首页> 外文期刊>Progress in Neuro-Psychopharmacology & Biological Psychiatry: An International Research, Review and News Journal >Multiple aberrations in shared inflammatory and oxidative & nitrosative stress (IO&NS) pathways explain the co-association of depression and cardiovascular disorder (CVD), and the increased risk for CVD and due mortality in depressed patients.
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Multiple aberrations in shared inflammatory and oxidative & nitrosative stress (IO&NS) pathways explain the co-association of depression and cardiovascular disorder (CVD), and the increased risk for CVD and due mortality in depressed patients.

机译:共有的炎症,氧化和亚硝化应激(IO&NS)途径中的多个畸变解释了抑郁症和心血管疾病(CVD)的共同关联,以及抑郁症患者的CVD风险增加和应有的死亡率。

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摘要

There is evidence that there is a bidirectional relationship between major depression and cardiovascular disorder (CVD): depressed patients are a population at risk for increased cardiac morbidity and mortality, and depression is more frequent in patients who suffer from CVD. There is also evidence that inflammatory and oxidative and nitrosative stress (IO&NS) pathways underpin the common pathophysiology of both CVD and major depression. Activation of these pathways may increase risk for both disorders and contribute to shared risk. The shared IO&NS pathways that may contribute to CVD and depression comprise the following: increased levels of pro-inflammatory cytokines, like interleukin-1beta (IL-1beta), IL-2, IL-6, IL-8, IL-12, tumor necrosis factor-alpha, and interferon-gamma; T cell activation; increased acute phase proteins, like C-reactive protein, haptoglobin, fibrinogen and alpha1-antitrypsin; complement factors; increased LPS load through bacterial translocation and subsequent gut-derived inflammation; induction of indoleamine 2,3-dioxygenase with increased levels of tryptophan catabolites; decreased levels of antioxidants, like coenzyme Q10, zinc, vitamin E, glutathione and glutathione peroxidase; increased O&NS characterized by oxidative damage to low density lipoprotein (LDL) and phospholipid inositol, increased malondialdehyde, and damage to DNA and mitochondria; increased nitrosative stress; and decreased omega3 polyunsaturated fatty acids (PUFAs). The complex interplay between the abovementioned IO&NS pathways in depression results in pro-atherogenic effects and should be regarded as a risk factor to future clinical CVD and due mortality. We suggest that major depression should be added as a risk factor to the Charlson "comorbidity" index. It is advised that patients with (sub)chronic or recurrent major depression should routinely be assessed by serology tests to predict if they have an increased risk to cardiovascular disorders.
机译:有证据表明,严重抑郁症与心血管疾病(CVD)之间存在双向关系:抑郁症患者有患心脏病和死亡率增加的风险,而患有CVD的患者抑郁症更为常见。也有证据表明炎性,氧化性和亚硝化应激(IO&NS)途径是CVD和严重抑郁症的常见病理生理的基础。这些途径的激活可能增加两种疾病的风险,并导致共同的风险。可能导致CVD和抑郁症的共有IO&NS途径包括:促炎性细胞因子水平升高,例如白介素-1β(IL-1beta),IL-2,IL-6,IL-8,IL-12,肿瘤坏死因子-α和干扰素-γ; T细胞活化;急性期蛋白增加,例如C反应蛋白,触珠蛋白,纤维蛋白原和α1-抗胰蛋白酶;互补因子通过细菌易位和随后的肠道源性炎症增加脂多糖负荷;色氨酸分解代谢物含量增加诱导吲哚胺2,3-二加氧酶;抗氧化剂水平降低,例如辅酶Q10,锌,维生素E,谷胱甘肽和谷胱甘肽过氧化物酶; O&NS增加,其特征在于对低密度脂蛋白(LDL)和磷脂肌醇的氧化损伤,丙二醛增加以及对DNA和线粒体的损​​害;亚硝化胁迫增加;并降低了omega3多不饱和脂肪酸(PUFA)。抑郁症中上述IO&NS途径之间的复杂相互作用导致了促动脉粥样硬化效应,应被视为未来临床CVD和应有的死亡率的危险因素。我们建议应将严重抑郁症作为查尔森“合并症”指数的危险因素添加。建议患有(亚)慢性或复发性重度抑郁症的患者应常规进行血清学检查,以评估他们是否罹患心血管疾病的风险增加。

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