Evidence map›Paper›PMID 26393143›Full record

ArticleJournal of clinical and diagnostic research : JCDR2015

Chromosomal Abnormalities in Infertile Men from Southern India.

Jaganathan Suganya, Smita B Kujur, Kamala Selvaraj, Muthiah S Suruli, Geetha Haripriya, Chandra R Samuel

Open access · goldAbstract read
In one paragraph

Article in Journal of clinical and diagnostic research : JCDR, 2015. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 18 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
18citing papers in PubMed, 1 pooled it
3.0field-weighted citation impact, top 8% 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

18 citing papers in PubMed, 1 synthesis or guideline pooled it, 35 citations in OpenAlex.

  1. Evidence-based guideline: unexplained infertility†.Human reproduction (Oxford, England) · 2023
    Guideline
  2. LncRNAiScience · 2026
    Article
  3. Article
  4. Review
  5. Article
  6. Article
  7. Article
  8. Review
  9. Article
  10. Article
  11. Article
  12. Clinical Features of Chromosome 6 Translocation in Male Carriers: A Report of 10 Cases and Review of the Literature.Medical science monitor : international medical journal of experimental and clinical research · 2018
    Review
  13. Article
  14. Article
  15. Review
  16. Asian journal of andrology
    Article
  17. Article
  18. 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

6 authors at 1 institution in 1 country.

Jaganathan SuganyaResearch Scholar, Department of Genetics, Dr. ALMPGIBMS, University of Madras , Taramani, Chennai, Tamil Nadu, India .
Smita B KujurProject Fellow, Department of Genetics, Dr. ALMPGIBMS, University of Madras , Taramani, Chennai, Tamil Nadu, India .
Kamala SelvarajObstetrician and Gynecologist, G.G Hospital , 6-E, Thirumoorthy Nagar, Nungambakkam High Road, Nungambakkam, Chennai, Tamil Nadu, India .
Muthiah S SuruliDirector & Embryologist, Kanmani Fertility Centre , 43, South Usman Road, T Nagar, Chennai, Tamil Nadu, India .
Geetha HaripriyaObstetrician & Gynaecologist, Prashanth Fertility Research Centre , 77, Harrington Road, Chetpet, Chennai, Tamil Nadu, India .
Chandra R SamuelAssociate Professor, Department of Genetics, Dr.ALMPGIBMS, University of Madras , Taramani, Chennai, Tamil Nadu, India .
University of Madras · IN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

BACKGROUND AND

objectiveMale infertility has been associated with aneuploidies and structural chromosomal abnormalities, Yq microdeletions and specific gene mutations and/or polymorphisms. Besides genetic factors, any block in sperm delivery, endocrine disorders, testicular tumours, infectious diseases, medications, lifestyle factors and environmental toxins can also play a causative role. This study aimed to determine the constitutional karyotype in infertile males having normal female partners in a south Indian population. MATERIALS AND

methodsA total of 180 men with a complaint of primary infertility ranging from 1 to 25 years were screened for chromosomal abnormalities through conventional analysis of GTG-banded metaphases from cultured lymphocytes.

resultsFour individuals were diagnosed to have Klinefelter syndrome. Two cases exhibited reciprocal translocations and one showed a maternally inherited insertion. Polymorphisms were seen in sixty-seven patients (37.2%).

conclusionThe occurrence of chromosomal abnormalities in 4.6% and variants involving the heterochromatic regions of Y, chromosome 9 and the acrocentric chromosomes in 38.2% of the infertile men with an abnormal seminogram strongly reiterates the inclusion of routine cytogenetic testing and counselling in the diagnostic work-up prior to the use of assisted reproduction technologies.

Indexed as

AzoospermiaChromosomal polymorphismsInsertionKlinefelter syndromeMale infertilityOligozoospermiaReciprocal translocation

Identifiers

PMID26393143
PMCPMC4572974
OpenAlexW2269068816

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.