{"title":"缺血性心脏病患者激素和代谢危险因素校正的特殊性","authors":"A. Dontsov","doi":"10.18087/RHJ.2016.6.2232","DOIUrl":null,"url":null,"abstract":"IL‑1β by 7.4 % (p=0.021), IL‑6 by 6.1 % (р=0.011), and IL‑8 by 12.3 % (р=0.18); the level of HDL CS increased by 7.9 % (р=0.02). In the SDT+D group, levels of TG decreased by 26.3 % (p<0.001), oxLDL by 14.4 % (р<0.001), insulin by 22.4 % (p<0.001), ACTH by 20.4 % ( p<0.001), cortisol by 23.9 % ( p<0.001), IL ‑ 1β by 52.1 % ( p<0.001), IL ‑ 6 by 56.3 % ( p<0.001), IL ‑ 8 by 60.2 % (p<0.001), the HOMA‑IR score by 38.8 % (p<0.001), and the depression score by 26.9 % (p<0.001); levels of HDL CS and β‑endorphin increased by 17.4 % and 32.6 %, respectively (p<0.001 for both). Conclusion. Using dalargin in the treatment of IHD patients with MS enhances the efficacy of correcting hypertriglyceridemia, HDL CS deficiency, insulin resistance, hypercortisolemia, proinflammatory cytokine activity, and depression. These effects may be due to activation of the opioidergic neuropeptide system possessing a stress ‑limiting capacity.","PeriodicalId":427424,"journal":{"name":"Russian Heart Journal","volume":"58 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Peculiarities of the correction of hormonal and metabolic risk factors in patients with ischemic heart disease\",\"authors\":\"A. Dontsov\",\"doi\":\"10.18087/RHJ.2016.6.2232\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"IL‑1β by 7.4 % (p=0.021), IL‑6 by 6.1 % (р=0.011), and IL‑8 by 12.3 % (р=0.18); the level of HDL CS increased by 7.9 % (р=0.02). In the SDT+D group, levels of TG decreased by 26.3 % (p<0.001), oxLDL by 14.4 % (р<0.001), insulin by 22.4 % (p<0.001), ACTH by 20.4 % ( p<0.001), cortisol by 23.9 % ( p<0.001), IL ‑ 1β by 52.1 % ( p<0.001), IL ‑ 6 by 56.3 % ( p<0.001), IL ‑ 8 by 60.2 % (p<0.001), the HOMA‑IR score by 38.8 % (p<0.001), and the depression score by 26.9 % (p<0.001); levels of HDL CS and β‑endorphin increased by 17.4 % and 32.6 %, respectively (p<0.001 for both). Conclusion. Using dalargin in the treatment of IHD patients with MS enhances the efficacy of correcting hypertriglyceridemia, HDL CS deficiency, insulin resistance, hypercortisolemia, proinflammatory cytokine activity, and depression. These effects may be due to activation of the opioidergic neuropeptide system possessing a stress ‑limiting capacity.\",\"PeriodicalId\":427424,\"journal\":{\"name\":\"Russian Heart Journal\",\"volume\":\"58 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"1900-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Russian Heart Journal\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.18087/RHJ.2016.6.2232\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Russian Heart Journal","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.18087/RHJ.2016.6.2232","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
IL - 1β7.4% (p = 0.021), IL - 6 6.1%(р= 0.011)和IL - 8 12.3%(р= 0.18);HDL - CS水平升高7.9% (p < 0.05)。在SDT+D组中,TG下降26.3% (p<0.001), oxLDL下降14.4% (p<0.001),胰岛素下降22.4% (p<0.001), ACTH下降20.4% (p<0.001),皮质醇下降23.9% (p<0.001), IL - 1β下降52.1% (p<0.001), IL - 6下降56.3% (p<0.001), IL - 8下降60.2% (p<0.001), HOMA - IR评分下降38.8% (p<0.001),抑郁评分下降26.9% (p<0.001);HDL - CS和β -内啡肽水平分别增加了17.4%和32.6% (p<0.001)。结论。使用dalargin治疗IHD合并MS患者可提高纠正高甘油三酯血症、HDL CS缺乏、胰岛素抵抗、高皮质醇血症、促炎细胞因子活性和抑郁症的疗效。这些影响可能是由于具有应激限制能力的阿片能神经肽系统的激活。
Peculiarities of the correction of hormonal and metabolic risk factors in patients with ischemic heart disease
IL‑1β by 7.4 % (p=0.021), IL‑6 by 6.1 % (р=0.011), and IL‑8 by 12.3 % (р=0.18); the level of HDL CS increased by 7.9 % (р=0.02). In the SDT+D group, levels of TG decreased by 26.3 % (p<0.001), oxLDL by 14.4 % (р<0.001), insulin by 22.4 % (p<0.001), ACTH by 20.4 % ( p<0.001), cortisol by 23.9 % ( p<0.001), IL ‑ 1β by 52.1 % ( p<0.001), IL ‑ 6 by 56.3 % ( p<0.001), IL ‑ 8 by 60.2 % (p<0.001), the HOMA‑IR score by 38.8 % (p<0.001), and the depression score by 26.9 % (p<0.001); levels of HDL CS and β‑endorphin increased by 17.4 % and 32.6 %, respectively (p<0.001 for both). Conclusion. Using dalargin in the treatment of IHD patients with MS enhances the efficacy of correcting hypertriglyceridemia, HDL CS deficiency, insulin resistance, hypercortisolemia, proinflammatory cytokine activity, and depression. These effects may be due to activation of the opioidergic neuropeptide system possessing a stress ‑limiting capacity.