“可能的”家族性高胆固醇血症冠状动脉病患者的诊断特点及降糖治疗的选择

O. Mitchenko, K. Timokhova, N. Chulaievska
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引用次数: 0

摘要

的目标。优化真“可能”家族性高胆固醇血症(FH)患者的诊断算法,并在合并内分泌疾病的背景下鉴别诊断为高胆固醇血症,以选择最佳的降血脂治疗方案。材料和方法。我们检查了130例伴有高胆固醇血症和合并症的患者(2型糖尿病、甲状腺功能减退、II-III级肥胖)。在每组中,选择低密度脂蛋白(LDL)≥5 mmol/l的亚组,并在他汀类药物的最大耐受剂量与旨在补偿共病病理的治疗的背景下进行随访。对照组为确诊FH患者20例。结果和讨论。1、3组合并血脂异常,2组单纯高胆固醇血症。脂质谱与共病病理特征之间的直接相关性被揭示。“可能”FH亚组患者的脂质谱具有较高的动脉粥样硬化性,与共病病理不稳定和颈动脉和冠状动脉粥样硬化的高比例相关。根据随访结果,可以确定他汀类药物治疗和共病病理补偿导致LDL达到目标水平(第3组)或LDL降低50%(第1,2组)。在对照组患者中,最大耐受剂量的他汀类药物治疗没有显示出这样的结果。结论。被定义为“可能”FH的患者队列是异质性的,可能包括在共病病理不稳定背景下的继发性血脂异常患者,及时的验证和治疗有助于实现降脂治疗的目标。考虑到只有肥胖患者达到LDL <1.8 mmol/l的目标水平,建议甲状腺功能减退合并糖尿病患者联合降脂治疗。证实“可能的”FH患者对他汀类药物治疗的难治性强调了联合降脂治疗的必要性(依折麦布、PCSK9抑制剂)。
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Diagnostic Features and Selection of Hypolipidemic Therapy in Patients with Coronary Artery Disease with “Possible” Familial Hypercholesterolemia
The aim. To optimize the diagnostic algorithm for patients with true “possible” familial hypercholesterolemia (FH) and differential diagnosis with hypercholesterolemia on the background of comorbid endocrinopathies for selection of optimal hypolipidemic therapy. Materials and methods. We examined 130 patients with hypercholesterolemia and comorbid pathology (type 2 diabetes mellitus, hypothyroidism, obesity grade II-III). In each group, subgroups with low-density lipoproteins (LDL) ≥5 mmol/l were selected and followed up on the background of maximum tolerated doses of statins in combination with therapy aimed to compensate comorbid pathology. The control group consisted of 20 patients with verified FH. Results and discussion. Combined dyslipidemia was detected in groups 1 and 3, pure hypercholesterolemia in group 2. Direct correlations between lipid profile and comorbid pathology characteristics were revealed. Patients of the subgroups with “possible” FH had higher atherogenicity of the lipid profile associated with comorbid pathology destabilization and high percentage of atherosclerosis of carotid and coronary arteries. According to the results of the follow-up, it was established that statin therapy and comorbid pathology compensation led to the achievement of target levels of LDL (group 3) or a reduction of LDL by 50% (group 1, 2). In patients of the control group, statin therapy with maximally tolerated doses did not show such results. Conclusions. The cohort of patients defined as having “possible” FH is heterogeneous and may include patients with secondary dyslipidemia on the background of comorbid pathology destabilization, timely verification and treatment of which contributes to achieving the goals of lipid-lowering therapy. Taking into account that only obese patients reached the target level of LDL <1.8 mmol/l, combined lipid-lowering therapy is recommended for patients with hypothyroidism and diabetes. Refractoriness to statin therapy in patients with verified “possible” FH emphasizes the need for combined lipid-lowering therapy (ezetimibe, PCSK9 inhibitors).
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