Evidence map›Paper›PMID 34768699›Full record

ArticleJournal of clinical medicine2021

The Utility of BDNF Detection in Assessing Severity of Huntington's Disease.

Klaudia Plinta, Andrzej Plewka, Krzysztof Pawlicki, Nikola Zmarzły, Magdalena Wójcik-Pędziwiatr, Marcin Rudziński, Agnieszka Krzak-Kubica, Magdalena Doręgowska-Stachera, Monika Rudzińska-Bar

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical medicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 5 papers.

0numbers the graph read from it
0cells of the map it votes in
5citing papers in PubMed
0.5field-weighted citation impact, top 42% 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

5 citing papers in PubMed, 10 citations in OpenAlex.

  1. 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

9 authors at 4 institutions in 1 country.

Klaudia PlintaNeurology Department, Institute of Medical Science, University of Opole, 45-040 Opole, Poland.
Andrzej PlewkaInstitute of Health Sciences, University of Opole, 45-040 Opole, Poland.ORCID 0000-0001-7129-9490
Krzysztof PawlickiFaculty of Medical Sciences, Medical University of Silesia, 40-055 Katowice, Poland.
Nikola ZmarzłyDepartment of Histology, Cytophysiology and Embryology, Faculty of Medicine, University of Technology in Katowice, 41-800 Zabrze, Poland.ORCID 0000-0002-7833-6167
Magdalena Wójcik-PędziwiatrDepartment of Neurology, Faculty of Medicine and Health Sciences, Andrzej Frycz Modrzewski Krakow University, 30-705 Krakow, Poland.ORCID 0000-0003-0600-6780
Marcin RudzińskiDepartment of Otolaryngology, Jagiellonian University Medical College, The University Hospital in Krakow, 30-688 Krakow, Poland.
Agnieszka Krzak-KubicaVito-Med Hospital in Gliwice, 44-100 Gliwice, Poland.
Magdalena Doręgowska-StacheraDepartment of Neurology, Faculty of Medicine and Health Sciences, Andrzej Frycz Modrzewski Krakow University, 30-705 Krakow, Poland.
Monika Rudzińska-BarDepartment of Neurology, Faculty of Medicine and Health Sciences, Andrzej Frycz Modrzewski Krakow University, 30-705 Krakow, Poland.ORCID 0000-0002-1453-6856
Andrzej Frycz Modrzewski Krakow University · PLUniversity of Opole · PLJagiellonian University · PLMedical University of Silesia · PL

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Brain-derived neurotrophic factor (BDNF) is involved in the survival and maturation of neurons, and also promotes and controls neurogenesis. Its levels are lowered in many neurodegenerative diseases, including Huntington's disease (HD). Clinical pictures of HD can be very diverse, which makes it difficult to assess its severity; however, molecular markers may be helpful. The aim of the study was to determine the relationship between HD severity and the plasma BDNF concentration in HD patients. The study recruited 42 patients with diagnosed and genetically confirmed HD and 40 healthy volunteers. BDNF levels were determined in plasma with the enzyme-linked immunosorbent assay (ELISA). Correlations between BDNF levels and clinical profiles and HD severity were also investigated. The BDNF level was significantly lower in HD patients compared to the control. There was no correlation between the BDNF level and motor symptoms and cognitive impairment. In the early disease stages, BDNF levels were associated with a better neurological examination, independence, and functional evaluation, in contrast to later HD stages, where the correlations were inverse. Multidirectional correlations between parameters of saccadic disorders and the BDNF level do not allow for drawing a conclusion, whether or not there is a relationship between the severity of saccadic disorders and the BDNF concentration.

Indexed as

BDNFdisease severityHuntington’s disease

Identifiers

PMID34768699
PMCPMC8584708
OpenAlexW3211541640

What OpenQuestion holds

Textmetadata
LicenceCC BY
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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 OpenQuestion graph.