Influence of obesity on soluble endoglin and transforming growth factor β1 in women with polycystic ovary syndrome
Chronic low-grade inflammation is a common feature of obesity and polycystic ovary syndrome (PCOS). There is dysregulation of transforming growth factor (TGF)-β1 in women with PCOS, soluble endoglin (sEng) is a non-signaling coreceptor of the TGF-β modulating its responses. We aimed for the first ti...
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Published in | Middle East Fertility Society journal Vol. 23; no. 4; pp. 418 - 424 |
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Main Authors | , , , |
Format | Journal Article |
Language | English |
Published |
Elsevier B.V
01.12.2018
SpringerOpen |
Subjects | |
Online Access | Get full text |
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Summary: | Chronic low-grade inflammation is a common feature of obesity and polycystic ovary syndrome (PCOS). There is dysregulation of transforming growth factor (TGF)-β1 in women with PCOS, soluble endoglin (sEng) is a non-signaling coreceptor of the TGF-β modulating its responses. We aimed for the first time to investigate the impact of obesity on sEng and TGF-β1 in women with PCOS.
Case control study enrolled seventy patients diagnosed with PCOS and50 control group. High sensitivity C-reactive protein (hs-CRP) and sEng levels were assessed using an enzyme-linked immunosorbent assay (ELISA).
Our results revealed that, PCOS patients had higher values of TGF-β1 and lower levels of sEng. Among both control and PCOS patients, obese subjects had higher values of TGF-β1 and lower levels of sEng. Receiver operating characteristic curve (ROC) analysis revealed that, the power of sEng was more sensitive and specific than TGF-β1 in diagnosis of PCOS and in differentiating obese from lean group. Nonetheless, the diagnostic power of both TGF-β1 and sEng was highly significant.
Obese subjects of control and PCOS groups had higher values of TGF-β1 and lower values of plasma sEng level than lean subjects, the diagnostic power of both TGF-β1 and sEng was highly significant thus, sEng and TGF-β1 could be a useful diagnostic biomarker of PCOS. |
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ISSN: | 1110-5690 |
DOI: | 10.1016/j.mefs.2018.07.003 |