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代谢综合征的血脂异常成分、脂联素水平以及抗糖尿病药物对合并冠心病的他汀类药物治疗糖尿病患者的丙二醛修饰的低密度脂蛋白水平的影响。

Impact of dyslipidemic components of metabolic syndrome, adiponectin levels, and anti-diabetes medications on malondialdehyde-modified low-density lipoprotein levels in statin-treated diabetes patients with coronary artery disease.

机构信息

Department of Cardiology, National Hospital Organization Kure Medical Center and Chugoku Cancer Center, 3-1 Aoyamacho, Kure, Hiroshima 737-0023, Japan.

出版信息

Diabetol Metab Syndr. 2013 Dec 6;5(1):77. doi: 10.1186/1758-5996-5-77.

DOI:10.1186/1758-5996-5-77
PMID:24314067
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC4029151/
Abstract

BACKGROUND

A residual risk of cardiovascular disease tends to persist despite standard prevention therapy with statins. This may stem partly from increased oxidized low-density lipoprotein (LDL) levels. However, how oxidized LDL can be further reduced beyond statin therapy in high-risk diabetes patients remains unclear. We aimed to clarify the clinical factors associated with oxidized LDL levels in statin-treated high-risk diabetes patients.

METHODS

This cross-sectional observational study included 210 diabetes patients with coronary artery diseases (CAD) who were treated with statins. We determined serum malondialdehyde-modified LDL (MDA-LDL), LDL cholesterol, high-density lipoprotein (HDL) cholesterol, triglyceride (TG), remnant lipoprotein cholesterol, hemoglobin (Hb) A1c, adiponectin, and C-reactive protein (CRP) levels and investigated the factors influencing the MDA-LDL level.

RESULTS

In univariate analysis, the MDA-LDL level was significantly correlated with LDL cholesterol (p < 0.0001), TG (p < 0.0001), HDL cholesterol (p = 0.017), and adiponectin (p = 0.001) levels but not with age, body mass index, waist circumference, blood pressure, or HbA1c levels. Even after adjusting for the LDL cholesterol level, the correlations between the MDA-LDL level and the TG, HDL cholesterol, and adiponectin levels were still significant. Among these significant factors, multivariate analysis revealed that the MDA-LDL level was independently associated with the LDL cholesterol, TG, and HDL cholesterol but not with adiponectin levels. The MDA-LDL level was also significantly associated with the CRP level (p = 0.014) and the remnant lipoprotein cholesterol level (p < 0.0001) independently of the LDL cholesterol level. The number of metabolic syndrome (MS) components was significantly associated with the MDA-LDL/LDL cholesterol ratio (p < 0.0001). Furthermore, the use of metformin and α-glucosidase inhibitors was inversely associated with high MDA-LDL levels (p = 0.033 and 0.018, respectively).

CONCLUSION

In statin-treated diabetes patients with CAD, the MDA-LDL level was significantly correlated with TG and HDL cholesterol levels. Adiponectin level was also significantly associated with the MDA-LDL level, but not independent of the above-mentioned factors. The management of dyslipidemic MS components, including the use of metformin or α-glucosidase inhibitors, may be important for reducing the oxidized LDL levels beyond statin therapy in high-risk diabetes patients.

摘要

背景

尽管使用他汀类药物进行标准预防治疗,心血管疾病的残余风险仍倾向于持续存在。这可能部分源于氧化型低密度脂蛋白(LDL)水平升高。然而,在高危糖尿病患者中,除了他汀类药物治疗之外,如何进一步降低氧化型 LDL 水平仍不清楚。我们旨在阐明与他汀类药物治疗的高危糖尿病患者的氧化型 LDL 水平相关的临床因素。

方法

这是一项横断面观察性研究,纳入了 210 名患有冠状动脉疾病(CAD)的糖尿病患者,这些患者正在接受他汀类药物治疗。我们测定了血清丙二醛修饰的 LDL(MDA-LDL)、LDL 胆固醇、高密度脂蛋白(HDL)胆固醇、甘油三酯(TG)、残粒脂蛋白胆固醇、血红蛋白(Hb)A1c、脂联素和 C 反应蛋白(CRP)水平,并探讨了影响 MDA-LDL 水平的因素。

结果

在单因素分析中,MDA-LDL 水平与 LDL 胆固醇(p<0.0001)、TG(p<0.0001)、HDL 胆固醇(p=0.017)和脂联素(p=0.001)水平显著相关,但与年龄、体重指数、腰围、血压或 HbA1c 水平无关。即使在校正 LDL 胆固醇水平后,MDA-LDL 水平与 TG、HDL 胆固醇和脂联素水平之间的相关性仍然显著。在这些显著因素中,多因素分析显示 MDA-LDL 水平与 LDL 胆固醇、TG 和 HDL 胆固醇独立相关,但与脂联素水平无关。MDA-LDL 水平还与 CRP 水平(p=0.014)和残粒脂蛋白胆固醇水平(p<0.0001)独立于 LDL 胆固醇水平显著相关。代谢综合征(MS)成分的数量与 MDA-LDL/LDL 胆固醇比值显著相关(p<0.0001)。此外,使用二甲双胍和α-葡萄糖苷酶抑制剂与高 MDA-LDL 水平呈负相关(p=0.033 和 0.018)。

结论

在接受他汀类药物治疗的 CAD 合并糖尿病患者中,MDA-LDL 水平与 TG 和 HDL 胆固醇水平显著相关。脂联素水平也与 MDA-LDL 水平显著相关,但不受上述因素的影响。管理血脂异常的 MS 成分,包括使用二甲双胍或α-葡萄糖苷酶抑制剂,可能对降低高危糖尿病患者除他汀类药物治疗之外的氧化型 LDL 水平很重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29ec/4029151/76b80dc4b235/1758-5996-5-77-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29ec/4029151/b148d95d6578/1758-5996-5-77-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29ec/4029151/2dd13e9f27b4/1758-5996-5-77-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29ec/4029151/76b80dc4b235/1758-5996-5-77-3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29ec/4029151/b148d95d6578/1758-5996-5-77-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29ec/4029151/2dd13e9f27b4/1758-5996-5-77-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/29ec/4029151/76b80dc4b235/1758-5996-5-77-3.jpg

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