Evidence map›Paper›PMID 36269558›Full record

ArticleJournal of endocrinological investigation2023

Congenital adrenal hyperplasia in patients with adrenal tumors: a population-based case-control study.

F Sahlander, J Patrova, B Mannheimer, J D Lindh, H Falhammar

Open access · hybridAbstract read
In one paragraph

Article in Journal of endocrinological investigation, 2023. 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
1.6field-weighted citation impact, top 16% 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, 19 citations in OpenAlex.

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  11. Adrenal Cysts: To Operate or Not to Operate?Journal of clinical medicine · 2024
    Review
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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

5 authors at 2 institutions in 1 country.

F Sahlander *Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden. fredrik.sahlander@regiondalarna.se.ORCID http://orcid.org/0000-0003-1572-0812
J Patrova *Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.
B MannheimerDepartment of Clinical Science and Education at Södersjukhuset, Karolinska Institutet, Stockholm, Sweden.ORCID http://orcid.org/0000-0001-5789-8470
J D LindhDepartment of Laboratory Medicine, Division of Clinical Pharmacology, Karolinska University Hospital Huddinge, Karolinska Institutet, Stockholm, Sweden.
H FalhammarDepartment of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden.ORCID http://orcid.org/0000-0002-5622-6987
Karolinska Institutet · SEKarolinska University Hospital · SE

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeCongenital adrenal hyperplasia (CAH) has been associated with adrenal tumors (ATs) but the relationship is still unclear. The aim was to investigate if CAH was more common in patients with adrenal tumors and their characteristics.

methodsUsing national registers all patients with an AT diagnosis (cases) and selected matched controls without AT diagnosis were included from 1st January 2005 to 31st December 2019. The patients with a CAH diagnosis were scrutinized in detail.

resultsATs were diagnosed in 26,573 individuals and in none of 144,124 controls. In 20 patients with ATs and 1 control, a CAH diagnosis was present. The odds for having CAH in patients with ATs was 109 (95% CI 15-809; P < 0.0001). Among cases, 5 had a CAH diagnosis before the discovery of ATs and 15 afterwards. Half were females and two had been screened for CAH neonatally. The mean age when the ATs was discovered was 55.6 years. Adrenalectomy was performed in seven patients. Five patients had unilateral adrenalectomy before the CAH diagnosis and did not have any glucocorticoid protection. After the CAH diagnosis, 15 were initiated on glucocorticoids and 6 on mineralocorticoids. The majority diagnosed with CAH before index date had classic CAH. In individual diagnosed after index date, only three had classic CAH. The rest had nonclassical CAH. During the follow-up time of 9 years, six deceased, two of them in an adrenal crisis.

conclusionsThe prevalence of CAH was greater in patients with ATs than in patients without. In all patients with ATs, CAH should be considered.

Indexed as

Adrenal Gland NeoplasmsAdrenal Hyperplasia, CongenitalAdrenalectomyCase-Control StudiesFemaleGlucocorticoidsHumansMaleMiddle AgedGlucocorticoids21-Hydroxylase deficiencyAdrenal crisisAdrenalectomyAdrenal incidentalomaAdrenocortical cancer

Identifiers

PMID36269558
PMCPMC9938068
OpenAlexW4306980387

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.