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Proteins and peptides biochemically changes of metabolism regulate in patients serum with polycystic ovary syndrome
Polycystic ovarian syndrome (PCOS) is a crucial aspect characterized as the most widespread endocrine disease. The pathogenesis of this complex for patients with PCOS has hyperandrogenism affecting women at reproductive age The metabolic pathways may be involved in the PCOS pathophysiology. Obesity and overweight are used to designate irregular or extreme weight growth that affects the production ability. This study aimed to quantity the nesfatin-1, preptin, and omentin levels in the serum of females who had polycystic ovarian syndrome, besides being overweight, and also to find the correlation between the variables. Likewise, this study focused on the peptides and proteins that might be interrelated with PCOS pathogenesis with the probability and efficacy of measuring their levels in clinical practice. The study included 84 women, ages 18 to 34 years, the first group included 42 women who have polycystic ovarian syndrome, and the second group comprised 42 women who appear to be in health besides serving by way of the control group. Women who smoke, have chronic circumstances like high blood pressure, and use illicit drugs were excluded from both groups. All women have a body mass index that is used to regulate their quantity of obesity. A considerable decrease in the level of Nesfatin-1 and Omentin, while rises in Preptin levels are observed. Polycystic ovarian syndrome women than the control group (p< 0.05) is significant. The results of this study revealed the proteins and peptides affect metabolic regulation and possibly can be measured as biomarkers in some clinical conditions like polycystic ovarian syndrome (PCOS nesfatin-1, preptin, and omentin were observed to increase significantly in patients with PCOS and correlated with BMI. © 2025 by SPC
Authors : Jassim S.M.; Hussein H.H.; Al-Asadi E.H.; Kadhum A.A.H.; Al-Amiery A.A.
Source : Sami Publishing Company
Article Information
| Year | 2025 |
| Type | Article |
| DOI | 10.48309/jmpcr.2025.474973.1405 |
| ISSN | 29810221 |
| Volume | 7 |
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