIMLS), Radboud University Medical Center, HB Nijmegen, the Netherlands.
Erica L T van den AkkerDepartment of Pediatrics, Division of Endocrinology, Erasmus MC, University Medical Center Rotterdam, DR Rotterdam, the Netherlands.ORCID 0000-0001-5352-9328
Gianni BoccaBeatrix Children's Hospital, Department of Pediatrics, University Medical Center Groningen, RB Groningen, the Netherlands.ORCID 0000-0002-2665-8738
Sabine E HannemaDepartment of Pediatrics, Leiden University Medical Centre, RC Leiden, the Netherlands.ORCID 0000-0002-8996-0993
Hetty J van der KampWilhelmina Children's Hospital, Utrecht University Medical Center, EA Utrecht, the Netherlands.
Sandra W K de KortDepartment of Pediatrics, Haga Teaching Hospital/Juliana Children's Hospital, AA The Hague, the Netherlands.
Christiaan F MooijDepartment of Pediatric Endocrinology, Emma Children's Hospital, Amsterdam University Medical Centers, University of Amsterdam, AZ Amsterdam, the Netherlands.
Dina A SchottDepartment of Pediatrics Endocrinology, Zuyderland medical center, PC Heerlen, the Netherlands.
Saartje StraetemansDepartment of Pediatric Endocrinology, Maastricht university medical center, HX Maastricht, the Netherlands.
Vera van TellingenDepartment of Pediatrics, Catharina Hospital, EJ Eindhoven, the Netherlands.
Janiëlle A van der VeldenAmalia Children's Hospital, Department of Pediatrics, Radboud University Medical Center, HB Nijmegen, the Netherlands.
Fred C G J SweepDepartment of Laboratory Medicine, Radboud Institute for Molecular Life Sciences (RIMLS), Radboud University Medical Center, HB Nijmegen, the Netherlands.
Hedi L Claahsen-van der GrintenAmalia Children's Hospital, Department of Pediatrics, Radboud University Medical Center, HB Nijmegen, the Netherlands.ORCID 0000-0003-0181-0403
Radboud University Nijmegen · NLEmma Kinderziekenhuis · NLErasmus MC · NLHaga Hospital · NLLeiden University · NLMaastricht University · NLUniversity Medical Center Groningen · NLUtrecht University · NLZuyderland Medisch Centrum · NL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

contextHydrocortisone treatment of young patients with 21-hydroxylase deficiency (21OHD) is given thrice daily, but there is debate about the optimal timing of the highest hydrocortisone dose, either mimicking the physiological diurnal rhythm (morning), or optimally suppressing androgen activity (evening).

objectiveWe aimed to compare 2 standard hydrocortisone timing strategies, either highest dosage in the morning or evening, with respect to hormonal status throughout the day, nocturnal blood pressure (BP), and sleep and activity scores.

methodsThis 6-week crossover study included 39 patients (aged 4-19 years) with 21OHD. Patients were treated for 3 weeks with the highest hydrocortisone dose in the morning, followed by 3 weeks with the highest dose in the evening (n = 21), or vice versa (n = 18). Androstenedione (A4) and 17-hydroxyprogesterone (17OHP) levels were quantified in saliva collected at 5 am; 7 am; 3 pm; and 11 pm during the last 2 days of each treatment period. The main outcome measure was comparison of saliva 17OHP and A4 levels between the 2 treatment strategies.

resultsAdministration of the highest dose in the evening resulted in significantly lower 17OHP levels at 5 am, whereas the highest dose in the morning resulted in significantly lower 17OHP and A4 levels in the afternoon. The 2 treatment dose regimens were comparable with respect to averaged daily hormone levels, nocturnal BP, and activity and sleep scores.

conclusionNo clear benefit for either treatment schedule was established. Given the variation in individual responses, we recommend individually optimizing dose distribution and monitoring disease control at multiple time points.

Indexed as

Adrenal Hyperplasia, CongenitalHydrocortisone17-alpha-HydroxyprogesteroneAdolescentAndrogensChildChild, PreschoolCross-Over StudiesFemaleHumansMaleYoung Adult17-alpha-HydroxyprogesteroneAndrogensHydrocortisone21-hydroxylase deficiencyCAHcongenital adrenal hyperplasiadosinghydrocortisone

Identifiers

PMID34788830
PMCPMC8947312
OpenAlexW3201205688

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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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 Socratic graph.