de Souza Bastos Alliny, Graves Dana T, de Melo Loureiro Ana Paula, Júnior Carlos Rossa, Corbi Sâmia Cruz Tfaile, Frizzera Fausto, Scarel-Caminaga Raquel Mantuaneli, Câmara Niels Olsen, Andriankaja Oelisoa M, Hiyane Meire I, Orrico Silvana Regina Perez
Department of Diagnosis and Surgery, Araraquara School of Dentistry UNESP-Univ Estadual Paulista, Araraquara, São Paulo, Brazil.
Department of Periodontics, School of Dental Medicine, University of Pennsylvania, Philadelphia, PA, United States.
J Diabetes Complications. 2016 Nov-Dec;30(8):1593-1599. doi: 10.1016/j.jdiacomp.2016.07.011. Epub 2016 Jul 21.
The effect of the interaction between type 2 diabetes and dyslipidemia on inflammation and lipid peroxidation (LPO) has not been assessed.
To investigate whether diabetes coupled with dyslipidemia alters oxidative metabolism leading to increased LPO products and inflammatory status.
100 patients were divided into four groups based upon diabetic and dyslipidemic status: poorly controlled diabetes with dyslipidemia (DM-PC/D), well-controlled diabetes with dyslipidemia (DM-WC/D), normoglycemic individuals with dyslipidemia (NG/D), and normoglycemic individuals without dyslipidemia (NG/ND). Plasma was evaluated for an LPO product (MDA), antioxidant levels and inflammatory cytokines.
Diabetics presented significantly higher levels of LPO (p<0.05) and the DM-PC/D had higher levels of proinflammatory cytokines and MDA in the plasma in comparison with normoglycemics (p<0.05). Interestingly IL1-β, IL-6, and TNF-α in DM-WC/D were not statistically different from those in DM-PC/D. Normoglycemic individuals with dyslipidemia presented significantly increased levels of IL-6 and TNF-α when compared to normoglycemic without dyslipidemia (p<0.05). MDA levels were also positively correlated with the presence of DM complications (r=0.42, p<0.01).
These findings show that dyslipidemia is associated with an increased inflammatory status, even in well-controlled diabetics and in normoglycemics. Our results suggest that lipid metabolism and peroxidation are important for the development of inflammation, which is elevated in several complications associated with diabetes.
2型糖尿病与血脂异常之间的相互作用对炎症和脂质过氧化(LPO)的影响尚未得到评估。
研究糖尿病合并血脂异常是否会改变氧化代谢,导致LPO产物增加和炎症状态改变。
根据糖尿病和血脂异常状况将100例患者分为四组:血糖控制不佳合并血脂异常的糖尿病患者(DM-PC/D)、血糖控制良好合并血脂异常的糖尿病患者(DM-WC/D)、血糖正常合并血脂异常的个体(NG/D)以及血糖正常且无血脂异常的个体(NG/ND)。评估血浆中的LPO产物(丙二醛)、抗氧化剂水平和炎性细胞因子。
糖尿病患者的LPO水平显著更高(p<0.05),与血糖正常者相比,DM-PC/D患者血浆中的促炎细胞因子和丙二醛水平更高(p<0.05)。有趣的是,DM-WC/D患者的IL1-β、IL-6和TNF-α与DM-PC/D患者相比无统计学差异。与无血脂异常的血糖正常个体相比,有血脂异常的血糖正常个体的IL-6和TNF-α水平显著升高(p<0.05)。丙二醛水平也与糖尿病并发症的存在呈正相关(r=0.42,p<0.01)。
这些发现表明,即使在血糖控制良好的糖尿病患者和血糖正常者中,血脂异常也与炎症状态增加有关。我们的结果表明,脂质代谢和过氧化对炎症的发展很重要,炎症在与糖尿病相关的几种并发症中会升高。