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The relationship between genetic variants associated with primary ovarian insufficiency and lipid profile in women recruited.pdf (735.96 kB)

The relationship between genetic variants associated with primary ovarian insufficiency and lipid profile in women recruited from MASHAD cohort study

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posted on 2023-06-10, 04:08 authored by Mohammad Reza Mirinezhad, Hamideh Ghazizadeh, Maliheh Aghsizadeh, Mohammad Zamiri Bidary, Alireza Naghipour, Elahe Hasanzadeh, Mahdiyeh Yaghooti-Khorasani, Ali Ebrahimi Dabagh, Mohammad Reza Shadmand Foumani Moghadam, Nazzanin Sheikh Andalibi, Zeynab Naseri Far, Habibollah Esmaily, Gordon FernsGordon Ferns, Tayebeh Hamzehloei, Alireza Pasdar, Majid Ghayour-Mobarhan
Background and aim: Primary Ovarian Insufficiency (POI) is defined by the occurrence of menopause before the age of 40 years. It is often associated with cardiovascular disease (CVD). The purpose of this study was to explore the relationship between POI-associated genotypes cardiometabolic disorder risk factors. Methods: One hundred seventeen women with POI and one hundred eighty-three healthy women without POI were recruited in this study. DNA was extracted and analyzed using ASO-PCR or Tetra ARMS-PCR. Lipid profiles were also assessed. Results: Multivariate logistic regression analysis showed that individuals with GG vs. TT genotype of the rs1046089 SNP were more likely to have a higher serum LDL (p = 0.03) compared to the control group. There was also a significant association between low serum HDL and rs2303369 and rs4806660 SNP genotypes in the POI group. In the POI group, the percentage of those with high total cholesterol was lower in those with a CC genotype compared to those with a TT genotype (p = 0.03). Conclusion: Some SNPs reported to be associated with POI appear to be independently associated with dyslipidemia. These results may be helpful to identify subjects with POI who may be susceptible to CVD.

History

Publication status

  • Published

File Version

  • Published version

Journal

BMC Women's Health

ISSN

1472-6874

Publisher

Springer Science and Business Media LLC

Volume

22

Page range

2

Event location

England

Department affiliated with

  • Division of Medical Education Publications

Full text available

  • Yes

Peer reviewed?

  • Yes

Legacy Posted Date

2022-07-04

First Open Access (FOA) Date

2022-07-04

First Compliant Deposit (FCD) Date

2022-07-04

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