Analysis of chromosome in 1 324 patients with oligozoospermia or azoosperm.
- Author:
Xiao Wei DAI
1
;
Ying XU
1
;
Lian Wen ZHENG
1
;
Ling Yun LI
1
;
Dan Dan LI
1
;
Xin TAN
2
;
Fei GAO
1
;
Yan WANG
1
;
Gui Jie WU
1
Author Information
1. Center for Reproduction Medicine, the Second Hospital of Jilin University, Changchun 130041, China.
2. Medical Insurance Office, the Second Hospital of Jilin University, Changchun 130041, China.
- Publication Type:Journal Article
- MeSH:
Azoospermia/genetics*;
Chromosome Aberrations;
Chromosome Deletion;
Chromosomes, Human, Y;
Humans;
Infertility, Male/genetics*;
Male;
Oligospermia/genetics*;
Retrospective Studies
- From:
Journal of Peking University(Health Sciences)
2018;50(5):774-777
- CountryChina
- Language:Chinese
-
Abstract:
OBJECTIVE:To explore the incidience of chromosome abnormality of the patients with oligozoospermia or azoospermia and male infertility, to discuss the relationship between the quantitative and structural abnormality of chromosome and to lay the foundation for the clinical diagnosis and consultation.
METHODS:A retrospective analysis was conducted from January 1, 2015 to May 1, 2016, in the Center for Reproduction Medicine, the Second Hospital of Jilin University, with male reproductive abnormalities history excluded. In the study, 1 324 cases were included with 448 cases of azoospermia and 876 cases of oligozoospermia. All the patients through ultrasound examination, color Doppler ultrasonography, the seminal plasma Zn determination, their hormone level determination, chromosome karyotype (the perinatal blood samples were obtained from the 1 324 patients with oligozoospermia or azoospermia for lymphocyte culture, then chromosomal specimens were prepared, G-banding analyses combined with clinical data were used to statistically analyze the incidence of chromosomal abnormality), Y chromosome azoospermia factor [PCR technique was used to detect SY157 locus, SY254 locus, and SY255 locus in male Y chromosome azoospermia factor (AZF) gene of the patients with oligozoospermia or azoospermia]. The relationship between chromosome abnormalities and oligozoospermia or azoospermia were analyzed.
RESULTS:Among the 876 cases of oligospermia patients, 78 cases were chromosome number abnormality and chromosomal structural abnormality, the abnormal number of sex chromosomes in 22 cases, and sex chromosomes and chromosome structural abnormalities in 56 cases; in the 448 cases of azoospermia patients, 91 cases were chromosomal structural abnormality and chromosome number abnormality, of them, 78 cases were of abnormal number of sex chromosomes, and 13 cases were of abnormal structure. In addition, 137 cases were of chromosome polymorphism in all the 1 324 patients, The incidence of Y chromosome abnormality in azoospermatism was higher than that of the 43 patients with Y chromosome AZF microdeletion. In addition, the asthenospermia and recurrent spontaneous abortion were closely related to Y chromosome abnormality and the chromosome translocations and inversions.
CONCLUSION:Oligozoospermia and azoospermia patients with abnormal chromosome karyotype have high incidence rate, and chromosome karyotype analyses were carried out on it, which is conducive to clinical diagnosis for the patients with abnormal chromosome karyotype. There is a close relationship between male infertility and abnormal karyotype. It is conducive to clinical diagnosis for the patients with infertility through chromosome karyotye analysis, which also provides evidence for genetic counseling.
