Evidence map›Paper›PMID 33718759›Full record

ArticleInternational journal of reproductive biomedicine2021

Y chromosome microdeletion and cytogenetic findings in male infertility: A cross-sectional descriptive study.

Meenakshi Arumugam, Deyyanthody Prashanth Shetty, Jayarama Shanker Kadandale, Suchetha Nalilu Kumari

Open access · goldAbstract read
In one paragraph

Article in International journal of reproductive biomedicine, 2021. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
1.9field-weighted citation impact, top 14% 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

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3 · Its place in the literature

Who cites it

3 citing papers in PubMed, 14 citations in OpenAlex.

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4 · The record

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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

4 authors at 1 institution in 1 country.

Meenakshi ArumugamKSHEMA Centre for Genetic Services, Kowdur Sadananda Hegde Medical Academy, Nitte University, Mangalore, Karnataka, India.
Deyyanthody Prashanth ShettyKSHEMA Centre for Genetic Services, Kowdur Sadananda Hegde Medical Academy, Nitte University, Mangalore, Karnataka, India.
Jayarama Shanker KadandaleKSHEMA Centre for Genetic Services, Kowdur Sadananda Hegde Medical Academy, Nitte University, Mangalore, Karnataka, India.
Suchetha Nalilu KumariDepartment of Biochemistry, Kowdur Sadananda Hegde Medical Academy, Nitte University, Mangalore, Karnataka, India.
K S Hegde Medical Academy · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundInfertility affects about 15% of couples worldwide, and the male factor alone is responsible for approximately 50% of the cases. Genetic factors have been found to play important roles in the etiology of azoospermia and severe oligospermia conditions that affect 30% of individuals seeking treatment at infertility clinics.

objectiveTo determine the frequency of chromosomal abnormalities and Y chromosome microdeletion in infertile men. MATERIALS AND

methodsA total of 100 infertile men with abnormal semen parameters were included in this study from 2014 to 2018. Chromosomal analysis was carried out using standard G-banding using Trypsin Giemsa protocol. Multiplex polymerase chain reaction was used to determine the Y microdeletion frequency.

resultsAll participants were aged between 22 and 48 yr with a mean and standard deviation of 35.5

conclusionThe present study emphasizes the importance of routine cytogenetic screening and Y microdeletion assessment for infertile men, which can provide specific and better treatment options before undergoing assisted reproductive technology during genetic counseling.

Indexed as

Chromosome aberrationsChromosome deletionInfertilityPolymerase chain reactionSequence tagged sites.

Identifiers

PMID33718759
PMCPMC7922297
OpenAlexW3130661063

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