Evidence map›Paper›PMID 34503413›Full record

ReviewCurrent neuropharmacology2022

The Role of Mitochondrial Genes in Neurodegenerative Disorders.

Rajesh Kumar, Seetha Harilal, Della Grace Thomas Parambi, S K Kanthlal, Md Atiar Rahman, Athanasios Alexiou, Gaber El-Saber Batiha, Bijo Mathew

Open access · greenAbstract readReview
In one paragraph

Review in Current neuropharmacology, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 13 papers.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed
0.8field-weighted citation impact, top 29% 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

13 citing papers in PubMed, 17 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

8 authors at 5 institutions in 4 countries.

Rajesh KumarDepartment of Pharmacy, Kerala University of Health Sciences, Thrissur, Kerala, India.
Seetha HarilalDepartment of Pharmacy, Kerala University of Health Sciences, Thrissur, Kerala, India.
Della Grace Thomas ParambiDepartment of Pharmaceutical Chemistry, College of Pharmacy, Jouf University, Sakaka, Al Jouf-2014, Saudi Arabia.
S K KanthlalDepartment of Pharmacology, Amrita School of Pharmacy, Amrita Vishwa Vidyapeetham, AIMS Health Sciences Campus, Kochi-682 041, India.
Md Atiar RahmanDepartment of Biochemistry and Molecular Biology, University of Chittagong, Chittagong, Bangladesh.
Athanasios AlexiouNovel Global Community Educational Foundation, Hebersham, Australia.
Gaber El-Saber BatihaDepartment of Pharmacology and Therapeutics, Faculty of Veterinary Medicine, Damanhour University, Damanhour 22511, AlBeheira, Egypt.
Bijo MathewDepartment of Pharmaceutical Chemistry, Amrita School of Pharmacy, Amrita Vishwa Vidyapeetham, AIMS Health Sciences Campus, Kochi-682 041, India.
Amrita Vishwa Vidyapeetham · INKerala University of Health Sciences · INAl Jouf University · SADamanhour University · EGUniversity of Chittagong · BD

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Mitochondrial disorders are clinically heterogeneous, resulting from nuclear gene and mitochondrial mutations that disturb the mitochondrial functions and dynamics. There is a lack of evidence linking mtDNA mutations to neurodegenerative disorders, mainly due to the absence of noticeable neuropathological lesions in postmortem samples. This review describes various gene mutations in Alzheimer's disease, Parkinson's disease, amyotrophic lateral sclerosis, multiple sclerosis, and stroke. These abnormalities, including PINK1, Parkin, and SOD1 mutations, seem to reveal mitochondrial dysfunctions due to either mtDNA mutation or deletion, the mechanism of which remains unclear in depth.

Indexed as

Amyotrophic Lateral SclerosisMitochondrial DiseasesNeurodegenerative DiseasesParkinson DiseaseDNA, MitochondrialGenes, MitochondrialHumansMutationDNA, MitochondrialAlzheimer's diseaseamyotrophic lateral sclerosismtDNAmultiple sclerosisneurodegenerationParkinson's diseasestroke

Identifiers

PMID34503413
PMCPMC9881096
OpenAlexW3197650194

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
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.