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首页> 外文期刊>Racional?naa Farmakoterapia v Kardiologii >Cross-Sectional Study to Estimate the Prevalence of Familial Hypercholesterolemia in Selected Regions of the Russian Federation: Relevance, Design of the Study and Initial Characteristics of the Participants
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Cross-Sectional Study to Estimate the Prevalence of Familial Hypercholesterolemia in Selected Regions of the Russian Federation: Relevance, Design of the Study and Initial Characteristics of the Participants

机译:横断面研究估算俄罗斯联邦所选地区家族性高胆固醇血症的患病率:相关性,参与者研究的研究和初始特征

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Aim. To study the prevalence of familial hypercholesterolemia (FH), the characteristics of the clinical features and treatment of the disease in selected regions of the Russian Federation, this article describes the design and initial characteristics of patients included in the study. Material and methods. The study participants were selected among those included in the study “Epidemiology of cardiovascular risk factors and diseases in the regions of the Russian Federation” (ESSE-RF) in different regions of the Russian Federation. The study included individuals with lowdensity lipoprotein cholesterol (LDL-C) levels 4.9 mmol/l or LDL-C levels 1.8 mmol/l, but ≤4.9 mmol/l during statin therapy, according to the data obtained in the ESSE-RF study. These persons are invited for examination and questioning by experts in the field of FH diagnostics. On the basis of the survey data and provided medical documentation, the following information is collected: age, sex, smoking status, presence of hypertension, history of coronary artery disease, stroke, atherosclerosis of cerebral and peripheral arteries, LDL-C level, type, volume and duration of lipid-lowering therapy throughout life, presence and dates of secondary causes of hyperlipidemia, information about the family history of development of early cardiovascular diseases and atherosclerotic diseases, increased levels of LDL-C in relatives of the 1st and 2nd degree of kinship. All patients are examined for the presence of tendon xanthomas (Achilles, metacarpal, elbow, knee tendons) and Corneal arcus. During the visit, blood is taken for subsequent biobanking, measurement of current blood lipid levels, elimination of secondary forms of hypercholesterolemia (for subsequent determination of liver enzymes, thyroid stimulating hormone) and genetic testing. The diagnosis of FH is based on Dutch Lipid Clinical Network Criteria (DLCN). Besides, all participants in the study are tested for compliance with the diagnosis of FH according to Simon Broome criteria. All patients with a definite or probable diagnosis of FH according to DLCN or Simon Broome criteria are subjected to ultrasound examination of carotid, femoral arteries and heart and molecular genetic testing for LDLR , APOB and PCSK9 gene variants. Results. Out of 16 360 participants of the ESSE-RF study in 10 regions, 1787 people (10,9%) met the criteria for inclusion in this study. Among them, men accounted for 35.4%, of which 1150 (7%) patients had a LDL-C level 4.9 mmol/l and 637 (3,9%) had a LDL-C level from 1,81 mmol/l to 4.9 mmol/l during lipid-lowering therapy. When compared to the original cohorts of participants from the 10 regions as compared to 3 previously surveyed regions and selected sub-groups within these cohorts we observed significant differences in several parameters such as age, total cholesterol level, triglycerides, LDL-C, the frequency of cardiovascular diseases, that may indicate regional differences in FH prevalence. Conclusion. The analysis of clinical data of the participants of the ESSE-RF study shows that more than 10% of individuals require an additional examination to verify the FH diagnosis, and regional differences in the FH prevalence are possible.
机译:目标。为了研究家族性高胆固醇血症(FH)的患病率,俄罗斯联邦所选地区临床特征和治疗的特点,本文介绍了研究中包括的患者的设计和初始特征。材料与方法。该研究参与者被选中在俄罗斯联邦不同地区的研究中包含在研究中“俄罗斯联邦地区的心血管危险因素和疾病的流行病学”(Esse-RF)。该研究包括低密度脂蛋白胆固醇(LDL-C)水平> 4.9mmol / L或LDL-C水平> 1.8mmol / L,但≤4.9mmol/ l,根据ESSE-RF中获得的数据,如肠疗法期间学习。这些人受到FH诊断领域专家的审查和质疑。在调查数据和提供医疗文件的基础上,收集了以下信息:年龄,性别,吸烟状态,高血压存在,冠状动脉疾病病史,脑卒中,脑粥样硬化的脑和外周动脉,LDL-C水平,类型脂质降低治疗的体积和持续时间在整个生命,存在和次要原因的次生原因的日期,有关早期心血管疾病和动脉粥样硬化疾病的新闻史的信息,在第1和第2度的亲属中增加的LDL-C水平亲属关系。检查所有患者是否存在肌腱xanthomas(achilles,御术,肘部,膝盖肌腱)和角膜弧菌的存在。在访问期间,采取血液用于后续生物库,测量目前的血脂水平,消除二级形式的高胆固醇血症(用于随后测定肝酶,甲状腺刺激激素)和遗传检测。 FH的诊断基于荷兰脂临床网络标准(DLCN)。此外,研究的所有参与者都会根据Simon Broome标准遵守FH的诊断。根据DLCN或Simon Broome标准的所有患有明确或可能的FH诊断的患者对LDLR,APOB和PCSK9基因变体进行超声检查颈动脉,股动脉和心脏和分子遗传检测。结果。在16个360个参与者中,在10个地区的Esse-RF研究中,1787人(10,9%)达到了本研究的纳入标准。其中,男性占35.4%,其中1150(7%)患者的LDL-C水平> 4.9 mmol / L和637(3,9%)的LDL-C水平为1,81 mmol / L.在降脂治疗过程中4.9 mmol / l。与来自10个地区的参与者的原始群组相比,与3个先前的调查区域和这些群组中的选定子组相比,我们观察到诸如年龄,总胆固醇水平,甘油三酯,LDL-C,频率的若干参数中的显着差异心血管疾病,可能表明FH流行率的区域差异。结论。 Esse-RF研究参与者的临床数据分析表明,超过10%的人需要额外的检查来验证FH诊断,并且FH流行率的区域差异是可能的。

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