Evidence map›Paper›PMID 39039641›Full record

ArticleClinical and experimental reproductive medicine2025

Contribution of chromosomal aberrations to the pathogenesis of primary and secondary amenorrhea: A study from Western Iran.

Azam Azimi, Matin Heidari, Reza Alibakhshi, Sara Hamani, Negar Salimi, Parham Nejati, Nazanin Jalilian

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Article in Clinical and experimental reproductive medicine, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

Authors and funding

7 authors.

Azam AzimiMedical Genetics Laboratory, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Matin HeidariStudent Research Committee, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Reza AlibakhshiDepartment of Clinical Biochemistry, School of Medicine, Kermanshah University of Medical sciences, Kermanshah, Iran.
Sara HamaniMedical Genetics Laboratory, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Negar SalimiMedical Genetics Laboratory, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Parham NejatiMedical Genetics Laboratory, Kermanshah University of Medical Sciences, Kermanshah, Iran.
Nazanin JalilianDepartment of Clinical Biochemistry, School of Medicine, Kermanshah University of Medical sciences, Kermanshah, Iran.

Funding

Deputy for Research and Technology, Kermanshah University of Medical Sciences 4010776
6 · The paper itself

Abstract

objectiveAmenorrhea is an abnormal condition characterized by the absence of menstruation in women of reproductive age. According to the World Health Organization, amenorrhea ranks as the sixth leading cause of female infertility. Approximately 2% to 5% of women of reproductive age experience amenorrhea, which can be classified as primary amenorrhea (PA) or secondary amenorrhea (SA). Several studies have named chromosomal abnormalities among the main causes of amenorrhea, though the prevalence of these abnormalities may differ across populations. The objective of this study was to ascertain the frequency and types of chromosomal abnormalities in women with amenorrhea in Kermanshah Province, Iran.

methodsThis retrospective study included patients with PA and SA who underwent standard cytogenetic analysis. We also conducted a review of the literature on chromosomal abnormalities and their prevalence in SA.

resultsAmong the 137 cases of PA in this study, 22% exhibited chromosomal abnormalities. Numerical changes were the most common finding (46.6%) in this group, including 45,X, mosaic, and 47,XXX karyotypes. These were followed by the 46,XY karyotype (40%). Of the 51 cases of SA that received chromosomal analysis, abnormalities were identified in only one case. Additionally, our review of the literature revealed that chromosomal aberrations are responsible for 7% of SA cases globally.

conclusionIn this study, we successfully characterized the cytogenetic causes of PA and SA in a substantial population from Kermanshah Province, Iran.

Indexed as

AmenorrheaChromosome aberrationsIran

Identifiers

PMID39039641
PMCPMC11900666

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