Evidence map›Paper›PMID 37543931›Full record

ArticleArchives of Iranian medicine2023

Prevalence of Chromosomal Abnormalities in Iranian Patients with Infertility.

Saima Abbaspour, Alireza Isazadeh, Matin Heidari, Masoud Heidari, Saba Hajazimian, Morteza Soleyman-Nejad, Mohammad Hossein Taskhiri, Manzar Bolhassani, Amir Hossein Ebrahimi, Parvaneh Keshavarz and 2 more

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Article in Archives of Iranian medicine, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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4citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

12 authors.

Saima AbbaspourCellular and Molecular Research Center, Faculty of Medicine, Guilan University of Medical Sciences, Rasht, Iran.ORCID 0009-0002-1867-4364
Alireza IsazadehImmunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.ORCID 0000-0002-8781-1177
Matin HeidariAriagene Medical Genetics Laboratory, Qom, Iran.
Masoud HeidariDepartment of Animal Biology, Faculty of Natural Sciences, University of Tabriz, Tabriz, Iran.
Saba HajazimianImmunology Research Center, Tabriz University of Medical Sciences, Tabriz, Iran.
Morteza Soleyman-NejadAriagene Medical Genetics Laboratory, Qom, Iran.
Mohammad Hossein TaskhiriAriagene Medical Genetics Laboratory, Qom, Iran.
Manzar BolhassaniAriagene Medical Genetics Laboratory, Qom, Iran.
Amir Hossein EbrahimiAriagene Medical Genetics Laboratory, Qom, Iran.
Parvaneh KeshavarzCellular and Molecular Research Center, Faculty of Medicine, Guilan University of Medical Sciences, Rasht, Iran.
Zahra ShiriAriagene Medical Genetics Laboratory, Qom, Iran.
Mansour HeidariAriagene Medical Genetics Laboratory, Qom, Iran.ORCID 0000-0001-6394-0970

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundThe numerical and structural abnormalities of chromosomes are the most common cause of infertility. Here, we evaluated the prevalence and types of chromosomal abnormalities in Iranian infertile patients.

methodsWe enrolled 1750 couples of reproductive age with infertility, who referred to infertility clinics in Tehran during 2014- 2019, in order to perform chromosomal analysis. Peripheral blood samples were obtained from all couples and chromosomal abnormalities were evaluated by G-banded metaphase karyotyping. In some cases, the detected abnormalities were confirmed using fluorescence

resultsWe detected various chromosomal abnormalities in 114/3500 (3.257%) patients with infertility. The prevalence of chromosomal abnormalities was 44/114 (38.596%) among infertile females and 70/114 (61.403%) among infertile males. Structural chromosomal abnormalities were found in 27/1750 infertile females and 35/1750 infertile males. Numerical chromosomal abnormalities were found in 17/1750 of females and 35/1750 of males. The 45, XY, rob (13;14) (p10q10) translocation and Klinefelter syndrome (47, XXY) were the most common structural and numerical chromosomal abnormalities in the Iranian infertile patients, respectively.

conclusionIn general, we found a high prevalence of chromosomal abnormalities in Iranian patients with reproductive problems. Our study highlights the importance of cytogenetic studies in infertile patients before starting infertility treatments approaches.

Indexed as

Infertility, FemaleInfertility, MaleChromosome AberrationsFemaleHumansIranKaryotypingMalePrevalenceChromosomal abnormalitiesCytogeneticsInfertilityKaryotyping

Identifiers

PMID37543931
PMCPMC10685900

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