Evidence map›Paper›PMID 34302265›Full record

ArticleMolecular biology reports2021

Genetic polymorphisms in the renin-angiotensin system and cognitive decline in Parkinson's disease.

Anna Pierzchlińska, Jarosław Sławek, Monika Mak, Barbara Gawrońska-Szklarz, Monika Białecka

Open access · hybridAbstract readMulticenter Study
In one paragraph

Article in Molecular biology reports, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.8field-weighted citation impact, top 26% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

  1. Genetic Polymorphisms in theInternational journal of molecular sciences · 2024
    Article
  2. Review
  3. 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

5 authors at 2 institutions in 1 country.

Anna PierzchlińskaDepartment of Pharmacokinetics and Therapeutic Drug Monitoring, Pomeranian Medical University, Powstańców Wlkp 72, 70-111, Szczecin, Poland. anna.pierzchlinska@pum.edu.pl.ORCID http://orcid.org/0000-0002-1606-7918
Jarosław SławekDepartment of Neurological-Psychiatric Nursing, Faculty of Health Sciences, Medical University of Gdansk, Gdansk, Poland.ORCID http://orcid.org/0000-0001-6816-0877
Monika MakDepartment of Health Psychology, Pomeranian Medical University, Szczecin, Poland.ORCID http://orcid.org/0000-0002-0565-2011
Barbara Gawrońska-SzklarzDepartment of Pharmacokinetics and Therapeutic Drug Monitoring, Pomeranian Medical University, Powstańców Wlkp 72, 70-111, Szczecin, Poland.ORCID http://orcid.org/0000-0002-8805-7217
Monika BiałeckaDepartment of Pharmacokinetics and Therapeutic Drug Monitoring, Pomeranian Medical University, Powstańców Wlkp 72, 70-111, Szczecin, Poland.ORCID http://orcid.org/0000-0002-3137-2224
Pomeranian Medical University · PLGdańsk Medical University · PL

Funding

institutional grants of the department of pharmacokinetics and therapeutic drug monitoring, pomeranian medical university, szczecin, poland WLA-129-01/S/16/2016-2020
6 · The paper itself

Abstract

backgroundRenin-angiotensin system (RAS) influences the central nervous system not only through its peripheral impact-the brain possesses its own local RAS. Studies showed altered RAS components in Parkinson's disease (PD) and their association with oxidative stress which may be linked to neurodegeneration and dementia. Moreover, the protective functions of RAS blockade antagonists against cognitive decline and dementia have been suggested. This study aimed to examine whether genetic variability in RAS genes correlates with cognitive decline in PD. METHODS AND

resultsWe genotyped single nucleotide polymorphisms (SNPs) in angiotensinogen (AGT: rs699, rs4762), angiotensin II receptors (AGTR1: rs5186 and AGTR2: rs5194, rs1403543) genes, as well as insertion/deletion polymorphism in the angiotensin-converting enzyme (ACE I/D) gene in 256 PD patients, divided into three groups: without cognitive decline, with mild cognitive impairment and with PD dementia. We did not find any significant differences in the frequencies of the analysed polymorphisms in any of the groups.

conclusionsDespite no direct correlation between the investigated polymorphisms in RAS genes and cognitive decline in PD, we believe the impact of those genotypes may be indirect, affecting RAS blockade treatment.

Indexed as

Cognitive DysfunctionGenetic Predisposition to DiseasePolymorphism, GeneticRenin-Angiotensin SystemAdultAgedAged, 80 and overAngiotensinogenFemaleHumansMaleMiddle AgedParkinson DiseasePeptidyl-Dipeptidase APolandReceptor, Angiotensin, Type 1ACE protein, humanAGT protein, humanAGTR1 protein, humanAGTR2 protein, humanAngiotensinogenPeptidyl-Dipeptidase AReceptor, Angiotensin, Type 1Receptor, Angiotensin, Type 2Cognitive declineDementiaGenetic polymorphismsParkinson’s diseaseRenin-angiotensin system

Identifiers

PMID34302265
PMCPMC8301732
OpenAlexW3183852497

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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.