Evidence map›Paper›PMID 37921983›Full record

ArticleMolecular biology reports2023

Single nucleotide polymorphism rs527236194 of the cytochrome B gene (MT-CYB) is associated with alterations in sperm parameters.

Yulia Yu Gromenko, Kamil S Galimov, Irina R Gilyazova, Elmira F Galimova, Kirill V Bulygin, Sergey N Ryagin, Shamil N Galimov, Peter F Litvitskiy, Gennadii A Piavchenko, Valentin N Pavlov

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Article in Molecular biology reports, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.5field-weighted citation impact, top 27% 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

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. FromiScience · 2024
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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 3 institutions in 1 country.

Yulia Yu GromenkoMedical Center "Family", Ufa, 450054, Russia.
Kamil S GalimovDepartment of Human Anatomy and Histology, I.M. Sechenov First Moscow State Medical University (Sechenov University, 8/2 Trubetskaya str, Moscow, 119991, Russian Federation.
Irina R GilyazovaBashkir State Medical University, Ufa, 450008, Russia.
Elmira F GalimovaBashkir State Medical University, Ufa, 450008, Russia.
Kirill V BulyginDepartment of Human Anatomy and Histology, I.M. Sechenov First Moscow State Medical University (Sechenov University, 8/2 Trubetskaya str, Moscow, 119991, Russian Federation.
Sergey N RyaginMoscow University for Industry and Finance «Synergy», Moscow, 125190, Russia.
Shamil N GalimovBashkir State Medical University, Ufa, 450008, Russia.
Peter F LitvitskiyDepartment of Human Anatomy and Histology, I.M. Sechenov First Moscow State Medical University (Sechenov University, 8/2 Trubetskaya str, Moscow, 119991, Russian Federation.
Gennadii A PiavchenkoDepartment of Human Anatomy and Histology, I.M. Sechenov First Moscow State Medical University (Sechenov University, 8/2 Trubetskaya str, Moscow, 119991, Russian Federation. gennadii.piavchenko@staff.sechenov.ru.ORCID http://orcid.org/0000-0001-7782-3468
Valentin N PavlovBashkir State Medical University, Ufa, 450008, Russia.
Bashkir State Medical University · RUSechenov University · RUMoscow University «Synergy» · RU

Funding

Bashkir State Medical University Strategic Academic Leadership Program (PRIORITY-2030) Bashkir State Medical University Strategic Academic Leadership Program (PRIORITY-2030)
6 · The paper itself

Abstract

backgroundThe mitochondrial genome is substantially susceptible to mutations and has high polymorphism due to structural features, location, and lack of recombinant variability, as its inheritance is strictly maternal. All of these events can be accompanied by the accumulation of mitochondrial single nucleotide polymorphisms (mtSNPs) in the sperm. The aim of this research was to analyze the influence of mutations in the MT-CYB gene on sperm quality. METHODS AND

resultsWe conducted a case‒control study to identify mutations in the mitochondrial cytochrome B (MT-CYB) gene in men with asthenoteratozoospermia (89 cases) and oligoasthenoteratozoospermia (65 cases). The comparison group consisted of 164 fertile men. Somatic cell lysis followed by mtDNA extraction was conducted to analyze three mtDNA polymorphisms, rs28357373 (T15629C (Leu295=), rs527236194 (T15784C (p.Pro346=), rs2853506 (A15218G, p.Thr158Ala). Detection and genotyping of polymorphic loci in the MT-CYB gene was performed using the TaqMan allelic discrimination assay. To verify mutations in the MT-CYB gene, automated Sanger DNA sequencing was used. We found that rs527236194 was associated with asthenoteratozoospermia. rs28357373 in the MT-CYB gene did not show any polymorphism in the analyzed groups, which indicates a rare frequency of the TT genotype in our region. Rs28357373 and rs2853506 are not associated with male sperm abnormalities in the Volga-Ural region.

conclusionThe association of the rs527236194 polymorphic variant with sperm parameter alterations suggests its role in the pathophysiology of male infertility and requires further investigation in larger samples.

Indexed as

AsthenozoospermiaCytochromes bCase-Control StudiesDNA, MitochondrialHumansMalePolymorphism, Single NucleotideSemenSpermatozoaCytochromes bDNA, MitochondrialAsthenoteratozoospermiaCytochrome BIdiopathic infertilityMitochondrial DNAMutationsOligoasthenoteratozoospermia

Identifiers

PMID37921983
OpenAlexW4388290061

What Socratic holds

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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 Socratic graph.