Division of Pediatric Gastroenterology, Hepatology, and Nutrition.
Department of Cardiology, Boston Children's Hospital.
J Pediatr Gastroenterol Nutr. 2019 Feb;68(2):175-181. doi: 10.1097/MPG.0000000000002174.
The aim of the study was to evaluate the hepatotoxicity of statins, as determined by serum alanine aminotransferase (ALT), in children and adolescents with dyslipidemia in real-world clinical practice.
Clinical and laboratory data were prospectively collected between September 2010 and March 2014. We compared ALT levels between patients prescribed versus not prescribed 3-hydroxy-3-methyl-glutaryl-coenzyme A reductase inhibitors (statins), and then compared ALT before and after initiation of statins.
Over the 3.5-year observation period, there were 2704 ALT measurements among 943 patients. The mean age was 14 years; 54% were boys, 47% obese, and 208 patients were treated with statins. Median follow-up after first ALT was 18 months. The mean (SD) ALT in statin and non-statin users was 23 (20) U/L and 28 (28) U/L, respectively. In models adjusted for age, sex, and race, ALT was 2.1 U/L (95% CI 0.1 to 4.4; P = 0.04) lower among statin users, which was attenuated after adjustment for weight category. Patients started on statins during the observation period did not demonstrate an increase in ALT over time (ALT 0.9 U/L [95% confidence interval -5.2 to 3.4] increase per year; P = 0.7).
In our study population, we did not observe a higher burden of ALT elevations among pediatric patients on statins as compared to those with dyslipidemia who are not on statins, supporting the hepatic safety of statin use in childhood.
本研究旨在评估他汀类药物的肝毒性,以血清丙氨酸氨基转移酶(ALT)为指标,在真实临床实践中评估患有血脂异常的儿童和青少年使用他汀类药物的情况。
2010 年 9 月至 2014 年 3 月期间前瞻性收集临床和实验室数据。我们比较了处方和未处方 3-羟基-3-甲基戊二酰基辅酶 A 还原酶抑制剂(他汀类药物)的患者的 ALT 水平,然后比较了开始使用他汀类药物前后的 ALT 水平。
在 3.5 年的观察期内,943 名患者中有 2704 次 ALT 测量。平均年龄为 14 岁;54%为男性,47%为肥胖,208 名患者接受了他汀类药物治疗。首次 ALT 后中位随访时间为 18 个月。他汀类药物使用者和非他汀类药物使用者的平均(SD)ALT 分别为 23(20)U/L 和 28(28)U/L。在调整年龄、性别和种族的模型中,他汀类药物使用者的 ALT 低 2.1 U/L(95%CI 0.1 至 4.4;P=0.04),但在调整体重类别后这一差异减弱。在观察期间开始使用他汀类药物的患者,其 ALT 随时间的变化并未增加(ALT 每年增加 0.9 U/L[95%置信区间 -5.2 至 3.4];P=0.7)。
在我们的研究人群中,与未使用他汀类药物治疗血脂异常的患者相比,使用他汀类药物的儿科患者的 ALT 升高负担并没有更高,这支持了儿童使用他汀类药物的安全性。