Evidence map›Paper›PMID 38538623›Full record

ArticleScientific reports2024

Vitamin D

Sabrina Ehnert, Stefan Hauser, Holger Hengel, Philip Höflinger, Rebecca Schüle, Tobias Lindig, Jonathan Baets, Tine Deconinck, Peter de Jonghe, Tina Histing and 3 more

Open access · goldAbstract read
In one paragraph

Article in Scientific reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
0.3field-weighted citation impact, top 49% 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

2 citing papers in PubMed, 1 citations in OpenAlex.

  1. Article
  2. Biomarkers in Hereditary Spastic Paraplegias.International journal of molecular sciences · 2025
    Review
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 4 institutions in 2 countries.

Sabrina EhnertSiegfried Weller Research Institute at the BG Unfallklinik Tübingen, Department of Trauma and Reconstructive Surgery, University of Tübingen, Schnarrenbergstr. 95, 72076, Tübingen, Germany.
Stefan HauserGerman Center of Neurodegenerative Diseases (DZNE), 72076, Tübingen, Germany.
Holger HengelGerman Center of Neurodegenerative Diseases (DZNE), 72076, Tübingen, Germany.
Philip HöflingerGerman Center of Neurodegenerative Diseases (DZNE), 72076, Tübingen, Germany.
Rebecca SchüleGerman Center of Neurodegenerative Diseases (DZNE), 72076, Tübingen, Germany.
Tobias LindigDepartment of Diagnostic and Interventional Neuroradiology, University Hospital Tübingen, 72076, Tübingen, Germany.
Jonathan BaetsNeurogenetics Group, Center for Molecular Neurology, VIB, 2610, Antwerp, Belgium.
Tine DeconinckNeurogenetics Group, Center for Molecular Neurology, VIB, 2610, Antwerp, Belgium.
Peter de JongheNeurogenetics Group, Center for Molecular Neurology, VIB, 2610, Antwerp, Belgium.
Tina HistingBG Unfallklinik Tübingen, Department of Trauma and Reconstructive Surgery, University of Tübingen, Schnarrenbergstr. 95, 72076, Tübingen, Germany.
Andreas K NüsslerSiegfried Weller Research Institute at the BG Unfallklinik Tübingen, Department of Trauma and Reconstructive Surgery, University of Tübingen, Schnarrenbergstr. 95, 72076, Tübingen, Germany.
Ludger SchölsGerman Center of Neurodegenerative Diseases (DZNE), 72076, Tübingen, Germany. ludger.schoels@uni-tuebingen.de.
Tim W RattayGerman Center of Neurodegenerative Diseases (DZNE), 72076, Tübingen, Germany.
German Center for Neurodegenerative Diseases · DEBG Klinik Tübingen · DEUniversity of Antwerp · BEUniversity Children's Hospital Tübingen · DE

Funding

University of Tübingen #386-0-0
6 · The paper itself

Abstract

Hereditary spastic paraplegia type 5 (SPG5) is an autosomal recessively inherited movement disorder characterized by progressive spastic gait disturbance and afferent ataxia. SPG5 is caused by bi-allelic loss of function mutations in CYP7B1 resulting in accumulation of the oxysterols 25-hydroxycholesterol and 27-hydroxycholesterol in serum and cerebrospinal fluid of SPG5 patients. An effect of 27- hydroxycholesterol via the estrogen and liver X receptors was previously shown on bone homeostasis. This study analyzed bone homeostasis and osteopenia in 14 SPG5 patients as a non-motor feature leading to a potential increased risk for bone fractures. T-Scores in CT bone density measurements were reduced, indicating osteopenia in SPG5 patients. Further, we analyzed various metabolites of bone homeostasis by ELISA in serum samples of these patients. We identified a lack of vitamin D

Indexed as

OxysterolsSpastic Paraplegia, HereditaryHomeostasisHumansMutationParaplegiaVitamin DOxysterolsVitamin D

Identifiers

PMID38538623
PMCPMC10973513
OpenAlexW4393217748

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.