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The Journal of clinical endocrinology and metabolism · 2010

Proteomic analysis of plasma in the polycystic ovary syndrome identifies novel markers involved in iron metabolism, acute-phase response, and inflammation.

СтатьяПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
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Insenser María, Martínez-García M Angeles, Montes Rafael, San-Millán José L, Escobar-Morreale Héctor F

Аннотация

CONTEXT: Hypothesis-free approaches such as proteomic analysis may identify novel biomarkers for disease.

OBJECTIVE: The objective of the study was to compare the plasma proteome of patients presenting with the polycystic ovary syndrome (PCOS) with that of women without hyperandrogenism.

DESIGN: This was a case-control study.

SETTINGS: The study was conducted at an academic hospital.

PATIENTS: Patients included 12 PCOS patients and 12 women without hyperandrogenism.

INTERVENTIONS: Interventions included basal blood sampling.

MAIN OUTCOME MEASURES: Two-dimensional difference in-gel electrophoresis, matrix-assisted laser desorption/ionization-time-of-flight mass spectrometry, Western blot, and ELISA analyses were measured.

RESULTS: Two-dimensional difference in-gel electrophoresis and matrix-assisted laser desorption/ionization-time-of-flight mass spectrometry analyses identified haptoglobin beta-chain and alpha2-macroglobulin as proteins underexpressed in PCOS samples, whereas transferrin and kappa-free light chain were overexpressed. We were able to confirm only the underexpression of haptoglobin beta-chain in subsequent Western blot and ELISA analyses.

CONCLUSIONS: Proteomic analysis of plasma from PCOS patients revealed changes in protein expression in several acute-phase response proteins including isoforms of plasma haptoglobin, alpha2-macroglobulin, and transferrin and in kappa-free light chain. In addition to their role as inflammatory markers, some of these molecules play major roles in iron metabolism, further suggesting that iron metabolism and low-grade chronic inflammation may be involved in the pathogenesis of insulin-resistant disorders such as PCOS.

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