Iughetti Lorenzo, Predieri Barbara, Bruzzi Patrizia
a Paediatric Unit, Department of Medical and Surgical Sciences of Mothers, Children and Adults, University of Modena and Reggio Emilia, Modena, Italy.
Expert Rev Endocrinol Metab. 2015 May;10(3):269-271. doi: 10.1586/17446651.2015.1033373. Epub 2015 Apr 6.
The diagnosis of dyslipidemia is increasing both in adulthood and in childhood because of not only the steadily increasing prevalence of obesity but also a rise of medical attention in detecting unfavorable genetic conditions in patients of all ages. Attempts in lifestyle changes are frequently failing and thus the pharmacological treatment of dyslipidemia is spreading in medical practice to reduce cardiovascular risk. In childhood, statins are authorized by 8 years of age. Nevertheless, data on their long-term safety and efficacy are still lacking, especially in ones with high cardiovascular risk and/or primary dyslipidemia such as homozygous familial hypercholesterolemia, considerable as a mainly exclusively pediatric disease. Thus, new pharmacological approaches are needed and have to be evaluated in all categories of patients. In this context, the update and the critical revision of new medications have become a new duty for scientists and clinicians.
由于肥胖患病率持续上升,以及各年龄段患者中检测不利遗传状况的医疗关注度提高,血脂异常在成人和儿童中的诊断率都在上升。改变生活方式的尝试常常失败,因此血脂异常的药物治疗在医学实践中不断推广,以降低心血管风险。在儿童中,他汀类药物在8岁时被批准使用。然而,关于其长期安全性和有效性的数据仍然缺乏,尤其是在心血管风险高和/或原发性血脂异常的患者中,如纯合子家族性高胆固醇血症,这是一种主要为儿科疾病。因此,需要新的药物治疗方法,并在所有类型的患者中进行评估。在这种背景下,新药的更新和批判性修订已成为科学家和临床医生的新职责。