Evidence map›Paper›PMID 22415247›Full record

ArticleJournal of assisted reproduction and genetics2012

Genetic screening for chromosomal abnormalities and Y chromosome microdeletions in Chinese infertile men.

Li Fu, Da-Ke Xiong, Xian-Ping Ding, Chuang Li, Li-Yuan Zhang, Min Ding, Shuang-Shuang Nie, Qiang Quan

Open access · bronzeAbstract read
In one paragraph

Article in Journal of assisted reproduction and genetics, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 1 pooled it
2.7field-weighted citation impact, top 10% 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

22 citing papers in PubMed, 1 synthesis or guideline pooled it, 60 citations in OpenAlex.

  1. Male fertility potential alteration in rheumatic diseases: a systematic review.International braz j urol : official journal of the Brazilian Society of Urology
    Pooled it
  2. Article
  3. Article
  4. Article
  5. Article
  6. Repetitive DNA Sequences in the Human Y Chromosome and Male Infertility.Frontiers in cell and developmental biology · 2022
    Review
  7. Review
  8. Article
  9. Genetic counseling prior to assisted reproductive technology.Reproductive medicine and biology · 2021
    Review
  10. Article
  11. Article
  12. Article
  13. Observational
  14. Observational
  15. Genetics of the human Y chromosome and its association with male infertility.Reproductive biology and endocrinology : RB&E · 2018
    Review
  16. Article
  17. Article
  18. Chromosomal Abnormalities in Infertile Men from Southern India.Journal of clinical and diagnostic research : JCDR · 2015
    Article
  19. Article
  20. Article
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

8 authors at 1 institution in 1 country.

Li FuInstitute of Medical Genetics, Key Laboratory of Bio-resources and Eco-environment, Ministry of Education, College of Life Science, Sichuan University, Chengdu 610064, China.
Da-Ke Xiong
Xian-Ping Ding
Chuang Li
Li-Yuan Zhang
Min Ding
Shuang-Shuang Nie
Qiang Quan
Sichuan University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposesTo investigate the frequency and type of both chromosomal abnormalities and Y chromosome microdeletions and analyze their association with defective spermatogenesis in Chinese infertile men.

methodsThis is a single center study. Karyotyping using G-banding and screening for Y chromosome microdeletion by multiplex polymerase chain reaction(PCR)were performed in 200 controls and 1,333 infertile men, including 945 patients with non-obstructive azoospermia and 388 patients with severe oligozoospermia.

resultsOut of 1,333 infertile patients, 154(11.55%) presented chromosomal abnormalities. Of these, 139 of 945 (14.71%) were from the azoospermic and 15 of 388 (3.87%) from the severe oligozoospermic patient groups. The incidence of sex chromosomal abnormalities in men with azoospermia was 11.53% compared with 1.03% in men with severe oligozoospermia (P < 0.01). Also 144 of 1,333(10.80%) patients presented Y chromosome microdeletions. The incidence of azoospermia factor(AZF) microdeletion was 11.75% and 8.51% in patients with azoospermia and severe oligozoospermia respectively. Deletion of AZFc was the most common and deletions in AZFa or AZFab or AZFabc were found in azoospermic men. In addition, 34 patients had chromosomal abnormalities among the 144 patients with Y chromosome microdeletions. No chromosomal abnormality and microdeletion in AZF region were detected in controls.

conclusionsThere was a high incidence (19.80%) of chromosomal abnormalities and Y chromosomal microdeletions in Chinese infertile males with azoospermia or severe oligozoospermia. These findings strongly suggest that genetic screening should be advised to infertile men before starting assisted reproductive treatments.

Indexed as

Chromosome AberrationsChromosomes, Human, YAsian PeopleAzoospermiaCase-Control StudiesChromosome DeletionGenetic TestingHumansInfertility, MaleKaryotypeMaleMultiplex Polymerase Chain ReactionOligospermiaSex Chromosome AberrationsSex Chromosome Disorders of Sex DevelopmentSpermatogenesis

Identifiers

PMID22415247
PMCPMC3370047
OpenAlexW1988943795

What OpenQuestion 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 OpenQuestion graph.