Evidence map›Paper›PMID 33967943›Full record

ArticleFrontiers in neurology2021

Serum BDNF as a Potential Biomarker of Alzheimer's Disease: Verification Through Assessment of Serum, Cerebrospinal Fluid, and Medial Temporal Lobe Atrophy.

Yukiko Mori, Mayumi Tsuji, Tatsunori Oguchi, Kensaku Kasuga, Atsushi Kimura, Akinori Futamura, Azusa Sugimoto, Hideyo Kasai, Takeshi Kuroda, Satoshi Yano and 4 more

Open access · goldAbstract read
In one paragraph

Article in Frontiers in neurology, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 51 papers.

0numbers the graph read from it
0cells of the map it votes in
51citing papers in PubMed
7.1field-weighted citation impact, top 2% 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

51 citing papers in PubMed, 77 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

14 authors at 2 institutions in 1 country.

Yukiko MoriDepartment of Pharmacology, School of Medicine, Showa University, Tokyo, Japan.
Mayumi TsujiPharmacological Research Center, Showa University, Tokyo, Japan.
Tatsunori OguchiDepartment of Pharmacology, School of Medicine, Showa University, Tokyo, Japan.
Kensaku KasugaDepartment of Molecular Genetics, Brain Research Institute, Niigata University, Niigata, Japan.
Atsushi KimuraDepartment of Pharmacology, School of Medicine, Showa University, Tokyo, Japan.
Akinori FutamuraDivision of Neurology, Department of Medicine, Showa University School of Medicine, Tokyo, Japan.
Azusa SugimotoDivision of Neurology, Department of Medicine, Showa University School of Medicine, Tokyo, Japan.
Hideyo KasaiDivision of Neurology, Department of Medicine, Showa University School of Medicine, Tokyo, Japan.
Takeshi KurodaDivision of Neurology, Department of Medicine, Showa University School of Medicine, Tokyo, Japan.
Satoshi YanoDivision of Neurology, Department of Medicine, Showa University School of Medicine, Tokyo, Japan.
Sotaro HiedaDivision of Neurology, Department of Medicine, Showa University School of Medicine, Tokyo, Japan.
Yuji KiuchiDepartment of Pharmacology, School of Medicine, Showa University, Tokyo, Japan.
Takeshi IkeuchiDepartment of Molecular Genetics, Brain Research Institute, Niigata University, Niigata, Japan.
Kenjiro OnoDivision of Neurology, Department of Medicine, Showa University School of Medicine, Tokyo, Japan.
Showa University · JPNiigata University · JP

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

There is an urgent need to establish blood biomarkers for Alzheimer's disease (AD). Although it has been speculated that brain-derived neurotrophic factor (BDNF) is associated with AD, whether it can be used as a blood biomarker has yet to be determined. We used serum, cerebrospinal fluid (CSF), and medial temporal lobe atrophy from patients with AD to evaluate the association of BDNF with AD and assess its severity. For the blood analysis, 66 participants [21 normal controls (NCs) with normal cognitive function, 22 patients with mild cognitive impairment (MCI) due to AD, and 23 patients with AD] were included. For the CSF analysis, 30 participants were included. Magnetic resonance imaging, including a voxel-based specific regional analysis system for AD, and a Mini Mental State Examination were performed. Serum levels of BDNF and CSF levels of amyloid-β

Indexed as

Alzheimer's diseaseBDNFblood biomarkermedial temporal lobe atrophymild cognitive impairment

Identifiers

PMID33967943
PMCPMC8102980
OpenAlexW3161277907

What OpenQuestion holds

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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.