Evidence map›Paper›PMID 34861061›Full record

ArticleJournal of clinical laboratory analysis2022

Oxidative stress parameters and keap 1 variants in T2DM: Association with T2DM, diabetic neuropathy, diabetic retinopathy, and obesity.

Farnaz Khalili, Asad Vaisi-Raygani, Ebrahim Shakiba, Maryam Kohsari, Maryam Dehbani, Rozita Naseri, Soheila Asadi, Ziba Rahimi, Mehrali Rahimi, Zohreh Rahimi

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical laboratory analysis, 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
1.6field-weighted citation impact, top 16% 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, 32 citations in OpenAlex.

  1. Article
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  7. Protective role ofHealth science reports · 2024
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  8. Antidiabetic and Anti-Inflammatory Effect ofPharmaceuticals (Basel, Switzerland) · 2024
    Article
  9. 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

10 authors at 1 institution in 1 country.

Farnaz KhaliliDepartment of Clinical Biochemistry, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Asad Vaisi-RayganiDepartment of Clinical Biochemistry, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Ebrahim ShakibaDepartment of Clinical Biochemistry, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Maryam KohsariDepartment of Clinical Biochemistry, Kermanshah University of Medical Sciences, Kermanshah, Iran.ORCID https://orcid.org/0000-0002-1817-9147
Maryam DehbaniMedical Biology Research Center, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Rozita NaseriDepartment of Internal Medicine, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Soheila AsadiDepartment of Clinical Biochemistry, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Ziba RahimiMedical Biology Research Center, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Mehrali RahimiDepartment of Internal Medicine, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Zohreh RahimiDepartment of Clinical Biochemistry, Kermanshah University of Medical Sciences, Kermanshah, Iran.ORCID https://orcid.org/0000-0001-7589-3307
Kermanshah University of Medical Sciences · IR

Funding

Kermanshah University of Medical Sciences 97937
6 · The paper itself

Abstract

introductionChronic hyperglycemia activates the inflammatory pathways and oxidative stress mechanisms with consequent damage to nerve tissue and retina. The Keap1-Nrf2 pathway acts as one of the most important antioxidant pathways of the organism. Variants of Keap1 could affect susceptibility to diabetes and its complications.

methodsIn a case-control study, 400 individuals included type 2 diabetes mellitus (T2DM) patients without complication, with neuropathy, with retinopathy, and healthy individuals were investigated. The levels of glutathione (GSH), glutathione peroxidase (GPx), malondialdehyde (MDA), and total antioxidant capacity (TAC) were measured using chemical methods. Using the PCR-RFLP method, the Keap1 (rs11085735) variants were identified.

resultsNeuropathic patients had significantly lower levels of GSH, GPx, and TAC and higher levels of total oxidative status (TOS), MDA, and oxidative stress index (OSI) compared to T2DM patients without complication and controls. Lower levels of GSH and GPx and a higher level of MDA were observed in patients with retinopathy compared with controls. Obesity was associated with significantly lower GPx activity and higher TOS. A significantly higher Keap1 AA genotype was found in patients with neuropathy than T2DM without complication and controls. The presence of Keap1 AA genotype correlated with lower GPx activity compared to CC genotype.

conclusionsOur study suggests the role of reduced antioxidant system and Keap1 variants in the pathogenesis of T2DM and its complications of neuropathy and retinopathy and also obesity in enhanced oxidative stress. Monitoring oxidative stress parameters in diabetic patients, especially those with complication and their treatment with antioxidants is suggested.

Indexed as

Diabetes Mellitus, Type 2Diabetic NeuropathiesDiabetic RetinopathyOxidative StressFemaleHumansKelch-Like ECH-Associated Protein 1MaleMiddle AgedObesityKEAP1 protein, humanKelch-Like ECH-Associated Protein 1diabetic neuropathydiabetic retinopathykeap1 variantsoxidative stresstype 2 diabetes

Identifiers

PMID34861061
PMCPMC8761405
OpenAlexW3216776539

What OpenQuestion holds

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LicenceCC BY
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Registered trials

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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.