4.2 Article

Serum INHB levels and ACE gene I/D polymorphism with increased risk for unexplained infertility

Journal

JOURNAL OF BIOCHEMISTRY
Volume 170, Issue 2, Pages 245-253

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/jb/mvab036

Keywords

angiotensin converting enzyme (ACE); anti-Mullerian hormone (AMH); inhibin-B (INHB); polymorphism; unexplained infertility (UI)

Funding

  1. GAZI University Projects of Scientific Investigation (GUBAP) [02/2015-03]

Ask authors/readers for more resources

The study found that UI patients had significantly higher serum INHB levels compared with controls, decreased serum ACE levels, and no significant difference in serum AMH levels. Analysis showed that the DD genotype of ACE insertion/deletion polymorphism may be associated with a higher risk for UI. Further studies with larger populations are needed to confirm these findings.
Angiotensin converting enzyme (ACE) has a significant role in the angiogenesis of ovarian endothelium and the resumption of meiosis and folicular growth. However, there is no any study concerning ACE polymorphism and unexplained infertility (UI). The main aim of this study is that both identify ACE polymorphism and measure the serum ACE, anti-Mullerian hormone (AMH) and inhibin-B (INHB) levels in UI patients and controls in Turkish population. Forty-seven UI patients and 41 controls were involved in this study. To determine the ACE polymorphisms, DNA isolation and PCR were performed. Then, serum ACE, AMH and INHB levels were measured spectrophotometrically. Patients with UI had significantly higher serum INHB levels compared with controls (P< 0.05). Serum ACE levels were decreased, compared to controls; however, the decrease was not significant. Serum AMH levels did not significantly differ from controls. When the relationship was analysed between ACE insertion/deletion (I/D) polymorphism and infertility risk, and ID genotype was chosen as reference, it was found to be 2.33 times more risk of UI than the women have DD genotype IDD versus ID: odds ratio = 2.33, 95% confidence interval (0.88-6.19); P = 0.086]. This finding indicates that DD genotype may be high risk for UI. Further studies are warranted to confirm this finding, especially with a larger population. [GRAPHICS] .

Authors

I am an author on this paper
Click your name to claim this paper and add it to your profile.

Reviews

Primary Rating

4.2
Not enough ratings

Secondary Ratings

Novelty
-
Significance
-
Scientific rigor
-
Rate this paper

Recommended

No Data Available
No Data Available