Sex Hormone-Binding Globulin (SHBG) as an Early Biomarker and Therapeutic Target in Polycystic Ovary Syndrome

被引:115
作者
Qu, Xianqin [1 ]
Donnelly, Richard [2 ]
机构
[1] Univ Technol Sydney, Sch Life Sci, Ultimo, NSW 2007, Australia
[2] Univ Nottingham, Sch Med, Derby DE22 3DT, England
关键词
adolescents; hepatic lipogenesis; human sex hormone-binding globulin; insulin resistance; non-alcoholic fatty liver disease; polycystic ovary syndrome; FATTY LIVER-DISEASE; METABOLIC SYNDROME; DOWN-REGULATION; INSULIN-RESISTANCE; GENE-EXPRESSION; OBESE WOMEN; RISK; TESTOSTERONE; ANDROGEN; ADOLESCENCE;
D O I
10.3390/ijms21218191
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Human sex hormone-binding globulin (SHBG) is a glycoprotein produced by the liver that binds sex steroids with high affinity and specificity. Clinical observations and reports in the literature have suggested a negative correlation between circulating SHBG levels and markers of non-alcoholic fatty liver disease (NAFLD) and insulin resistance. Decreased SHBG levels increase the bioavailability of androgens, which in turn leads to progression of ovarian pathology, anovulation and the phenotypic characteristics of polycystic ovarian syndrome (PCOS). This review will use a case report to illustrate the inter-relationships between SHBG, NAFLD and PCOS. In particular, we will review the evidence that low hepatic SHBG production may be a key step in the pathogenesis of PCOS. Furthermore, there is emerging evidence that serum SHBG levels may be useful as a diagnostic biomarker and therapeutic target for managing women with PCOS.
引用
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页码:1 / 17
页数:17
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