首页> 美国卫生研究院文献>Frontiers in Endocrinology >The Effect of Atorvastatin (and Subsequent Metformin) on Adipose Tissue Acylation-Stimulatory-Protein Concentration and Inflammatory Biomarkers in Overweight/Obese Women With Polycystic Ovary Syndrome
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The Effect of Atorvastatin (and Subsequent Metformin) on Adipose Tissue Acylation-Stimulatory-Protein Concentration and Inflammatory Biomarkers in Overweight/Obese Women With Polycystic Ovary Syndrome

机译:阿托伐他汀(及随后的二甲双胍)对超重/肥胖多囊卵巢综合征女性脂肪组织酰化-刺激性蛋白质浓度和炎性生物标志物的影响

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摘要

>Background: Atorvastatin has been shown to improve cardiovascular risk (CVR) indices in women with polycystic ovary syndrome (PCOS). Low-grade chronic inflammation of adipose tissue may link PCOS and adverse CVR. In pro-inflammatory states such as PCOS, spontaneous activation of the alternative pathway of complement results in increased generation of acylation stimulating protein (ASP) from adipocytes irrespective of body mass index.>Methods: The objective of this study was to determine the effect of atorvastatin on markers of adipose tissue dysfunction and inflammation; acylation-stimulating-protein (ASP), interleukin-6 (IL-6), and monocyte-chemoattractant-protein-1 (MCP-1) in PCOS. This was a randomized, double-blind, placebo-controlled study where 40 medication-naive women with PCOS and biochemical hyperandrogenaemia were randomized to either atorvastatin 20 mg daily or placebo for 12 weeks. Following the 12 week randomization; both group of women with PCOS were subsequently started on metformin 1,500 mg daily for further 12 weeks to assess whether pre-treatment with atorvastatin potentiates the effects of metformin on markers of adipose tissue function We conducted a post-hoc review to detect plasma ASP and the pro-inflammatory cytokines IL6 and MCP-1 before and after 12 and 24 weeks of treatment.>Results: There was significant reduction in ASP (156.7 ± 16.2 vs. 124.4 ± 14.8 ng/ml p <0.01), IL-6 (1.48 ± 0.29 vs.0.73 ± 0.34 pg/ml p = 0.01) and MCP-1 (30.4 ± 4.2 vs. 23.0 ± 4.5 pg/ml p = 0.02) after 12 weeks of atorvastatin that was maintained subsequently with 12 weeks treatment with metformin. There was a significant positive correlation between ASP levels with CRP (p < 0.01), testosterone (p < 0.01) and HOMA-IR (p < 0.01); IL-6 levels with CRP (p <0.01) and testosterone (p < 0.01) and MCP-1 with CRP (p < 0.01); testosterone (p < 0.01) and HOMA-IR (p < 0.02).>Conclusions: This post-hoc analysis revealed that 12 weeks of atorvastatin treatment significantly decreased the markers of adipose tissue dysfunction and inflammation, namely ASP, IL-6 and MCP-1 in obese women with PCOS. Changes in adipose tissue markers were significantly associative with substantial improvements in HOMA-IR, testosterone and hs-CRP levels.>ISRCTN Number: ISRCTN24474824.
机译:>背景:阿托伐他汀已被证明可以改善多囊卵巢综合征(PCOS)妇女的心血管风险(CVR)指数。脂肪组织的轻度慢性炎症可能与PCOS和不良CVR相关。在PCOS等促炎状态下,补体替代途径的自发激活导致脂肪细胞产生的酰化刺激蛋白(ASP)的产生与体重指数无关。>方法:旨在确定阿托伐他汀对脂肪组织功能障碍和炎症标志物的作用; PCOS中的酰化刺激蛋白(ASP),白介素6(IL-6)和单核细胞趋化蛋白1(MCP-1)。这是一项随机,双盲,安慰剂对照的研究,其中将40名未接受过药物治疗的PCOS和生化高雄激素血症的女性随机分为阿托伐他汀每天20 mg或安慰剂12周。在12周随机分组后;两组患有PCOS的女性随后均开始每日1,500 mg二甲双胍治疗,持续12周,以评估阿托伐他汀预处理是否能增强二甲双胍对脂肪组织功能指标的影响。我们进行了事后评估,以检测血浆ASP和在治疗12和24周之前和之后促炎细胞因子IL6和MCP-1。>结果:ASP显着降低(156.7±16.2 vs. 124.4±14.8 ng / ml p <0.01) ,阿托伐他汀治疗12周后,IL-6(1.48±0.29 vs.0.73±0.34 pg / ml p = 0.01)和MCP-1(30.4±4.2 vs. 23.0±4.5 pg / ml p = 0.02),随后维持用二甲双胍治疗12周。 ASP水平与CRP(p <0.01),睾丸激素(p <0.01)和HOMA-IR(p <0.01)之间存在显着的正相关。 CRP(p <0.01)和睾丸激素(p <0.01)的IL-6水平以及CRP(p <0.01)的MCP-1水平;睾丸激素(p <0.01)和HOMA-IR(p <0.02)。>结论:此事后分析显示,阿托伐他汀治疗12周可显着降低脂肪组织功能障碍和炎症标志物,即ASP ,肥胖妇女患有PCOS时,IL-6,IL-6和MCP-1升高。脂肪组织标志物的变化与HOMA-IR,睾丸激素和hs-CRP水平的显着改善显着相关。> ISRCTN编号: ISRCTN24474824。

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