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作 者:曾瑶池 赵恒侠[2] 李金花[2] 刘燕平[2] 王太芬[2] 穆桂萍[3]
机构地区:[1]深圳市中医院营养科,深圳518033 [2]深圳市中医院营养科内分泌科,深圳518033 [3]深圳市中医院中心实验室,深圳518033
出 处:《营养学报》2013年第3期268-272,共5页Acta Nutrimenta Sinica
基 金:广东省深圳市科技计划项目(No.201103377);广东省医学科研基金立项课题(No.A2012568)
摘 要:目的探讨2型糖尿病(T2DM)患者血清炎症因子水平与颈动脉内膜中层厚度(CIMT)的关系及番茄红素(Lyc)的干预效果。方法选取T2DM患者130例随机分为:A组(干预组)64例,给予Lyc胶囊30mg/d;B组(对照组)66例,不服用Lyc但给予安慰剂。两组患者均采集入组时和干预后6个月的空腹血清,监测血糖、生化指标、炎症因子和CIMT。结果 Lyc干预6个月后,A组IL-6、TNF-α、hs-CRP、NF-κB水平显著降低,均低于B组(P<0.05),B组上述炎症因子水平变化差异无统计学意义(P>0.05);干预后A组患者CIMT及颈动脉斑块发生率较干预前及B组明显下降;T2DM患者CIMT与炎症因子水平相关,多元回归分析表明NF-κB、HbAlc和hs-CRP是CIMT的独立影响因素(决定系数R2=0.612,P=0.000)。结论 T2DM患者炎症因子水平是CIMT的独立预测因素,Lyc可能通过降低炎症因子水平而抑制T2DM患者早期动脉粥样硬化的发生、发展。Objective To examine whether inflammatory cytokines were related to carotid artery intima media thickness (CIMT) in type 2 diabetic patients and evaluate the effect of lycopene (Lyc) on them. Methods One hundred and thirty T2DM patients without major vascular complications were recruited and randomly divided into two groups: Lyc treated group (A group, n=64) and control group (B group, n-66). In A group, the patients were given orally Lyc 30 mg twice daily for 6 months. In B group, the patients were given the placebo for 6 mo. Their biochemical indicators and inflammatory cytokines and carotid intima-media thickness were measured before and after the treatment. Results After treatment with Lyc, the interleukin-6 (IL-6), tumor necrosis factor (TNF-a ), (hypersensitive 3 C-reactive, hs-CRP), and nuclear factor kappa B (NF-KB) decreased significantly (P〈0.05). Most data had no marked changes in the B group (P〉0.05). After treatment with Lyc, CIMT and the incidence of carotid atherosclerotic (AS) plaque decreased significantly (P〈0.05). Pearson correlation analysis showed that CIMT was positively correlated with IL-6, TNF-ct, hs-CRP and NF-B (P〈0.05). Multivariate regression analysis showed that NF-B, HbAlc and hs-CRP concentration were independent predictors of CIMT in this cohort (R2 =0.612, P=0.000). Conclusion High concentration of inflammatory cytokines is risk factor for preclinical AS in T2DM patients. Lyc may delay the occurrence and development of AS via decreased inflammatory cytokines concentration.
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