Indices of low-grade chronic inflammation in polycystic ovary syndrome and the beneficial effect of metformin

被引:199
作者
Diamanti-Kandarakis, Evanthia
Paterakis, Thomas
Alexandraki, Krystallenia
Piperi, Christina
Aessopos, Athanasios
Katsikis, Ilias
Katsilambros, Nikolaos
Kreatsas, George
Panidis, Dimitrios
机构
[1] Univ Athens, Sch Med, Laiko Gen Hosp, Endocrine Sect,Dept Internal Med 1, Athens 14578, Greece
[2] Univ Athens, Sch Med, Biol Chem Lab, Athens, Greece
[3] Aristotle Univ Thessaloniki, Sch Med, Div Endocrinol & Human Reprod, Dept Obstet & Gynecol 2, Thessaloniki, Greece
[4] Univ Athens, Sch Med, Laiko Gen Hosp, Dept Propedeut Med, Athens, Greece
[5] Univ Athens, Sch Med, Aretaieion Hosp Athens, Dept Obstet & Gynaecol, Athens, Greece
关键词
cellular adhesion molecules; inflammation; insulin resistance; metformin; PCOS;
D O I
10.1093/humrep/del003
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
BACKGROUND: Women with polycystic ovary syndrome (PCOS) have an increased prevalence of insulin resistance (IR) and related disorders. Elevated serum levels of cellular adhesion molecules (CAMs) reflect low-grade chronic inflammation and have been associated with several insulin-resistant states. The objective of this study is to investigate whether soluble inflammatory markers [soluble intercellular adhesion molecule-1 (sICAM-1), soluble endothelial leukocyte adhesion molecule-1 (sE-selectin), soluble vascular cell adhesion molecule-1 (sVCAM-1) and C-reactive protein (CRP)] are altered in PCOS and to further elucidate the effect of metformin treatment on their levels. METHODS: Two young populations were studied [62 women with PCOS and 45 normal women of similar age, BMI and waist-to-hip ratio (WHR)]. Plasma levels of sICAM-1, sVCAM-1, sE-selectin and high-sensitivity CRP (hsCRP) were measured in both groups. Additionally, the effect of metformin on these molecules was investigated in 22 women with PCOS who accepted to metformin protocol (1700 mg daily for a 6-month period). RESULTS: In the total population studied, plasma levels of hsCRP (mg/l), sICAM-1 (ng/ml) and sE-selectin (ng/ml) were higher in the PCOS group compared with those in controls (hsCRP 1.31 +/- 0.22 versus 0.92 +/- 0.27, P = 0.014, sICAM-1 301.21 +/- 24.80 versus 209.86 +/- 17.05, P = 0.025, sE-selectin 57.37 +/- 4.08 versus 45.67 +/- 4.62, P = 0.045, respectively). sVCAM-1 (ng/ml) did not differ statistically among the two groups (P = 0.896). A significant reduction in hsCRP and sVCAM-1 was achieved after 6 months of metformin administration: PCOS pretreatment hsCRP 1.92 +/- 0.60 versus PCOS post-treatment hsCRP 0.52 +/- 0.26, P = 0.005; PCOS pretreatment sVCAM-1 668.09 +/- 98.38 versus PCOS post-treatment sVCAM-1 365.82 +/- 99.77, P = 0.039. CONCLUSION: These findings imply the presence of chronic inflammation in women with PCOS. Metformin decreases the levels of plasma inflammatory indices. Further investigation is required to determine whether these findings may prove to be of clinical significance for PCOS patients.
引用
收藏
页码:1426 / 1431
页数:6
相关论文
共 65 条
[61]   Alterations in cardiac flow parameters in patients with polycystic ovarian syndrome [J].
Tíras, MB ;
Yalçìn, R ;
Noyan, V ;
Maral, I ;
Yìldìrìm, M ;
Dörtlemez, O ;
Daya, S .
HUMAN REPRODUCTION, 1999, 14 (08) :1949-1952
[62]   Effect of intensive blood-glucose control with metformin on complications in overweight patients with type 2 diabetes (UKPDS 34) [J].
Turner, RC ;
Holman, RR ;
Stratton, IM ;
Cull, CA ;
Matthews, DR ;
Manley, SE ;
Frighi, V ;
Wright, D ;
Neil, A ;
Kohner, E ;
McElroy, H ;
Fox, C ;
Hadden, D .
LANCET, 1998, 352 (9131) :854-865
[63]   METFORMIN THERAPY IN POLYCYSTIC-OVARY-SYNDROME REDUCES HYPERINSULINEMIA, INSULIN-RESISTANCE, HYPERANDROGENEMIA, AND SYSTOLIC BLOOD-PRESSURE, WHILE FACILITATING NORMAL MENSES AND PREGNANCY [J].
VELAZQUEZ, EM ;
MENDOZA, S ;
HAMER, T ;
SOSA, F ;
GLUECK, CJ .
METABOLISM-CLINICAL AND EXPERIMENTAL, 1994, 43 (05) :647-654
[64]   The -597 G→A and -174 G→C polymorphisms in the promoter of the IL-6 gene are associated with hyperandrogenism [J].
Villuendas, G ;
San Millán, JL ;
Sancho, J ;
Escobar-Morreale, HF .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2002, 87 (03) :1134-1141
[65]   Clustering of metabolic factors and coronary heart disease [J].
Wilson, PWF ;
Kannel, WB ;
Silbershatz, H ;
D'Agostino, RB .
ARCHIVES OF INTERNAL MEDICINE, 1999, 159 (10) :1104-1109