Evidence map›Paper›PMID 34129647›Full record

ArticlePloS one2021

Sperm parameters and mitochondrial DNA sequence variants among patients at a fertility clinic in Ghana.

Bartholomew Dzudzor, Bismarck Bimah, Vincent Amarh, Augustine Ocloo

Erratum issuedOpen access · goldAbstract read
In one paragraph

Article in PloS one, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
2.3field-weighted citation impact, top 12% of its field
1 · What the graph read from it

What it found

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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

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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

8 citing papers in PubMed, 13 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors at 1 institution in 1 country.

Bartholomew DzudzorDepartment of Medical Biochemistry, University of Ghana Medical School, Korle Bu, Accra, Ghana.
Bismarck BimahDepartment of Medical Biochemistry, University of Ghana Medical School, Korle Bu, Accra, Ghana.
Vincent AmarhDepartment of Medical Biochemistry, University of Ghana Medical School, Korle Bu, Accra, Ghana.
Augustine OclooDepartment of Biochemistry, Cell and Molecular Biology, University of Ghana, Legon, Accra, Ghana.ORCID 0000-0003-1249-5349
University of Ghana · GH

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeThe present study sought to investigate the common abnormalities and mtDNA mutations in the sperm of Ghanaian men attending the fertility Clinic at the Korle-Bu Teaching Hospital (KBTH). The study therefore provides a baseline data mtDNA mutations in a cross-section of Ghanaian men on referral to the fertility clinic at the KBTH. MATERIALS AND

methodsThe semen of 55 men attending the fertility clinic were collected from the Urology and the Obstetrics and Gynaecology Departments of the KBTH. Demographic and clinical data were also collected using questionnaires. Semen analyses were performed and were followed by amplification and purification of mtDNA from total DNA extracted from the semen. Sequencing of the mtDNA amplicons was performed using the next generation sequencer (Illumina-MiSeq).

resultsAsthenozoospermia, oligospermia and oligoasthenoteratozoospermia were observed in 1.79%, 5.36% and 28.57%, respectively, of the study participants. There was no association between drinking and/or smoking and history of gonorrhea infection on sperm status/morphology. A total of 785 point mutations were detected in the non-coding control regions, rRNA genes, tRNA genes and the coding regions of the mtDNA samples from the participants. Amongst these mutations, 16 transition mutations were predominantly detected in the mtDNA samples. Missense mutations that were present in only specific sperm abnormalities were identified and they may contribute to infertility in the study population.

conclusionThe present study has identified various abnormal sperm phenotypes that are prevalent in the study population and provided a baseline data on mtDNA mutations in the spermatozoa of the patients. A wide range of sperm abnormalities were detected in the study population with no association with life style or history of gonorrhea infection. The mtDNA point mutations detected in the selected genes that were analysed were mostly transition mutations. These transition mutations might be critical for the development of abnormal sperm phenotypes underlying male infertility in the Ghanaian population.

Indexed as

Mutation, MissenseAdultCross-Sectional StudiesDNA, MitochondrialFertility ClinicsGhanaHigh-Throughput Nucleotide SequencingHumansInfertility, MaleMaleMiddle AgedMitochondriaSequence Analysis, DNASpermatozoaYoung AdultDNA, Mitochondrial

Identifiers

PMID34129647
PMCPMC8205148
OpenAlexW3168455889

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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.