Treatment strategies and LDL cholesterol target attainment in patients with statin intolerance: Insights from the multicentre statin intolerance registry
Paulina E. Stürzebecher , Julius L. Katzmann , Ionna Gouni-Berthold , Christina Mateev , Ole Frenzel , Ulrike Schatz , Andrea Baessler , Wolfgang Koenig , Stephan H. Schirmer , Irina Müller-Kozarez , Oliver Weingärtner , Ursula Kassner , Ulrich Laufs , Statin Intolerance Registry investigators
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引用次数: 0
Abstract
Objective and methods
Statin intolerance (SI) is an important cause of insufficient low-density lipoprotein cholesterol (LDL-C) target attainment. Contemporary treatment strategies and symptoms in patients with SI are incompletely understood. We report baseline lipid-lowering therapies (LLTs) and LDL-C target attainment in the Statin Intolerance Registry, an observational, prospective, multicenter study that recruited 1,111 patients with SI between 2021 and 2023 in Germany.
Results
The mean age was 66.1 (SD 9.9) years, 57.7 % were female. At study inclusion, 83.1 % received at least one LLT, and 47.0 % received combination LLT. A higher number of LLTs was associated with lower LDL-C, lower systolic blood pressure, more atherosclerotic disease, more elevations of creatine kinase and liver enzymes but not with impaired quality of life as measured by EuroQol (EQ-5D-5L). PCSK9 inhibitors were most frequently prescribed (48.0 %), followed by ezetimibe (39.2 %), statins (26.9 %), most commonly rosuvastatin, and bempedoic acid (25.4 %). Patients who had been prescribed multiple statins before were more likely to take a statin at baseline. Patients on a statin, even at low intensity, had lower LDL-C levels compared to patients without statin therapy (mean [SD] 2.4 [1.2] vs. 2.9 [1.6] mmol/L, p < 0.001). Significantly more men than women achieved the LDL-C target (21.7 % vs. 11.4 %, p < 0.001, total cohort: 15.8 %).
Conclusion
LDL-C target attainment is low in patients with SI, especially among women, despite high cardiovascular risk. The use of a greater number of LLTs, including statins, is not associated with reduced quality of life but is associated with lower LDL-C levels.
目的与方法他汀类药物不耐受(SI)是导致低密度脂蛋白胆固醇(LDL-C)达标的重要原因。SI患者的当代治疗策略和症状尚不完全清楚。我们报告了基线降脂疗法(LLTs)和LDL-C目标达到的他汀类药物不耐受注册,这是一项观察性、前瞻性、多中心研究,在2021年至2023年期间在德国招募了1111名SI患者。结果患者平均年龄66.1岁(SD 9.9),女性占57.7%。在纳入研究时,83.1%接受了至少一种LLT, 47.0%接受了联合LLT。较高数量的llt与较低的LDL-C、较低的收缩压、更多的动脉粥样硬化疾病、更多的肌酸激酶和肝酶升高相关,但与EuroQol (EQ-5D-5L)测量的生活质量受损无关。最常见的处方是PCSK9抑制剂(48.0%),其次是依折替米贝(39.2%),他汀类药物(26.9%),最常见的是瑞舒伐他汀和苯甲多酸(25.4%)。以前服用过多种他汀类药物的患者更有可能在基线时服用他汀类药物。接受他汀类药物治疗的患者,即使是低剂量,其LDL-C水平也低于未接受他汀类药物治疗的患者(平均[SD] 2.4[1.2]对2.9 [1.6]mmol/L, p <;0.001)。达到LDL-C目标的男性明显多于女性(21.7% vs 11.4%, p <;0.001,总队列:15.8%)。结论SI患者ldl - c目标达标率较低,尤其是女性患者,尽管心血管风险较高。使用更多的llt,包括他汀类药物,与生活质量的降低无关,但与较低的LDL-C水平有关。