Metabolic syndrome and hyperuricemia: features of patient management (clinical case)

V. Zhdan, Y. Kitura, M. Babanina, H. Volchenko, M. Tkachenko, O.A. Kyrіan, I. Ivanitsky, V. Lebid
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Abstract

Metabolic syndrome (MS) is a group of interrelated metabolic disorders such as high blood pressure, central obesity, insulin resistance (IR), dyslipidemia. The main mechanisms that indicate a metabolic disorder and contribute to its development are IR and a large amount of circulating free fatty acids. In turn, tissue IR is often combined with other abnormalities including disorders of uric acid metabolism, changes in the hemostasis system, endothelial dysfunction, increased levels of C-reactive protein. At the same time, metabo­lic disorders are a risk factor for hyperuricemia. MS occurs in 25–60 to 90 % of all gout patients. About 50 % of patients with hyperuricemia have symptoms of MS. Hyperuricemia as a component of MS is a predictor of cardiovascular mortality, development of diabetes mellitus, hypertension and nephrolithiasis. Hyperuricemia is closely related to diabetes, obesity, coronary heart disease, hypertension. On the example of a clinical case, the main components of MS are considered, as well as the issue of the relationship between hyperuricemia, gout and the components of MS. The main idea behind the creation of the MS concept is to select a population of patients at a high cardiovascular risk in whom preventive measures such as lifestyle modification and the use of adequate drugs can significantly affect the main health indicators. The goal of managing patients with MS is to minimize cardiovascular risk and mortality as much as possible. Accordingly, the therapeutic strategy should include optimal ways to modify the lifestyle; lowering blood pressure to the target level and treating comorbid conditions; reducing low-density lipoprotein cholesterol according to the risk profile: > 50 %, and < 70 mg/dL (1.4 mmol/L) in patients at a very high cardiovascular risk; > 50 %, and < 100 mg/dL (1.8 mmol/l) in high-risk patients; reducing fasting serum glucose < 126 mg/dl (7 mmol/l) or glycated hemoglobin < 7 % (53 mmol/mol); maintaining uric acid level < 6.5 mg/dL (0.387 mmol/L), in patients with gout — below 6 mg/dL (0.357 mmol/L). Thus, according to the results of the research, a causal relationship was found between insulin resistance and serum uric acid levels in patients with metabolic syndrome. The strategy for managing patients with metabolic syndrome should include screening and correction of hypertension, carbohydrate purine metabolism, dyslipidemia, and prevention of cardiovascular events.
代谢综合征和高尿酸血症:患者管理的特点(临床病例)
代谢综合征(MS)是一组相互关联的代谢紊乱,如高血压、中心性肥胖、胰岛素抵抗(IR)和血脂异常。胰岛素抵抗和大量循环游离脂肪酸是导致代谢紊乱的主要机制。反过来,组织胰岛素抵抗往往与其他异常情况结合在一起,包括尿酸代谢紊乱、止血系统变化、内皮功能障碍、C 反应蛋白水平升高。同时,代谢紊乱也是高尿酸血症的一个危险因素。在所有痛风患者中,25%-60% 至 90% 会出现多发性硬化症。大约 50% 的高尿酸血症患者有 MS 症状。高尿酸血症是多发性硬化症的一个组成部分,是心血管疾病死亡率、糖尿病、高血压和肾结石发病的预测因素。高尿酸血症与糖尿病、肥胖症、冠心病、高血压密切相关。以一个临床病例为例,考虑了多发性硬化症的主要组成部分,以及高尿酸血症、痛风和多发性硬化症组成部分之间的关系问题。多发性硬化症概念背后的主要理念是选择心血管风险较高的患者群体,对这些患者采取预防措施,如改变生活方式和使用适当的药物,可以显著影响主要健康指标。管理多发性硬化症患者的目标是尽可能降低心血管风险和死亡率。因此,治疗策略应包括改变生活方式的最佳方法;将血压降至目标水平并治疗合并症;根据风险情况降低低密度脂蛋白胆固醇:在心血管风险极高的患者中,> 50%,< 70 mg/dL (1.4 mmol/L);在心血管风险高的患者中,> 50%,< 100 mg/dL (1. 8 mmol/L)。8毫摩尔/升);降低空腹血清葡萄糖< 126毫克/分升(7毫摩尔/升)或糖化血红蛋白< 7 %(53毫摩尔/摩尔);维持尿酸水平< 6.5毫克/分升(0.387毫摩尔/升),痛风患者--低于6毫克/分升(0.357毫摩尔/升)。因此,研究结果表明,代谢综合征患者的胰岛素抵抗与血清尿酸水平之间存在因果关系。管理代谢综合征患者的策略应包括筛查和纠正高血压、碳水化合物嘌呤代谢、血脂异常和预防心血管事件。
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