Evidence map›Paper›PMID 38665259›Full record

ReviewFrontiers in endocrinology2024

Persistent hypercalcaemia associated with two pathogenic variants in the

Dorota Leszczyńska, Alicja Szatko, Julia Latocha, Magdalena Kochman, Maria Duchnowska, Anna Wójcicka, Waldemar Misiorowski, Wojciech Zgliczyníski, Piotr Glinicki

Open access · goldAbstract readCase ReportsReview
In one paragraph

Review in Frontiers in endocrinology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
3.8field-weighted citation impact, top 7% 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

8 citing papers in PubMed, 9 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

9 authors at 2 institutions in 1 country.

Dorota LeszczyńskaDepartment of Endocrinology, Centre of Postgraduate Medical Education, Warsaw, Poland.
Alicja SzatkoDepartment of Endocrinology, Centre of Postgraduate Medical Education, Warsaw, Poland.
Julia LatochaStudents' Scientific Group Affiliated with the Department of Endocrinology, Centre of Postgraduate Medical Education, Warsaw, Poland.
Magdalena KochmanDepartment of Endocrinology, Centre of Postgraduate Medical Education, Warsaw, Poland.
Maria DuchnowskaDepartment of Endocrinology, Centre of Postgraduate Medical Education, Warsaw, Poland.
Anna WójcickaWarsaw Genomics, Warsaw, Poland.
Waldemar MisiorowskiDepartment of Endocrinology, Centre of Postgraduate Medical Education, Warsaw, Poland.
Wojciech ZgliczynískiDepartment of Endocrinology, Centre of Postgraduate Medical Education, Warsaw, Poland.
Piotr GlinickiDepartment of Endocrinology, Centre of Postgraduate Medical Education, Warsaw, Poland.
Postgraduate School of Molecular Medicine · PLGenomed (Poland) · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: 24-Hydroxylase, encoded by the Aim of the study: We report a rare case of an adult with primary hyperparathyroidism and loss-of-function mutations in the Case presentation: We report the case of a 58-year-old woman diagnosed initially with primary hyperparathyroidism. Preoperatively, the suspected mass adjoining the upper pole of the left lobe of the thyroid gland was found via ultrasonography and confirmed by 99mTc scintigraphy and biopsy as the parathyroid gland. The patient underwent parathyroidectomy (a histopathology report revealed parathyroid adenoma), which led to normocalcaemia. After 10 months, vitamin D supplementation was introduced due to deficiency, and the calcium level remained within the reference range. Two years later, biochemical tests showed recurrence of hypercalcaemia with suppressed parathyroid hormone levels and elevated 1,25(OH) Conclusions: The diagnostic process for hypercalcaemia becomes complicated when multiple causes of hypercalcaemia coexist. The measurement of vitamin D metabolites using LC-MS/MS may help to identify carriers of

Indexed as

AdenomaHypercalcemiaParathyroid NeoplasmsVitamin D3 24-HydroxylaseFemaleHumansMiddle AgedMutationParathyroidectomyCYP24A1 protein, humanVitamin D3 24-Hydroxylase1,25(OH)2D324,25(OH)2D324-hydroxylase deficiency25(OH)D3CYP24A1 genehypercalcaemiaprimary hyperparathyroidismvitamin D

Identifiers

PMID38665259
PMCPMC11043563
OpenAlexW4394724242

What OpenQuestion holds

Textmetadata
LicenceCC BY
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.